Item | Value |
---|---|
geneid | 397 |
ensemblid | ENSG00000111348.9 |
hgncid | 679 |
symbol | ARHGDIB |
name | Rho GDP dissociation inhibitor beta |
refseq_nuc | NM_001175.7 |
refseq_prot | NP_001166.3 |
ensembl_nuc | ENST00000228945.9 |
ensembl_prot | ENSP00000228945.4 |
mane_status | MANE Select |
chr | chr12 |
start | 14942031 |
end | 14961601 |
strand | - |
ver | v1.2 |
region | chr12:14942031-14961601 |
region5000 | chr12:14937031-14966601 |
regionname0 | ARHGDIB_chr12_14942031_14961601 |
regionname5000 | ARHGDIB_chr12_14937031_14966601 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 201 | 462 | 98 | 70 | 233 | 15 | 44 | 185 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | MTEKA others(196): Show |
chr12 | 14937031 | 14966601 |
a0002 | 0/0 | 201 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | MTEKA others(196): Show |
chr12 | 14937031 | 14966601 |
a0003 | 0/0 | 201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | MTEKA others(196): Show |
chr12 | 14937031 | 14966601 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 603 | 237 | 46 | 43 | 119 | 9 | 19 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | ATGAC others(598): Show |
chr12 | 14937031 | 14966601 | ||
a0001c0002 | 1/0 | 603 | 225 | 52 | 27 | 114 | 6 | 25 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | ATGAC others(598): Show |
chr12 | 14937031 | 14966601 | ||
a0002c0003 | 0/0 | 603 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | ATGAC others(598): Show |
chr12 | 14937031 | 14966601 | ||
a0003c0004 | 0/0 | 603 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | ATGAC others(598): Show |
chr12 | 14937031 | 14966601 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1174 | 215 | 39 | 35 | 114 | 7 | 19 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0001c0001t0002 | 0/0 | 1174 | 9 | 0 | 4 | 3 | 2 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0001c0001t0003 | 0/0 | 1174 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0001c0001t0005 | 0/0 | 1174 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0001c0001t0007 | 0/0 | 1174 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0001c0001t0008 | 0/0 | 1174 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0001c0001t0009 | 0/0 | 1174 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0001c0001t0010 | 0/0 | 1174 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0001c0001t0011 | 0/0 | 1174 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0001c0002t0001 | 1/0 | 1174 | 215 | 48 | 27 | 108 | 6 | 25 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0001c0002t0003 | 0/0 | 1174 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0001c0002t0004 | 0/0 | 1174 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0001c0002t0006 | 0/0 | 1174 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0001c0002t0007 | 0/0 | 1174 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0002c0003t0001 | 0/0 | 1174 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
a0003c0004t0001 | 0/0 | 1174 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | GCCAG others(1169): Show |
chr12 | 14937031 | 14966601 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 21 | 0 | 4 | 17 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0003 | 0/0 | 9 | 0 | 5 | 1 | 2 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 5 | 1 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0033 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0035 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0061 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0063 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0065 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0070 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0071 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0072 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0175 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0002g0068 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0003g0074 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0007g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0008g0069 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0009g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0010g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0001t0011g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0002 | 0/0 | 19 | 0 | 1 | 16 | 0 | 2 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0014 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0030 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0032 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0034 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0036 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0057 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0059 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0060 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0062 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0066 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0067 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0245 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0003g0073 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0004g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0006g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0001c0002t0007g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
a0003c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | GBR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0116 | EUR | GBR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0111 | EUR | GBR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0284 | EUR | FIN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | FIN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0115 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0200 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01081 | hp1 | a0001 | c0001 | t0008 | g0069 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01099 | hp2 | a0001 | c0001 | t0009 | g0210 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0117 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01358 | hp2 | a0001 | c0001 | t0008 | g0069 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01515 | hp1 | a0002 | c0003 | t0001 | g0090 | EUR | IBS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0285 | EUR | IBS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0286 | EUR | IBS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0240 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0287 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0251 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02074 | hp2 | a0001 | c0002 | t0007 | g0244 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02135 | hp1 | a0001 | c0001 | t0007 | g0280 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0250 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | CDX | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CDX | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02258 | hp2 | a0001 | c0002 | t0006 | g0042 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0073 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | KHV | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0178 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0262 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0081 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0279 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02897 | hp2 | a0001 | c0001 | t0010 | g0288 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0164 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0238 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | MSL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | MSL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0281 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0278 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | MSL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0130 | AFR | MSL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0289 | AFR | MSL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0030 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | MSL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0030 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0091 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | ESN | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | MSL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0239 | SAS | STU | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0131 | SAS | STU | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0246 | SAS | BEB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0201 | SAS | BEB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | BEB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | STU | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0248 | SAS | STU | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | BEB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0112 | SAS | BEB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | STU | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | STU | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0132 | SAS | STU | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | YRI | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | YRI | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0123 | AFR | YRI | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18946 | hp1 | a0001 | c0002 | t0004 | g0022 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18962 | hp1 | a0001 | c0002 | t0004 | g0211 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18966 | hp1 | a0001 | c0002 | t0004 | g0022 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18991 | hp2 | a0001 | c0002 | t0004 | g0129 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18993 | hp1 | a0003 | c0004 | t0001 | g0154 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19000 | hp1 | a0001 | c0002 | t0004 | g0022 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0271 | AFR | LWK | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0165 | AFR | LWK | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19055 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19074 | hp2 | a0001 | c0001 | t0011 | g0291 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | ASW | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ASW | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0100 | EUR | TSI | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0196 | EUR | TSI | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0276 | EUR | TSI | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0273 | EUR | TSI | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | GIH | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | GIH | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | CLM | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02486 | hp1 | a0001 | c0002 | t0006 | g0042 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0290 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | ACB | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03471 | hp1 | a0001 | c0002 | t0003 | g0073 | AFR | MSL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | USA | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0066 | AFR | USA | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0277 | AFR | LWK | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0175 | REF | REF | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0245 | REF | REF | ARHGDIB_chr12_14937031_14966601 | ARHGDIB | chr12 | 14937031 | 14966601 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:14942682 | C | T | 1 | a0003 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.446G>A | p.Arg149Gln | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 6/6 | 523/1174 | 446/606 | 149/201 | chr12 | 14942682 | |||
