Item | Value |
---|---|
geneid | 84100 |
ensemblid | ENSG00000113966.11 |
hgncid | 13210 |
symbol | ARL6 |
name | ADP ribosylation factor like GTPase 6 |
refseq_nuc | NM_001278293.3 |
refseq_prot | NP_001265222.1 |
ensembl_nuc | ENST00000463745.6 |
ensembl_prot | ENSP00000419619.1 |
mane_status | MANE Select |
chr | chr3 |
start | 97764758 |
end | 97801229 |
strand | + |
ver | v1.2 |
region | chr3:97764758-97801229 |
region5000 | chr3:97759758-97806229 |
regionname0 | ARL6_chr3_97764758_97801229 |
regionname5000 | ARL6_chr3_97759758_97806229 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 186 | 362 | 92 | 72 | 140 | 16 | 40 | 106 | ARL6_chr3_97759758_97806229 | ARL6 | MGLLD others(181): Show |
chr3 | 97759758 | 97806229 |
a0002 | 0/0 | 186 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | MGLLD others(181): Show |
chr3 | 97759758 | 97806229 |
a0003 | 0/0 | 186 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | MGLLD others(181): Show |
chr3 | 97759758 | 97806229 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 558 | 359 | 92 | 71 | 138 | 16 | 40 | ARL6_chr3_97759758_97806229 | ARL6 | ATGGG others(553): Show |
chr3 | 97759758 | 97806229 | ||
a0001c0003 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | ATGGG others(553): Show |
chr3 | 97759758 | 97806229 | ||
a0001c0004 | 0/0 | 558 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | ATGGG others(553): Show |
chr3 | 97759758 | 97806229 | ||
a0001c0006 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | ATGGG others(553): Show |
chr3 | 97759758 | 97806229 | ||
a0002c0005 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | ATGGG others(553): Show |
chr3 | 97759758 | 97806229 | ||
a0003c0002 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | ATGGG others(553): Show |
chr3 | 97759758 | 97806229 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3988 | 224 | 70 | 39 | 89 | 7 | 19 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0002 | 0/0 | 3988 | 65 | 5 | 17 | 29 | 5 | 9 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0003 | 0/0 | 3988 | 19 | 0 | 4 | 7 | 0 | 8 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0004 | 1/1 | 3988 | 11 | 1 | 4 | 1 | 2 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0005 | 0/0 | 3989 | 6 | 1 | 4 | 0 | 1 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3984): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0006 | 0/0 | 3988 | 4 | 0 | 0 | 4 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0007 | 0/0 | 3988 | 4 | 0 | 0 | 3 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0008 | 0/0 | 3988 | 4 | 4 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0009 | 0/0 | 3988 | 3 | 0 | 0 | 3 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0010 | 0/0 | 3988 | 3 | 3 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0011 | 0/0 | 3988 | 2 | 0 | 0 | 0 | 0 | 2 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0012 | 0/0 | 3988 | 2 | 2 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0013 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0014 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0015 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0016 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0017 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0018 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0019 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0020 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0021 | 0/0 | 3988 | 1 | 0 | 0 | 0 | 1 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0022 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0023 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0001t0024 | 0/0 | 3989 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3984): Show |
chr3 | 97759758 | 97806229 |
a0001c0003t0002 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0004t0002 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0001c0006t0001 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0002c0005t0001 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
a0003c0002t0001 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | AAGGC others(3983): Show |
chr3 | 97759758 | 97806229 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 6 | 0 | 2 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 0 | 5 | 0 | 3 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0003 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0044 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0057 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0058 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0003g0006 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0003g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0004g0001 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0004g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0004g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0004g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0004g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0005g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0007g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0008g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0009g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0009g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0009g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0010g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0010g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0011g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0011g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0012g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0013g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0014g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0015g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0016g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0017g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0018g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0019g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0020g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0021g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0022g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0023g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0001t0024g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0004t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0001c0006t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0002c0005t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
a0003c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0058 | EUR | GBR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00099 | hp2 | a0001 | c0001 | t0021 | g0010 | EUR | GBR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | GBR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0053 | EUR | FIN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0053 | EUR | FIN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00423 | hp2 | a0001 | c0001 | t0007 | g0072 | EAS | CHS | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00733 | hp2 | a0001 | c0001 | t0013 | g0066 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0143 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01109 | hp1 | a0001 | c0004 | t0002 | g0231 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0176 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0017 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0017 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0046 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0046 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0045 | EUR | IBS | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0223 | EUR | IBS | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0045 | EUR | IBS | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01943 | hp1 | a0001 | c0001 | t0014 | g0016 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01981 | hp2 | a0001 | c0001 | t0024 | g0043 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02055 | hp2 | a0001 | c0001 | t0018 | g0103 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02071 | hp1 | a0001 | c0001 | t0019 | g0043 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02135 | hp1 | a0001 | c0003 | t0002 | g0259 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0254 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02145 | hp2 | a0001 | c0001 | t0010 | g0059 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | CDX | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02165 | hp1 | a0001 | c0001 | t0006 | g0119 | EAS | CDX | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02257 | hp2 | a0001 | c0001 | t0010 | g0025 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02717 | hp1 | a0002 | c0005 | t0001 | g0109 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02717 | hp2 | a0001 | c0001 | t0012 | g0070 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0047 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02976 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03195 | hp2 | a0001 | c0001 | t0022 | g0062 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03209 | hp1 | a0001 | c0001 | t0020 | g0076 | AFR | MSL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03225 | hp2 | a0003 | c0002 | t0001 | g0064 | AFR | MSL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0005 | AFR | MSL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03486 | hp2 | a0001 | c0001 | t0012 | g0071 | AFR | MSL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03516 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03516 | hp2 | a0001 | c0001 | t0023 | g0114 | AFR | ESN | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03540 | hp2 | a0001 | c0001 | t0016 | g0055 | AFR | GWD | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0005 | AFR | MSL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03654 | hp2 | a0001 | c0001 | t0011 | g0091 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03704 | hp1 | a0001 | c0001 | t0011 | g0208 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0123 | SAS | BEB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | BEB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | BEB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03927 | hp2 | a0001 | c0001 | t0007 | g0073 | SAS | BEB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | STU | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | STU | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | STU | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | YRI | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0069 | EAS | CHB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18944 | hp1 | a0001 | c0001 | t0009 | g0060 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18971 | hp2 | a0001 | c0001 | t0007 | g0027 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18974 | hp1 | a0001 | c0006 | t0001 | g0048 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18979 | hp2 | a0001 | c0001 | t0009 | g0061 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18991 | hp2 | a0001 | c0001 | t0006 | g0068 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19011 | hp1 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19063 | hp1 | a0001 | c0001 | t0015 | g0247 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19066 | hp2 | a0001 | c0001 | t0007 | g0027 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19082 | hp2 | a0001 | c0001 | t0006 | g0067 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | YRI | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ASW | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ASW | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0195 | EUR | TSI | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0120 | EUR | TSI | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | TSI | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | GIH | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02559 | hp1 | a0001 | c0001 | t0010 | g0025 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG02559 | hp2 | a0001 | c0001 | t0017 | g0019 | AFR | ACB | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | USA | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | USA | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | USA | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | USA | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0243 | REF | REF | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0001 | REF | REF | ARL6_chr3_97759758_97806229 | ARL6 | chr3 | 97759758 | 97806229 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:97780674 | A | G | 1 | a0002 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.245A>G | p.His82Arg | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/8 | 492/3988 | 245/561 | 82/186 | chr3 | 97780674 | |||
chr3:97788082 | T | G | 1 | a0003 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.442T>G | p.Cys148Gly | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/8 | 689/3988 | 442/561 | 148/186 | chr3 | 97788082 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:97780621 | A | G | 1 | a0001c0006 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.192A>G | p.Ser64Ser | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/8 | 439/3988 | 192/561 | 64/186 | chr3 | 97780621 | |||
chr3:97788108 | C | A | 1 | a0001c0003 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.468C>A | p.Pro156Pro | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/8 | 715/3988 | 468/561 | 156/186 | chr3 | 97788108 | |||
chr3:97791777 | T | C | 1 | a0001c0004 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.486T>C | p.Ser162Ser | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/8 | 733/3988 | 486/561 | 162/186 | chr3 | 97791777 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:97764765 | C | T | 1 | a0001c0001t0012 | 2 | HG02717.hp2 HG03486.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-240C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/8 | chr3 | 97764765 | |||||||
chr3:97764868 | A | C | 1 | a0001c0001t0024 | 1 | HG01981.hp2 | 5_prime_UTR_variant | MODIFIER | c.-137A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/8 | 3240 | chr3 | 97764868 | ||||||
chr3:97764883 | G | T | 1 | a0001c0001t0023 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-122G>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/8 | 3225 | chr3 | 97764883 | ||||||
chr3:97764925 | C | G | 1 | a0001c0001t0022 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80C>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/8 | 3183 | chr3 | 97764925 | ||||||
chr3:97764934 | C | G | 1 | a0001c0001t0021 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-71C>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/8 | 3174 | chr3 | 97764934 | ||||||
chr3:97798274 | G | C | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(25): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
3_prime_UTR_variant | MODIFIER | c.*225G>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 225 | chr3 | 97798274 | ||||||
chr3:97798304 | C | T | 1 | a0001c0001t0010 | 3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*255C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 255 | chr3 | 97798304 | ||||||
chr3:97798333 | C | A | 2 | a0001c0001t0006 a0001c0001t0013 |
5 | HG00733.hp2 HG02165.hp1 NA18747.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*284C>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 284 | chr3 | 97798333 | ||||||
chr3:97798519 | G | A | 1 | a0001c0001t0013 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*470G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 470 | chr3 | 97798519 | ||||||
chr3:97798544 | C | T | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG02071.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*495C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 495 | chr3 | 97798544 | ||||||
chr3:97798594 | G | T | 1 | a0001c0001t0009 | 3 | NA18944.hp1 NA18979.hp2 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*545G>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 545 | chr3 | 97798594 | ||||||
chr3:97798628 | C | T | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0018 others(2): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*579C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 579 | chr3 | 97798628 | ||||||
chr3:97798802 | T | C | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0018 others(2): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*753T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 753 | chr3 | 97798802 | ||||||
chr3:97799079 | G | T | 1 | a0001c0001t0017 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1030G>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 1030 | chr3 | 97799079 | ||||||
chr3:97799160 | T | C | 1 | a0001c0001t0010 | 3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1111T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 1111 | chr3 | 97799160 | ||||||
chr3:97799243 | G | C | 4 | a0001c0001t0002 a0001c0001t0009 a0001c0003t0002 others(1): Show |
70 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1194G>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 1194 | chr3 | 97799243 | ||||||
chr3:97799354 | G | A | 4 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0012 others(1): Show |
11 | HG00423.hp2 HG00733.hp2 HG02165.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1305G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 1305 | chr3 | 97799354 | ||||||
chr3:97799398 | A | G | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0018 others(2): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1349A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 1349 | chr3 | 97799398 | ||||||
chr3:97799452 | T | C | 1 | a0001c0001t0022 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1403T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 1403 | chr3 | 97799452 | ||||||
chr3:97799684 | A | C | 1 | a0001c0001t0010 | 3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1635A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 1635 | chr3 | 97799684 | ||||||
chr3:97799870 | A | T | 1 | a0001c0001t0020 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1821A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 1821 | chr3 | 97799870 | ||||||
chr3:97799971 | A | T | 1 | a0001c0001t0016 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1922A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 1922 | chr3 | 97799971 | ||||||
chr3:97800011 | T | G | 1 | a0001c0001t0014 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1962T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 1962 | chr3 | 97800011 | ||||||
chr3:97800073 | A | G | 1 | a0001c0001t0016 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2024A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 2024 | chr3 | 97800073 | ||||||
chr3:97800075 | A | C | 1 | a0001c0001t0016 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2026A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 2026 | chr3 | 97800075 | ||||||
chr3:97800203 | G | T | 1 | a0001c0001t0003 | 19 | HG01256.hp2 HG01257.hp1 HG02004.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2154G>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 2154 | chr3 | 97800203 | ||||||
chr3:97800207 | T | C | 1 | a0001c0001t0003 | 19 | HG01256.hp2 HG01257.hp1 HG02004.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2158T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 2158 | chr3 | 97800207 | ||||||
chr3:97800208 | T | A | 1 | a0001c0001t0003 | 19 | HG01256.hp2 HG01257.hp1 HG02004.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2159T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 2159 | chr3 | 97800208 | ||||||
chr3:97800561 | G | GT | 2 | a0001c0001t0005 a0001c0001t0024 |
7 | HG01070.hp2 HG01074.hp1 HG01168.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2518dupT | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 2519 | INFO_REALIGN_3_PRIME | chr3 | 97800561 | |||||
chr3:97800904 | A | C | 1 | a0001c0001t0011 | 2 | HG03654.hp2 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2855A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 2855 | chr3 | 97800904 | ||||||
chr3:97800971 | A | C | 1 | a0001c0001t0008 | 4 | HG02976.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2922A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 2922 | chr3 | 97800971 | ||||||
chr3:97801070 | A | G | 1 | a0001c0001t0015 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3021A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 8/8 | 3021 | chr3 | 97801070 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:97765129 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-28+152C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97765129 | |||||||
chr3:97765207 | TGG | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0244 others(11): Show |
18 | HG00099.hp2 HG00408.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.-28+234_-28+235del others(2): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765207 | ||||||
chr3:97765208 | G | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-28+231G>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97765208 | |||||||
chr3:97765209 | GGGGT | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0015 others(30): Show |
45 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-28+234_-28+237del others(4): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765209 | ||||||
chr3:97765209 | GGGGTGT | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(47): Show |
63 | HG00140.hp2 HG00423.hp1 HG01255.hp2 others(60): Show |
intron_variant | MODIFIER | c.-28+234_-28+239del others(6): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765209 | ||||||
chr3:97765209 | GGGGTGTG others(3): Show |
G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0125 a0001c0001t0001g0146 others(2): Show |
7 | NA18954.hp2 NA18970.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28+234_-28+243del others(10): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765209 | ||||||
chr3:97765209 | GGGGTGTG others(13): Show |
G | 6 | a0001c0001t0004g0045 a0001c0001t0004g0046 a0001c0001t0004g0047 others(3): Show |
