Item | Value |
---|---|
geneid | 4010 |
ensemblid | ENSG00000136944.19 |
hgncid | 6654 |
symbol | LMX1B |
name | LIM homeobox transcription factor 1 beta |
refseq_nuc | NM_001174147.2 |
refseq_prot | NP_001167618.1 |
ensembl_nuc | ENST00000373474.9 |
ensembl_prot | ENSP00000362573.3 |
mane_status | MANE Select |
chr | chr9 |
start | 126613928 |
end | 126701032 |
strand | + |
ver | v1.2 |
region | chr9:126613928-126701032 |
region5000 | chr9:126608928-126706032 |
regionname0 | LMX1B_chr9_126613928_126701032 |
regionname5000 | LMX1B_chr9_126608928_126706032 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1206 | 166 | 33 | 30 | 72 | 7 | 22 | LMX1B_chr9_126608928_126706032 | LMX1B | ATGGA others(1201): Show |
chr9 | 126608928 | 126706032 | ||
a0001c0002 | 0/0 | 1206 | 132 | 12 | 27 | 74 | 3 | 16 | LMX1B_chr9_126608928_126706032 | LMX1B | ATGGA others(1201): Show |
chr9 | 126608928 | 126706032 | ||
a0001c0003 | 0/0 | 1206 | 15 | 13 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | ATGGA others(1201): Show |
chr9 | 126608928 | 126706032 | ||
a0001c0004 | 0/0 | 1206 | 12 | 9 | 3 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | ATGGA others(1201): Show |
chr9 | 126608928 | 126706032 | ||
a0001c0005 | 0/0 | 1206 | 6 | 6 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | ATGGA others(1201): Show |
chr9 | 126608928 | 126706032 | ||
a0001c0006 | 0/0 | 1206 | 3 | 3 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | ATGGA others(1201): Show |
chr9 | 126608928 | 126706032 | ||
a0001c0007 | 0/0 | 1206 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | ATGGA others(1201): Show |
chr9 | 126608928 | 126706032 | ||
a0001c0008 | 0/0 | 1206 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | ATGGA others(1201): Show |
chr9 | 126608928 | 126706032 | ||
a0001c0009 | 0/0 | 1206 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | ATGGA others(1201): Show |
chr9 | 126608928 | 126706032 | ||
a0001c0010 | 0/0 | 1206 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | ATGGA others(1201): Show |
chr9 | 126608928 | 126706032 | ||
a0001c0011 | 0/0 | 1206 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | ATGGA others(1201): Show |
chr9 | 126608928 | 126706032 | ||
a0001c0012 | 0/0 | 1206 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | ATGGA others(1201): Show |
chr9 | 126608928 | 126706032 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 6305 | 16 | 4 | 4 | 2 | 2 | 4 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0003 | 0/0 | 6307 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0004 | 0/0 | 6317 | 10 | 0 | 1 | 9 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6312): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0005 | 0/0 | 6291 | 6 | 0 | 3 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6286): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0007 | 0/0 | 6305 | 5 | 0 | 0 | 5 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0008 | 0/0 | 6310 | 5 | 0 | 0 | 3 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0010 | 0/0 | 6306 | 4 | 0 | 0 | 4 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6301): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0011 | 0/0 | 6312 | 4 | 0 | 1 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0018 | 0/0 | 6305 | 3 | 0 | 0 | 2 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0019 | 0/0 | 6310 | 3 | 0 | 2 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0020 | 0/0 | 6317 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6312): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0021 | 0/0 | 6322 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6317): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0025 | 0/0 | 6305 | 3 | 2 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0026 | 0/0 | 6308 | 2 | 0 | 1 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6303): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0027 | 0/0 | 6315 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6310): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0028 | 0/0 | 6313 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6308): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0029 | 0/0 | 6307 | 2 | 0 | 0 | 0 | 1 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0030 | 0/0 | 6309 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6304): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0035 | 0/0 | 6305 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0036 | 0/0 | 6300 | 2 | 0 | 0 | 0 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6295): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0037 | 0/0 | 6305 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0038 | 0/0 | 6312 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0039 | 0/0 | 6310 | 2 | 0 | 1 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0040 | 0/0 | 6317 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6312): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0041 | 0/0 | 6315 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6310): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0042 | 0/0 | 6296 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6291): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0051 | 0/0 | 6307 | 2 | 1 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0052 | 0/0 | 6310 | 2 | 1 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0056 | 0/1 | 6311 | 1 | 0 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6306): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0058 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6310): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0059 | 0/0 | 6308 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6303): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0060 | 0/0 | 6315 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6310): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0061 | 0/0 | 6313 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6308): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0064 | 0/0 | 6325 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6320): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0065 | 0/0 | 6313 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6308): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0066 | 0/0 | 6313 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6308): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0067 | 0/0 | 6313 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6308): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0068 | 0/0 | 6325 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6320): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0078 | 0/0 | 6309 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6304): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0079 | 0/0 | 6307 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0080 | 0/0 | 6307 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0081 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0082 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0083 | 0/0 | 6309 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6304): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0084 | 0/0 | 6314 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6309): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0086 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0095 | 0/0 | 6306 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6301): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0096 | 0/0 | 6308 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6303): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0097 | 0/0 | 6313 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6308): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0098 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6287): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0099 | 0/0 | 6316 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6311): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0101 | 0/0 | 6308 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6303): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0106 | 0/0 | 6317 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6312): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0117 | 0/0 | 6305 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0118 | 0/0 | 6302 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6297): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0119 | 0/0 | 6307 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0120 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0121 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0122 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0123 | 0/0 | 6307 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0124 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0125 | 0/0 | 6305 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0126 | 0/0 | 6305 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0127 | 0/0 | 6305 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0128 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0129 | 0/0 | 6310 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0130 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0131 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0132 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0133 | 0/0 | 6310 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0134 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0135 | 0/0 | 6310 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0136 | 0/0 | 6312 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0137 | 0/0 | 6291 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6286): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0138 | 0/0 | 6291 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6286): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0139 | 0/0 | 6291 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6286): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0140 | 0/0 | 6317 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6312): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0141 | 0/0 | 6315 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6310): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0142 | 0/0 | 6320 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6315): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0143 | 0/0 | 6320 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6315): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0144 | 0/0 | 6322 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6317): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0146 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0147 | 0/0 | 6310 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0148 | 0/0 | 6325 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6320): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0149 | 0/0 | 6310 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0164 | 0/0 | 6297 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6292): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0169 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0170 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6295): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0171 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0172 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0173 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0174 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0175 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0176 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0177 | 1/0 | 6312 | 1 | 0 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0178 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0179 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0181 | 0/0 | 6317 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6312): Show |
chr9 | 126608928 | 126706032 |
a0001c0001t0194 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6295): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0001 | 0/0 | 6312 | 27 | 0 | 2 | 25 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0002 | 0/0 | 6305 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0003 | 0/0 | 6307 | 11 | 0 | 1 | 10 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0006 | 0/0 | 6297 | 6 | 0 | 2 | 0 | 2 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6292): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0009 | 0/0 | 6309 | 4 | 0 | 1 | 2 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6304): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0013 | 0/0 | 6307 | 4 | 0 | 2 | 0 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0014 | 0/0 | 6310 | 4 | 0 | 2 | 0 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0015 | 0/0 | 6314 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6309): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0016 | 0/0 | 6312 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0017 | 0/0 | 6312 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0022 | 0/0 | 6312 | 3 | 0 | 1 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0023 | 0/0 | 6308 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6303): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0031 | 0/0 | 6307 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0032 | 0/0 | 6309 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6304): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0033 | 0/0 | 6313 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6308): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0044 | 0/0 | 6307 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0045 | 0/0 | 6310 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0046 | 0/0 | 6312 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0047 | 0/0 | 6311 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6306): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0053 | 0/0 | 6300 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6295): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0054 | 0/0 | 6299 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6294): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0055 | 0/0 | 6302 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6297): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0069 | 0/0 | 6305 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0070 | 0/0 | 6308 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6303): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0071 | 0/0 | 6320 