Item | Value |
---|---|
geneid | 84944 |
ensemblid | ENSG00000143194.13 |
hgncid | 25929 |
symbol | MAEL |
name | maelstrom spermatogenic transposon silencer |
refseq_nuc | NM_032858.3 |
refseq_prot | NP_116247.1 |
ensembl_nuc | ENST00000367872.9 |
ensembl_prot | ENSP00000356846.4 |
mane_status | MANE Select |
chr | chr1 |
start | 166989280 |
end | 167022214 |
strand | + |
ver | v1.2 |
region | chr1:166989280-167022214 |
region5000 | chr1:166984280-167027214 |
regionname0 | MAEL_chr1_166989280_167022214 |
regionname5000 | MAEL_chr1_166984280_167027214 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 434 | 278 | 53 | 56 | 127 | 13 | 29 | 101 | MAEL_chr1_166984280_167027214 | MAEL | MPNRK others(429): Show |
chr1 | 166984280 | 167027214 |
a0002 | 0/0 | 434 | 123 | 35 | 16 | 60 | 1 | 11 | 50 | MAEL_chr1_166984280_167027214 | MAEL | MPNRK others(429): Show |
chr1 | 166984280 | 167027214 |
a0003 | 0/0 | 434 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | MPNRK others(429): Show |
chr1 | 166984280 | 167027214 |
a0004 | 0/0 | 434 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | MPNRK others(429): Show |
chr1 | 166984280 | 167027214 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1302 | 254 | 32 | 53 | 127 | 13 | 29 | MAEL_chr1_166984280_167027214 | MAEL | ATGCC others(1297): Show |
chr1 | 166984280 | 167027214 | ||
a0001c0003 | 0/0 | 1302 | 21 | 21 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ATGCC others(1297): Show |
chr1 | 166984280 | 167027214 | ||
a0001c0005 | 0/0 | 1302 | 3 | 0 | 3 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ATGCC others(1297): Show |
chr1 | 166984280 | 167027214 | ||
a0002c0002 | 0/0 | 1302 | 120 | 34 | 16 | 58 | 1 | 11 | MAEL_chr1_166984280_167027214 | MAEL | ATGCC others(1297): Show |
chr1 | 166984280 | 167027214 | ||
a0002c0006 | 0/0 | 1302 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ATGCC others(1297): Show |
chr1 | 166984280 | 167027214 | ||
a0002c0008 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ATGCC others(1297): Show |
chr1 | 166984280 | 167027214 | ||
a0003c0004 | 0/0 | 1302 | 4 | 4 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ATGCC others(1297): Show |
chr1 | 166984280 | 167027214 | ||
a0004c0007 | 0/0 | 1302 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ATGCC others(1297): Show |
chr1 | 166984280 | 167027214 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1737 | 254 | 32 | 53 | 127 | 13 | 29 | MAEL_chr1_166984280_167027214 | MAEL | ACTTA others(1732): Show |
chr1 | 166984280 | 167027214 |
a0001c0003t0001 | 0/0 | 1737 | 21 | 21 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ACTTA others(1732): Show |
chr1 | 166984280 | 167027214 |
a0001c0005t0001 | 0/0 | 1737 | 3 | 0 | 3 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ACTTA others(1732): Show |
chr1 | 166984280 | 167027214 |
a0002c0002t0001 | 0/0 | 1737 | 117 | 33 | 16 | 56 | 1 | 11 | MAEL_chr1_166984280_167027214 | MAEL | ACTTA others(1732): Show |
chr1 | 166984280 | 167027214 |
a0002c0002t0002 | 0/0 | 1737 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ACTTA others(1732): Show |
chr1 | 166984280 | 167027214 |
a0002c0002t0003 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ACTTA others(1732): Show |
chr1 | 166984280 | 167027214 |
a0002c0006t0001 | 0/0 | 1737 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ACTTA others(1732): Show |
chr1 | 166984280 | 167027214 |
a0002c0008t0005 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ACTTA others(1732): Show |
chr1 | 166984280 | 167027214 |
a0003c0004t0001 | 0/0 | 1737 | 3 | 3 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ACTTA others(1732): Show |
chr1 | 166984280 | 167027214 |
a0003c0004t0004 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ACTTA others(1732): Show |
chr1 | 166984280 | 167027214 |
a0004c0007t0001 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | ACTTA others(1732): Show |
chr1 | 166984280 | 167027214 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 17 | 1 | 1 | 13 | 0 | 2 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0004 | 0/0 | 9 | 1 | 7 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0009 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0014 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0003t0001g0006 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0003t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0001c0005t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0002 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0003 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0005 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0012 | 0/0 | 5 | 0 | 0 | 0 | 0 | 5 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0023 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0002t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0006t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0002c0008t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0003c0004t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0003c0004t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0003c0004t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0003c0004t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
a0004c0007t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | GBR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | FIN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | FIN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00639 | hp1 | a0001 | c0005 | t0001 | g0007 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01070 | hp1 | a0001 | c0005 | t0001 | g0007 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0149 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0141 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0261 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01192 | hp1 | a0001 | c0005 | t0001 | g0007 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0057 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0229 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | IBS | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0228 | EUR | IBS | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0235 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0227 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0205 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CDX | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CDX | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CDX | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0241 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0202 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0133 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0226 | AMR | PEL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0049 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0201 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0232 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0256 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0225 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0239 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0044 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0198 | AFR | ESN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02922 | hp2 | a0003 | c0004 | t0001 | g0156 | AFR | ESN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0252 | AFR | ESN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0208 | AFR | ESN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0012 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0251 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03098 | hp1 | a0003 | c0004 | t0004 | g0159 | AFR | MSL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0204 | AFR | MSL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | ESN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0258 | AFR | ESN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0263 | AFR | MSL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0044 | AFR | MSL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0242 | AFR | MSL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0203 | AFR | MSL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | MSL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0012 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0012 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03516 | hp1 | a0003 | c0004 | t0001 | g0158 | AFR | ESN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | ESN | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03540 | hp2 | a0002 | c0002 | t0003 | g0265 | AFR | GWD | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0197 | AFR | MSL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0264 | AFR | MSL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0247 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0012 | SAS | STU | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0219 | SAS | BEB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | BEB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | YRI | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18522 | hp2 | a0001 | c0003 | t0001 | g0199 | AFR | YRI | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | CHB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | CHB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18906 | hp2 | a0003 | c0004 | t0001 | g0152 | AFR | YRI | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18947 | hp1 | a0002 | c0006 | t0001 | g0070 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18987 | hp2 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0243 | AFR | LWK | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19055 | hp2 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19058 | hp2 | a0004 | c0007 | t0001 | g0217 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19072 | hp1 | a0002 | c0006 | t0001 | g0066 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | YRI | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | ASW | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0255 | AFR | ASW | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | TSI | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | TSI | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0012 | SAS | GIH | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | GIH | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02109 | hp1 | a0002 | c0008 | t0005 | g0262 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0253 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0260 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0207 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0257 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | ACB | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | MSL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | MSL | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0213 | AFR | USA | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0200 | AFR | USA | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0254 | AFR | USA | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0259 | AFR | LWK | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | MAEL_chr1_166984280_167027214 | MAEL | chr1 | 166984280 | 167027214 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:166989473 | T | G | 2 | a0002 a0004 |
124 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(121): Show |
missense_variant | MODERATE | c.121T>G | p.Ser41Ala | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 1/12 | 194/1737 | 121/1305 | 41/434 | chr1 | 166989473 | |||
chr1:166989782 | G | C | 1 | a0004 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.178G>C | p.Glu60Gln | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 2/12 | 251/1737 | 178/1305 | 60/434 | chr1 | 166989782 | |||
chr1:167004291 | C | A | 1 | a0003 | 4 | HG02922.hp2 HG03098.hp1 HG03516.hp1 others(1): Show |
missense_variant | MODERATE | c.635C>A | p.Pro212His | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 6/12 | 708/1737 | 635/1305 | 212/434 | chr1 | 167004291 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:166989364 | T | C | 4 | a0001c0003 a0002c0002 a0002c0008 others(1): Show |
143 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(140): Show |
synonymous_variant | LOW | c.12T>C | p.Arg4Arg | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 1/12 | 85/1737 | 12/1305 | 4/434 | chr1 | 166989364 | |||
chr1:166989370 | C | G | 1 | a0001c0005 | 3 | HG00639.hp1 HG01070.hp1 HG01192.hp1 |
synonymous_variant | LOW | c.18C>G | p.Ala6Ala | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 1/12 | 91/1737 | 18/1305 | 6/434 | chr1 | 166989370 | |||
chr1:167017875 | A | G | 1 | a0002c0008 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.957A>G | p.Thr319Thr | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/12 | 1030/1737 | 957/1305 | 319/434 | chr1 | 167017875 | |||
chr1:167017956 | C | T | 1 | a0002c0008 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.1038C>T | p.Tyr346Tyr | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/12 | 1111/1737 | 1038/1305 | 346/434 | chr1 | 167017956 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:166989344 | C | T | 1 | a0002c0002t0002 | 2 | NA18987.hp2 NA19055.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-9C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 1/12 | chr1 | 166989344 | |||||||