9 | HG00738.hp2 HG01168.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28+234_-28+253del others(20): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765209 | ||||||
chr3:97765211 | G | GGGGTGTG others(5): Show |
2 | a0001c0001t0009g0060 a0001c0001t0009g0061 |
2 | NA18944.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.-28+235_-28+236ins others(12): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765211 | ||||||
chr3:97765211 | G | GGT | 29 | a0001c0001t0001g0020 a0001c0001t0001g0055 a0001c0001t0001g0197 others(26): Show |
33 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-28+273_-28+274dup others(2): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765211 | ||||||
chr3:97765211 | G | GGTGT | 26 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0222 others(23): Show |
40 | HG00323.hp2 HG00408.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-28+271_-28+274dup others(4): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765211 | ||||||
chr3:97765211 | G | GGTGTGT | 4 | a0001c0001t0001g0240 a0001c0001t0002g0057 a0001c0001t0002g0058 others(1): Show |
6 | HG00099.hp1 HG00597.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+269_-28+274dup others(6): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765211 | ||||||
chr3:97765211 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0002g0242 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-28+265_-28+274dup others(10): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765211 | ||||||
chr3:97765211 | G | T | 5 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0001t0001g0258 others(2): Show |
5 | HG00621.hp1 HG02135.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+234G>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97765211 | |||||||
chr3:97765211 | GGT | G | 32 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0029 others(29): Show |
39 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.-28+273_-28+274del others(2): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765211 | ||||||
chr3:97765211 | GGTGT | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0089 others(6): Show |
17 | HG01243.hp1 HG02280.hp1 HG02723.hp2 others(14): Show |
intron_variant | MODIFIER | c.-28+271_-28+274del others(4): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765211 | ||||||
chr3:97765211 | GGTGTGT | G | 18 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 others(15): Show |
19 | HG00423.hp2 HG00741.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-28+269_-28+274del others(6): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765211 | ||||||
chr3:97765211 | GGTGTGTG others(1): Show |
G | 3 | a0001c0001t0002g0065 a0001c0001t0010g0025 a0003c0002t0001g0064 |
4 | HG02257.hp2 HG02559.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28+267_-28+274del others(8): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765211 | ||||||
chr3:97765211 | GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0010g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-28+265_-28+274del others(10): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765211 | ||||||
chr3:97765211 | GGTGTGTG others(15): Show |
G | 1 | a0001c0001t0002g0063 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-28+253_-28+274del others(22): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97765211 | ||||||
chr3:97765213 | T | G | 1 | a0001c0001t0001g0026 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-28+236T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97765213 | |||||||
chr3:97765217 | T | G | 1 | a0001c0001t0022g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-28+240T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97765217 | |||||||
chr3:97765221 | T | G | 1 | a0001c0001t0010g0025 | 2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-28+244T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97765221 | |||||||
chr3:97765223 | T | G | 1 | a0001c0001t0010g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-28+246T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97765223 | |||||||
chr3:97765248 | G | A | 6 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(3): Show |
6 | HG00733.hp2 HG02717.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+271G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97765248 | |||||||
chr3:97765249 | T | A | 6 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(3): Show |
6 | HG00733.hp2 HG02717.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+272T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97765249 | |||||||
chr3:97765687 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-28+710T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97765687 | |||||||
chr3:97765808 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(121): Show |
166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-28+831G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97765808 | |||||||
chr3:97765869 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-28+892T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97765869 | |||||||
chr3:97765930 | T | G | 1 | a0001c0001t0002g0221 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-28+953T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97765930 | |||||||
chr3:97765983 | T | C | 1 | a0001c0001t0008g0005 | 4 | HG02976.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+1006T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97765983 | |||||||
chr3:97766092 | A | C | 1 | a0001c0001t0002g0221 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-28+1115A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97766092 | |||||||
chr3:97766169 | G | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0244 others(4): Show |
9 | HG01192.hp2 HG01952.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.-28+1192G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97766169 | |||||||
chr3:97766354 | T | C | 1 | a0001c0001t0001g0004 | 5 | HG02280.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+1377T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97766354 | |||||||
chr3:97766620 | A | T | 1 | a0001c0001t0001g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-27-1461A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97766620 | |||||||
chr3:97766778 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0177 a0001c0001t0001g0197 |
3 | HG03239.hp1 HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-27-1303G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97766778 | |||||||
chr3:97766882 | T | C | 4 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0198 others(1): Show |
4 | HG02615.hp1 HG02809.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27-1199T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97766882 | |||||||
chr3:97766952 | C | CTTT | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-27-1129_-27-1128i others(5): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97766952 | |||||||
chr3:97766953 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-27-1128C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97766953 | |||||||
chr3:97767088 | A | T | 1 | a0001c0001t0002g0239 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-27-993A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97767088 | |||||||
chr3:97767437 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0115 a0001c0001t0023g0114 |
4 | HG01256.hp1 HG01975.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27-644A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97767437 | |||||||
chr3:97767467 | T | C | 1 | a0001c0001t0002g0223 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-27-614T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97767467 | |||||||
chr3:97767531 | CA | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.-27-541delA | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 97767531 | ||||||
chr3:97767734 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-27-347G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97767734 | |||||||
chr3:97767844 | A | C | 1 | a0001c0001t0004g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-27-237A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97767844 | |||||||
chr3:97768018 | C | G | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-27-63C>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 1/7 | chr3 | 97768018 | |||||||
chr3:97768395 | C | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.123+165C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97768395 | |||||||
chr3:97768403 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.123+173A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97768403 | |||||||
chr3:97768438 | G | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0209 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.123+208G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97768438 | |||||||
chr3:97768535 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.123+305G>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97768535 | |||||||
chr3:97768628 | A | T | 1 | a0001c0001t0002g0196 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.123+398A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97768628 | |||||||
chr3:97768744 | T | C | 9 | a0001c0001t0002g0022 a0001c0001t0002g0102 a0001c0001t0002g0210 others(6): Show |
11 | HG01123.hp1 HG01255.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.123+514T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97768744 | |||||||
chr3:97768888 | C | T | 4 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(1): Show |
4 | NA18964.hp2 NA18973.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+658C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97768888 | |||||||
chr3:97768931 | C | G | 1 | a0001c0001t0015g0247 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.123+701C>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97768931 | |||||||
chr3:97768942 | A | G | 6 | a0001c0001t0004g0045 a0001c0001t0004g0046 a0001c0001t0004g0047 others(3): Show |
9 | HG00738.hp2 HG01168.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.123+712A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97768942 | |||||||
chr3:97769014 | T | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0230 |
7 | HG00642.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+784T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97769014 | |||||||
chr3:97769031 | A | T | 1 | a0001c0001t0002g0196 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.123+801A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97769031 | |||||||
chr3:97769214 | T | A | 3 | a0001c0001t0007g0027 a0001c0001t0007g0072 a0001c0001t0007g0073 |
4 | HG00423.hp2 HG03927.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+984T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97769214 | |||||||
chr3:97769285 | T | C | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.123+1055T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97769285 | |||||||
chr3:97769334 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.123+1104A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97769334 | |||||||