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6315): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0072 | 0/0 | 6315 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6310): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0073 | 0/0 | 6315 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6310): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0074 | 0/0 | 6315 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6310): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0075 | 0/0 | 6331 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6326): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0077 | 0/0 | 6309 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6304): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0087 | 0/0 | 6299 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6294): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0088 | 0/0 | 6304 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6299): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0089 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0090 | 0/0 | 6309 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6304): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0091 | 0/0 | 6309 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6304): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0092 | 0/0 | 6309 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6304): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0093 | 0/0 | 6314 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6309): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0094 | 0/0 | 6314 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6309): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0100 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6308): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0103 | 0/0 | 6313 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6308): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0104 | 0/0 | 6311 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6306): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0105 | 0/0 | 6301 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6296): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0107 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0151 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0152 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0153 | 0/0 | 6310 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0154 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0155 | 0/0 | 6312 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0156 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0157 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0158 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0159 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0160 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0161 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6295): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0162 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6295): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0163 | 0/0 | 6312 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0166 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0186 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0187 | 0/0 | 6305 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0188 | 0/0 | 6307 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0189 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6302): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0190 | 0/0 | 6310 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0191 | 0/0 | 6310 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0002t0192 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6295): Show |
chr9 | 126608928 | 126706032 |
a0001c0003t0024 | 0/0 | 6312 | 3 | 3 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0003t0049 | 0/0 | 6312 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0003t0057 | 0/0 | 6314 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6309): Show |
chr9 | 126608928 | 126706032 |
a0001c0003t0076 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6308): Show |
chr9 | 126608928 | 126706032 |
a0001c0003t0108 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6306): Show |
chr9 | 126608928 | 126706032 |
a0001c0003t0109 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6306): Show |
chr9 | 126608928 | 126706032 |
a0001c0003t0110 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6306): Show |
chr9 | 126608928 | 126706032 |
a0001c0003t0111 | 0/0 | 6302 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6297): Show |
chr9 | 126608928 | 126706032 |
a0001c0003t0112 | 0/0 | 6305 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0003t0113 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0003t0114 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0003t0165 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0004t0037 | 0/0 | 6305 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6300): Show |
chr9 | 126608928 | 126706032 |
a0001c0004t0043 | 0/0 | 6322 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6317): Show |
chr9 | 126608928 | 126706032 |
a0001c0004t0062 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6310): Show |
chr9 | 126608928 | 126706032 |
a0001c0004t0063 | 0/0 | 6320 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6315): Show |
chr9 | 126608928 | 126706032 |
a0001c0004t0145 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6322): Show |
chr9 | 126608928 | 126706032 |
a0001c0004t0150 | 0/0 | 6320 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6315): Show |
chr9 | 126608928 | 126706032 |
a0001c0004t0180 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6310): Show |
chr9 | 126608928 | 126706032 |
a0001c0004t0182 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6310): Show |
chr9 | 126608928 | 126706032 |
a0001c0004t0183 | 0/0 | 6317 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6312): Show |
chr9 | 126608928 | 126706032 |
a0001c0004t0184 | 0/0 | 6320 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6315): Show |
chr9 | 126608928 | 126706032 |
a0001c0004t0185 | 0/0 | 6322 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6317): Show |
chr9 | 126608928 | 126706032 |
a0001c0005t0012 | 0/0 | 6310 | 4 | 4 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0005t0167 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0005t0168 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6305): Show |
chr9 | 126608928 | 126706032 |
a0001c0006t0050 | 0/0 | 6312 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0006t0115 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0007t0048 | 0/0 | 6300 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6295): Show |
chr9 | 126608928 | 126706032 |
a0001c0008t0034 | 0/0 | 6312 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0009t0102 | 0/0 | 6308 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6303): Show |
chr9 | 126608928 | 126706032 |
a0001c0010t0193 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0011t0085 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6307): Show |
chr9 | 126608928 | 126706032 |
a0001c0012t0116 | 0/0 | 6309 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | AGCCC others(6304): Show |
chr9 | 126608928 | 126706032 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0007g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0007g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0007g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0008g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0008g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0010g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0010g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0010g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0010g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0011g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0011g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0011g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0011g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0018g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0018g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0018g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0019g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0019g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0019g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0020g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0020g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0020g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0021g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0021g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0021g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0025g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0025g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0025g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0026g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0026g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0027g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0027g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0028g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0028g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0029g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0029g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0030g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0030g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0035g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0035g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0036g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0037g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0038g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0038g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0039g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0039g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0040g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0040g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0041g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0041g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0042g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0042g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0051g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0051g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0052g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0052g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0056g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0058g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0059g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0060g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0061g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0064g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0065g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0066g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0067g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0068g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0078g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0079g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0080g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0081g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0082g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0083g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0084g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0086g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0095g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0096g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0097g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0098g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0099g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0101g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0106g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0117g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0118g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0119g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0120g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0121g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0122g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0123g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0124g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0125g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0126g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0127g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0128g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0129g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0130g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0131g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0132g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0133g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0134g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0135g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0136g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0137g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0138g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0139g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0140g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0141g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0142g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0143g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0144g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0146g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0147g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0148g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0149g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0164g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0169g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0170g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0171g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0172g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0173g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0174g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0175g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0176g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0177g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0178g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