chr1:167022018 | G | A | 1 | a0002c0002t0003 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*163G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 12/12 | 163 | chr1 | 167022018 | ||||||
chr1:167022099 | G | A | 1 | a0003c0004t0004 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*244G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 12/12 | 244 | chr1 | 167022099 | ||||||
chr1:167022175 | T | A | 1 | a0002c0008t0005 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*320T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 12/12 | 320 | chr1 | 167022175 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:166989589 | C | G | 19 | a0002c0002t0001g0005 a0002c0002t0001g0048 a0002c0002t0001g0049 others(16): Show |
29 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.132+105C>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 1/11 | chr1 | 166989589 | |||||||
chr1:166989621 | C | T | 4 | a0002c0002t0001g0263 a0002c0002t0001g0264 a0002c0002t0003g0265 others(1): Show |
4 | HG02109.hp1 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-116C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 1/11 | chr1 | 166989621 | |||||||
chr1:166989690 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.133-47G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 1/11 | chr1 | 166989690 | |||||||
chr1:166989700 | G | T | 69 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(66): Show |
118 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.133-37G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 1/11 | chr1 | 166989700 | |||||||
chr1:166989966 | TC | T | 3 | a0001c0003t0001g0044 a0001c0003t0001g0207 a0001c0003t0001g0208 |
4 | HG02486.hp2 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+141delC | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 166989966 | ||||||
chr1:166990043 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.225+214A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 2/11 | chr1 | 166990043 | |||||||
chr1:166990191 | T | TG | 53 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(50): Show |
91 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.225+368dupG | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 166990191 | ||||||
chr1:166990200 | G | A | 1 | a0002c0002t0001g0243 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.225+371G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 2/11 | chr1 | 166990200 | |||||||
chr1:166990218 | C | G | 55 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0003t0001g0207 others(52): Show |
93 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.225+389C>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 2/11 | chr1 | 166990218 | |||||||
chr1:166990348 | G | A | 5 | a0002c0002t0001g0250 a0002c0002t0001g0263 a0002c0002t0001g0264 others(2): Show |
5 | HG02109.hp1 HG03209.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+519G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 2/11 | chr1 | 166990348 | |||||||
chr1:166990525 | A | G | 30 | a0001c0003t0001g0006 a0001c0003t0001g0044 a0001c0003t0001g0197 others(27): Show |
49 | HG01081.hp2 HG01175.hp2 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.225+696A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 2/11 | chr1 | 166990525 | |||||||
chr1:166990653 | T | C | 54 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0003t0001g0006 others(51): Show |
100 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.226-725T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 2/11 | chr1 | 166990653 | |||||||
chr1:166990737 | A | G | 1 | a0002c0002t0001g0246 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.226-641A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 2/11 | chr1 | 166990737 | |||||||
chr1:166990833 | A | G | 72 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(69): Show |
124 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.226-545A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 2/11 | chr1 | 166990833 | |||||||
chr1:166990911 | G | T | 1 | a0001c0001t0001g0185 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.226-467G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 2/11 | chr1 | 166990911 | |||||||
chr1:166990917 | A | G | 3 | a0001c0003t0001g0207 a0001c0003t0001g0208 a0002c0002t0001g0251 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.226-461A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 2/11 | chr1 | 166990917 | |||||||
chr1:166991045 | A | C | 22 | a0001c0003t0001g0198 a0001c0003t0001g0199 a0001c0003t0001g0200 others(19): Show |
32 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.226-333A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 2/11 | chr1 | 166991045 | |||||||
chr1:166991567 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.325+90T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 3/11 | chr1 | 166991567 | |||||||
chr1:166991662 | G | GT | 15 | a0002c0002t0001g0005 a0002c0002t0001g0048 a0002c0002t0001g0049 others(12): Show |
25 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.325+195dupT | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 166991662 | ||||||
chr1:166991828 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.325+351C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 3/11 | chr1 | 166991828 | |||||||
chr1:166991893 | G | A | 4 | a0001c0003t0001g0198 a0001c0003t0001g0199 a0001c0003t0001g0200 others(1): Show |
4 | HG02572.hp2 HG02922.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+416G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 3/11 | chr1 | 166991893 | |||||||
chr1:166992027 | G | T | 1 | a0002c0002t0001g0046 | 2 | HG01081.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.325+550G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 3/11 | chr1 | 166992027 | |||||||
chr1:166992174 | G | A | 1 | a0002c0002t0001g0057 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.326-512G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 3/11 | chr1 | 166992174 | |||||||
chr1:166992247 | T | C | 94 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(91): Show |
156 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.326-439T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 3/11 | chr1 | 166992247 | |||||||
chr1:166992530 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.326-156G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 3/11 | chr1 | 166992530 | |||||||
chr1:166992620 | G | A | 72 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(69): Show |
124 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.326-66G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 3/11 | chr1 | 166992620 | |||||||
chr1:166993137 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.481+296G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 4/11 | chr1 | 166993137 | |||||||
chr1:166993302 | A | G | 2 | a0002c0002t0001g0264 a0002c0002t0003g0265 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.481+461A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 4/11 | chr1 | 166993302 | |||||||
chr1:166993366 | C | CTCT | 22 | a0001c0003t0001g0198 a0001c0003t0001g0199 a0001c0003t0001g0200 others(19): Show |
32 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.481+528_481+530dup others(3): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 166993366 | ||||||
chr1:166993441 | T | C | 46 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
68 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.482-587T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 4/11 | chr1 | 166993441 | |||||||
chr1:166993499 | A | G | 16 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(13): Show |
22 | HG00323.hp2 HG01081.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.482-529A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 4/11 | chr1 | 166993499 | |||||||
chr1:166993714 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0088 |
2 | NA18968.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.482-314A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 4/11 | chr1 | 166993714 | |||||||
chr1:166993749 | G | A | 1 | a0002c0002t0001g0241 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.482-279G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 4/11 | chr1 | 166993749 | |||||||
chr1:166993997 | T | C | 94 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(91): Show |
156 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.482-31T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 4/11 | chr1 | 166993997 | |||||||
chr1:166994243 | T | G | 1 | a0001c0001t0001g0059 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.523+174T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166994243 | |||||||
chr1:166994254 | T | C | 1 | a0002c0002t0001g0210 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.523+185T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166994254 | |||||||
chr1:166994441 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.523+372C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166994441 | |||||||
chr1:166994489 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.523+420C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166994489 | |||||||
chr1:166994589 | G | A | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+520G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166994589 | |||||||
chr1:166994613 | T | A | 21 | a0001c0003t0001g0198 a0001c0003t0001g0199 a0001c0003t0001g0200 others(18): Show |
31 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.523+544T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166994613 | |||||||
chr1:166994666 | A | AT | 73 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0053 others(70): Show |
120 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.523+619dupT | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 166994666 | ||||||
chr1:166994694 | G | A | 1 | a0002c0002t0001g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.523+625G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166994694 | |||||||
chr1:166994731 | G | A | 2 | a0001c0001t0001g0186 a0001c0003t0001g0044 |
3 | HG02280.hp1 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.523+662G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166994731 | |||||||
chr1:166994738 | T | C | 185 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(182): Show |
287 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.523+669T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166994738 | |||||||
chr1:166994880 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.523+811G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166994880 | |||||||
chr1:166994974 | A | AT | 42 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0039 others(39): Show |
50 | HG00323.hp2 HG00741.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.523+927dupT | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 166994974 | ||||||
chr1:166995002 | G | A | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+933G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995002 | |||||||
chr1:166995006 | C | T | 3 | a0001c0003t0001g0207 a0001c0003t0001g0208 a0002c0002t0001g0251 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.523+937C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995006 | |||||||
chr1:166995085 | T | C | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+1016T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995085 | |||||||
chr1:166995138 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0086 |
2 | NA18981.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.523+1069A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995138 | |||||||
chr1:166995290 | G | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1221G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995290 | |||||||
chr1:166995292 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1223G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995292 | |||||||
chr1:166995294 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1225G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995294 | |||||||
chr1:166995299 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1230G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995299 | |||||||
chr1:166995318 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1249G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995318 | |||||||
chr1:166995321 | A | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1252A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995321 | |||||||
chr1:166995324 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1255T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995324 | |||||||
chr1:166995326 | C | T | 1 | a0002c0002t0001g0233 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.523+1257C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995326 | |||||||
chr1:166995357 | C | T | 93 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(90): Show |
155 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.523+1288C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995357 | |||||||
chr1:166995383 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1314G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995383 | |||||||
chr1:166995387 | G | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1318G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995387 | |||||||
chr1:166995388 | C | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1319C>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995388 | |||||||