chr3:97769490 | G | A | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.123+1260G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97769490 | |||||||
chr3:97769548 | A | T | 1 | a0001c0001t0002g0196 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.123+1318A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97769548 | |||||||
chr3:97769657 | T | G | 1 | a0001c0001t0002g0196 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.123+1427T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97769657 | |||||||
chr3:97769731 | A | G | 1 | a0001c0001t0002g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.123+1501A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97769731 | |||||||
chr3:97769780 | T | C | 55 | a0001c0001t0002g0009 a0001c0001t0002g0018 a0001c0001t0002g0022 others(52): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.123+1550T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97769780 | |||||||
chr3:97769799 | G | A | 3 | a0001c0001t0002g0212 a0001c0001t0002g0241 a0001c0004t0002g0231 |
3 | HG01074.hp2 HG01109.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.123+1569G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97769799 | |||||||
chr3:97769821 | T | C | 1 | a0001c0001t0005g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.123+1591T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97769821 | |||||||
chr3:97769870 | T | A | 1 | a0001c0001t0022g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.123+1640T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97769870 | |||||||
chr3:97770706 | A | G | 1 | a0001c0001t0022g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.123+2476A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97770706 | |||||||
chr3:97770792 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.123+2562A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97770792 | |||||||
chr3:97770984 | G | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0209 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.123+2754G>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97770984 | |||||||
chr3:97771045 | T | C | 28 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0031 others(25): Show |
39 | HG01175.hp1 HG01256.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.123+2815T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97771045 | |||||||
chr3:97771218 | A | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.123+2988A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97771218 | |||||||
chr3:97771340 | C | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.123+3110C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97771340 | |||||||
chr3:97771484 | T | G | 1 | a0001c0001t0002g0196 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.123+3254T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97771484 | |||||||
chr3:97771545 | T | G | 1 | a0001c0001t0002g0196 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.123+3315T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97771545 | |||||||
chr3:97771611 | G | GTATATTA others(32): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0230 |
7 | HG00642.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+3382_123+3383i others(41): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 97771611 | ||||||
chr3:97771613 | T | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0230 |
7 | HG00642.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+3383T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97771613 | |||||||
chr3:97771615 | T | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0230 |
7 | HG00642.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+3385T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97771615 | |||||||
chr3:97771617 | C | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0230 |
7 | HG00642.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+3387C>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97771617 | |||||||
chr3:97771715 | A | G | 3 | a0001c0001t0007g0027 a0001c0001t0007g0072 a0001c0001t0007g0073 |
4 | HG00423.hp2 HG03927.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+3485A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97771715 | |||||||
chr3:97771944 | G | C | 1 | a0001c0001t0022g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.123+3714G>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97771944 | |||||||
chr3:97771963 | A | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.123+3733A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97771963 | |||||||
chr3:97772045 | A | G | 1 | a0001c0001t0002g0195 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.123+3815A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97772045 | |||||||
chr3:97772094 | T | C | 55 | a0001c0001t0002g0009 a0001c0001t0002g0018 a0001c0001t0002g0022 others(52): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.123+3864T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97772094 | |||||||
chr3:97772177 | T | A | 1 | a0001c0001t0002g0196 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.123+3947T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97772177 | |||||||
chr3:97772221 | A | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0209 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.123+3991A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97772221 | |||||||
chr3:97772223 | G | A | 3 | a0001c0001t0002g0212 a0001c0001t0002g0241 a0001c0004t0002g0231 |
3 | HG01074.hp2 HG01109.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.123+3993G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97772223 | |||||||
chr3:97772350 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0260 |
3 | NA18957.hp1 NA19065.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.123+4120G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97772350 | |||||||
chr3:97772353 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.123+4123G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97772353 | |||||||
chr3:97772617 | T | A | 1 | a0001c0001t0002g0196 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.123+4387T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97772617 | |||||||
chr3:97772618 | A | C | 1 | a0001c0001t0002g0196 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.123+4388A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97772618 | |||||||
chr3:97772619 | C | CT | 15 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0005g0254 others(12): Show |
17 | HG00423.hp2 HG00733.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.123+4408dupT | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 97772619 | ||||||
chr3:97772619 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.123+4389C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97772619 | |||||||
chr3:97772748 | A | C | 1 | a0001c0001t0001g0209 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.123+4518A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97772748 | |||||||
chr3:97772817 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123+4587C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97772817 | |||||||
chr3:97772911 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.123+4681C>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97772911 | |||||||
chr3:97773038 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.123+4808G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97773038 | |||||||
chr3:97773178 | A | G | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.123+4948A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97773178 | |||||||
chr3:97773399 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0209 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.123+5169C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97773399 | |||||||
chr3:97773574 | C | T | 1 | a0001c0001t0015g0247 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.123+5344C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97773574 | |||||||
chr3:97773713 | T | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG02109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.123+5483T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97773713 | |||||||
chr3:97773751 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.123+5521G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97773751 | |||||||
chr3:97774213 | A | C | 1 | a0001c0001t0001g0166 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.124-5946A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97774213 | |||||||
chr3:97774284 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | NA18984.hp1 NA19058.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.124-5875C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97774284 | |||||||
chr3:97774346 | A | G | 2 | a0001c0001t0012g0070 a0001c0001t0012g0071 |
2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.124-5813A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97774346 | |||||||
chr3:97774360 | C | T | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.124-5799C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97774360 | |||||||
chr3:97774364 | G | GTGC | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.124-5795_124-5794i others(5): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97774364 | |||||||
chr3:97774365 | G | T | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.124-5794G>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97774365 | |||||||
chr3:97774367 | A | C | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.124-5792A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97774367 | |||||||
chr3:97774369 | T | A | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.124-5790T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97774369 | |||||||
chr3:97774372 | G | GGA | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.124-5786_124-5785i others(4): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 97774372 | ||||||
chr3:97774431 | T | C | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.124-5728T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97774431 | |||||||
chr3:97774501 | T | G | 5 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(2): Show |
5 | HG00733.hp2 HG02165.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-5658T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97774501 | |||||||
chr3:97774727 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.124-5432T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97774727 | |||||||
chr3:97774871 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.124-5288T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97774871 | |||||||
chr3:97775127 | C | T | 1 | a0001c0001t0022g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.124-5032C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97775127 | |||||||
chr3:97775158 | C | G | 1 | a0001c0001t0001g0165 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.124-5001C>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97775158 | |||||||