0179g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0181g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0194g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0006g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0006g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0006g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0006g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0006g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0006g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0009g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0009g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0009g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0009g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0013g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0013g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0013g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0013g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0014g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0014g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0014g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0014g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0015g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0015g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0015g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0016g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0016g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0016g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0017g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0017g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0017g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0022g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0022g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0022g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0023g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0023g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0023g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0031g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0031g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0032g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0033g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0033g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0044g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0044g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0045g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0045g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0046g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0046g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0047g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0047g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0053g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0053g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0054g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0055g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0069g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0070g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0071g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0072g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0073g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0074g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0075g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0077g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0087g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0088g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0089g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0090g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0091g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0092g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0093g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0094g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0100g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0103g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0104g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0105g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0107g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0151g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0152g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0153g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0154g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0155g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0156g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0157g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0158g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0159g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0160g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0161g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0162g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0163g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0166g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0186g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0187g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0188g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0189g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0190g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0191g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0192g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0024g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0024g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0024g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0049g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0049g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0057g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0076g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0108g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0109g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0110g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0111g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0112g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0113g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0114g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0165g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0037g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0043g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0043g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0062g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0063g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0145g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0150g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0180g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0182g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0183g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0184g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0185g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0005t0012g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0005t0012g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0005t0012g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0005t0012g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0005t0167g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0005t0168g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0006t0050g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0006t0050g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0006t0115g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0007t0048g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0007t0048g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0008t0034g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0008t0034g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0009t0102g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0010t0193g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0011t0085g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0012t0116g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0039 | g0282 | EUR | GBR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0207 | EUR | GBR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00280 | hp1 | a0001 | c0002 | t0006 | g0188 | EUR | FIN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00280 | hp2 | a0001 | c0001 | t0068 | g0078 | EUR | FIN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00323 | hp1 | a0001 | c0001 | t0080 | g0080 | EUR | FIN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00323 | hp2 | a0001 | c0002 | t0006 | g0186 | EUR | FIN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0258 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00438 | hp2 | a0001 | c0001 | t0008 | g0030 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00558 | hp1 | a0001 | c0001 | t0011 | g0328 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00558 | hp2 | a0001 | c0001 | t0135 | g0299 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00597 | hp1 | a0001 | c0001 | t0040 | g0259 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00597 | hp2 | a0001 | c0001 | t0008 | g0054 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00609 | hp1 | a0001 | c0002 | t0191 | g0192 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00621 | hp1 | a0001 | c0001 | t0021 | g0320 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00621 | hp2 | a0001 | c0002 | t0009 | g0121 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00639 | hp1 | a0001 | c0003 | t0049 | g0169 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00639 | hp2 | a0001 | c0001 | t0019 | g0334 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0275 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00642 | hp2 | a0001 | c0001 | t0026 | g0100 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00735 | hp1 | a0001 | c0001 | t0123 | g0232 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00735 | hp2 | a0001 | c0001 | t0019 | g0335 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00738 | hp1 | a0001 | c0002 | t0013 | g0176 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00738 | hp2 | a0001 | c0001 | t0065 | g0119 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00741 | hp1 | a0001 | c0002 | t0087 | g0103 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00741 | hp2 | a0001 | c0002 | t0188 | g0144 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01069 | hp1 | a0001 | c0002 | t0014 | g0183 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01069 | hp2 | a0001 | c0001 | t0136 | g0008 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01070 | hp1 | a0001 | c0002 | t0014 | g0198 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01070 | hp2 | a0001 | c0002 | t0031 | g0096 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01074 | hp1 | a0001 | c0001 | t0147 | g0206 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01074 | hp2 | a0001 | c0002 | t0031 | g0095 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01081 | hp1 | a0001 | c0001 | t0039 | g0316 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01081 | hp2 | a0001 | c0001 | t0059 | g0120 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01099 | hp2 | a0001 | c0001 | t0125 | g0203 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01106 | hp1 | a0001 | c0001 | t0079 | g0104 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01109 | hp1 | a0001 | c0001 | t0051 | g0158 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01109 | hp2 | a0001 | c0003 | t0049 | g0150 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01167 | hp1 | a0001 | c0002 | t0032 | g0002 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01167 | hp2 | a0001 | c0004 | t0037 | g0227 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01168 | hp1 | a0001 | c0002 | t0045 | g0229 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01168 | hp2 | a0001 | c0001 | t0142 | g0281 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01169 | hp1 | a0001 | c0002 | t0032 | g0002 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01169 | hp2 | a0001 | c0002 | t0045 | g0212 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01175 | hp1 | a0001 | c0001 | t0127 | g0209 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01175 | hp2 | a0001 | c0001 | t0028 | g0076 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01192 | hp1 | a0001 | c0002 | t0103 | g0196 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01192 | hp2 | a0001 | c0002 | t0104 | g0197 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01243 | hp1 | a0001 | c0001 | t0052 | g0201 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01243 | hp2 | a0001 | c0004 | t0185 | g0088 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01257 | hp1 | a0001 | c0002 | t0013 | g0128 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01257 | hp2 | a0001 | c0002 | t0022 | g0001 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0056 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01346 | hp2 | a0001 | c0002 | t0006 | g0190 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01358 | hp1 | a0001 | c0002 | t0047 | g0001 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01358 | hp2 | a0001 | c0002 | t0190 | g0199 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01361 | hp1 | a0001 | c0001 | t0011 | g0224 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01361 | hp2 | a0001 | c0002 | t0047 | g0044 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01496 | hp1 | a0001 | c0001 | t0028 | g0081 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01496 | hp2 | a0001 | c0004 | t0063 | g0087 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01516 | hp1 | a0001 | c0001 | t0029 | g0127 | EUR | IBS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01516 | hp2 | a0001 | c0001 | t0149 | g0283 | EUR | IBS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01884 | hp1 | a0001 | c0011 | t0085 | g0082 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01884 | hp2 | a0001 | c0005 | t0012 | g0140 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0221 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01952 | hp2 | a0001 | c0002 | t0006 | g0184 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01975 | hp1 | a0001 | c0002 | t0009 | g0097 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01975 | hp2 | a0001 | c0001 | t0164 | g0241 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01978 | hp1 | a0001 | c0001 | t0141 | g0204 