chr1:166995389 | A | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1320A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995389 | |||||||
chr1:166995398 | C | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1329C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995398 | |||||||
chr1:166995401 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1332G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995401 | |||||||
chr1:166995409 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1340T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995409 | |||||||
chr1:166995411 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1342G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995411 | |||||||
chr1:166995412 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1343T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995412 | |||||||
chr1:166995415 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1346T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995415 | |||||||
chr1:166995416 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1347T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995416 | |||||||
chr1:166995426 | C | A | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+1357C>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995426 | |||||||
chr1:166995427 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1358G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995427 | |||||||
chr1:166995428 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1359G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995428 | |||||||
chr1:166995429 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1360G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995429 | |||||||
chr1:166995431 | G | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1362G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995431 | |||||||
chr1:166995433 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1364T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995433 | |||||||
chr1:166995434 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1365T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995434 | |||||||
chr1:166995436 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1367T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995436 | |||||||
chr1:166995437 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.523+1368C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995437 | |||||||
chr1:166995503 | G | C | 93 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(90): Show |
155 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.523+1434G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995503 | |||||||
chr1:166995509 | G | A | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+1440G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995509 | |||||||
chr1:166995554 | T | C | 1 | a0002c0002t0001g0235 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.523+1485T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995554 | |||||||
chr1:166995584 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1515T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995584 | |||||||
chr1:166995585 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1516G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995585 | |||||||
chr1:166995586 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1517G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995586 | |||||||
chr1:166995589 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1520G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995589 | |||||||
chr1:166995592 | A | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1523A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995592 | |||||||
chr1:166995593 | A | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1524A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995593 | |||||||
chr1:166995595 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1526T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995595 | |||||||
chr1:166995596 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1527T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995596 | |||||||
chr1:166995598 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1529T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995598 | |||||||
chr1:166995599 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1530G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995599 | |||||||
chr1:166995600 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1531T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995600 | |||||||
chr1:166995603 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1534T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995603 | |||||||
chr1:166995654 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1585G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995654 | |||||||
chr1:166995655 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1586G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995655 | |||||||
chr1:166995660 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1591T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995660 | |||||||
chr1:166995661 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1592G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995661 | |||||||
chr1:166995665 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1596T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995665 | |||||||
chr1:166995667 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1598G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995667 | |||||||
chr1:166995671 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1602G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995671 | |||||||
chr1:166995674 | G | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1605G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995674 | |||||||
chr1:166995675 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1606T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995675 | |||||||
chr1:166995676 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1607T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995676 | |||||||
chr1:166995676 | T | TA | 83 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(80): Show |
145 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.523+1619dupA | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 166995676 | ||||||
chr1:166995683 | A | AT | 4 | a0001c0003t0001g0199 a0001c0003t0001g0200 a0001c0003t0001g0201 others(1): Show |
4 | HG02572.hp2 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+1614_523+1615i others(3): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995683 | |||||||
chr1:166995683 | A | T | 1 | a0001c0001t0001g0038 | 2 | NA18951.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.523+1614A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995683 | |||||||
chr1:166995689 | T | A | 3 | a0001c0003t0001g0198 a0002c0002t0001g0231 a0002c0002t0001g0237 |
3 | HG02922.hp1 NA19003.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.523+1620T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995689 | |||||||
chr1:166995690 | A | T | 4 | a0001c0001t0001g0166 a0001c0003t0001g0198 a0002c0002t0001g0231 others(1): Show |
4 | HG02145.hp2 HG02922.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.523+1621A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995690 | |||||||
chr1:166995740 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1671G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995740 | |||||||
chr1:166995752 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1683G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995752 | |||||||
chr1:166995753 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1684G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995753 | |||||||
chr1:166995756 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1687T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995756 | |||||||
chr1:166995764 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1695T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995764 | |||||||
chr1:166995765 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1696G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995765 | |||||||
chr1:166995776 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1707T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995776 | |||||||
chr1:166995777 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1708G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995777 | |||||||
chr1:166995778 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1709G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995778 | |||||||
chr1:166995785 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1716T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995785 | |||||||
chr1:166995814 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.523+1745C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995814 | |||||||
chr1:166995826 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1757T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995826 | |||||||
chr1:166995840 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1771T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995840 | |||||||
chr1:166995842 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1773T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995842 | |||||||
chr1:166995843 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1774T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995843 | |||||||
chr1:166995844 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1775T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995844 | |||||||
chr1:166995845 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1776T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995845 | |||||||
chr1:166995846 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1777G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995846 | |||||||
chr1:166995847 | A | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1778A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995847 | |||||||
chr1:166995848 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1779T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995848 | |||||||
chr1:166995849 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1780T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995849 | |||||||
chr1:166995851 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1782T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995851 | |||||||
chr1:166995852 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1783G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995852 | |||||||
chr1:166995853 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1784T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995853 | |||||||
chr1:166995854 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1785T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995854 | |||||||
chr1:166995856 | A | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1787A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995856 | |||||||
chr1:166995858 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1789T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995858 | |||||||
chr1:166995860 | C | G | 21 | a0001c0003t0001g0198 a0001c0003t0001g0199 a0001c0003t0001g0200 others(18): Show |
31 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.523+1791C>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995860 | |||||||
chr1:166995861 | T | G | 1 | a0001c0001t0001g0125 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.523+1792T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995861 | |||||||
chr1:166995871 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1802T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995871 | |||||||
chr1:166995887 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1818T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995887 | |||||||
chr1:166995888 | A | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1819A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995888 | |||||||
chr1:166995889 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1820T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995889 | |||||||
chr1:166995900 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1831T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995900 | |||||||
chr1:166995914 | A | G | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+1845A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995914 | |||||||
chr1:166995932 | G | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1863G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995932 | |||||||
chr1:166995951 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1882T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995951 | |||||||
chr1:166995952 | A | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1883A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995952 | |||||||
chr1:166995955 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1886G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995955 | |||||||
chr1:166995957 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1888T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995957 | |||||||