chr12:14949865 | C | G | 1 | a0002 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.202G>C | p.Val68Leu | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/6 | 279/1174 | 202/606 | 68/201 | chr12 | 14949865 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:14942624 | C | G | 2 | a0001c0001 a0003c0004 |
237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
synonymous_variant | LOW | c.504G>C | p.Ala168Ala | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 6/6 | 581/1174 | 504/606 | 168/201 | chr12 | 14942624 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:14942197 | T | C | 1 | a0001c0002t0006 | 2 | HG02258.hp2 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*325A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 6/6 | 325 | chr12 | 14942197 | ||||||
chr12:14942228 | G | A | 3 | a0001c0001t0002 a0001c0001t0008 a0001c0002t0004 |
16 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*294C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 6/6 | 294 | chr12 | 14942228 | ||||||
chr12:14942394 | T | C | 1 | a0001c0002t0004 | 5 | NA18946.hp1 NA18962.hp1 NA18966.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*128A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 6/6 | 128 | chr12 | 14942394 | ||||||
chr12:14942508 | A | C | 2 | a0001c0001t0005 a0001c0001t0010 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*14T>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 6/6 | 14 | chr12 | 14942508 | ||||||
chr12:14942509 | G | A | 2 | a0001c0001t0007 a0001c0002t0007 |
2 | HG02074.hp2 HG02135.hp1 |
3_prime_UTR_variant | MODIFIER | c.*13C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 6/6 | 13 | chr12 | 14942509 | ||||||
chr12:14942511 | G | C | 2 | a0001c0001t0008 a0001c0001t0009 |
3 | HG01081.hp1 HG01099.hp2 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 6/6 | 11 | chr12 | 14942511 | ||||||
chr12:14961554 | T | A | 3 | a0001c0001t0003 a0001c0001t0010 a0001c0002t0003 |
8 | HG01934.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-30A>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/6 | 10842 | chr12 | 14961554 | ||||||
chr12:14961561 | G | A | 1 | a0001c0001t0011 | 1 | NA19074.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-37C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/6 | chr12 | 14961561 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:14942773 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(208): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.407-52A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14942773 | |||||||
chr12:14942776 | A | G | 2 | a0001c0002t0001g0044 a0001c0002t0003g0073 |
4 | HG02451.hp2 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.407-55T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14942776 | |||||||
chr12:14942806 | T | C | 1 | a0001c0002t0001g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.407-85A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14942806 | |||||||
chr12:14942870 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(206): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.407-149T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14942870 | |||||||
chr12:14942872 | CT | C | 9 | a0001c0001t0001g0103 a0001c0001t0001g0236 a0001c0001t0001g0268 others(6): Show |
11 | HG02145.hp1 HG02451.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.407-152delA | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14942872 | |||||||
chr12:14942901 | T | C | 2 | a0001c0002t0001g0279 a0001c0002t0001g0281 |
2 | HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.407-180A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14942901 | |||||||
chr12:14942976 | C | CT | 2 | a0001c0001t0001g0071 a0001c0001t0007g0280 |
3 | HG02135.hp1 HG02135.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.407-256dupA | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14942976 | |||||||
chr12:14943018 | G | A | 1 | a0001c0002t0001g0260 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.407-297C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943018 | |||||||
chr12:14943088 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.407-367C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943088 | |||||||
chr12:14943115 | G | A | 1 | a0001c0002t0001g0201 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.407-394C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943115 | |||||||
chr12:14943158 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0007g0280 |
3 | HG02135.hp1 HG02135.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.407-437C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943158 | |||||||
chr12:14943183 | A | T | 4 | a0001c0002t0001g0049 a0001c0002t0001g0265 a0001c0002t0001g0279 others(1): Show |
5 | HG02895.hp2 HG03130.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.407-462T>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943183 | |||||||
chr12:14943268 | T | G | 1 | a0001c0001t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.407-547A>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943268 | |||||||
chr12:14943312 | A | C | 1 | a0001c0002t0001g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.407-591T>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943312 | |||||||
chr12:14943377 | G | GT | 32 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(29): Show |
53 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.407-657dupA | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943377 | |||||||
chr12:14943377 | GT | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(124): Show |
197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.407-657delA | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943377 | |||||||
chr12:14943389 | T | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0016 others(68): Show |
107 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.407-668A>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943389 | |||||||
chr12:14943389 | T | TG | 19 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0075 others(16): Show |
28 | HG00408.hp2 HG01074.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.407-669_407-668ins others(1): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943389 | |||||||
chr12:14943391 | TG | T | 23 | a0001c0001t0001g0015 a0001c0001t0001g0048 a0001c0001t0001g0072 others(20): Show |
33 | HG00099.hp2 HG00609.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.407-671delC | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943391 | |||||||
chr12:14943392 | G | T | 12 | a0001c0001t0001g0230 a0001c0001t0001g0268 a0001c0001t0001g0269 others(9): Show |
19 | HG02083.hp2 HG02145.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.407-671C>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943392 | |||||||
chr12:14943395 | G | T | 5 | a0001c0002t0001g0010 a0001c0002t0001g0271 a0001c0002t0001g0272 others(2): Show |
8 | HG00733.hp1 HG02280.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.407-674C>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943395 | |||||||
chr12:14943398 | G | T | 4 | a0001c0002t0001g0010 a0001c0002t0001g0271 a0001c0002t0001g0272 others(1): Show |
7 | HG00733.hp1 HG02280.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.407-677C>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943398 | |||||||
chr12:14943400 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0007g0280 |
3 | HG02135.hp1 HG02135.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.407-679A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943400 | |||||||
chr12:14943401 | G | GT | 3 | a0001c0001t0001g0261 a0001c0001t0003g0290 a0001c0001t0005g0130 |
3 | HG02486.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.407-681dupA | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943401 | |||||||
chr12:14943401 | G | T | 2 | a0001c0002t0001g0271 a0001c0002t0001g0272 |
2 | HG00733.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.407-680C>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943401 | |||||||
chr12:14943403 | T | G | 2 | a0001c0002t0001g0271 a0001c0002t0001g0272 |
2 | HG00733.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.407-682A>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943403 | |||||||
chr12:14943404 | G | GT | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(127): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.407-684dupA | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943404 | |||||||
chr12:14943404 | G | T | 5 | a0001c0001t0001g0261 a0001c0001t0003g0290 a0001c0001t0005g0130 others(2): Show |
5 | HG00733.hp1 HG02486.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.407-683C>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943404 | |||||||
chr12:14943406 | T | TG | 45 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0101 others(42): Show |
57 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.407-686_407-685ins others(1): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943406 | |||||||
chr12:14943502 | A | G | 4 | a0001c0002t0001g0271 a0001c0002t0001g0272 a0001c0002t0001g0279 others(1): Show |
4 | HG00733.hp1 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-781T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943502 | |||||||
chr12:14943628 | T | C | 1 | a0001c0002t0001g0138 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.407-907A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943628 | |||||||