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01978 | hp2 | a0001 | c0002 | t0069 | g0079 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01981 | hp1 | a0001 | c0001 | t0025 | g0191 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01993 | hp1 | a0001 | c0002 | t0003 | g0228 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01993 | hp2 | a0001 | c0001 | t0137 | g0307 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02004 | hp1 | a0001 | c0002 | t0163 | g0302 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02015 | hp1 | a0001 | c0001 | t0175 | g0125 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02015 | hp2 | a0001 | c0002 | t0016 | g0019 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02027 | hp1 | a0001 | c0001 | t0124 | g0252 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02027 | hp2 | a0001 | c0002 | t0017 | g0016 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0313 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02040 | hp2 | a0001 | c0002 | t0107 | g0023 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02055 | hp1 | a0001 | c0005 | t0012 | g0137 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02055 | hp2 | a0001 | c0004 | t0180 | g0083 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02071 | hp1 | a0001 | c0001 | t0026 | g0107 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02071 | hp2 | a0001 | c0001 | t0007 | g0292 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02074 | hp2 | a0001 | c0001 | t0133 | g0018 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02080 | hp1 | a0001 | c0002 | t0016 | g0024 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02080 | hp2 | a0001 | c0001 | t0096 | g0230 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02083 | hp1 | a0001 | c0001 | t0143 | g0285 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02083 | hp2 | a0001 | c0001 | t0007 | g0051 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02129 | hp1 | a0001 | c0002 | t0157 | g0047 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02129 | hp2 | a0001 | c0001 | t0021 | g0270 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0268 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02132 | hp2 | a0001 | c0002 | t0017 | g0014 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02145 | hp1 | a0001 | c0001 | t0101 | g0170 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02145 | hp2 | a0001 | c0009 | t0102 | g0167 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | CDX | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02155 | hp2 | a0001 | c0001 | t0061 | g0077 | EAS | CDX | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02165 | hp1 | a0001 | c0001 | t0018 | g0006 | EAS | CDX | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02165 | hp2 | a0001 | c0001 | t0042 | g0309 | EAS | CDX | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02257 | hp1 | a0001 | c0001 | t0041 | g0314 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02257 | hp2 | a0001 | c0005 | t0012 | g0139 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02258 | hp1 | a0001 | c0001 | t0131 | g0305 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02258 | hp2 | a0001 | c0001 | t0025 | g0157 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02280 | hp1 | a0001 | c0001 | t0173 | g0159 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02280 | hp2 | a0001 | c0002 | t0053 | g0177 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0288 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0061 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02523 | hp1 | a0001 | c0002 | t0154 | g0027 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02523 | hp2 | a0001 | c0001 | t0097 | g0325 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02572 | hp1 | a0001 | c0001 | t0181 | g0143 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02572 | hp2 | a0001 | c0002 | t0189 | g0172 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02602 | hp1 | a0001 | c0001 | t0126 | g0276 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0243 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02615 | hp1 | a0001 | c0002 | t0161 | g0068 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02615 | hp2 | a0001 | c0001 | t0194 | g0216 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02630 | hp2 | a0001 | c0002 | t0162 | g0327 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02647 | hp1 | a0001 | c0001 | t0106 | g0218 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02647 | hp2 | a0001 | c0003 | t0110 | g0069 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02683 | hp1 | a0001 | c0002 | t0006 | g0187 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02683 | hp2 | a0001 | c0002 | t0088 | g0122 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02698 | hp1 | a0001 | c0002 | t0013 | g0178 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02698 | hp2 | a0001 | c0002 | t0093 | g0108 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02717 | hp1 | a0001 | c0001 | t0172 | g0160 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02717 | hp2 | a0001 | c0008 | t0034 | g0149 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02723 | hp1 | a0001 | c0002 | t0054 | g0146 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02723 | hp2 | a0001 | c0003 | t0165 | g0141 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02735 | hp1 | a0001 | c0001 | t0064 | g0091 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02735 | hp2 | a0001 | c0002 | t0091 | g0135 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02738 | hp1 | a0001 | c0002 | t0187 | g0179 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02738 | hp2 | a0001 | c0002 | t0014 | g0193 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02818 | hp1 | a0001 | c0003 | t0111 | g0233 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02886 | hp1 | a0001 | c0004 | t0150 | g0067 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02886 | hp2 | a0001 | c0001 | t0121 | g0277 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02895 | hp1 | a0001 | c0001 | t0025 | g0084 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02895 | hp2 | a0001 | c0007 | t0048 | g0319 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02897 | hp1 | a0001 | c0007 | t0048 | g0318 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02922 | hp1 | a0001 | c0001 | t0169 | g0152 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02922 | hp2 | a0001 | c0002 | t0053 | g0180 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02965 | hp1 | a0001 | c0001 | t0078 | g0090 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02965 | hp2 | a0001 | c0001 | t0120 | g0238 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02976 | hp1 | a0001 | c0001 | t0051 | g0153 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02976 | hp2 | a0001 | c0006 | t0050 | g0173 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03041 | hp1 | a0001 | c0003 | t0024 | g0202 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03041 | hp2 | a0001 | c0003 | t0108 | g0253 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03098 | hp1 | a0001 | c0001 | t0170 | g0155 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03098 | hp2 | a0001 | c0002 | t0192 | g0171 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03130 | hp1 | a0001 | c0001 | t0058 | g0089 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03130 | hp2 | a0001 | c0001 | t0171 | g0151 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03139 | hp1 | a0001 | c0006 | t0050 | g0174 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03139 | hp2 | a0001 | c0001 | t0041 | g0284 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03195 | hp1 | a0001 | c0004 | t0182 | g0154 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03195 | hp2 | a0001 | c0005 | t0012 | g0138 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03209 | hp1 | a0001 | c0008 | t0034 | g0148 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03209 | hp2 | a0001 | c0003 | t0112 | g0225 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03225 | hp1 | a0001 | c0004 | t0043 | g0214 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03225 | hp2 | a0001 | c0002 | t0100 | g0147 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03239 | hp1 | a0001 | c0001 | t0148 | g0333 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03239 | hp2 | a0001 | c0001 | t0060 | g0106 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03453 | hp1 | a0001 | c0004 | t0145 | g0222 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03453 | hp2 | a0001 | c0001 | t0179 | g0195 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03486 | hp1 | a0001 | c0003 | t0109 | g0136 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03486 | hp2 | a0001 | c0002 | t0186 | g0133 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03490 | hp1 | a0001 | c0001 | t0008 | g0005 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03490 | hp2 | a0001 | c0002 | t0092 | g0113 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03491 | hp1 | a0001 | c0001 | t0036 | g0003 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03491 | hp2 | a0001 | c0002 | t0009 | g0098 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03492 | hp1 | a0001 | c0001 | t0008 | g0005 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03492 | hp2 | a0001 | c0001 | t0036 | g0003 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03516 | hp1 | a0001 | c0006 | t0115 | g0235 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03516 | hp2 | a0001 | c0004 | t0183 | g0101 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03540 | hp1 | a0001 | c0001 | t0037 | g0234 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03540 | hp2 | a0001 | c0004 | t0062 | g0085 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03579 | hp1 | a0001 | c0004 | t0184 | g0086 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03579 | hp2 | a0001 | c0003 | t0024 | g0165 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03654 | hp1 | a0001 | c0001 | t0084 | g0071 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03654 | hp2 | a0001 | c0001 | t0029 | g0094 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03688 | hp1 | a0001 | c0001 | t0095 | g0247 | SAS | STU | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03688 | hp2 | a0001 | c0002 | t0006 | g0189 | SAS | STU | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03704 | hp1 | a0001 | c0002 | t0013 | g0185 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03704 | hp2 | a0001 | c0001 | t0129 | g0220 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03710 | hp2 | a0001 | c0002 | t0014 | g0194 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03927 | hp1 | a0001 | c0001 | t0117 | g0245 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03927 | hp2 | a0001 | c0001 | t0119 | g0217 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03942 | hp1 | a0001 | c0001 | t0018 | g0290 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03942 | hp2 | a0001 | c0001 | t0066 | g0126 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG04184 | hp1 | a0001 | c0002 | t0071 | g0092 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG04204 | hp1 | a0001 | c0002 | t0090 | g0099 | SAS | STU | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG04204 | hp2 | a0001 | c0002 | t0155 | g0310 | SAS | STU | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG04228 | hp1 | a0001 | c0002 | t0072 | g0074 | SAS | STU | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG04228 | hp2 | a0001 | c0001 | t0067 | g0073 | SAS | STU | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18522 | hp1 | a0001 | c0003 | t0076 | g0132 | AFR | YRI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18522 | hp2 | a0001 | c0005 | t0168 | g0164 | AFR | YRI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18747 | hp1 | a0001 | c0002 | t0009 | g0109 | EAS | CHB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18747 | hp2 | a0001 | c0001 | t0140 | g0269 | EAS | CHB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18906 | hp1 | a0001 | c0002 | t0166 | g0181 | AFR | YRI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18906 | hp2 | a0001 | c0001 | t0130 | g0237 | AFR | YRI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18941 | hp1 | a0001 | c0001 | t0083 | g0131 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18942 | hp2 | a0001 | c0001 | t0134 | g0066 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18943 | hp2 | a0001 | c0001 | t0020 | g0267 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18945 | hp1 | a0001 | c0002 | t0089 | g0111 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18945 | hp2 | a0001 | c0001 | t0019 | g0031 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18946 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18950 | hp1 | a0001 | c0002 | t0033 | g0012 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18950 | hp2 | a0001 | c0002 | t0074 | g0114 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18953 | hp1 | a0001 | c0001 | t0027 | g0129 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18953 | hp2 | a0001 | c0002 | t0046 | g0257 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18954 | hp1 | a0001 | c0002 | t0022 | g0293 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18954 | hp2 | a0001 | c0002 | t0023 | g0028 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18959 | hp1 | a0001 | c0002 | t0151 | g0026 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18959 | hp2 | a0001 | c0001 | t0010 | g0007 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18960 | hp1 | a0001 | c0002 | t0152 | g0295 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18961 | hp1 | a0001 | c0001 | t0010 | g0326 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18961 | hp2 | a0001 | c0002 | t0023 | g0052 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18962 | hp2 | a0001 | c0002 | t0003 | g0041 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18963 | hp1 | a0001 | c0001 | t0010 | g0006 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18966 | hp2 | a0001 | c0002 | t0070 | g0105 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18970 | hp1 | a0001 | c0001 | t0008 | g0331 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18971 | hp2 | a0001 | c0001 | t0020 | g0266 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18973 | hp1 | a0001 | c0001 | t0081 | g0102 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18973 | hp2 | a0001 | c0001 | t0038 | g0332 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18975 | hp1 | a0001 | c0002 | t0003 | g0287 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18975 | hp2 | a0001 | c0001 | t0099 | g0038 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18980 | hp1 | a0001 | c0001 | t0007 | g0317 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18983 | hp1 | a0001 | c0001 | t0035 | g0020 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18983 | hp2 | a0001 | c0001 | t0030 | g0117 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18984 | hp1 | a0001 | c0002 | t0015 | g0110 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18984 | hp2 | a0001 | c0001 | t0020 | g0323 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18985 | hp1 | a0001 | c0001 | t0128 | g0298 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18985 | hp2 | a0001 | c0002 | t0156 | g0053 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18986 | hp1 | a0001 | c0002 | t0094 | g0115 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18986 | hp2 | a0001 | c0002 | t0077 | g0075 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18993 | hp1 | a0001 | c0002 | t0046 | g0256 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18993 | hp2 | a0001 | c0001 | t0011 | g0063 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18994 | hp1 | a0001 | c0001 | t0007 | g0330 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18994 | hp2 | a0001 | c0002 | t0016 | g0013 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18995 | hp1 | a0001 | c0002 | t0159 | g0010 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18995 | hp2 | a0001 | c0002 | t0044 | g0286 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18997 | hp1 | a0001 | c0001 | t0021 | g0255 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18997 | hp2 | a0001 | c0001 | t0086 | g0116 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18999 | hp1 | a0001 | c0001 | t0042 | g0308 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18999 | hp2 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19002 | hp1 | a0001 | c0002 | t0158 | g0291 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19002 | hp2 | a0001 | c0001 | t0010 | g0315 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19003 | hp1 | a0001 | c0001 | t0018 | g0007 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19004 | hp1 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19004 | hp2 | a0001 | c0001 | t0082 | g0124 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19005 | hp1 | a0001 | c0001 | t0040 | g0039 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19005 | hp2 | a0001 | c0001 | t0132 | g0004 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19006 | hp1 | a0001 | c0001 | t0098 | g0322 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19009 | hp2 | a0001 | c0001 | t0038 | g0004 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19010 | hp1 | a0001 | c0002 | t0022 | g0011 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19010 | hp2 | a0001 | c0002 | t0153 | g0303 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19012 | hp2 | a0001 | c0001 | t0027 | g0072 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19030 | hp1 | a0001 | c0012 | t0116 | g0142 | AFR | LWK | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19030 | hp2 | a0001 | c0004 | t0043 | g0213 | AFR | LWK | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19054 | hp1 | a0001 | c0002 | t0015 | g0123 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19056 | hp1 | a0001 | c0001 | t0005 | g0280 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19057 | hp1 | a0001 | c0002 | t0003 | g0049 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19060 | hp2 | a0001 | c0002 | t0033 | g0022 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19064 | hp1 | a0001 | c0002 | t0044 | g0294 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19068 | hp2 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19074 | hp2 | a0001 | c0001 | t0011 | g0321 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19077 | hp1 | a0001 | c0002 | t0015 | g0112 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19077 | hp2 | a0001 | c0002 | t0017 | g0021 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19079 | hp1 | a0001 | c0002 | t0023 | g0045 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19079 | hp2 | a0001 | c0001 | t0118 | g0297 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19080 | hp2 | a0001 | c0002 | t0003 | g0312 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19083 | hp2 | a0001 | c0002 | t0073 | g0130 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19084 | hp1 | a0001 | c0002 | t0003 | g0296 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19084 | hp2 | a0001 | c0002 | t0160 | g0033 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19088 | hp2 | a0001 | c0001 | t0138 | g0306 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19090 | hp1 | a0001 | c0002 | t0003 | g0244 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19090 | hp2 | a0001 | c0001 | t0030 | g0118 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19091 | hp1 | a0001 | c0001 | t0139 | g0251 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19091 | hp2 | a0001 | c0001 | t0035 | g0062 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19240 | hp1 | a0001 | c0003 | t0113 | g0223 | AFR | YRI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19240 | hp2 | a0001 | c0001 | t0146 | g0254 | AFR | YRI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA20129 | hp1 | a0001 | c0010 | t0193 | g0168 | AFR | ASW | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | ASW | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0215 | EUR | TSI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA20752 | hp2 | a0001 | c0002 | t0075 | g0093 | EUR | TSI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02109 | hp1 | a0001 | c0003 | t0057 | g0134 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02109 | hp2 | a0001 | c0001 | t0176 | g0161 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02559 | hp1 | a0001 | c0005 | t0167 | g0175 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02559 | hp2 | a0001 | c0002 | t0055 | g0145 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03471 | hp1 | a0001 | c0003 | t0114 | g0210 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03471 | hp2 | a0001 | c0001 | t0122 | g0236 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG06807 | hp1 | a0001 | c0001 | t0052 | g0182 | AFR | USA | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG06807 | hp2 | a0001 | c0002 | t0105 | g0166 | AFR | USA | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA20300 | hp1 | a0001 | c0003 | t0024 | g0163 | AFR | USA | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA20300 | hp2 | a0001 | c0001 | t0178 | g0200 | AFR | USA | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA21309 | hp1 | a0001 | c0001 | t0174 | g0156 | AFR | LWK | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA21309 | hp2 | a0001 | c0001 | t0144 | g0205 | AFR | LWK | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
homoSapiens | chm13v2 | a0001 | c0001 | t0056 | g0070 | REF | REF | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
homoSapiens | grch38p0 | a0001 | c0001 | t0177 | g0162 | REF | REF | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:126690950 | A | G | 9 | a0001c0002 a0001c0003 a0001c0004 others(6): Show |
173 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(170): Show |
synonymous_variant | LOW | c.441A>G | p.Glu147Glu | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/8 | 963/6312 | 441/1209 | 147/402 | chr9 | 126690950 | |||
chr9:126691043 | C | A | 2 | a0001c0010 a0001c0011 |
2 | HG01884.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.534C>A | p.Ser178Ser | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/8 | 1056/6312 | 534/1209 | 178/402 | chr9 | 126691043 | |||
chr9:126691055 | C | T | 1 | a0001c0009 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.546C>T | p.Asp182Asp | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/8 | 1068/6312 | 546/1209 | 182/402 | chr9 | 126691055 | |||
chr9:126693308 | G | C | 7 | a0001c0002 a0001c0003 a0001c0005 others(4): Show |
159 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
synonymous_variant | LOW | c.726G>C | p.Ser242Ser | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 4/8 | 1248/6312 | 726/1209 | 242/402 | chr9 | 126693308 | |||
chr9:126693796 | C | A | 1 | a0001c0008 | 2 | HG02717.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.870C>A | p.Ser290Ser | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/8 | 1392/6312 | 870/1209 | 290/402 | chr9 | 126693796 | |||
chr9:126695882 | G | A | 1 | a0001c0005 | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
synonymous_variant | LOW | c.930G>A | p.Thr310Thr | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 7/8 | 1452/6312 | 930/1209 | 310/402 | chr9 | 126695882 | |||
chr9:126696301 | C | T | 1 | a0001c0012 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1059C>T | p.Asp353Asp | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1581/6312 | 1059/1209 | 353/402 | chr9 | 126696301 | |||
chr9:126696349 | C | T | 5 | a0001c0003 a0001c0006 a0001c0008 others(2): Show |
22 | HG00639.hp1 HG01109.hp2 HG02109.hp1 others(19): Show |
synonymous_variant | LOW | c.1107C>T | p.Ser369Ser | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1629/6312 | 1107/1209 | 369/402 | chr9 | 126696349 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:126613982 | G | C | 2 | a0001c0002t0054 a0001c0002t0055 |
2 | HG02559.hp2 HG02723.hp1 |
5_prime_UTR_variant | MODIFIER | c.-468G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 468 | chr9 | 126613982 | ||||||
chr9:126614010 | C | T | 1 | a0001c0001t0194 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-440C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 440 | chr9 | 126614010 | ||||||
chr9:126614046 | G | GC | 15 | a0001c0001t0010 a0001c0001t0095 a0001c0001t0096 others(12): Show |
20 | HG01192.hp1 HG01192.hp2 HG02080.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-396dupC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 126614046 | |||||
chr9:126614046 | G | GCC | 26 | a0001c0001t0029 a0001c0001t0030 a0001c0001t0078 others(23): Show |
35 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-397_-396dupCC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 126614046 | |||||
chr9:126614046 | G | GCCC | 21 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0028 others(18): Show |
24 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-398_-396dupCCC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 126614046 | |||||
chr9:126614087 | C | A | 5 | a0001c0001t0035 a0001c0001t0106 a0001c0002t0016 others(2): Show |
10 | HG02015.hp2 HG02027.hp2 HG02040.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-363C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 363 | chr9 | 126614087 | ||||||
chr9:126614099 | T | C | 100 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(97): Show |
209 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(206): Show |
5_prime_UTR_variant | MODIFIER | c.-351T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 351 | chr9 | 126614099 | ||||||
chr9:126614230 | G | A | 1 | a0001c0003t0165 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-220G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 220 | chr9 | 126614230 | ||||||
chr9:126614265 | C | T | 1 | a0001c0001t0164 | 1 | HG01975.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-185C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | chr9 | 126614265 | |||||||
chr9:126614345 | G | GGGGCCGC others(15): Show |
1 | a0001c0002t0075 | 1 | NA20752.hp2 | 5_prime_UTR_variant | MODIFIER | c.-96_-75dupCCTCCCCG others(14): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 74 | INFO_REALIGN_3_PRIME | chr9 | 126614345 | |||||
chr9:126696478 | G | A | 21 | a0001c0002t0100 a0001c0002t0166 a0001c0003t0024 others(18): Show |
29 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*27G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 27 | chr9 | 126696478 | ||||||
chr9:126696489 | G | A | 2 | a0001c0001t0095 a0001c0001t0117 |
2 | HG03688.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*38G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 38 | chr9 | 126696489 | ||||||
chr9:126696502 | A | G | 22 | a0001c0002t0055 a0001c0002t0100 a0001c0002t0166 others(19): Show |
30 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*51A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 51 | chr9 | 126696502 | ||||||
chr9:126696530 | G | A | 22 | a0001c0002t0055 a0001c0002t0100 a0001c0002t0166 others(19): Show |
30 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*79G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 79 | chr9 | 126696530 | ||||||
chr9:126696578 | C | T | 3 | a0001c0002t0054 a0001c0007t0048 a0001c0010t0193 |
4 | HG02723.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*127C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 127 | chr9 | 126696578 | ||||||
chr9:126696606 | G | A | 1 | a0001c0001t0010 | 4 | NA18959.hp2 NA18961.hp1 NA18963.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*155G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 155 | chr9 | 126696606 | ||||||
chr9:126696624 | G | A | 5 | a0001c0003t0057 a0001c0003t0076 a0001c0003t0108 others(2): Show |
5 | HG02109.hp1 HG02647.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*173G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 173 | chr9 | 126696624 | ||||||
chr9:126696651 | C | T | 1 | a0001c0012t0116 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 200 | chr9 | 126696651 | ||||||
chr9:126696701 | G | A | 1 | a0001c0002t0077 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*250G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 250 | chr9 | 126696701 | ||||||
chr9:126696731 | G | A | 2 | a0001c0002t0054 a0001c0007t0048 |
3 | HG02723.hp1 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*280G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 280 | chr9 | 126696731 | ||||||
chr9:126696891 | G | T | 1 | a0001c0002t0163 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*440G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 440 | chr9 | 126696891 | ||||||
chr9:126696902 | C | T | 29 | a0001c0002t0001 a0001c0002t0014 a0001c0002t0017 others(26): Show |
69 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*451C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 451 | chr9 | 126696902 | ||||||
chr9:126696966 | A | G | 2 | a0001c0002t0054 a0001c0007t0048 |