chr1:166995960 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1891T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995960 | |||||||
chr1:166995962 | G | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1893G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995962 | |||||||
chr1:166995965 | A | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1896A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995965 | |||||||
chr1:166995966 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1897T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995966 | |||||||
chr1:166995996 | A | C | 1 | a0001c0001t0001g0015 | 4 | HG00558.hp2 HG00609.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+1927A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166995996 | |||||||
chr1:166996013 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1944T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996013 | |||||||
chr1:166996023 | A | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1954A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996023 | |||||||
chr1:166996024 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1955G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996024 | |||||||
chr1:166996025 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1956G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996025 | |||||||
chr1:166996027 | A | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1958A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996027 | |||||||
chr1:166996030 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1961T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996030 | |||||||
chr1:166996031 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1962T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996031 | |||||||
chr1:166996034 | A | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1965A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996034 | |||||||
chr1:166996036 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1967T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996036 | |||||||
chr1:166996037 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1968G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996037 | |||||||
chr1:166996038 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1969T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996038 | |||||||
chr1:166996039 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1970T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996039 | |||||||
chr1:166996040 | T | C | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+1971T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996040 | |||||||
chr1:166996041 | G | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1972G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996041 | |||||||
chr1:166996042 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1973G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996042 | |||||||
chr1:166996044 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+1975G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996044 | |||||||
chr1:166996072 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2003G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996072 | |||||||
chr1:166996079 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2010T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996079 | |||||||
chr1:166996080 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2011G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996080 | |||||||
chr1:166996081 | A | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2012A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996081 | |||||||
chr1:166996082 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2013T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996082 | |||||||
chr1:166996085 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2016T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996085 | |||||||
chr1:166996086 | C | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2017C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996086 | |||||||
chr1:166996089 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2020G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996089 | |||||||
chr1:166996090 | G | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2021G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996090 | |||||||
chr1:166996091 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2022G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996091 | |||||||
chr1:166996093 | A | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2024A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996093 | |||||||
chr1:166996094 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.523+2025A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996094 | |||||||
chr1:166996098 | G | A | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+2029G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996098 | |||||||
chr1:166996100 | C | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2031C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996100 | |||||||
chr1:166996103 | T | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2034T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996103 | |||||||
chr1:166996106 | A | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2037A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996106 | |||||||
chr1:166996108 | T | G | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2039T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996108 | |||||||
chr1:166996111 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2042G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996111 | |||||||
chr1:166996114 | A | G | 1 | a0002c0002t0001g0046 | 2 | HG01081.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.523+2045A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996114 | |||||||
chr1:166996115 | A | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2046A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996115 | |||||||
chr1:166996117 | A | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2048A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996117 | |||||||
chr1:166996123 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2054T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996123 | |||||||
chr1:166996164 | A | G | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+2095A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996164 | |||||||
chr1:166996170 | A | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2101A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996170 | |||||||
chr1:166996171 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2102T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996171 | |||||||
chr1:166996172 | G | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2103G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996172 | |||||||
chr1:166996176 | T | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2107T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996176 | |||||||
chr1:166996180 | G | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2111G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996180 | |||||||
chr1:166996183 | G | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2114G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996183 | |||||||
chr1:166996188 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2119G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996188 | |||||||
chr1:166996189 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2120G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996189 | |||||||
chr1:166996191 | G | C | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2122G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996191 | |||||||
chr1:166996192 | G | A | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2123G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996192 | |||||||
chr1:166996217 | A | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523+2148A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996217 | |||||||
chr1:166996272 | G | A | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+2203G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996272 | |||||||
chr1:166996308 | T | A | 4 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+2239T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996308 | |||||||
chr1:166996350 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.523+2281T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996350 | |||||||
chr1:166996649 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.523+2580T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996649 | |||||||
chr1:166996722 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0126 |
3 | NA18949.hp2 NA18960.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.523+2653T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996722 | |||||||
chr1:166996768 | A | G | 94 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(91): Show |
156 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.523+2699A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166996768 | |||||||
chr1:166997095 | G | C | 44 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(41): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.523+3026G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166997095 | |||||||
chr1:166997220 | A | G | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+3151A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166997220 | |||||||
chr1:166997291 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.523+3222G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166997291 | |||||||
chr1:166997314 | T | C | 1 | a0002c0002t0001g0213 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.523+3245T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166997314 | |||||||
chr1:166997320 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.523+3251A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166997320 | |||||||
chr1:166997349 | G | A | 13 | a0002c0002t0001g0005 a0002c0002t0001g0048 a0002c0002t0001g0049 others(10): Show |
23 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.523+3280G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166997349 | |||||||
chr1:166997375 | G | A | 70 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0013 others(67): Show |
102 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.523+3306G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166997375 | |||||||
chr1:166997379 | T | C | 3 | a0001c0003t0001g0207 a0001c0003t0001g0208 a0002c0002t0001g0251 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.523+3310T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166997379 | |||||||
chr1:166997736 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0081 |
3 | NA18978.hp1 NA19000.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.523+3667A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166997736 | |||||||
chr1:166997757 | G | A | 1 | a0002c0002t0001g0211 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.523+3688G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166997757 | |||||||
chr1:166997786 | C | T | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+3717C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166997786 | |||||||
chr1:166997846 | A | G | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+3777A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166997846 | |||||||
chr1:166997878 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
8 | HG00408.hp2 HG00558.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.523+3809A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166997878 | |||||||
chr1:166997987 | A | G | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+3918A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166997987 | |||||||
chr1:166998111 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.523+4042C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166998111 | |||||||
chr1:166998228 | T | G | 1 | a0002c0002t0001g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.523+4159T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166998228 | |||||||
chr1:166998271 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.523+4202A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166998271 | |||||||
chr1:166998487 | C | G | 2 | a0002c0002t0001g0253 a0002c0002t0001g0259 |
2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.523+4418C>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166998487 | |||||||
chr1:166998635 | C | A | 1 | a0001c0001t0001g0033 | 2 | NA19080.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.523+4566C>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166998635 | |||||||
chr1:166998653 | G | T | 1 | a0001c0001t0001g0071 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.523+4584G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166998653 | |||||||
chr1:166998673 | G | T | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523+4604G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166998673 | |||||||
chr1:166998728 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.523+4659T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166998728 | |||||||