chr12:14943631 | A | G | 1 | a0001c0001t0002g0273 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.407-910T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943631 | |||||||
chr12:14943681 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0007g0280 |
3 | HG02135.hp1 HG02135.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.407-960C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943681 | |||||||
chr12:14943689 | C | G | 3 | a0001c0001t0001g0078 a0001c0002t0001g0044 a0001c0002t0003g0073 |
5 | HG02257.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.407-968G>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943689 | |||||||
chr12:14943735 | T | C | 2 | a0001c0002t0001g0279 a0001c0002t0001g0281 |
2 | HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.407-1014A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943735 | |||||||
chr12:14943776 | T | C | 11 | a0001c0001t0001g0039 a0001c0001t0001g0101 a0001c0001t0001g0103 others(8): Show |
14 | HG00558.hp2 HG02071.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.406+1000A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943776 | |||||||
chr12:14943851 | C | T | 1 | a0001c0002t0001g0207 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.406+925G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14943851 | |||||||
chr12:14944128 | T | C | 2 | a0001c0002t0001g0279 a0001c0002t0001g0281 |
2 | HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.406+648A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14944128 | |||||||
chr12:14944215 | A | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(173): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.406+561T>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14944215 | |||||||
chr12:14944249 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.406+527C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14944249 | |||||||
chr12:14944315 | A | G | 18 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0101 others(15): Show |
22 | HG00140.hp2 HG00558.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.406+461T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14944315 | |||||||
chr12:14944392 | G | C | 29 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0101 others(26): Show |
36 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.406+384C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14944392 | |||||||
chr12:14944402 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0003g0290 a0001c0001t0005g0130 |
3 | HG02486.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.406+374A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14944402 | |||||||
chr12:14944441 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA18978.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.406+335G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14944441 | |||||||
chr12:14944525 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.406+251G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14944525 | |||||||
chr12:14944563 | C | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(173): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.406+213G>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14944563 | |||||||
chr12:14944600 | G | A | 1 | a0001c0002t0001g0010 | 4 | HG02280.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+176C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14944600 | |||||||
chr12:14944614 | A | C | 3 | a0001c0001t0001g0261 a0001c0001t0003g0290 a0001c0001t0005g0130 |
3 | HG02486.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.406+162T>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14944614 | |||||||
chr12:14944693 | A | G | 1 | a0001c0002t0001g0206 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.406+83T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14944693 | |||||||
chr12:14944729 | T | C | 13 | a0001c0001t0001g0015 a0001c0001t0001g0071 a0001c0001t0001g0072 others(10): Show |
18 | HG00733.hp1 HG02083.hp1 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.406+47A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 5/5 | chr12 | 14944729 | |||||||
chr12:14944857 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.343-18G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14944857 | |||||||
chr12:14944866 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0003g0290 a0001c0001t0005g0130 |
3 | HG02486.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.343-27A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14944866 | |||||||
chr12:14944978 | A | G | 3 | a0001c0001t0001g0078 a0001c0002t0001g0044 a0001c0002t0003g0073 |
5 | HG02257.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-139T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14944978 | |||||||
chr12:14945029 | T | C | 1 | a0002c0003t0001g0090 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.343-190A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14945029 | |||||||
chr12:14945131 | A | G | 1 | a0001c0002t0001g0202 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.343-292T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14945131 | |||||||
chr12:14945146 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.343-307T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14945146 | |||||||
chr12:14945177 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.343-338G>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14945177 | |||||||
chr12:14945507 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.343-668G>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14945507 | |||||||
chr12:14945598 | T | A | 18 | a0001c0001t0001g0015 a0001c0001t0001g0071 a0001c0001t0001g0072 others(15): Show |
26 | HG00733.hp1 HG01891.hp2 HG02083.hp1 others(23): Show |
intron_variant | MODIFIER | c.343-759A>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14945598 | |||||||
chr12:14945617 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.343-778G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14945617 | |||||||
chr12:14945642 | A | C | 1 | a0001c0001t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.343-803T>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14945642 | |||||||
chr12:14945645 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.343-806C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14945645 | |||||||
chr12:14945706 | T | C | 17 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0029 others(14): Show |
29 | HG00597.hp2 HG00621.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.343-867A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14945706 | |||||||
chr12:14945740 | C | T | 53 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0101 others(50): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.343-901G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14945740 | |||||||
chr12:14945861 | G | C | 1 | a0001c0002t0001g0080 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.343-1022C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14945861 | |||||||
chr12:14945874 | G | GACTGTGA others(20): Show |
1 | a0001c0002t0001g0205 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.343-1062_343-1036d others(29): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14945874 | |||||||
chr12:14946066 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.343-1227G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14946066 | |||||||
chr12:14946182 | T | C | 1 | a0001c0002t0001g0100 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.343-1343A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14946182 | |||||||
chr12:14946544 | C | T | 1 | a0001c0002t0001g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.342+1329G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14946544 | |||||||
chr12:14946549 | G | T | 3 | a0001c0002t0001g0038 a0001c0002t0001g0093 a0001c0002t0001g0097 |
4 | NA18947.hp1 NA18979.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+1324C>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14946549 | |||||||
chr12:14946643 | C | CCA | 1 | a0001c0002t0001g0010 | 4 | HG02280.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+1228_342+1229d others(4): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14946643 | |||||||
chr12:14946667 | C | A | 7 | a0001c0001t0001g0075 a0001c0001t0001g0270 a0001c0001t0003g0289 others(4): Show |
7 | HG00733.hp1 HG02145.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.342+1206G>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14946667 | |||||||
chr12:14946778 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.342+1095G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14946778 | |||||||
chr12:14946793 | A | G | 1 | a0001c0002t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.342+1080T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14946793 | |||||||
chr12:14946953 | T | C | 7 | a0001c0001t0001g0075 a0001c0001t0001g0270 a0001c0001t0003g0289 others(4): Show |
7 | HG00733.hp1 HG02145.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.342+920A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14946953 | |||||||
chr12:14947033 | A | ACCTGTAT others(6): Show |
1 | a0001c0001t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.342+839_342+840ins others(13): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947033 | |||||||
chr12:14947034 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.342+839A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947034 | |||||||
chr12:14947049 | A | G | 3 | a0001c0001t0001g0078 a0001c0002t0001g0044 a0001c0002t0003g0073 |
5 | HG02257.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+824T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947049 | |||||||
chr12:14947112 | C | A | 1 | a0001c0002t0001g0250 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.342+761G>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947112 | |||||||
chr12:14947165 | C | T | 3 | a0001c0001t0001g0078 a0001c0002t0001g0044 a0001c0002t0003g0073 |
5 | HG02257.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+708G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947165 | |||||||
chr12:14947166 | G | T | 18 | a0001c0001t0001g0015 a0001c0001t0001g0071 a0001c0001t0001g0072 others(15): Show |
26 | HG00733.hp1 HG01891.hp2 HG02083.hp1 others(23): Show |
intron_variant | MODIFIER | c.342+707C>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947166 | |||||||
chr12:14947273 | T | G | 1 | a0001c0001t0001g0252 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.342+600A>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947273 | |||||||
chr12:14947304 | T | A | 3 | a0001c0001t0001g0261 a0001c0001t0003g0290 a0001c0001t0005g0130 |