3 | HG02723.hp1 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*515A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 515 | chr9 | 126696966 | ||||||
chr9:126697035 | C | T | 33 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0006 others(30): Show |
62 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*584C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 584 | chr9 | 126697035 | ||||||
chr9:126697083 | AACAC | A | 1 | a0001c0002t0023 | 3 | NA18954.hp2 NA18961.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*640_*643delCACA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 640 | INFO_REALIGN_3_PRIME | chr9 | 126697083 | |||||
chr9:126697132 | C | T | 1 | a0001c0002t0153 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*681C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 681 | chr9 | 126697132 | ||||||
chr9:126697159 | G | A | 31 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0006 others(28): Show |
59 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*708G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 708 | chr9 | 126697159 | ||||||
chr9:126697199 | C | T | 37 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0006 others(34): Show |
67 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*748C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 748 | chr9 | 126697199 | ||||||
chr9:126697236 | C | T | 1 | a0001c0004t0150 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*785C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 785 | chr9 | 126697236 | ||||||
chr9:126697246 | C | T | 1 | a0001c0001t0149 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*795C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 795 | chr9 | 126697246 | ||||||
chr9:126697335 | G | A | 2 | a0001c0001t0058 a0001c0001t0169 |
2 | HG02922.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*884G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 884 | chr9 | 126697335 | ||||||
chr9:126697349 | C | T | 8 | a0001c0001t0058 a0001c0001t0065 a0001c0001t0066 others(5): Show |
8 | HG00280.hp2 HG00738.hp2 HG01074.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*898C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 898 | chr9 | 126697349 | ||||||
chr9:126697383 | G | T | 48 | a0001c0001t0146 a0001c0002t0001 a0001c0002t0014 others(45): Show |
95 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*932G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 932 | chr9 | 126697383 | ||||||
chr9:126697519 | T | A | 1 | a0001c0001t0106 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1068T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1068 | chr9 | 126697519 | ||||||
chr9:126697556 | CTT | C | 7 | a0001c0002t0053 a0001c0002t0054 a0001c0002t0105 others(4): Show |
9 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1106_*1107delTT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1106 | chr9 | 126697556 | ||||||
chr9:126697582 | C | T | 1 | a0001c0002t0160 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1131C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1131 | chr9 | 126697582 | ||||||
chr9:126697706 | A | G | 48 | a0001c0001t0146 a0001c0002t0001 a0001c0002t0014 others(45): Show |
95 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*1255A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1255 | chr9 | 126697706 | ||||||
chr9:126697755 | G | A | 13 | a0001c0001t0146 a0001c0002t0055 a0001c0002t0100 others(10): Show |
17 | HG00639.hp1 HG01109.hp2 HG02559.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1304G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1304 | chr9 | 126697755 | ||||||
chr9:126697837 | C | CTGTTT | 15 | a0001c0001t0004 a0001c0001t0020 a0001c0001t0040 others(12): Show |
29 | HG00597.hp1 HG01346.hp1 HG01496.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1437_*1441dupTGTT others(1): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1442 | INFO_REALIGN_3_PRIME | chr9 | 126697837 | |||||
chr9:126697837 | C | CTGTTTTG others(3): Show |
10 | a0001c0001t0021 a0001c0001t0064 a0001c0001t0068 others(7): Show |
13 | HG00280.hp2 HG00621.hp1 HG01168.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1432_*1441dupTGTT others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1442 | INFO_REALIGN_3_PRIME | chr9 | 126697837 | |||||
chr9:126697837 | C | CTGTTTTG others(8): Show |
2 | a0001c0001t0148 a0001c0004t0145 |
2 | HG03239.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1427_*1441dupTGTT others(11): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1442 | INFO_REALIGN_3_PRIME | chr9 | 126697837 | |||||
chr9:126697837 | CTGTTT | C | 59 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(56): Show |
109 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*1437_*1441delTGTT others(1): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1437 | INFO_REALIGN_3_PRIME | chr9 | 126697837 | |||||
chr9:126697837 | CTGTTTTG others(3): Show |
C | 15 | a0001c0001t0036 a0001c0001t0118 a0001c0001t0170 others(12): Show |
18 | HG01978.hp2 HG02280.hp2 HG02559.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1432_*1441delTGTT others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1432 | INFO_REALIGN_3_PRIME | chr9 | 126697837 | |||||
chr9:126697837 | CTGTTTTG others(8): Show |
C | 3 | a0001c0001t0164 a0001c0002t0006 a0001c0002t0087 |
8 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1427_*1441delTGTT others(11): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1427 | INFO_REALIGN_3_PRIME | chr9 | 126697837 | |||||
chr9:126697839 | G | GGTTTT | 4 | a0001c0002t0001 a0001c0002t0014 a0001c0005t0012 others(1): Show |
8 | HG00609.hp2 HG01884.hp2 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1388_*1389insGTTT others(1): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1389 | chr9 | 126697839 | ||||||
chr9:126697839 | GTTTTGTT others(2): Show |
G | 3 | a0001c0002t0047 a0001c0008t0034 a0001c0012t0116 |
5 | HG01358.hp1 HG01361.hp2 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1389_*1397delTTTT others(5): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1389 | chr9 | 126697839 | ||||||
chr9:126697839 | GTTTTGTT others(7): Show |
G | 5 | a0001c0003t0057 a0001c0003t0076 a0001c0003t0108 others(2): Show |
5 | HG02109.hp1 HG02647.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1389_*1402delTTTT others(10): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1389 | chr9 | 126697839 | ||||||
chr9:126697839 | GTTTTGTT others(12): Show |
G | 1 | a0001c0010t0193 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1389_*1407delTTTT others(15): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1389 | chr9 | 126697839 | ||||||
chr9:126697840 | T | G | 24 | a0001c0002t0001 a0001c0002t0014 a0001c0002t0017 others(21): Show |
59 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1389T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1389 | chr9 | 126697840 | ||||||
chr9:126697844 | G | T | 24 | a0001c0002t0001 a0001c0002t0014 a0001c0002t0017 others(21): Show |
58 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1393G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1393 | chr9 | 126697844 | ||||||
chr9:126697853 | TG | T | 3 | a0001c0002t0047 a0001c0008t0034 a0001c0012t0116 |
5 | HG01358.hp1 HG01361.hp2 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1403delG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1403 | chr9 | 126697853 | ||||||
chr9:126697858 | TG | T | 5 | a0001c0003t0057 a0001c0003t0076 a0001c0003t0108 others(2): Show |
5 | HG02109.hp1 HG02647.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1408delG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1408 | chr9 | 126697858 | ||||||
chr9:126697924 | G | A | 32 | a0001c0002t0001 a0001c0002t0014 a0001c0002t0017 others(29): Show |
72 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1473G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1473 | chr9 | 126697924 | ||||||
chr9:126697989 | C | G | 2 | a0001c0002t0100 a0001c0002t0166 |
2 | HG03225.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1538C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1538 | chr9 | 126697989 | ||||||
chr9:126698025 | G | A | 1 | a0001c0001t0119 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1574G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1574 | chr9 | 126698025 | ||||||
chr9:126698025 | G | T | 3 | a0001c0005t0012 a0001c0005t0167 a0001c0005t0168 |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1574G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1574 | chr9 | 126698025 | ||||||
chr9:126698033 | A | G | 75 | a0001c0001t0003 a0001c0001t0067 a0001c0002t0001 others(72): Show |
148 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*1582A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1582 | chr9 | 126698033 | ||||||
chr9:126698055 | A | G | 6 | a0001c0003t0057 a0001c0003t0076 a0001c0003t0108 others(3): Show |
7 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1604A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1604 | chr9 | 126698055 | ||||||
chr9:126698088 | TGGTCTCC others(14): Show |
T | 6 | a0001c0001t0005 a0001c0001t0042 a0001c0001t0098 others(3): Show |
12 | HG00408.hp1 HG00642.hp1 HG01934.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1641_*1661delCTCC others(17): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1641 | INFO_REALIGN_3_PRIME | chr9 | 126698088 | |||||
chr9:126698095 | C | G | 6 | a0001c0003t0057 a0001c0003t0076 a0001c0003t0108 others(3): Show |
7 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1644C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1644 | chr9 | 126698095 | ||||||
chr9:126698115 | T | A | 1 | a0001c0004t0180 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1664T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1664 | chr9 | 126698115 | ||||||
chr9:126698117 | C | T | 34 | a0001c0001t0003 a0001c0001t0067 a0001c0002t0003 others(31): Show |
62 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1666C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1666 | chr9 | 126698117 | ||||||
chr9:126698124 | C | G | 1 | a0001c0001t0020 | 3 | NA18943.hp2 NA18971.hp2 NA18984.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1673C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1673 | chr9 | 126698124 | ||||||
chr9:126698154 | C | T | 6 | a0001c0003t0057 a0001c0003t0076 a0001c0003t0108 others(3): Show |
7 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1703C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1703 | chr9 | 126698154 | ||||||
chr9:126698167 | A | G | 9 | a0001c0003t0057 a0001c0003t0076 a0001c0003t0108 others(6): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1716A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1716 | chr9 | 126698167 | ||||||
chr9:126698226 | T | C | 1 | a0001c0012t0116 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1775T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1775 | chr9 | 126698226 | ||||||
chr9:126698443 | T | C | 43 | a0001c0001t0037 a0001c0001t0078 a0001c0001t0120 others(40): Show |
86 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1992T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1992 | chr9 | 126698443 | ||||||
chr9:126698446 | C | G | 3 | a0001c0001t0146 a0001c0003t0024 a0001c0003t0165 |
5 | HG02723.hp2 HG03041.hp1 HG03579.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1995C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1995 | chr9 | 126698446 | ||||||
chr9:126698448 | G | A | 43 | a0001c0001t0037 a0001c0001t0078 a0001c0001t0120 others(40): Show |
86 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1997G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1997 | chr9 | 126698448 | ||||||
chr9:126698463 | A | G | 1 | a0001c0004t0063 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2012A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2012 | chr9 | 126698463 | ||||||
chr9:126698611 | C | T | 1 | a0001c0001t0139 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2160C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2160 | chr9 | 126698611 | ||||||
chr9:126698635 | A | G | 98 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(95): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*2184A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2184 | chr9 | 126698635 | ||||||
chr9:126698686 | T | G | 1 | a0001c0002t0154 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2235T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2235 | chr9 | 126698686 | ||||||
chr9:126698796 | G | A | 5 | a0001c0001t0120 a0001c0003t0108 a0001c0003t0109 others(2): Show |
6 | HG02559.hp1 HG02717.hp2 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2345G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2345 | chr9 | 126698796 | ||||||
chr9:126698844 | T | C | 167 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(164): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*2393T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2393 | chr9 | 126698844 | ||||||
chr9:126698845 | G | C | 85 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(82): Show |
128 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*2394G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2394 | chr9 | 126698845 | ||||||
chr9:126699034 | C | A | 1 | a0001c0001t0025 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2583C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2583 | chr9 | 126699034 | ||||||
chr9:126699039 | CTT | C | 69 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(66): Show |
117 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*2590_*2591delTT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2590 | INFO_REALIGN_3_PRIME | chr9 | 126699039 | |||||
chr9:126699101 | G | T | 1 | a0001c0001t0059 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2650G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2650 | chr9 | 126699101 | ||||||
chr9:126699126 | C | T | 1 | a0001c0001t0174 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2675C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2675 | chr9 | 126699126 | ||||||
chr9:126699165 | G | A | 1 | a0001c0010t0193 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2714G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2714 | chr9 | 126699165 | ||||||
chr9:126699190 | C | A | 1 | a0001c0002t0015 | 3 | NA18984.hp1 NA19054.hp1 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2739C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2739 | chr9 | 126699190 | ||||||