chr1:166998803 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.523+4734C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166998803 | |||||||
chr1:166998904 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.523+4835C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166998904 | |||||||
chr1:166999213 | G | A | 1 | a0002c0002t0001g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.524-4967G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166999213 | |||||||
chr1:166999359 | A | G | 1 | a0002c0006t0001g0070 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.524-4821A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166999359 | |||||||
chr1:166999490 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.524-4690T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166999490 | |||||||
chr1:166999577 | C | T | 93 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(90): Show |
155 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.524-4603C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166999577 | |||||||
chr1:166999583 | C | T | 21 | a0001c0003t0001g0198 a0001c0003t0001g0199 a0001c0003t0001g0200 others(18): Show |
31 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.524-4597C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166999583 | |||||||
chr1:166999658 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG00280.hp2 HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.524-4522C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166999658 | |||||||
chr1:166999690 | C | T | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.524-4490C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166999690 | |||||||
chr1:166999735 | G | A | 85 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(82): Show |
125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.524-4445G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166999735 | |||||||
chr1:166999748 | G | C | 48 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0003t0001g0006 others(45): Show |
94 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.524-4432G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166999748 | |||||||
chr1:166999782 | T | C | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.524-4398T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166999782 | |||||||
chr1:166999832 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.524-4348G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166999832 | |||||||
chr1:166999895 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.524-4285A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166999895 | |||||||
chr1:166999912 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.524-4268C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 166999912 | |||||||
chr1:167000096 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.524-4084C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167000096 | |||||||
chr1:167000324 | C | T | 93 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(90): Show |
155 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.524-3856C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167000324 | |||||||
chr1:167000685 | T | G | 94 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(91): Show |
156 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.524-3495T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167000685 | |||||||
chr1:167000699 | T | A | 3 | a0002c0002t0001g0048 a0002c0002t0001g0255 a0002c0002t0001g0261 |
4 | HG01175.hp2 HG01496.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-3481T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167000699 | |||||||
chr1:167000778 | C | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0037 others(12): Show |
20 | HG00741.hp2 HG01168.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.524-3402C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167000778 | |||||||
chr1:167001090 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.524-3090G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167001090 | |||||||
chr1:167001134 | CTG | C | 3 | a0001c0003t0001g0207 a0001c0003t0001g0208 a0002c0002t0001g0251 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.524-3044_524-3043d others(4): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 167001134 | ||||||
chr1:167001203 | G | A | 94 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(91): Show |
156 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.524-2977G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167001203 | |||||||
chr1:167001321 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.524-2859C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167001321 | |||||||
chr1:167001429 | A | G | 2 | a0001c0001t0001g0186 a0001c0003t0001g0044 |
3 | HG02280.hp1 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.524-2751A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167001429 | |||||||
chr1:167001486 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.524-2694C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167001486 | |||||||
chr1:167001505 | T | C | 21 | a0001c0003t0001g0198 a0001c0003t0001g0199 a0001c0003t0001g0200 others(18): Show |
31 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.524-2675T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167001505 | |||||||
chr1:167001513 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.524-2667T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167001513 | |||||||
chr1:167001859 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.524-2321A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167001859 | |||||||
chr1:167001868 | G | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0054 others(7): Show |
16 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.524-2312G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167001868 | |||||||
chr1:167001946 | A | G | 3 | a0001c0003t0001g0202 a0001c0003t0001g0204 a0001c0003t0001g0205 |
3 | HG02145.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.524-2234A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167001946 | |||||||
chr1:167001990 | A | G | 1 | a0002c0002t0001g0245 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.524-2190A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167001990 | |||||||
chr1:167002076 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.524-2104G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167002076 | |||||||
chr1:167002113 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.524-2067T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167002113 | |||||||
chr1:167002502 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.524-1678G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167002502 | |||||||
chr1:167002600 | A | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0097 others(13): Show |
26 | HG00642.hp2 HG00735.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.524-1580A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167002600 | |||||||
chr1:167002775 | G | C | 1 | a0002c0002t0001g0214 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.524-1405G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167002775 | |||||||
chr1:167002870 | T | G | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.524-1310T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167002870 | |||||||
chr1:167002935 | C | G | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.524-1245C>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167002935 | |||||||
chr1:167002943 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.524-1237G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167002943 | |||||||
chr1:167002944 | C | G | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.524-1236C>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167002944 | |||||||
chr1:167002948 | C | CT | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.524-1231dupT | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 167002948 | ||||||
chr1:167003077 | T | A | 1 | a0002c0002t0001g0215 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.524-1103T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167003077 | |||||||
chr1:167003078 | C | A | 1 | a0002c0002t0001g0215 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.524-1102C>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167003078 | |||||||
chr1:167003419 | A | C | 1 | a0001c0001t0001g0183 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.524-761A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167003419 | |||||||
chr1:167003466 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.524-714T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167003466 | |||||||
chr1:167003648 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG00323.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.524-532T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167003648 | |||||||
chr1:167003832 | C | A | 94 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(91): Show |
156 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.524-348C>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167003832 | |||||||
chr1:167004121 | C | T | 44 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(41): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.524-59C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 5/11 | chr1 | 167004121 | |||||||
chr1:167004382 | T | G | 1 | a0002c0002t0001g0216 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.648+78T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 6/11 | chr1 | 167004382 | |||||||
chr1:167004421 | C | T | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.648+117C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 6/11 | chr1 | 167004421 | |||||||
chr1:167004504 | CA | C | 40 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(37): Show |
56 | HG00323.hp2 HG01081.hp1 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.648+204delA | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 167004504 | ||||||
chr1:167004520 | A | T | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.648+216A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 6/11 | chr1 | 167004520 | |||||||
chr1:167004571 | A | G | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.648+267A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 6/11 | chr1 | 167004571 | |||||||
chr1:167004614 | C | T | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.648+310C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 6/11 | chr1 | 167004614 | |||||||
chr1:167004940 | A | T | 1 | a0002c0002t0001g0230 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.649-136A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 6/11 | chr1 | 167004940 | |||||||
chr1:167004971 | C | T | 3 | a0001c0003t0001g0207 a0001c0003t0001g0208 a0002c0002t0001g0251 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.649-105C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 6/11 | chr1 | 167004971 | |||||||
chr1:167005183 | T | C | 53 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0003t0001g0006 others(50): Show |
99 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.703+53T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 7/11 | chr1 | 167005183 | |||||||
chr1:167005481 | A | G | 1 | a0002c0002t0001g0233 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.845+84A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167005481 | |||||||
chr1:167005555 | ATT | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0033 others(42): Show |
72 | HG00280.hp1 HG00423.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.845+159_845+160del others(2): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167005555 | |||||||
chr1:167005965 | G | A | 13 | a0002c0002t0001g0005 a0002c0002t0001g0048 a0002c0002t0001g0049 others(10): Show |
23 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.845+568G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167005965 | |||||||
chr1:167005992 | C | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | NA18954.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.845+595C>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167005992 | |||||||
chr1:167006115 | G | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0167 |
2 | HG01243.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.845+718G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006115 | |||||||
chr1:167006190 | C | G | 1 | a0001c0001t0001g0167 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.845+793C>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006190 | |||||||
chr1:167006306 | G | A | 4 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.845+909G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006306 | |||||||
chr1:167006361 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.845+964G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006361 | |||||||
chr1:167006596 | T | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(82): Show |
125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.845+1199T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006596 | |||||||
chr1:167006601 | C | CCATATAT others(1): Show |
3 | a0001c0003t0001g0200 a0001c0003t0001g0202 a0001c0003t0001g0205 |
3 | HG02145.hp1 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.845+1204_845+1205i others(10): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006601 | |||||||