3 | HG02486.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.342+569A>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947304 | |||||||
chr12:14947365 | T | C | 21 | a0001c0001t0001g0015 a0001c0001t0001g0071 a0001c0001t0001g0072 others(18): Show |
29 | HG00733.hp1 HG01891.hp2 HG02083.hp1 others(26): Show |
intron_variant | MODIFIER | c.342+508A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947365 | |||||||
chr12:14947366 | C | T | 5 | a0001c0001t0001g0133 a0001c0002t0001g0163 a0001c0002t0001g0164 others(2): Show |
5 | HG02723.hp1 HG02976.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+507G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947366 | |||||||
chr12:14947440 | T | C | 12 | a0001c0002t0001g0020 a0001c0002t0001g0041 a0001c0002t0001g0060 others(9): Show |
18 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.342+433A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947440 | |||||||
chr12:14947462 | A | G | 7 | a0001c0002t0001g0007 a0001c0002t0001g0171 a0001c0002t0001g0194 others(4): Show |
11 | HG00408.hp1 HG02056.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+411T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947462 | |||||||
chr12:14947672 | C | T | 1 | a0001c0002t0001g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.342+201G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947672 | |||||||
chr12:14947748 | C | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0270 a0001c0001t0003g0289 |
3 | HG02145.hp2 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.342+125G>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947748 | |||||||
chr12:14947749 | C | T | 49 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0101 others(46): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.342+124G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947749 | |||||||
chr12:14947750 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0025 others(44): Show |
72 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.342+123G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947750 | |||||||
chr12:14947760 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.342+113C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947760 | |||||||
chr12:14947804 | C | A | 1 | a0001c0002t0001g0054 | 2 | HG00738.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.342+69G>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947804 | |||||||
chr12:14947806 | A | G | 7 | a0001c0001t0001g0230 a0001c0002t0001g0046 a0001c0002t0001g0059 others(4): Show |
11 | HG02083.hp2 HG03669.hp1 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.342+67T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947806 | |||||||
chr12:14947840 | A | G | 2 | a0001c0002t0001g0279 a0001c0002t0001g0281 |
2 | HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.342+33T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4/5 | chr12 | 14947840 | |||||||
chr12:14948099 | T | TGCGC | 4 | a0001c0001t0001g0144 a0001c0001t0001g0146 a0001c0001t0001g0179 others(1): Show |
4 | HG00639.hp2 HG02155.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-151_266-150ins others(4): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948099 | |||||||
chr12:14948099 | T | TGCGCGC | 3 | a0001c0001t0001g0089 a0001c0001t0001g0147 a0001c0001t0001g0180 |
3 | HG02602.hp1 NA19030.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.266-151_266-150ins others(6): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948099 | |||||||
chr12:14948100 | G | GCA | 38 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0065 others(35): Show |
55 | HG00280.hp1 HG00408.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.266-153_266-152dup others(2): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | G | GCACA | 33 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0058 others(30): Show |
57 | HG00140.hp1 HG00423.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.266-155_266-152dup others(4): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | G | GCACACA | 3 | a0001c0001t0001g0247 a0001c0002t0001g0096 a0001c0002t0001g0124 |
3 | HG01109.hp1 HG02523.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.266-157_266-152dup others(6): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | G | GCACACAC others(1): Show |
3 | a0001c0001t0001g0009 a0001c0002t0001g0041 a0001c0002t0001g0254 |
8 | HG00738.hp1 HG01175.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.266-159_266-152dup others(8): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | G | GCACACAC others(3): Show |
2 | a0001c0001t0001g0063 a0001c0002t0001g0248 |
3 | HG01433.hp1 HG02004.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.266-161_266-152dup others(10): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | G | GCGCGCA | 4 | a0001c0001t0001g0047 a0001c0001t0001g0083 a0001c0001t0001g0134 others(1): Show |
5 | HG00438.hp1 HG02886.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-152_266-151ins others(6): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | G | GCGCGCAC others(1): Show |
47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(44): Show |
91 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.266-152_266-151ins others(8): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | G | GCGCGCAC others(3): Show |
16 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0076 others(13): Show |
21 | HG00280.hp2 HG00733.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.266-152_266-151ins others(10): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | G | GCGCGCAC others(5): Show |
8 | a0001c0001t0001g0048 a0001c0001t0001g0137 a0001c0001t0001g0227 others(5): Show |
9 | HG02004.hp1 HG02109.hp1 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.266-152_266-151ins others(12): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | G | GCGCGCAC others(7): Show |
2 | a0001c0001t0002g0273 a0001c0002t0001g0054 |
3 | HG00738.hp2 HG01257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.266-152_266-151ins others(14): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | G | GCGCGCGC others(1): Show |
6 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0035 others(3): Show |
13 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.266-152_266-151ins others(8): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | G | GCGCGCGC others(3): Show |
4 | a0001c0001t0001g0186 a0001c0001t0001g0224 a0001c0001t0001g0274 others(1): Show |
4 | HG01099.hp1 HG01517.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-152_266-151ins others(10): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | G | GCGCGCGC others(5): Show |
3 | a0001c0001t0001g0027 a0001c0001t0001g0084 a0001c0001t0003g0074 |
6 | HG02055.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.266-152_266-151ins others(12): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | GCA | G | 15 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0001c0001t0001g0261 others(12): Show |
21 | HG00597.hp1 HG01081.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.266-153_266-152del others(2): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | GCACA | G | 11 | a0001c0001t0001g0078 a0001c0002t0001g0010 a0001c0002t0001g0011 others(8): Show |
21 | HG00140.hp2 HG00733.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.266-155_266-152del others(4): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | GCACACA | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0282 others(3): Show |
10 | HG02083.hp1 HG03491.hp2 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.266-157_266-152del others(6): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948100 | GCACACAC others(3): Show |
G | 17 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0002t0001g0018 others(14): Show |
22 | HG00099.hp2 HG00609.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.266-161_266-152del others(10): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948100 | |||||||
chr12:14948102 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA18978.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.266-153T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948102 | |||||||
chr12:14948138 | T | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(177): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.266-189A>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948138 | |||||||
chr12:14948163 | G | A | 2 | a0001c0002t0001g0271 a0001c0002t0001g0272 |
2 | HG00733.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.266-214C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948163 | |||||||
chr12:14948224 | A | G | 2 | a0001c0001t0001g0261 a0001c0001t0003g0290 |
2 | HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.266-275T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948224 | |||||||
chr12:14948425 | A | G | 3 | a0001c0002t0001g0163 a0001c0002t0001g0164 a0001c0002t0001g0165 |
3 | HG02976.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.266-476T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948425 | |||||||
chr12:14948485 | G | T | 4 | a0001c0001t0001g0085 a0001c0002t0001g0086 a0001c0002t0001g0087 others(1): Show |
4 | HG01891.hp2 HG02109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-536C>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948485 | |||||||
chr12:14948501 | T | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(27): Show |
61 | HG00140.hp1 HG00408.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.266-552A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948501 | |||||||
chr12:14948544 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(111): Show |
177 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.266-595C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948544 | |||||||
chr12:14948622 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.266-673G>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948622 | |||||||
chr12:14948624 | C | G | 4 | a0001c0002t0001g0163 a0001c0002t0001g0164 a0001c0002t0001g0165 others(1): Show |
4 | HG02976.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-675G>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948624 | |||||||
chr12:14948673 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0282 others(2): Show |
12 | HG02083.hp1 HG02280.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.266-724A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948673 | |||||||
chr12:14948825 | T | C | 1 | a0001c0002t0001g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.266-876A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948825 | |||||||
chr12:14948868 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0282 others(1): Show |