chr9:126699231 | G | A | 1 | a0001c0002t0156 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2780G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2780 | chr9 | 126699231 | ||||||
chr9:126699435 | C | T | 61 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(58): Show |
102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*2984C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2984 | chr9 | 126699435 | ||||||
chr9:126699633 | A | G | 67 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(64): Show |
108 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3182A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3182 | chr9 | 126699633 | ||||||
chr9:126699682 | T | C | 1 | a0001c0002t0189 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3231T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3231 | chr9 | 126699682 | ||||||
chr9:126699687 | G | A | 1 | a0001c0001t0141 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3236G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3236 | chr9 | 126699687 | ||||||
chr9:126699789 | C | G | 1 | a0001c0001t0127 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3338C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3338 | chr9 | 126699789 | ||||||
chr9:126699793 | T | C | 64 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(61): Show |
103 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*3342T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3342 | chr9 | 126699793 | ||||||
chr9:126699797 | G | A | 35 | a0001c0001t0003 a0001c0001t0027 a0001c0001t0040 others(32): Show |
66 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*3346G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3346 | chr9 | 126699797 | ||||||
chr9:126700023 | G | C | 1 | a0001c0003t0109 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3572G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3572 | chr9 | 126700023 | ||||||
chr9:126700222 | G | T | 117 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(114): Show |
217 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*3771G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3771 | chr9 | 126700222 | ||||||
chr9:126700284 | A | G | 118 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(115): Show |
218 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*3833A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3833 | chr9 | 126700284 | ||||||
chr9:126700315 | T | C | 118 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(115): Show |
218 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*3864T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3864 | chr9 | 126700315 | ||||||
chr9:126700316 | G | A | 33 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0011 others(30): Show |
60 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*3865G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3865 | chr9 | 126700316 | ||||||
chr9:126700332 | G | T | 33 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0011 others(30): Show |
60 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*3881G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3881 | chr9 | 126700332 | ||||||
chr9:126700408 | C | A | 113 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(110): Show |
212 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*3957C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3957 | chr9 | 126700408 | ||||||
chr9:126700431 | T | A | 1 | a0001c0003t0114 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3980T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3980 | chr9 | 126700431 | ||||||
chr9:126700463 | C | T | 1 | a0001c0001t0125 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4012C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 4012 | chr9 | 126700463 | ||||||
chr9:126700503 | A | G | 1 | a0001c0001t0140 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4052A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 4052 | chr9 | 126700503 | ||||||
chr9:126700581 | G | A | 2 | a0001c0003t0076 a0001c0003t0110 |
2 | HG02647.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4130G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 4130 | chr9 | 126700581 | ||||||
chr9:126700616 | G | A | 4 | a0001c0003t0114 a0001c0004t0063 a0001c0004t0185 others(1): Show |
4 | HG01243.hp2 HG01496.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4165G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 4165 | chr9 | 126700616 | ||||||
chr9:126700622 | T | C | 119 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(116): Show |
222 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*4171T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 4171 | chr9 | 126700622 | ||||||
chr9:126700661 | G | C | 1 | a0001c0009t0102 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4210G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 4210 | chr9 | 126700661 | ||||||
chr9:126700824 | A | G | 2 | a0001c0002t0100 a0001c0002t0166 |
2 | HG03225.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4373A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 4373 | chr9 | 126700824 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:126614787 | G | A | 1 | a0001c0001t0136g0008 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.139+199G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126614787 | |||||||
chr9:126614797 | C | T | 3 | a0001c0001t0019g0334 a0001c0001t0019g0335 a0001c0001t0148g0333 |
3 | HG00639.hp2 HG00735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.139+209C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126614797 | |||||||
chr9:126614883 | G | A | 60 | a0001c0001t0004g0056 a0001c0001t0007g0040 a0001c0001t0007g0051 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.139+295G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126614883 | |||||||
chr9:126614956 | C | T | 100 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(97): Show |
101 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.139+368C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126614956 | |||||||
chr9:126615075 | G | A | 2 | a0001c0002t0161g0068 a0001c0004t0150g0067 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.140-308G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126615075 | |||||||
chr9:126615117 | A | G | 44 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(41): Show |
45 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.140-266A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126615117 | |||||||
chr9:126615121 | C | T | 1 | a0001c0001t0038g0332 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.140-262C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126615121 | |||||||
chr9:126615301 | G | A | 1 | a0001c0003t0110g0069 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.140-82G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126615301 | |||||||
chr9:126615576 | G | C | 66 | a0001c0001t0025g0084 a0001c0001t0026g0100 a0001c0001t0026g0107 others(63): Show |
67 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(64): Show |
splice_region_variant&intron_variant | LOW | c.326+7G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126615576 | |||||||
chr9:126615747 | G | C | 290 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(287): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.326+178G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126615747 | |||||||
chr9:126615856 | T | C | 1 | a0001c0001t0004g0240 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.326+287T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126615856 | |||||||
chr9:126615857 | A | G | 1 | a0001c0003t0024g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.326+288A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126615857 | |||||||
chr9:126615947 | C | T | 1 | a0001c0001t0052g0201 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.326+378C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126615947 | |||||||
chr9:126616049 | GCCCC | G | 4 | a0001c0001t0011g0063 a0001c0001t0134g0066 a0001c0002t0001g0064 others(1): Show |
4 | NA18942.hp2 NA18946.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+482_326+485del others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126616049 | ||||||
chr9:126616105 | A | T | 100 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(97): Show |
101 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.326+536A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616105 | |||||||
chr9:126616118 | C | G | 1 | a0001c0001t0008g0331 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.326+549C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616118 | |||||||
chr9:126616193 | A | G | 60 | a0001c0001t0004g0056 a0001c0001t0007g0040 a0001c0001t0007g0051 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+624A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616193 | |||||||
chr9:126616213 | T | C | 1 | a0001c0001t0164g0241 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.326+644T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616213 | |||||||
chr9:126616304 | C | T | 5 | a0001c0001t0178g0200 a0001c0002t0014g0198 a0001c0002t0103g0196 others(2): Show |
5 | HG01070.hp1 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+735C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616304 | |||||||
chr9:126616685 | G | A | 60 | a0001c0001t0004g0056 a0001c0001t0007g0040 a0001c0001t0007g0051 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+1116G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616685 | |||||||
chr9:126616766 | C | T | 1 | a0001c0002t0091g0135 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.326+1197C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616766 | |||||||
chr9:126616951 | G | C | 66 | a0001c0001t0025g0084 a0001c0001t0026g0100 a0001c0001t0026g0107 others(63): Show |
67 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.326+1382G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616951 | |||||||
chr9:126617028 | A | G | 1 | a0001c0001t0052g0201 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.326+1459A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617028 | |||||||
chr9:126617239 | G | A | 44 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(41): Show |
45 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.326+1670G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617239 | |||||||
chr9:126617277 | G | A | 1 | a0001c0001t0084g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.326+1708G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617277 | |||||||
chr9:126617492 | T | TA | 61 | a0001c0001t0003g0243 a0001c0001t0004g0056 a0001c0001t0007g0040 others(58): Show |
61 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.326+1934dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126617492 | ||||||
chr9:126617681 | C | T | 3 | a0001c0002t0186g0133 a0001c0003t0057g0134 a0001c0003t0076g0132 |
3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.326+2112C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617681 | |||||||
chr9:126617801 | G | A | 1 | a0001c0003t0109g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+2232G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617801 | |||||||
chr9:126617829 | C | A | 5 | a0001c0003t0165g0141 a0001c0005t0012g0137 a0001c0005t0012g0138 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+2260C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617829 | |||||||
chr9:126617864 | G | A | 1 | a0001c0001t0125g0203 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.326+2295G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617864 | |||||||
chr9:126617868 | A | G | 1 | a0001c0001t0179g0195 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.326+2299A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617868 | |||||||
chr9:126617904 | C | T | 1 | a0001c0001t0007g0330 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.326+2335C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617904 | |||||||
chr9:126617918 | T | TG | 9 | a0001c0001t0027g0072 a0001c0001t0117g0245 a0001c0001t0141g0204 others(6): Show |
9 | HG00741.hp2 HG01978.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.326+2355dupG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126617918 | ||||||
chr9:126618037 | T | A | 1 | a0001c0001t0002g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.326+2468T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126618037 | |||||||
chr9:126618273 | G | A | 1 | a0001c0001t0095g0247 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.326+2704G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126618273 | |||||||
chr9:126618653 | G | A | 1 | a0001c0001t0067g0073 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.326+3084G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126618653 | |||||||
chr9:126619106 | G | A | 1 | a0001c0003t0110g0069 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.326+3537G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126619106 | |||||||
chr9:126619287 | C | A | 2 | a0001c0001t0002g0246 a0001c0001t0002g0248 |
2 | HG03834.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.326+3718C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126619287 | |||||||
chr9:126619560 | A | G | 1 | a0001c0001t0002g0329 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.326+3991A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126619560 | |||||||
chr9:126619602 | G | A | 1 | a0001c0002t0072g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.326+4033G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126619602 | |||||||
chr9:126619772 | G | A | 1 | a0001c0002t0022g0011 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.326+4203G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126619772 | |||||||
chr9:126619946 | G | A | 1 | a0001c0002t0103g0196 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.326+4377G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126619946 | |||||||
chr9:126620141 | C | T | 1 | a0001c0001t0011g0328 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.326+4572C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126620141 | |||||||
chr9:126620281 | A | G | 29 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0052g0182 others(26): Show |
29 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.326+4712A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126620281 | |||||||
chr9:126620519 | G | A | 1 | a0001c0002t0077g0075 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.326+4950G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126620519 | |||||||
chr9:126620920 | G | A | 165 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(162): Show |