chr3:97775178 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.124-4981C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97775178 | |||||||
chr3:97775270 | G | T | 2 | a0001c0001t0001g0019 a0001c0001t0017g0019 |
3 | HG01106.hp2 HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.124-4889G>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97775270 | |||||||
chr3:97775353 | C | T | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.124-4806C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97775353 | |||||||
chr3:97775392 | G | A | 1 | a0001c0001t0022g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.124-4767G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97775392 | |||||||
chr3:97775443 | AG | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.124-4715delG | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97775443 | |||||||
chr3:97775586 | C | T | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.124-4573C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97775586 | |||||||
chr3:97775654 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.124-4505A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97775654 | |||||||
chr3:97775811 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(183): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.124-4348T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97775811 | |||||||
chr3:97775854 | A | G | 1 | a0001c0001t0007g0027 | 2 | NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.124-4305A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97775854 | |||||||
chr3:97775861 | A | G | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.124-4298A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97775861 | |||||||
chr3:97775912 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.124-4247G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97775912 | |||||||
chr3:97776299 | G | A | 13 | a0001c0001t0001g0197 a0001c0001t0006g0067 a0001c0001t0006g0068 others(10): Show |
15 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.124-3860G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97776299 | |||||||
chr3:97776386 | A | G | 1 | a0001c0001t0002g0051 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.124-3773A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97776386 | |||||||
chr3:97776399 | G | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0031 others(25): Show |
39 | HG01175.hp1 HG01256.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.124-3760G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97776399 | |||||||
chr3:97776468 | T | G | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.124-3691T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97776468 | |||||||
chr3:97776662 | A | AT | 42 | a0001c0001t0001g0097 a0001c0001t0002g0009 a0001c0001t0002g0018 others(39): Show |
57 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.124-3485dupT | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 97776662 | ||||||
chr3:97776662 | A | T | 1 | a0001c0001t0022g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.124-3497A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97776662 | |||||||
chr3:97776666 | T | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.124-3493T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97776666 | |||||||
chr3:97776750 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.124-3409G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97776750 | |||||||
chr3:97776948 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0017g0019 |
3 | HG01106.hp2 HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.124-3211C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97776948 | |||||||
chr3:97777097 | A | C | 1 | a0001c0001t0002g0237 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.124-3062A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97777097 | |||||||
chr3:97777185 | C | A | 3 | a0001c0001t0003g0006 a0001c0001t0003g0034 a0001c0001t0003g0123 |
7 | HG02004.hp2 HG02300.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-2974C>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97777185 | |||||||
chr3:97777713 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.124-2446G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97777713 | |||||||
chr3:97777811 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.124-2348A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97777811 | |||||||
chr3:97777825 | G | T | 55 | a0001c0001t0002g0009 a0001c0001t0002g0018 a0001c0001t0002g0022 others(52): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.124-2334G>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97777825 | |||||||
chr3:97777991 | A | G | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.124-2168A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97777991 | |||||||
chr3:97778078 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.124-2081G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97778078 | |||||||
chr3:97778098 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.124-2061A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97778098 | |||||||
chr3:97778248 | G | A | 6 | a0001c0001t0004g0045 a0001c0001t0004g0046 a0001c0001t0004g0047 others(3): Show |
9 | HG00738.hp2 HG01168.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.124-1911G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97778248 | |||||||
chr3:97778364 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.124-1795G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97778364 | |||||||
chr3:97778961 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.124-1198G>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97778961 | |||||||
chr3:97779091 | A | C | 1 | a0001c0001t0001g0225 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.124-1068A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97779091 | |||||||
chr3:97779120 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.124-1039T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97779120 | |||||||
chr3:97779126 | C | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.124-1033C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97779126 | |||||||
chr3:97779168 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.124-991T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97779168 | |||||||
chr3:97779198 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.124-961G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97779198 | |||||||
chr3:97779308 | A | G | 12 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0110 others(9): Show |
16 | HG01175.hp1 HG02451.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.124-851A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97779308 | |||||||
chr3:97779559 | C | A | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.124-600C>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97779559 | |||||||
chr3:97779637 | C | T | 1 | a0001c0001t0022g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.124-522C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97779637 | |||||||
chr3:97779735 | G | A | 55 | a0001c0001t0002g0009 a0001c0001t0002g0018 a0001c0001t0002g0022 others(52): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.124-424G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97779735 | |||||||
chr3:97779865 | C | CA | 11 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0001t0001g0128 others(8): Show |
12 | HG00140.hp2 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-280dupA | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 97779865 | ||||||
chr3:97780017 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124-142A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 2/7 | chr3 | 97780017 | |||||||
chr3:97780305 | A | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0230 |
7 | HG00642.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+85A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 3/7 | chr3 | 97780305 | |||||||
chr3:97780502 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.186-113C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 3/7 | chr3 | 97780502 | |||||||
chr3:97780597 | T | C | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.186-18T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 3/7 | chr3 | 97780597 | |||||||
chr3:97780787 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.254+104A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97780787 | |||||||
chr3:97780810 | T | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.254+127T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97780810 | |||||||
chr3:97780822 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.254+139T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97780822 | |||||||
chr3:97780885 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.254+202T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97780885 | |||||||
chr3:97780993 | T | C | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.254+310T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97780993 | |||||||
chr3:97781024 | T | C | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.254+341T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97781024 | |||||||
chr3:97781214 | A | AT | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.254+534dupT | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 97781214 | ||||||
chr3:97781269 | T | C | 2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | HG01169.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.254+586T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97781269 | |||||||
chr3:97781299 | A | G | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.254+616A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97781299 | |||||||
chr3:97781300 | GTCAAGTG others(44): Show |
G | 10 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(7): Show |
11 | HG00423.hp2 HG00733.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.254+620_254+670del others(51): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 97781300 | ||||||
chr3:97781384 | T | C | 1 | a0001c0001t0001g0249 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.254+701T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97781384 | |||||||
chr3:97781475 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(183): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.254+792A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97781475 | |||||||
chr3:97781492 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.254+809C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97781492 | |||||||
chr3:97781569 | T | G | 28 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0031 others(25): Show |
39 | HG01175.hp1 HG01256.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.254+886T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97781569 | |||||||
chr3:97781640 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0017g0019 |
3 | HG01106.hp2 HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.254+957C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97781640 | |||||||