8 | HG02083.hp1 HG03491.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.266-919G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948868 | |||||||
chr12:14948874 | G | A | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0002t0001g0079 |
3 | HG02145.hp1 HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.266-925C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948874 | |||||||
chr12:14948932 | G | A | 1 | a0001c0002t0001g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.265+870C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14948932 | |||||||
chr12:14949070 | G | A | 1 | a0001c0002t0001g0106 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.265+732C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14949070 | |||||||
chr12:14949106 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(95): Show |
160 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.265+696A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14949106 | |||||||
chr12:14949149 | G | A | 4 | a0001c0001t0001g0085 a0001c0002t0001g0086 a0001c0002t0001g0087 others(1): Show |
4 | HG01891.hp2 HG02109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+653C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14949149 | |||||||
chr12:14949166 | T | G | 5 | a0001c0001t0001g0071 a0001c0001t0001g0268 a0001c0001t0001g0269 others(2): Show |
6 | HG02135.hp1 HG02135.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+636A>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14949166 | |||||||
chr12:14949169 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.265+633G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14949169 | |||||||
chr12:14949212 | C | T | 4 | a0001c0001t0001g0085 a0001c0002t0001g0086 a0001c0002t0001g0087 others(1): Show |
4 | HG01891.hp2 HG02109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+590G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14949212 | |||||||
chr12:14949253 | C | T | 1 | a0001c0002t0001g0010 | 4 | HG02280.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+549G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14949253 | |||||||
chr12:14949321 | T | C | 1 | a0001c0001t0001g0053 | 2 | HG03654.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.265+481A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14949321 | |||||||
chr12:14949513 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.265+289C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14949513 | |||||||
chr12:14949587 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(109): Show |
174 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.265+215C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14949587 | |||||||
chr12:14949734 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.265+68T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14949734 | |||||||
chr12:14949747 | G | C | 18 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0001g0284 others(15): Show |
23 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.265+55C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14949747 | |||||||
chr12:14949790 | G | A | 5 | a0001c0001t0001g0071 a0001c0001t0001g0268 a0001c0001t0001g0269 others(2): Show |
6 | HG02135.hp1 HG02135.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+12C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | 14949790 | |||||||
chr12:14949893 | A | T | 1 | a0001c0002t0001g0178 | 1 | HG02735.hp1 | splice_region_variant&intron_variant | LOW | c.182-8T>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 2/5 | chr12 | 14949893 | |||||||
chr12:14949896 | G | A | 5 | a0001c0001t0001g0071 a0001c0001t0001g0268 a0001c0001t0001g0269 others(2): Show |
6 | HG02135.hp1 HG02135.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-11C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 2/5 | chr12 | 14949896 | |||||||
chr12:14950066 | A | T | 8 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(5): Show |
9 | HG01891.hp2 HG02109.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.182-181T>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 2/5 | chr12 | 14950066 | |||||||
chr12:14950083 | G | A | 3 | a0001c0001t0001g0253 a0001c0002t0001g0034 a0001c0002t0001g0254 |
5 | HG02056.hp2 NA18939.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.182-198C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 2/5 | chr12 | 14950083 | |||||||
chr12:14950153 | A | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0282 others(1): Show |
8 | HG02083.hp1 HG03491.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.182-268T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 2/5 | chr12 | 14950153 | |||||||
chr12:14950200 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.182-315G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 2/5 | chr12 | 14950200 | |||||||
chr12:14950282 | T | A | 3 | a0001c0001t0001g0078 a0001c0002t0001g0044 a0001c0002t0003g0073 |
5 | HG02257.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.181+250A>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 2/5 | chr12 | 14950282 | |||||||
chr12:14950442 | C | T | 6 | a0001c0002t0001g0021 a0001c0002t0001g0066 a0001c0002t0001g0088 others(3): Show |
9 | HG01167.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.181+90G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 2/5 | chr12 | 14950442 | |||||||
chr12:14950792 | G | A | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-68C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14950792 | |||||||
chr12:14950892 | A | C | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-168T>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14950892 | |||||||
chr12:14951213 | C | T | 1 | a0001c0002t0001g0177 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-12-489G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951213 | |||||||
chr12:14951448 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-12-724A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951448 | |||||||
chr12:14951521 | G | A | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-797C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951521 | |||||||
chr12:14951671 | T | G | 2 | a0001c0001t0001g0191 a0001c0002t0001g0054 |
3 | HG00738.hp2 HG01257.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-12-947A>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951671 | |||||||
chr12:14951698 | T | TAAAACAT others(313): Show |
1 | a0001c0001t0001g0283 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-12-975_-12-974ins others(320): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(314): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0282 a0001c0002t0001g0010 |
9 | HG02280.hp2 HG02922.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12-975_-12-974ins others(321): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(315): Show |
1 | a0001c0001t0001g0072 | 2 | HG03492.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.-12-975_-12-974ins others(322): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(307): Show |
1 | a0001c0001t0001g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-12-975_-12-974ins others(314): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(319): Show |
1 | a0001c0002t0001g0165 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12-975_-12-974ins others(326): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(331): Show |
1 | a0001c0002t0001g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-12-975_-12-974ins others(338): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(334): Show |
1 | a0001c0002t0001g0163 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-12-975_-12-974ins others(341): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(335): Show |
1 | a0001c0002t0001g0164 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-12-975_-12-974ins others(342): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(304): Show |
1 | a0001c0001t0001g0113 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-12-975_-12-974ins others(311): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(318): Show |
8 | a0001c0001t0001g0284 a0001c0002t0001g0036 a0001c0002t0001g0037 others(5): Show |
10 | HG00280.hp1 HG01261.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-975_-12-974ins others(325): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(319): Show |
5 | a0001c0002t0001g0038 a0001c0002t0001g0095 a0001c0002t0001g0096 others(2): Show |
6 | HG00423.hp2 HG01106.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-975_-12-974ins others(326): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(320): Show |
5 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0001g0099 others(2): Show |
5 | HG00558.hp2 HG01981.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-975_-12-974ins others(327): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(321): Show |
10 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0121 others(7): Show |
13 | HG00609.hp2 HG00735.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12-975_-12-974ins others(328): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(322): Show |
10 | a0001c0001t0001g0039 a0001c0002t0001g0017 a0001c0002t0001g0019 others(7): Show |
15 | HG00639.hp1 HG01884.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12-975_-12-974ins others(329): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(323): Show |
4 | a0001c0001t0001g0040 a0001c0002t0001g0110 a0001c0002t0001g0116 others(1): Show |
5 | HG00099.hp2 HG01168.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-975_-12-974ins others(330): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(324): Show |
3 | a0001c0002t0001g0111 a0001c0002t0001g0117 a0001c0002t0001g0118 |
3 | HG00140.hp2 HG01258.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-12-975_-12-974ins others(331): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(325): Show |
2 | a0001c0002t0001g0119 a0001c0002t0001g0120 |
2 | HG01123.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.-12-975_-12-974ins others(332): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951698 | T | TAAAACAT others(326): Show |
1 | a0001c0002t0001g0112 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-12-975_-12-974ins others(333): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951698 | |||||||
chr12:14951741 | G | A | 59 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(56): Show |
78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.-12-1017C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951741 | |||||||
chr12:14951962 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0007g0280 |