chr1:167006601 | C | CCATATAT others(3): Show |
1 | a0001c0003t0001g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.845+1204_845+1205i others(12): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006601 | |||||||
chr1:167006601 | C | CCATATAT others(5): Show |
3 | a0001c0003t0001g0201 a0001c0003t0001g0207 a0002c0002t0001g0251 |
3 | HG02486.hp2 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.845+1204_845+1205i others(14): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006601 | |||||||
chr1:167006601 | C | CCATATAT others(9): Show |
1 | a0001c0003t0001g0208 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.845+1204_845+1205i others(18): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006601 | |||||||
chr1:167006601 | C | CTA | 44 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(41): Show |
71 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.845+1239_845+1240d others(4): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006601 | ||||||
chr1:167006601 | C | CTATA | 28 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0032 others(25): Show |
33 | HG00408.hp2 HG00423.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.845+1237_845+1240d others(6): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006601 | ||||||
chr1:167006601 | C | CTATATA | 23 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(20): Show |
41 | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.845+1235_845+1240d others(8): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006601 | ||||||
chr1:167006601 | C | CTATATAT others(1): Show |
7 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(4): Show |
7 | HG01074.hp2 HG01346.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.845+1233_845+1240d others(10): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006601 | ||||||
chr1:167006601 | C | CTATATAT others(3): Show |
10 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0114 others(7): Show |
11 | HG00099.hp2 HG00738.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.845+1231_845+1240d others(12): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006601 | ||||||
chr1:167006601 | C | CTATATAT others(5): Show |
4 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(1): Show |
4 | HG02258.hp1 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.845+1229_845+1240d others(14): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006601 | ||||||
chr1:167006601 | C | CTATATAT others(7): Show |
1 | a0001c0001t0001g0126 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.845+1227_845+1240d others(16): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006601 | ||||||
chr1:167006601 | C | CTATATAT others(11): Show |
1 | a0001c0001t0001g0111 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.845+1223_845+1240d others(20): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006601 | ||||||
chr1:167006601 | CTA | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG00280.hp1 NA18981.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.845+1239_845+1240d others(4): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006601 | ||||||
chr1:167006601 | CTATATAT others(5): Show |
C | 14 | a0001c0001t0001g0090 a0002c0002t0001g0005 a0002c0002t0001g0048 others(11): Show |
24 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.845+1229_845+1240d others(14): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006601 | ||||||
chr1:167006601 | CTATATAT others(7): Show |
C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0089 a0001c0001t0001g0091 others(1): Show |
5 | HG01256.hp2 HG01258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.845+1227_845+1240d others(16): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006601 | ||||||
chr1:167006601 | CTATATAT others(13): Show |
C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0110 |
2 | HG01433.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.845+1221_845+1240d others(22): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006601 | ||||||
chr1:167006601 | CTATATAT others(15): Show |
C | 2 | a0001c0001t0001g0186 a0001c0003t0001g0044 |
3 | HG02280.hp1 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.845+1219_845+1240d others(24): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006601 | ||||||
chr1:167006601 | CTATATAT others(17): Show |
C | 53 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0003t0001g0006 others(50): Show |
99 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.845+1217_845+1240d others(26): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006601 | ||||||
chr1:167006602 | T | C | 16 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(13): Show |
21 | HG00323.hp2 HG01081.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.845+1205T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006602 | |||||||
chr1:167006610 | T | C | 1 | a0002c0002t0001g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.845+1213T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006610 | |||||||
chr1:167006614 | T | C | 12 | a0002c0002t0001g0005 a0002c0002t0001g0048 a0002c0002t0001g0049 others(9): Show |
22 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.845+1217T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006614 | |||||||
chr1:167006622 | T | C | 13 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(10): Show |
18 | HG00323.hp2 HG01081.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.845+1225T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006622 | |||||||
chr1:167006624 | T | C | 3 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0003t0001g0044 |
4 | HG02280.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.845+1227T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006624 | |||||||
chr1:167006624 | TATATATA others(7): Show |
T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0188 a0001c0001t0001g0195 others(1): Show |
6 | HG01891.hp1 HG02572.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.845+1230_845+1243d others(16): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006624 | ||||||
chr1:167006624 | TATATATA others(8): Show |
T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0187 others(6): Show |
12 | HG00323.hp2 HG01081.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.845+1228_845+1242d others(17): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006624 | |||||||
chr1:167006626 | T | C | 53 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0003t0001g0006 others(50): Show |
99 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.845+1229T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006626 | |||||||
chr1:167006626 | TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0189 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.845+1230_845+1242d others(15): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006626 | |||||||
chr1:167006628 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.845+1231T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006628 | |||||||
chr1:167006629 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0118 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.845+1234_845+1244d others(13): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167006629 | ||||||
chr1:167006634 | T | C | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.845+1237T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006634 | |||||||
chr1:167006636 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.845+1239T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006636 | |||||||
chr1:167006638 | C | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0081 a0001c0001t0001g0084 others(4): Show |
8 | HG01123.hp2 NA18522.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.845+1241C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006638 | |||||||
chr1:167006639 | A | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0173 a0001c0001t0001g0188 others(3): Show |
8 | HG01891.hp1 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.845+1242A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006639 | |||||||
chr1:167006640 | T | A | 1 | a0001c0001t0001g0081 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.845+1243T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006640 | |||||||
chr1:167006640 | T | TATATACA | 3 | a0001c0001t0001g0028 a0001c0001t0001g0180 a0001c0003t0001g0199 |
4 | NA18522.hp2 NA18973.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.845+1243_845+1244i others(9): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006640 | |||||||
chr1:167006867 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG00099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.845+1470C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167006867 | |||||||
chr1:167007131 | T | TA | 8 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0001c0001t0001g0123 others(5): Show |
9 | HG00438.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.845+1747dupA | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167007131 | ||||||
chr1:167007145 | G | C | 93 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(90): Show |
155 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.845+1748G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167007145 | |||||||
chr1:167007160 | C | A | 1 | a0002c0002t0001g0133 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.845+1763C>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167007160 | |||||||
chr1:167007457 | T | C | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.845+2060T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167007457 | |||||||
chr1:167007557 | T | TTG | 10 | a0001c0001t0001g0034 a0001c0001t0001g0040 a0001c0001t0001g0063 others(7): Show |
12 | HG00099.hp2 HG01243.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.845+2200_845+2201d others(4): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167007557 | ||||||
chr1:167007557 | TTG | T | 74 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(71): Show |
113 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.845+2200_845+2201d others(4): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167007557 | ||||||
chr1:167007557 | TTGTG | T | 26 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0032 others(23): Show |
31 | HG00733.hp1 HG01993.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.845+2198_845+2201d others(6): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167007557 | ||||||
chr1:167007557 | TTGTGTG | T | 7 | a0001c0001t0001g0029 a0001c0001t0001g0097 a0001c0001t0001g0111 others(4): Show |
8 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.845+2196_845+2201d others(8): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167007557 | ||||||
chr1:167007557 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0127 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.845+2190_845+2201d others(14): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167007557 | ||||||
chr1:167007583 | GTGTGTGT others(9): Show |
G | 2 | a0001c0001t0001g0190 a0002c0002t0001g0258 |
2 | HG03195.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.845+2190_845+2205d others(18): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167007583 | ||||||
chr1:167007585 | GTGTGTGT others(7): Show |
G | 12 | a0001c0001t0001g0186 a0001c0001t0001g0191 a0001c0003t0001g0044 others(9): Show |
13 | HG00323.hp2 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.845+2192_845+2205d others(16): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167007585 | ||||||
chr1:167007587 | GTGTGTGT others(5): Show |
G | 24 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(21): Show |
39 | HG01081.hp1 HG01099.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.845+2194_845+2205d others(14): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167007587 | ||||||
chr1:167007589 | GTGTGTGT others(3): Show |
G | 3 | a0002c0002t0001g0218 a0002c0002t0001g0219 a0002c0002t0001g0220 |
3 | HG03834.hp1 NA18612.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.845+2196_845+2205d others(12): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167007589 | ||||||
chr1:167007591 | GTGTGTGT others(1): Show |
G | 34 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0002c0002t0001g0002 others(31): Show |
63 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.845+2198_845+2205d others(10): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167007591 | ||||||
chr1:167007593 | GTGTGTA | G | 11 | a0001c0003t0001g0006 a0001c0003t0001g0197 a0001c0003t0001g0207 others(8): Show |
26 | HG00408.hp1 HG00642.hp1 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.845+2200_845+2205d others(8): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167007593 | ||||||
chr1:167007595 | GTGTA | G | 6 | a0002c0002t0001g0023 a0002c0002t0001g0225 a0002c0002t0001g0226 others(3): Show |
8 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.845+2203_845+2206d others(6): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167007595 | ||||||
chr1:167007599 | A | G | 1 | a0002c0002t0001g0229 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.845+2202A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167007599 | |||||||
chr1:167007646 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0093 others(21): Show |
34 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.845+2249A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167007646 | |||||||