chr3:97781641 | G | A | 4 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0209 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.254+958G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97781641 | |||||||
chr3:97781690 | A | T | 55 | a0001c0001t0002g0009 a0001c0001t0002g0018 a0001c0001t0002g0022 others(52): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.254+1007A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97781690 | |||||||
chr3:97782210 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.254+1527T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97782210 | |||||||
chr3:97782294 | A | C | 2 | a0001c0001t0003g0160 a0001c0001t0003g0161 |
2 | NA18998.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.254+1611A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97782294 | |||||||
chr3:97782304 | T | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(41): Show |
60 | HG00323.hp2 HG00423.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.254+1621T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97782304 | |||||||
chr3:97782431 | A | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0209 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.254+1748A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97782431 | |||||||
chr3:97782474 | T | C | 1 | a0001c0001t0022g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.254+1791T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97782474 | |||||||
chr3:97782511 | A | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0209 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.254+1828A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97782511 | |||||||
chr3:97782522 | T | C | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | NA18984.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.254+1839T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97782522 | |||||||
chr3:97782598 | T | C | 1 | a0001c0001t0002g0191 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.254+1915T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97782598 | |||||||
chr3:97782646 | A | C | 1 | a0001c0001t0001g0159 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.254+1963A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97782646 | |||||||
chr3:97782825 | T | TA | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.255-2118dupA | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 97782825 | ||||||
chr3:97783027 | A | G | 1 | a0001c0001t0006g0069 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.255-1928A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783027 | |||||||
chr3:97783049 | A | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0209 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.255-1906A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783049 | |||||||
chr3:97783079 | A | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0167 |
2 | HG00639.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.255-1876A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783079 | |||||||
chr3:97783285 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.255-1670A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783285 | |||||||
chr3:97783418 | A | C | 1 | a0001c0001t0001g0157 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.255-1537A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783418 | |||||||
chr3:97783434 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.255-1521T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783434 | |||||||
chr3:97783526 | G | A | 1 | a0001c0001t0020g0076 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.255-1429G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783526 | |||||||
chr3:97783576 | T | G | 11 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0110 others(8): Show |
12 | HG01175.hp1 HG02451.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.255-1379T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783576 | |||||||
chr3:97783592 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.255-1363T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783592 | |||||||
chr3:97783628 | G | A | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.255-1327G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783628 | |||||||
chr3:97783677 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.255-1278T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783677 | |||||||
chr3:97783684 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.255-1271A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783684 | |||||||
chr3:97783700 | G | A | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.255-1255G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783700 | |||||||
chr3:97783761 | T | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.255-1194T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783761 | |||||||
chr3:97783824 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.255-1131T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783824 | |||||||
chr3:97783842 | G | C | 1 | a0001c0001t0002g0210 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.255-1113G>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783842 | |||||||
chr3:97783859 | G | C | 1 | a0001c0001t0001g0078 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.255-1096G>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97783859 | |||||||
chr3:97784037 | C | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA19009.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.255-918C>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97784037 | |||||||
chr3:97784427 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.255-528A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97784427 | |||||||
chr3:97784480 | T | TA | 6 | a0001c0001t0001g0087 a0001c0001t0001g0132 a0001c0001t0001g0168 others(3): Show |
6 | HG02055.hp2 HG03654.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.255-461dupA | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 97784480 | ||||||
chr3:97784480 | T | TAA | 10 | a0001c0001t0006g0067 a0001c0001t0006g0069 a0001c0001t0006g0119 others(7): Show |
12 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.255-462_255-461dup others(2): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 97784480 | ||||||
chr3:97784906 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.255-49A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | chr3 | 97784906 | |||||||
chr3:97785323 | A | ATAAT | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(183): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.349+275_349+276ins others(4): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 97785323 | ||||||
chr3:97785335 | CA | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.349+302delA | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 97785335 | ||||||
chr3:97785448 | TTG | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.349+407_349+408del others(2): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 97785448 | ||||||
chr3:97785487 | CAT | C | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.349+457_349+458del others(2): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 97785487 | ||||||
chr3:97785563 | A | G | 1 | a0001c0001t0004g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.349+514A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97785563 | |||||||
chr3:97785753 | G | A | 2 | a0001c0001t0002g0104 a0001c0001t0002g0105 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.349+704G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97785753 | |||||||
chr3:97785777 | G | C | 1 | a0001c0001t0003g0142 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.349+728G>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97785777 | |||||||
chr3:97786016 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0209 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.349+967C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97786016 | |||||||
chr3:97786125 | T | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0230 |
7 | HG00642.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+1076T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97786125 | |||||||
chr3:97786169 | G | A | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.349+1120G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97786169 | |||||||
chr3:97786381 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0115 a0001c0001t0023g0114 |
4 | HG01256.hp1 HG01975.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+1332G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97786381 | |||||||
chr3:97786441 | T | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(183): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.349+1392T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97786441 | |||||||
chr3:97786604 | T | C | 1 | a0001c0001t0003g0034 | 2 | HG02004.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.350-1386T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97786604 | |||||||
chr3:97786638 | T | A | 2 | a0001c0001t0005g0143 a0001c0001t0005g0254 |
2 | HG01070.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.350-1352T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97786638 | |||||||
chr3:97786785 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0230 |
7 | HG00642.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-1205G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97786785 | |||||||
chr3:97786803 | G | A | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-1187G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97786803 | |||||||
chr3:97786945 | C | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0115 a0001c0001t0023g0114 |
4 | HG01256.hp1 HG01975.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-1045C>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97786945 | |||||||
chr3:97787104 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.350-886C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97787104 | |||||||
chr3:97787273 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.350-717T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97787273 | |||||||
chr3:97787599 | A | T | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-391A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97787599 | |||||||
chr3:97787670 | C | A | 13 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(10): Show |
15 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.350-320C>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97787670 | |||||||
chr3:97787718 | T | A | 4 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0198 others(1): Show |
4 | HG02615.hp1 HG02809.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-272T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 5/7 | chr3 | 97787718 | |||||||
chr3:97788268 | T | A | 1 | a0001c0001t0004g0169 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.479+149T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97788268 | |||||||
chr3:97788345 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0017g0019 |