3 | HG02135.hp1 HG02135.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.-12-1238G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951962 | |||||||
chr12:14951963 | A | G | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-1239T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14951963 | |||||||
chr12:14952030 | A | G | 1 | a0001c0002t0001g0198 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-12-1306T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952030 | |||||||
chr12:14952042 | A | T | 1 | a0001c0001t0001g0055 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-12-1318T>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952042 | |||||||
chr12:14952076 | G | T | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-1352C>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952076 | |||||||
chr12:14952130 | T | C | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-1406A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952130 | |||||||
chr12:14952215 | A | G | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-1491T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952215 | |||||||
chr12:14952270 | A | G | 1 | a0001c0002t0001g0165 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12-1546T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952270 | |||||||
chr12:14952277 | C | CA | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(129): Show |
200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-12-1554dupT | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952277 | |||||||
chr12:14952277 | C | CAA | 23 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0113 others(20): Show |
32 | HG00099.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.-12-1555_-12-1554d others(4): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952277 | |||||||
chr12:14952277 | C | CAAA | 7 | a0001c0001t0001g0085 a0001c0002t0001g0010 a0001c0002t0001g0086 others(4): Show |
10 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12-1556_-12-1554d others(5): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952277 | |||||||
chr12:14952277 | CA | C | 21 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0001g0078 others(18): Show |
27 | HG00733.hp1 HG01109.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.-12-1554delT | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952277 | |||||||
chr12:14952278 | A | G | 1 | a0001c0002t0001g0196 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-12-1554T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952278 | |||||||
chr12:14952384 | T | A | 59 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(56): Show |
78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.-12-1660A>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952384 | |||||||
chr12:14952473 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-12-1749T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952473 | |||||||
chr12:14952486 | C | T | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-1762G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952486 | |||||||
chr12:14952530 | T | G | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-1806A>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952530 | |||||||
chr12:14952598 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0007g0280 |
3 | HG02135.hp1 HG02135.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.-12-1874C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952598 | |||||||
chr12:14952602 | C | T | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-1878G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952602 | |||||||
chr12:14952626 | A | T | 68 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(65): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-12-1902T>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952626 | |||||||
chr12:14952697 | A | G | 68 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(65): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-12-1973T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952697 | |||||||
chr12:14952712 | G | C | 2 | a0001c0002t0001g0271 a0001c0002t0001g0272 |
2 | HG00733.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-12-1988C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952712 | |||||||
chr12:14952762 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-12-2038C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952762 | |||||||
chr12:14952769 | C | T | 59 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(56): Show |
78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.-12-2045G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952769 | |||||||
chr12:14952799 | A | C | 6 | a0001c0001t0001g0085 a0001c0001t0001g0268 a0001c0001t0001g0269 others(3): Show |
6 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-2075T>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952799 | |||||||
chr12:14952820 | G | A | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-2096C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952820 | |||||||
chr12:14952973 | G | C | 1 | a0001c0001t0001g0261 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12-2249C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952973 | |||||||
chr12:14952983 | A | AAG | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-2261_-12-2260d others(4): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952983 | |||||||
chr12:14952990 | C | A | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-2266G>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14952990 | |||||||
chr12:14953002 | T | C | 1 | a0001c0002t0001g0216 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12-2278A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953002 | |||||||
chr12:14953050 | T | C | 68 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(65): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-12-2326A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953050 | |||||||
chr12:14953088 | C | T | 68 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(65): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-12-2364G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953088 | |||||||
chr12:14953095 | T | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0173 a0001c0001t0001g0236 others(2): Show |
8 | HG02040.hp2 HG02071.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-2371A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953095 | |||||||
chr12:14953096 | C | T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0270 a0001c0001t0003g0289 others(1): Show |
4 | HG02145.hp2 HG02486.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-2372G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953096 | |||||||
chr12:14953134 | A | G | 7 | a0001c0001t0001g0085 a0001c0001t0001g0268 a0001c0001t0001g0269 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-2410T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953134 | |||||||
chr12:14953216 | C | T | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-2492G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953216 | |||||||
chr12:14953225 | G | C | 1 | a0001c0001t0007g0280 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-12-2501C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953225 | |||||||
chr12:14953466 | C | T | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-2742G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953466 | |||||||
chr12:14953520 | G | C | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-2796C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953520 | |||||||
chr12:14953634 | GA | G | 72 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(69): Show |
92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.-12-2911delT | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953634 | |||||||
chr12:14953680 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0007g0280 |
3 | HG02135.hp1 HG02135.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.-12-2956C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953680 | |||||||
chr12:14953818 | G | GCT | 6 | a0001c0001t0001g0078 a0001c0001t0001g0261 a0001c0001t0005g0130 others(3): Show |
8 | HG00741.hp1 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-3096_-12-3095d others(4): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953818 | |||||||
chr12:14953818 | G | GCTCTCTC others(3): Show |
2 | a0001c0002t0001g0241 a0001c0002t0001g0242 |
2 | NA18967.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-12-3104_-12-3095d others(12): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953818 | |||||||
chr12:14953818 | GCTCT | G | 4 | a0001c0001t0001g0156 a0001c0002t0001g0080 a0001c0002t0001g0217 others(1): Show |
5 | HG00609.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-3098_-12-3095d others(6): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953818 | |||||||
chr12:14953821 | C | CTT | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-3098_-12-3097i others(4): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953821 | |||||||
chr12:14953823 | C | T | 59 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(56): Show |
78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.-12-3099G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953823 | |||||||
chr12:14953833 | C | A | 1 | a0001c0002t0001g0218 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-12-3109G>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953833 | |||||||
chr12:14953833 | C | T | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-3109G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953833 | |||||||
chr12:14953835 | CTCTCTTT others(5): Show |
C | 2 | a0001c0001t0001g0270 a0001c0001t0003g0290 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-12-3123_-12-3112d others(14): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953835 | |||||||
chr12:14953851 | C | T | 2 | a0001c0001t0001g0270 a0001c0001t0003g0290 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-12-3127G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953851 | |||||||
chr12:14953883 | G | C | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-3159C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953883 | |||||||
chr12:14953954 | TTTCC | T | 10 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(7): Show |
14 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-3234_-12-3231d others(6): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953954 | |||||||
chr12:14953960 | T | C | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-3236A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14953960 | |||||||