chr1:167007739 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.845+2342A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167007739 | |||||||
chr1:167007827 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.845+2430A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167007827 | |||||||
chr1:167008053 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.845+2656T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167008053 | |||||||
chr1:167008255 | G | A | 46 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0003t0001g0006 others(43): Show |
91 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.845+2858G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167008255 | |||||||
chr1:167008518 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.845+3121G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167008518 | |||||||
chr1:167008534 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.845+3137T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167008534 | |||||||
chr1:167008549 | G | A | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.845+3152G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167008549 | |||||||
chr1:167008578 | A | G | 1 | a0002c0002t0001g0220 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.845+3181A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167008578 | |||||||
chr1:167008619 | G | C | 1 | a0002c0002t0001g0049 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.845+3222G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167008619 | |||||||
chr1:167008633 | T | C | 21 | a0001c0003t0001g0198 a0001c0003t0001g0199 a0001c0003t0001g0200 others(18): Show |
31 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.845+3236T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167008633 | |||||||
chr1:167008735 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.845+3338G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167008735 | |||||||
chr1:167008752 | A | G | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.845+3355A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167008752 | |||||||
chr1:167008798 | G | A | 184 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(181): Show |
286 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.845+3401G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167008798 | |||||||
chr1:167008948 | T | G | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.845+3551T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167008948 | |||||||
chr1:167008965 | TA | T | 93 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(90): Show |
155 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.845+3569delA | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167008965 | |||||||
chr1:167009135 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.845+3738T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167009135 | |||||||
chr1:167009277 | C | G | 1 | a0002c0002t0001g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.845+3880C>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167009277 | |||||||
chr1:167009300 | T | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG02451.hp1 HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.845+3903T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167009300 | |||||||
chr1:167009321 | T | G | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.845+3924T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167009321 | |||||||
chr1:167009432 | G | A | 4 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02451.hp1 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.845+4035G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167009432 | |||||||
chr1:167009511 | C | G | 93 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(90): Show |
155 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.845+4114C>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167009511 | |||||||
chr1:167009590 | A | AT | 57 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(54): Show |
86 | HG00323.hp2 HG01081.hp1 HG01099.hp2 others(83): Show |
intron_variant | MODIFIER | c.845+4207dupT | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167009590 | ||||||
chr1:167009590 | AT | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0064 a0001c0001t0001g0099 others(2): Show |
6 | HG01168.hp2 HG01169.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.845+4207delT | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167009590 | ||||||
chr1:167009639 | C | T | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.845+4242C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167009639 | |||||||
chr1:167009835 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.845+4438T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167009835 | |||||||
chr1:167009876 | A | C | 1 | a0001c0001t0001g0020 | 3 | HG01081.hp1 HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.845+4479A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167009876 | |||||||
chr1:167010031 | C | T | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.845+4634C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167010031 | |||||||
chr1:167010067 | T | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0068 a0001c0001t0001g0080 |
6 | NA18943.hp1 NA18957.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.845+4670T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167010067 | |||||||
chr1:167010076 | G | A | 1 | a0004c0007t0001g0217 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.845+4679G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167010076 | |||||||
chr1:167010101 | T | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0120 |
3 | HG02602.hp2 HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.845+4704T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167010101 | |||||||
chr1:167010285 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.845+4888C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167010285 | |||||||
chr1:167010295 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.845+4898T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167010295 | |||||||
chr1:167010342 | T | C | 94 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(91): Show |
156 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.845+4945T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167010342 | |||||||
chr1:167010351 | G | A | 93 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(90): Show |
155 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.845+4954G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167010351 | |||||||
chr1:167010374 | G | A | 94 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(91): Show |
156 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.845+4977G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167010374 | |||||||
chr1:167010415 | G | T | 1 | a0002c0002t0001g0209 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.845+5018G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167010415 | |||||||
chr1:167010555 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.845+5158C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167010555 | |||||||
chr1:167010704 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0175 |
3 | HG00738.hp2 HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.845+5307T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167010704 | |||||||
chr1:167010888 | C | A | 13 | a0002c0002t0001g0005 a0002c0002t0001g0048 a0002c0002t0001g0049 others(10): Show |
23 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.846-5334C>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167010888 | |||||||
chr1:167011019 | A | G | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.846-5203A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167011019 | |||||||
chr1:167011104 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.846-5118G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167011104 | |||||||
chr1:167011138 | A | G | 1 | a0002c0006t0001g0066 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.846-5084A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167011138 | |||||||
chr1:167011235 | T | C | 13 | a0002c0002t0001g0005 a0002c0002t0001g0048 a0002c0002t0001g0049 others(10): Show |
23 | HG01175.hp2 HG01243.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.846-4987T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167011235 | |||||||
chr1:167011262 | A | C | 2 | a0001c0001t0001g0186 a0001c0003t0001g0044 |
3 | HG02280.hp1 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.846-4960A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167011262 | |||||||
chr1:167011346 | G | A | 70 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0013 others(67): Show |
102 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.846-4876G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167011346 | |||||||
chr1:167011512 | G | A | 1 | a0002c0002t0001g0247 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.846-4710G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167011512 | |||||||
chr1:167011661 | A | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG02451.hp1 HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.846-4561A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167011661 | |||||||
chr1:167012553 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.846-3669A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167012553 | |||||||
chr1:167012782 | T | G | 1 | a0001c0001t0001g0115 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.846-3440T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167012782 | |||||||
chr1:167012804 | C | T | 2 | a0002c0002t0002g0212 a0002c0002t0002g0224 |
2 | NA18987.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.846-3418C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167012804 | |||||||
chr1:167012893 | T | TGG | 93 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(90): Show |
155 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.846-3325_846-3324d others(4): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 167012893 | ||||||
chr1:167012916 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.846-3306A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167012916 | |||||||
chr1:167012927 | G | T | 1 | a0001c0001t0001g0063 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.846-3295G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167012927 | |||||||
chr1:167012989 | G | A | 1 | a0002c0002t0001g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.846-3233G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167012989 | |||||||
chr1:167012991 | C | T | 1 | a0002c0002t0001g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.846-3231C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167012991 | |||||||
chr1:167013047 | C | T | 1 | a0002c0002t0001g0223 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.846-3175C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013047 | |||||||
chr1:167013048 | A | G | 94 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(91): Show |
156 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.846-3174A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013048 | |||||||
chr1:167013121 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.846-3101G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013121 | |||||||
chr1:167013166 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0106 |
2 | HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.846-3056G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013166 | |||||||
chr1:167013201 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.846-3021C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013201 | |||||||
chr1:167013296 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.846-2926C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013296 | |||||||
chr1:167013297 | G | A | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.846-2925G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013297 | |||||||
chr1:167013365 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.846-2857C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013365 | |||||||
chr1:167013384 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.846-2838C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013384 | |||||||
chr1:167013449 | T | A | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.846-2773T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013449 | |||||||
chr1:167013482 | T | G | 93 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(90): Show |
155 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.846-2740T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013482 | |||||||
chr1:167013572 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.846-2650T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013572 | |||||||
chr1:167013630 | T | G | 2 | a0001c0001t0001g0168 a0002c0002t0001g0255 |
2 | HG02027.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.846-2592T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013630 | |||||||
chr1:167013734 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.846-2488G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013734 | |||||||
chr1:167013838 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.846-2384A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013838 | |||||||