3 | HG01106.hp2 HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.479+226T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97788345 | |||||||
chr3:97788348 | T | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0230 |
7 | HG00642.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.479+229T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97788348 | |||||||
chr3:97788447 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.479+328C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97788447 | |||||||
chr3:97788466 | T | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0200 others(2): Show |
8 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.479+347T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97788466 | |||||||
chr3:97788614 | T | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(228): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.479+495T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97788614 | |||||||
chr3:97788642 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.479+523G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97788642 | |||||||
chr3:97788675 | A | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.479+556A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97788675 | |||||||
chr3:97788687 | T | A | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.479+568T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97788687 | |||||||
chr3:97788950 | C | A | 1 | a0001c0001t0004g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.479+831C>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97788950 | |||||||
chr3:97789095 | G | A | 12 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(9): Show |
14 | HG00423.hp2 HG00733.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.479+976G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97789095 | |||||||
chr3:97789248 | G | A | 55 | a0001c0001t0002g0009 a0001c0001t0002g0018 a0001c0001t0002g0022 others(52): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.479+1129G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97789248 | |||||||
chr3:97789430 | C | T | 1 | a0001c0001t0022g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.479+1311C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97789430 | |||||||
chr3:97789488 | C | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0144 |
3 | NA18950.hp2 NA18968.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.479+1369C>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97789488 | |||||||
chr3:97789509 | A | G | 10 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(7): Show |
11 | HG00423.hp2 HG00733.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.479+1390A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97789509 | |||||||
chr3:97789547 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.479+1428A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97789547 | |||||||
chr3:97789597 | A | C | 10 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(7): Show |
11 | HG00423.hp2 HG00733.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.479+1478A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97789597 | |||||||
chr3:97789699 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.479+1580A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97789699 | |||||||
chr3:97789856 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.479+1737C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97789856 | |||||||
chr3:97789926 | T | TA | 113 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.479+1810dupA | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 97789926 | ||||||
chr3:97789941 | T | G | 4 | a0001c0001t0001g0087 a0001c0001t0001g0108 a0001c0001t0001g0217 others(1): Show |
4 | HG01884.hp2 HG02717.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.479+1822T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97789941 | |||||||
chr3:97790051 | T | TTG | 44 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0041 others(41): Show |
54 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.480-1681_480-1680d others(4): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 97790051 | ||||||
chr3:97790051 | T | TTGTG | 51 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(48): Show |
65 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.480-1683_480-1680d others(6): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 97790051 | ||||||
chr3:97790051 | T | TTGTGTG | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(23): Show |
39 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.480-1685_480-1680d others(8): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 97790051 | ||||||
chr3:97790051 | T | TTGTGTGT others(1): Show |
13 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0078 others(10): Show |
16 | HG00423.hp1 HG01255.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.480-1687_480-1680d others(10): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 97790051 | ||||||
chr3:97790051 | T | TTGTGTGT others(3): Show |
4 | a0001c0001t0001g0036 a0001c0001t0001g0084 a0001c0001t0001g0140 others(1): Show |
5 | HG01346.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.480-1689_480-1680d others(12): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 97790051 | ||||||
chr3:97790051 | T | TTGTGTGT others(5): Show |
1 | a0001c0001t0001g0033 | 2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.480-1691_480-1680d others(14): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 97790051 | ||||||
chr3:97790051 | TTG | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0030 others(16): Show |
24 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(21): Show |
intron_variant | MODIFIER | c.480-1681_480-1680d others(4): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 97790051 | ||||||
chr3:97790051 | TTGTG | T | 7 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0100 others(4): Show |
7 | HG01256.hp1 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.480-1683_480-1680d others(6): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 97790051 | ||||||
chr3:97790051 | TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0001g0240 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.480-1689_480-1680d others(12): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 97790051 | ||||||
chr3:97790085 | G | A | 1 | a0001c0001t0022g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.480-1686G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97790085 | |||||||
chr3:97790141 | A | C | 1 | a0001c0001t0001g0012 | 3 | HG03130.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.480-1630A>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97790141 | |||||||
chr3:97790202 | TAAGAG | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.480-1566_480-1562d others(7): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 97790202 | ||||||
chr3:97790388 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.480-1383G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97790388 | |||||||
chr3:97790791 | A | T | 1 | a0001c0001t0001g0185 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.480-980A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97790791 | |||||||
chr3:97790888 | A | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.480-883A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97790888 | |||||||
chr3:97790899 | C | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0230 |
7 | HG00642.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.480-872C>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97790899 | |||||||
chr3:97791015 | C | A | 1 | a0001c0001t0001g0163 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.480-756C>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97791015 | |||||||
chr3:97791073 | C | A | 1 | a0001c0001t0022g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.480-698C>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97791073 | |||||||
chr3:97791732 | G | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.480-39G>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97791732 | |||||||
chr3:97791763 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
splice_region_variant&intron_variant | LOW | c.480-8C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 6/7 | chr3 | 97791763 | |||||||
chr3:97791904 | TTATTA | T | 10 | a0001c0001t0006g0067 a0001c0001t0006g0068 a0001c0001t0006g0069 others(7): Show |
11 | HG00423.hp2 HG00733.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.535+82_535+86delTA others(3): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 97791904 | ||||||
chr3:97791906 | A | G | 30 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0019 others(27): Show |
42 | HG01106.hp2 HG01175.hp1 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.535+80A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97791906 | |||||||
chr3:97792259 | C | T | 1 | a0001c0001t0008g0005 | 4 | HG02976.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.535+433C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97792259 | |||||||
chr3:97792260 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0188 |
2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.535+434G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97792260 | |||||||
chr3:97792289 | C | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.535+463C>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97792289 | |||||||
chr3:97792317 | T | A | 1 | a0001c0001t0003g0123 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.535+491T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97792317 | |||||||
chr3:97792406 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.535+580C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97792406 | |||||||
chr3:97792510 | A | G | 9 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0080 others(6): Show |
9 | HG01891.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.535+684A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97792510 | |||||||
chr3:97792640 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.535+814G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97792640 | |||||||
chr3:97792713 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0165 |
2 | NA18944.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.535+887C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97792713 | |||||||
chr3:97792870 | G | GA | 9 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0111 others(6): Show |
10 | HG01175.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.535+1046dupA | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 97792870 | ||||||
chr3:97792934 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.535+1108A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97792934 | |||||||
chr3:97792976 | A | T | 2 | a0001c0001t0002g0053 a0001c0001t0002g0086 |
3 | HG00280.hp2 HG00323.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.535+1150A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97792976 | |||||||
chr3:97792978 | ATCT | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0074 |