chr12:14954018 | A | T | 1 | a0001c0001t0002g0219 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-12-3294T>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954018 | |||||||
chr12:14954092 | C | T | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-3368G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954092 | |||||||
chr12:14954119 | C | T | 2 | a0001c0002t0001g0279 a0001c0002t0001g0281 |
2 | HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-12-3395G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954119 | |||||||
chr12:14954122 | G | A | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-3398C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954122 | |||||||
chr12:14954139 | G | C | 2 | a0001c0002t0001g0279 a0001c0002t0001g0281 |
2 | HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-12-3415C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954139 | |||||||
chr12:14954213 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-12-3489T>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954213 | |||||||
chr12:14954262 | T | G | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-3538A>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954262 | |||||||
chr12:14954292 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-12-3568G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954292 | |||||||
chr12:14954387 | C | A | 1 | a0001c0002t0001g0158 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-12-3663G>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954387 | |||||||
chr12:14954500 | T | C | 5 | a0001c0001t0001g0075 a0001c0001t0001g0270 a0001c0001t0003g0289 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-3776A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954500 | |||||||
chr12:14954502 | C | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(169): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.-12-3778G>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954502 | |||||||
chr12:14954511 | T | C | 8 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(5): Show |
9 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-3787A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954511 | |||||||
chr12:14954518 | A | G | 10 | a0001c0002t0001g0020 a0001c0002t0001g0041 a0001c0002t0001g0067 others(7): Show |
15 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-12-3794T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954518 | |||||||
chr12:14954767 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-12-4043A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954767 | |||||||
chr12:14954829 | T | G | 6 | a0001c0001t0001g0085 a0001c0001t0001g0268 a0001c0001t0001g0269 others(3): Show |
6 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-4105A>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954829 | |||||||
chr12:14954853 | G | A | 1 | a0001c0002t0001g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-12-4129C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954853 | |||||||
chr12:14954856 | A | G | 1 | a0001c0002t0001g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-12-4132T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954856 | |||||||
chr12:14954857 | C | T | 1 | a0001c0002t0001g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-12-4133G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954857 | |||||||
chr12:14954915 | G | A | 1 | a0001c0001t0002g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-12-4191C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14954915 | |||||||
chr12:14955009 | C | T | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-4285G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14955009 | |||||||
chr12:14955212 | C | T | 2 | a0001c0002t0001g0194 a0001c0002t0001g0195 |
2 | HG00408.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.-12-4488G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14955212 | |||||||
chr12:14955328 | C | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0282 others(1): Show |
8 | HG02083.hp1 HG03491.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-4604G>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14955328 | |||||||
chr12:14955409 | G | A | 1 | a0001c0001t0001g0055 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-12-4685C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14955409 | |||||||
chr12:14955418 | T | C | 1 | a0001c0002t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-12-4694A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14955418 | |||||||
chr12:14955550 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-12-4826G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14955550 | |||||||
chr12:14955758 | T | A | 1 | a0001c0002t0004g0129 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-12-5034A>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14955758 | |||||||
chr12:14955894 | T | C | 3 | a0001c0001t0001g0230 a0001c0002t0001g0046 a0001c0002t0001g0231 |
4 | HG02083.hp2 NA18612.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-5170A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14955894 | |||||||
chr12:14956122 | A | G | 72 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(69): Show |
92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.-12-5398T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956122 | |||||||
chr12:14956286 | G | A | 6 | a0001c0001t0001g0085 a0001c0001t0001g0268 a0001c0001t0001g0269 others(3): Show |
6 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+5251C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956286 | |||||||
chr12:14956349 | G | A | 8 | a0001c0001t0001g0085 a0001c0001t0001g0261 a0001c0001t0001g0268 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+5188C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956349 | |||||||
chr12:14956398 | G | C | 1 | a0001c0001t0001g0065 | 2 | HG02293.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-13+5139C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956398 | |||||||
chr12:14956420 | G | C | 3 | a0001c0002t0001g0163 a0001c0002t0001g0164 a0001c0002t0001g0165 |
3 | HG02976.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-13+5117C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956420 | |||||||
chr12:14956427 | G | A | 2 | a0001c0002t0001g0271 a0001c0002t0001g0272 |
2 | HG00733.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-13+5110C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956427 | |||||||
chr12:14956451 | G | A | 1 | a0001c0002t0001g0260 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-13+5086C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956451 | |||||||
chr12:14956510 | C | A | 1 | a0001c0001t0001g0261 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-13+5027G>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956510 | |||||||
chr12:14956637 | T | C | 98 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0029 others(95): Show |
132 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-13+4900A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956637 | |||||||
chr12:14956640 | A | G | 8 | a0001c0001t0001g0085 a0001c0001t0001g0268 a0001c0001t0001g0269 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+4897T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956640 | |||||||
chr12:14956646 | T | A | 1 | a0001c0002t0001g0158 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-13+4891A>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956646 | |||||||
chr12:14956732 | C | G | 4 | a0001c0002t0001g0046 a0001c0002t0001g0059 a0001c0002t0001g0238 others(1): Show |
6 | HG02083.hp2 HG03017.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+4805G>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956732 | |||||||
chr12:14956753 | G | A | 1 | a0001c0002t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-13+4784C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956753 | |||||||
chr12:14956771 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-13+4766A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956771 | |||||||
chr12:14956820 | C | A | 1 | a0001c0001t0001g0232 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-13+4717G>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956820 | |||||||
chr12:14956843 | A | C | 1 | a0001c0001t0003g0287 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-13+4694T>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14956843 | |||||||
chr12:14957151 | T | C | 7 | a0001c0001t0001g0085 a0001c0001t0001g0268 a0001c0001t0001g0269 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+4386A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957151 | |||||||
chr12:14957174 | C | T | 63 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0089 others(60): Show |
84 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.-13+4363G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957174 | |||||||
chr12:14957237 | G | A | 1 | a0001c0001t0003g0287 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-13+4300C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957237 | |||||||
chr12:14957273 | T | C | 72 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0075 others(69): Show |
93 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.-13+4264A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957273 | |||||||
chr12:14957403 | T | C | 1 | a0001c0002t0006g0042 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-13+4134A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957403 | |||||||
chr12:14957588 | T | C | 1 | a0001c0001t0001g0070 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-13+3949A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957588 | |||||||
chr12:14957639 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-13+3898G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957639 | |||||||
chr12:14957770 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-13+3767T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957770 | |||||||
chr12:14957783 | G | A | 1 | a0001c0001t0003g0287 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-13+3754C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957783 | |||||||
chr12:14957784 | G | A | 1 | a0001c0002t0001g0004 | 7 | HG00621.hp2 HG00673.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+3753C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957784 | |||||||
chr12:14957819 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-13+3718G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957819 | |||||||
chr12:14957828 | A | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0058 a0001c0001t0001g0233 others(5): Show |
12 | HG02040.hp2 HG02071.hp1 NA18959.hp2 others(9): Show |