chr1:167013863 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.846-2359A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013863 | |||||||
chr1:167013888 | T | C | 1 | a0002c0002t0001g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.846-2334T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013888 | |||||||
chr1:167013925 | T | A | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.846-2297T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013925 | |||||||
chr1:167013934 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0033 others(42): Show |
72 | HG00280.hp1 HG00423.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.846-2288G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167013934 | |||||||
chr1:167014141 | A | G | 1 | a0002c0002t0001g0226 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.846-2081A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167014141 | |||||||
chr1:167014200 | C | A | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.846-2022C>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167014200 | |||||||
chr1:167014217 | G | A | 5 | a0002c0002t0001g0242 a0002c0002t0001g0250 a0002c0002t0001g0263 others(2): Show |
5 | HG03209.hp1 HG03225.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.846-2005G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167014217 | |||||||
chr1:167014250 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.846-1972G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167014250 | |||||||
chr1:167014288 | T | C | 3 | a0001c0003t0001g0207 a0001c0003t0001g0208 a0002c0002t0001g0251 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.846-1934T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167014288 | |||||||
chr1:167014445 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.846-1777G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167014445 | |||||||
chr1:167014617 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0188 a0001c0001t0001g0195 others(1): Show |
6 | HG01891.hp1 HG02572.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.846-1605T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167014617 | |||||||
chr1:167014748 | C | T | 3 | a0001c0003t0001g0207 a0001c0003t0001g0208 a0002c0002t0001g0251 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.846-1474C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167014748 | |||||||
chr1:167014792 | G | A | 1 | a0001c0003t0001g0197 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.846-1430G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167014792 | |||||||
chr1:167014877 | G | A | 16 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(13): Show |
22 | HG00323.hp2 HG01081.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.846-1345G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167014877 | |||||||
chr1:167014897 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.846-1325C>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167014897 | |||||||
chr1:167014917 | A | G | 94 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(91): Show |
156 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.846-1305A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167014917 | |||||||
chr1:167014936 | A | T | 2 | a0002c0002t0002g0212 a0002c0002t0002g0224 |
2 | NA18987.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.846-1286A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167014936 | |||||||
chr1:167014948 | C | T | 2 | a0001c0001t0001g0186 a0001c0003t0001g0044 |
3 | HG02280.hp1 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.846-1274C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167014948 | |||||||
chr1:167015139 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.846-1083A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167015139 | |||||||
chr1:167015168 | G | T | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.846-1054G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167015168 | |||||||
chr1:167015383 | A | G | 1 | a0001c0003t0001g0203 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.846-839A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167015383 | |||||||
chr1:167015420 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.846-802T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167015420 | |||||||
chr1:167015562 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.846-660T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167015562 | |||||||
chr1:167015738 | T | C | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.846-484T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167015738 | |||||||
chr1:167015751 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.846-471T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167015751 | |||||||
chr1:167015936 | A | G | 1 | a0002c0002t0001g0222 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.846-286A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167015936 | |||||||
chr1:167016163 | T | A | 1 | a0001c0001t0001g0090 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.846-59T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167016163 | |||||||
chr1:167016164 | A | T | 1 | a0001c0001t0001g0090 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.846-58A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 8/11 | chr1 | 167016164 | |||||||
chr1:167016337 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.908+53C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 9/11 | chr1 | 167016337 | |||||||
chr1:167016388 | A | G | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.908+104A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 9/11 | chr1 | 167016388 | |||||||
chr1:167016937 | A | G | 2 | a0002c0002t0001g0221 a0002c0002t0001g0230 |
2 | NA18954.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.908+653A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 9/11 | chr1 | 167016937 | |||||||
chr1:167017169 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.909-658C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 9/11 | chr1 | 167017169 | |||||||
chr1:167017190 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.909-637C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 9/11 | chr1 | 167017190 | |||||||
chr1:167017305 | A | G | 1 | a0002c0002t0001g0023 | 3 | HG01167.hp2 HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.909-522A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 9/11 | chr1 | 167017305 | |||||||
chr1:167017415 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0123 a0001c0001t0001g0172 |
4 | HG01891.hp2 HG02055.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.909-412G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 9/11 | chr1 | 167017415 | |||||||
chr1:167017423 | G | C | 2 | a0002c0006t0001g0066 a0002c0006t0001g0070 |
2 | NA18947.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.909-404G>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 9/11 | chr1 | 167017423 | |||||||
chr1:167017822 | T | C | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | splice_region_variant&intron_variant | LOW | c.909-5T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 9/11 | chr1 | 167017822 | |||||||
chr1:167017987 | G | T | 1 | a0001c0001t0001g0065 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1041+28G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167017987 | |||||||
chr1:167018015 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1041+56A>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167018015 | |||||||
chr1:167018029 | A | C | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1041+70A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167018029 | |||||||
chr1:167018031 | A | G | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1041+72A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167018031 | |||||||
chr1:167018371 | CTTA | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0175 |
3 | HG00738.hp2 HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1041+416_1041+418d others(5): Show |
MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 167018371 | ||||||
chr1:167018689 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1041+730T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167018689 | |||||||
chr1:167018761 | A | C | 53 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0003t0001g0006 others(50): Show |
99 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1041+802A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167018761 | |||||||
chr1:167018951 | A | G | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1041+992A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167018951 | |||||||
chr1:167019041 | T | A | 93 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(90): Show |
155 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1041+1082T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167019041 | |||||||
chr1:167019056 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1041+1097C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167019056 | |||||||
chr1:167019059 | T | C | 1 | a0002c0002t0001g0243 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1041+1100T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167019059 | |||||||
chr1:167019088 | A | C | 1 | a0001c0001t0001g0031 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1041+1129A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167019088 | |||||||
chr1:167019097 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1041+1138C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167019097 | |||||||
chr1:167019191 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1041+1232G>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167019191 | |||||||
chr1:167019222 | A | G | 1 | a0001c0001t0001g0015 | 4 | HG00558.hp2 HG00609.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1041+1263A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167019222 | |||||||
chr1:167019330 | A | G | 5 | a0002c0002t0001g0003 a0002c0002t0001g0047 a0002c0002t0001g0218 others(2): Show |
15 | HG02015.hp2 HG02071.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.1041+1371A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167019330 | |||||||
chr1:167019529 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1042-1556C>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167019529 | |||||||
chr1:167019939 | C | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0041 others(10): Show |
20 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1042-1146C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167019939 | |||||||
chr1:167019965 | C | T | 1 | a0002c0002t0001g0229 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1042-1120C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167019965 | |||||||
chr1:167020060 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1042-1025G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167020060 | |||||||
chr1:167020221 | T | C | 1 | a0002c0008t0005g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1042-864T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167020221 | |||||||
chr1:167020280 | T | G | 4 | a0003c0004t0001g0152 a0003c0004t0001g0156 a0003c0004t0001g0158 others(1): Show |
4 | HG02922.hp2 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1042-805T>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167020280 | |||||||
chr1:167020292 | T | A | 2 | a0001c0001t0001g0137 a0002c0002t0001g0244 |
2 | NA19054.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1042-793T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167020292 | |||||||
chr1:167020460 | T | C | 1 | a0002c0002t0001g0227 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1042-625T>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167020460 | |||||||
chr1:167020494 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1042-591A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167020494 | |||||||
chr1:167020517 | A | C | 3 | a0002c0002t0001g0048 a0002c0002t0001g0255 a0002c0002t0001g0261 |
4 | HG01175.hp2 HG01496.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1042-568A>C | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167020517 | |||||||
chr1:167020671 | A | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(83): Show |
126 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1042-414A>G | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167020671 | |||||||
chr1:167020846 | C | T | 53 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0003t0001g0006 others(50): Show |
99 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1042-239C>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167020846 | |||||||
chr1:167020865 | T | A | 93 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(90): Show |
155 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1042-220T>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 10/11 | chr1 | 167020865 | |||||||
chr1:167021222 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1117+62C>A | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 11/11 | chr1 | 167021222 | |||||||
chr1:167021231 | G | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0123 a0001c0001t0001g0172 |
4 | HG01891.hp2 HG02055.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1117+71G>T | MAEL | ENSG00000143194.13 | transcript | ENST00000367872.9 | protein_coding | 11/11 | chr1 | 167021231 |