3 | HG02622.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.535+1156_535+1158d others(5): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 97792978 | ||||||
chr3:97793083 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.535+1257C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97793083 | |||||||
chr3:97793084 | G | A | 2 | a0001c0001t0002g0227 a0001c0001t0002g0228 |
2 | NA19004.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.535+1258G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97793084 | |||||||
chr3:97793223 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.535+1397G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97793223 | |||||||
chr3:97793245 | A | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.535+1419A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97793245 | |||||||
chr3:97793272 | A | G | 2 | a0001c0001t0002g0104 a0001c0001t0002g0105 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.535+1446A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97793272 | |||||||
chr3:97793541 | T | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.535+1715T>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97793541 | |||||||
chr3:97793576 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.535+1750C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97793576 | |||||||
chr3:97793621 | A | G | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0165 |
3 | NA18944.hp2 NA19010.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.535+1795A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97793621 | |||||||
chr3:97793861 | GA | G | 11 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0001t0001g0079 others(8): Show |
13 | HG00558.hp2 HG00597.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.535+2047delA | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 97793861 | ||||||
chr3:97793912 | A | G | 54 | a0001c0001t0002g0009 a0001c0001t0002g0018 a0001c0001t0002g0022 others(51): Show |
70 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.535+2086A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97793912 | |||||||
chr3:97794110 | G | A | 9 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0080 others(6): Show |
9 | HG01891.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.535+2284G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97794110 | |||||||
chr3:97794177 | T | TTG | 103 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(100): Show |
143 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.535+2391_535+2392d others(4): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 97794177 | ||||||
chr3:97794177 | T | TTGTG | 71 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(68): Show |
94 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.535+2389_535+2392d others(6): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 97794177 | ||||||
chr3:97794177 | T | TTGTGTG | 23 | a0001c0001t0001g0017 a0001c0001t0001g0078 a0001c0001t0001g0080 others(20): Show |
26 | HG00423.hp2 HG00733.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.535+2387_535+2392d others(8): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 97794177 | ||||||
chr3:97794177 | T | TTGTGTGT others(1): Show |
12 | a0001c0001t0001g0037 a0001c0001t0001g0144 a0001c0001t0001g0152 others(9): Show |
13 | HG03195.hp2 HG03654.hp2 NA18942.hp2 others(10): Show |
intron_variant | MODIFIER | c.535+2385_535+2392d others(10): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 97794177 | ||||||
chr3:97794177 | T | TTGTGTGT others(3): Show |
3 | a0001c0001t0001g0019 a0001c0001t0003g0160 a0001c0001t0017g0019 |
4 | HG01106.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+2383_535+2392d others(12): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 97794177 | ||||||
chr3:97794177 | T | TTGTGTGT others(5): Show |
4 | a0001c0001t0001g0113 a0001c0001t0001g0147 a0001c0001t0001g0156 others(1): Show |
4 | HG02622.hp1 NA18964.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+2381_535+2392d others(14): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 97794177 | ||||||
chr3:97794177 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0001g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.535+2379_535+2392d others(16): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 97794177 | ||||||
chr3:97794177 | TTG | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0184 a0001c0001t0001g0225 others(10): Show |
21 | HG00642.hp2 HG01071.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.535+2391_535+2392d others(4): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 97794177 | ||||||
chr3:97794205 | GTGTGTGT others(7): Show |
G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.535+2381_535+2394d others(16): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 97794205 | ||||||
chr3:97794219 | T | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0238 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.535+2393T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97794219 | |||||||
chr3:97794438 | A | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.535+2612A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97794438 | |||||||
chr3:97794803 | G | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0230 |
7 | HG00642.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.535+2977G>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97794803 | |||||||
chr3:97794882 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0115 |
3 | HG01256.hp1 HG01975.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.535+3056T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97794882 | |||||||
chr3:97794883 | C | A | 1 | a0001c0001t0003g0042 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.535+3057C>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97794883 | |||||||
chr3:97795076 | A | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.536-2948A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97795076 | |||||||
chr3:97795095 | T | G | 1 | a0001c0001t0002g0193 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.536-2929T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97795095 | |||||||
chr3:97795374 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.536-2650G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97795374 | |||||||
chr3:97795422 | A | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(43): Show |
64 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.536-2602A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97795422 | |||||||
chr3:97795640 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.536-2384A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97795640 | |||||||
chr3:97795723 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0209 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.536-2301C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97795723 | |||||||
chr3:97795866 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.536-2158G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97795866 | |||||||
chr3:97795911 | G | C | 1 | a0001c0001t0002g0065 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.536-2113G>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97795911 | |||||||
chr3:97796099 | A | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.536-1925A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97796099 | |||||||
chr3:97796213 | C | G | 1 | a0001c0001t0002g0051 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.536-1811C>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97796213 | |||||||
chr3:97796246 | C | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.536-1778C>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97796246 | |||||||
chr3:97796263 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.536-1761G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97796263 | |||||||
chr3:97796355 | A | T | 1 | a0001c0001t0001g0136 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.536-1669A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97796355 | |||||||
chr3:97796452 | A | G | 30 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0019 others(27): Show |
42 | HG01106.hp2 HG01175.hp1 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.536-1572A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97796452 | |||||||
chr3:97796558 | C | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.536-1466C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97796558 | |||||||
chr3:97796575 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.536-1449A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97796575 | |||||||
chr3:97796600 | A | G | 1 | a0001c0001t0002g0210 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.536-1424A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97796600 | |||||||
chr3:97796684 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.536-1340G>A | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97796684 | |||||||
chr3:97797051 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.536-973C>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97797051 | |||||||
chr3:97797156 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.536-868A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97797156 | |||||||
chr3:97797209 | T | G | 1 | a0001c0001t0001g0136 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.536-815T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97797209 | |||||||
chr3:97797307 | A | G | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.536-717A>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97797307 | |||||||
chr3:97797319 | A | T | 1 | a0001c0001t0001g0136 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.536-705A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97797319 | |||||||
chr3:97797424 | G | T | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.536-600G>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97797424 | |||||||
chr3:97797448 | T | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0059 |
3 | HG02145.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.536-576T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97797448 | |||||||
chr3:97797781 | T | G | 1 | a0001c0001t0001g0136 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.536-243T>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97797781 | |||||||
chr3:97797816 | A | T | 1 | a0001c0001t0020g0076 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.536-208A>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97797816 | |||||||
chr3:97797817 | G | T | 1 | a0001c0001t0020g0076 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.536-207G>T | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97797817 | |||||||
chr3:97797821 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.536-203T>C | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97797821 | |||||||
chr3:97797888 | C | G | 13 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0080 others(10): Show |
14 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.536-136C>G | ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 7/7 | chr3 | 97797888 |