intron_variant | MODIFIER | c.-13+3709T>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957828 | |||||||
chr12:14957840 | G | A | 12 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(9): Show |
13 | HG02109.hp2 HG02135.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-13+3697C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957840 | |||||||
chr12:14957856 | A | AGAGAAAG others(2): Show |
76 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(73): Show |
103 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-13+3672_-13+3680d others(11): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957856 | |||||||
chr12:14957981 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-13+3556A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14957981 | |||||||
chr12:14958044 | G | A | 2 | a0001c0002t0001g0049 a0001c0002t0001g0265 |
3 | NA18990.hp2 NA19070.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-13+3493C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14958044 | |||||||
chr12:14958334 | A | G | 48 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0204 others(45): Show |
84 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-13+3203T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14958334 | |||||||
chr12:14958343 | A | C | 1 | a0001c0001t0001g0070 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-13+3194T>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14958343 | |||||||
chr12:14958554 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-13+2983T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14958554 | |||||||
chr12:14958570 | A | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0016 others(55): Show |
92 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.-13+2967T>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14958570 | |||||||
chr12:14958744 | T | A | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG02109.hp2 HG02135.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+2793A>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14958744 | |||||||
chr12:14958785 | C | T | 3 | a0001c0001t0001g0134 a0001c0002t0001g0044 a0001c0002t0003g0073 |
5 | HG02451.hp2 HG02970.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+2752G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14958785 | |||||||
chr12:14958878 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-13+2659C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14958878 | |||||||
chr12:14959128 | A | G | 76 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(73): Show |
103 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-13+2409T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959128 | |||||||
chr12:14959330 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-13+2207T>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959330 | |||||||
chr12:14959334 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-13+2203G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959334 | |||||||
chr12:14959359 | C | T | 76 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(73): Show |
103 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-13+2178G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959359 | |||||||
chr12:14959361 | C | CA | 4 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0282 others(1): Show |
8 | HG02083.hp1 HG03491.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+2175dupT | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959361 | |||||||
chr12:14959407 | T | C | 2 | a0001c0002t0001g0131 a0001c0002t0001g0132 |
2 | HG03688.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-13+2130A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959407 | |||||||
chr12:14959513 | C | A | 3 | a0001c0001t0001g0274 a0001c0001t0002g0275 a0001c0001t0002g0276 |
3 | HG01099.hp1 HG02004.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-13+2024G>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959513 | |||||||
chr12:14959584 | C | G | 9 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(6): Show |
10 | HG02109.hp2 HG02135.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+1953G>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959584 | |||||||
chr12:14959604 | T | C | 1 | a0001c0002t0001g0043 | 2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-13+1933A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959604 | |||||||
chr12:14959644 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
4 | HG00099.hp1 HG00733.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+1893T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959644 | |||||||
chr12:14959652 | C | T | 1 | a0001c0001t0003g0287 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-13+1885G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959652 | |||||||
chr12:14959676 | G | A | 1 | a0001c0002t0001g0267 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-13+1861C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959676 | |||||||
chr12:14959713 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-13+1824G>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959713 | |||||||
chr12:14959715 | A | T | 76 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0040 others(73): Show |
103 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-13+1822T>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959715 | |||||||
chr12:14959965 | A | G | 62 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0089 others(59): Show |
82 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.-13+1572T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959965 | |||||||
chr12:14959982 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0007g0280 |
3 | HG02135.hp1 HG02135.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.-13+1555C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14959982 | |||||||
chr12:14960000 | T | G | 11 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0268 others(8): Show |
12 | HG00733.hp1 HG02109.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13+1537A>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14960000 | |||||||
chr12:14960063 | C | A | 6 | a0001c0001t0001g0085 a0001c0001t0001g0269 a0001c0002t0001g0086 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13+1474G>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14960063 | |||||||
chr12:14960205 | C | A | 3 | a0001c0001t0001g0270 a0001c0001t0003g0289 a0001c0001t0003g0290 |
3 | HG02145.hp2 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-13+1332G>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14960205 | |||||||
chr12:14960245 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0282 others(2): Show |
12 | HG02083.hp1 HG02280.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13+1292T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14960245 | |||||||
chr12:14960440 | C | T | 1 | a0001c0002t0001g0010 | 4 | HG02280.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+1097G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14960440 | |||||||
chr12:14960624 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0003g0289 a0001c0001t0003g0290 |
3 | HG02145.hp2 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-13+913G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14960624 | |||||||
chr12:14960782 | C | T | 1 | a0001c0002t0001g0010 | 4 | HG02280.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+755G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14960782 | |||||||
chr12:14960783 | G | A | 3 | a0001c0001t0001g0270 a0001c0001t0003g0289 a0001c0001t0003g0290 |
3 | HG02145.hp2 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-13+754C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14960783 | |||||||
chr12:14960795 | G | A | 1 | a0001c0002t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-13+742C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14960795 | |||||||
chr12:14960809 | T | C | 2 | a0001c0002t0001g0271 a0001c0002t0001g0272 |
2 | HG00733.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-13+728A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14960809 | |||||||
chr12:14960907 | T | C | 1 | a0001c0002t0001g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-13+630A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14960907 | |||||||
chr12:14961037 | T | G | 6 | a0001c0001t0001g0274 a0001c0001t0002g0068 a0001c0001t0002g0273 others(3): Show |
8 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+500A>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14961037 | |||||||
chr12:14961042 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(93): Show |
152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-13+495T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14961042 | |||||||
chr12:14961046 | T | C | 18 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0072 others(15): Show |
24 | HG01934.hp2 HG02083.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-13+491A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14961046 | |||||||
chr12:14961053 | A | AT | 13 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0078 others(10): Show |
15 | HG01934.hp2 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-13+483dupA | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14961053 | |||||||
chr12:14961143 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-13+394G>A | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14961143 | |||||||
chr12:14961155 | G | A | 3 | a0001c0001t0001g0070 a0001c0002t0001g0278 a0001c0002t0001g0279 |
4 | HG02723.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+382C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14961155 | |||||||
chr12:14961176 | C | A | 3 | a0001c0001t0001g0071 a0001c0001t0007g0280 a0001c0002t0001g0281 |
4 | HG02135.hp1 HG02135.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+361G>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14961176 | |||||||
chr12:14961276 | G | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0282 others(1): Show |
8 | HG02083.hp1 HG03491.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+261C>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14961276 | |||||||
chr12:14961404 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-13+133T>C | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14961404 | |||||||
chr12:14961415 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-13+122A>G | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14961415 | |||||||
chr12:14961476 | G | A | 2 | a0001c0002t0001g0285 a0001c0002t0001g0286 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-13+61C>T | ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | 14961476 |