167 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.326+5351G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126620920 | |||||||
chr9:126621006 | G | A | 61 | a0001c0001t0004g0056 a0001c0001t0007g0040 a0001c0001t0007g0051 others(58): Show |
61 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.326+5437G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621006 | |||||||
chr9:126621063 | GA | G | 4 | a0001c0001t0027g0072 a0001c0001t0027g0129 a0001c0001t0083g0131 others(1): Show |
4 | NA18941.hp1 NA18953.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+5495delA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621063 | |||||||
chr9:126621411 | T | C | 1 | a0001c0001t0028g0076 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.326+5842T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621411 | |||||||
chr9:126621620 | C | T | 14 | a0001c0001t0101g0170 a0001c0002t0189g0172 a0001c0002t0192g0171 others(11): Show |
14 | HG00639.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.326+6051C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621620 | |||||||
chr9:126621621 | G | A | 67 | a0001c0001t0025g0084 a0001c0001t0026g0100 a0001c0001t0026g0107 others(64): Show |
68 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.326+6052G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621621 | |||||||
chr9:126621652 | CTTCTTTT others(2): Show |
C | 5 | a0001c0001t0027g0129 a0001c0001t0061g0077 a0001c0001t0068g0078 others(2): Show |
6 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.326+6086_326+6094d others(11): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621652 | ||||||
chr9:126621652 | CTTCTTTT others(3): Show |
C | 61 | a0001c0001t0025g0084 a0001c0001t0026g0100 a0001c0001t0026g0107 others(58): Show |
61 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.326+6086_326+6095d others(12): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621652 | ||||||
chr9:126621655 | C | CT | 10 | a0001c0001t0002g0219 a0001c0001t0002g0226 a0001c0001t0101g0170 others(7): Show |
10 | HG01069.hp2 HG01167.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.326+6112dupT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621655 | ||||||
chr9:126621655 | CTTTTT | C | 10 | a0001c0001t0010g0315 a0001c0001t0018g0006 a0001c0001t0040g0259 others(7): Show |
10 | HG00597.hp1 HG02040.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.326+6108_326+6112d others(7): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621655 | ||||||
chr9:126621655 | CTTTTTT | C | 87 | a0001c0001t0002g0231 a0001c0001t0002g0246 a0001c0001t0002g0248 others(84): Show |
88 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.326+6107_326+6112d others(8): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621655 | ||||||
chr9:126621655 | CTTTTTTT | C | 28 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0215 others(25): Show |
29 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.326+6106_326+6112d others(9): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621655 | ||||||
chr9:126621655 | CTTTTTTT others(3): Show |
C | 82 | a0001c0001t0003g0243 a0001c0001t0004g0056 a0001c0001t0007g0051 others(79): Show |
82 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.326+6103_326+6112d others(12): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621655 | ||||||
chr9:126621655 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0007g0040 a0001c0001t0019g0031 a0001c0002t0001g0036 others(1): Show |
4 | HG01069.hp1 NA18945.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+6102_326+6112d others(13): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621655 | ||||||
chr9:126621661 | T | C | 1 | a0001c0012t0116g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326+6092T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621661 | |||||||
chr9:126621662 | T | C | 5 | a0001c0001t0027g0129 a0001c0001t0061g0077 a0001c0001t0068g0078 others(2): Show |
6 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.326+6093T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621662 | |||||||
chr9:126621663 | T | C | 61 | a0001c0001t0025g0084 a0001c0001t0026g0100 a0001c0001t0026g0107 others(58): Show |
61 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.326+6094T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621663 | |||||||
chr9:126621664 | T | C | 3 | a0001c0001t0139g0251 a0001c0002t0001g0249 a0001c0002t0001g0250 |
3 | NA18966.hp1 NA19068.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.326+6095T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621664 | |||||||
chr9:126621677 | T | C | 1 | a0001c0003t0110g0069 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.326+6108T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621677 | |||||||
chr9:126621691 | G | C | 1 | a0001c0001t0124g0252 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.326+6122G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621691 | |||||||
chr9:126621703 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.326+6134A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621703 | |||||||
chr9:126621942 | C | T | 1 | a0001c0001t0178g0200 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.326+6373C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621942 | |||||||
chr9:126621943 | C | T | 1 | a0001c0002t0013g0128 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.326+6374C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621943 | |||||||
chr9:126622168 | C | T | 7 | a0001c0001t0037g0234 a0001c0001t0120g0238 a0001c0001t0122g0236 others(4): Show |
7 | HG00735.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.326+6599C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126622168 | |||||||
chr9:126622511 | G | A | 1 | a0001c0003t0109g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+6942G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126622511 | |||||||
chr9:126622530 | C | T | 1 | a0001c0002t0105g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.326+6961C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126622530 | |||||||
chr9:126622690 | C | T | 2 | a0001c0001t0002g0231 a0001c0001t0096g0230 |
2 | HG02080.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.326+7121C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126622690 | |||||||
chr9:126623171 | G | A | 15 | a0001c0001t0035g0020 a0001c0001t0035g0062 a0001c0001t0133g0018 others(12): Show |
15 | HG00438.hp1 HG02015.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.326+7602G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623171 | |||||||
chr9:126623174 | G | A | 2 | a0001c0002t0054g0146 a0001c0002t0055g0145 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.326+7605G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623174 | |||||||
chr9:126623304 | G | C | 1 | a0001c0003t0108g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.326+7735G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623304 | |||||||
chr9:126623391 | T | C | 320 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(317): Show |
323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.326+7822T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623391 | |||||||
chr9:126623545 | T | C | 2 | a0001c0001t0038g0004 a0001c0001t0132g0004 |
2 | NA19005.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.326+7976T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623545 | |||||||
chr9:126623752 | ACCT | A | 44 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(41): Show |
45 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.326+8188_326+8190d others(5): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126623752 | ||||||
chr9:126623764 | C | T | 61 | a0001c0001t0004g0056 a0001c0001t0007g0040 a0001c0001t0007g0051 others(58): Show |
61 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.326+8195C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623764 | |||||||
chr9:126623796 | G | T | 4 | a0001c0003t0024g0163 a0001c0003t0024g0165 a0001c0003t0024g0202 others(1): Show |
4 | HG03041.hp1 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+8227G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623796 | |||||||
chr9:126623850 | G | A | 1 | a0001c0001t0061g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.326+8281G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623850 | |||||||
chr9:126623907 | A | G | 77 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(74): Show |
78 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.326+8338A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623907 | |||||||
chr9:126623966 | G | C | 1 | a0001c0001t0080g0080 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.326+8397G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623966 | |||||||
chr9:126623969 | T | C | 1 | a0001c0001t0144g0205 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.326+8400T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623969 | |||||||
chr9:126624062 | G | A | 4 | a0001c0002t0100g0147 a0001c0002t0105g0166 a0001c0008t0034g0148 others(1): Show |
4 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+8493G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624062 | |||||||
chr9:126624346 | C | T | 165 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(162): Show |
167 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.326+8777C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624346 | |||||||
chr9:126624352 | G | A | 1 | a0001c0001t0146g0254 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.326+8783G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624352 | |||||||
chr9:126624485 | G | T | 1 | a0001c0001t0029g0127 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.326+8916G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624485 | |||||||
chr9:126624499 | T | C | 20 | a0001c0001t0002g0273 a0001c0001t0004g0260 a0001c0001t0004g0261 others(17): Show |
20 | HG00408.hp1 HG00597.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.326+8930T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624499 | |||||||
chr9:126624581 | C | T | 66 | a0001c0001t0025g0084 a0001c0001t0026g0100 a0001c0001t0026g0107 others(63): Show |
67 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.326+9012C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624581 | |||||||
chr9:126624663 | C | T | 320 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(317): Show |
323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.326+9094C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624663 | |||||||
chr9:126624666 | GT | G | 306 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.326+9110delT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126624666 | ||||||
chr9:126624683 | T | C | 1 | a0001c0001t0002g0274 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.326+9114T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624683 | |||||||
chr9:126624985 | C | G | 4 | a0001c0002t0100g0147 a0001c0002t0105g0166 a0001c0008t0034g0148 others(1): Show |
4 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+9416C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624985 | |||||||
chr9:126625044 | C | T | 3 | a0001c0002t0186g0133 a0001c0003t0057g0134 a0001c0003t0076g0132 |
3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.326+9475C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625044 | |||||||
chr9:126625062 | C | G | 1 | a0001c0001t0175g0125 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.326+9493C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625062 | |||||||
chr9:126625108 | T | C | 1 | a0001c0003t0024g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.326+9539T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625108 | |||||||
chr9:126625224 | T | C | 4 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0127g0209 others(1): Show |
4 | HG00099.hp2 HG01074.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.326+9655T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625224 | |||||||
chr9:126625493 | G | A | 1 | a0001c0001t0028g0081 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.326+9924G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625493 | |||||||
chr9:126625754 | C | A | 28 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0052g0182 others(25): Show |
28 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.326+10185C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625754 | |||||||
chr9:126625757 | C | G | 1 | a0001c0001t0082g0124 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.326+10188C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625757 | |||||||
chr9:126625947 | G | C | 1 | a0001c0002t0100g0147 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.326+10378G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625947 | |||||||
chr9:126626129 | T | C | 2 | a0001c0009t0102g0167 a0001c0010t0193g0168 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.326+10560T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126626129 | |||||||
chr9:126626389 | C | A | 1 | a0001c0001t0008g0005 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.326+10820C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126626389 | |||||||
chr9:126626435 | A | G | 1 | a0001c0003t0109g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+10866A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126626435 | |||||||
chr9:126626783 | C | A | 2 | a0001c0007t0048g0318 a0001c0007t0048g0319 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.326+11214C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126626783 | |||||||
chr9:126627183 | A | AC | 15 | a0001c0001t0035g0020 a0001c0001t0035g0062 a0001c0001t0133g0018 others(12): Show |
15 | HG00438.hp1 HG02015.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.326+11620dupC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126627183 | ||||||
chr9:126627431 | C | T | 320 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(317): Show |
323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.326+11862C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126627431 | |||||||
chr9:126627449 | C | T | 2 | a0001c0002t0014g0193 a0001c0002t0014g0194 |
2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.326+11880C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126627449 | |||||||
chr9:126627555 | G | A | 1 | a0001c0001t0005g0275 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.326+11986G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126627555 | |||||||
chr9:126627556 | C | A | 1 | a0001c0001t0005g0275 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.326+11987C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126627556 | |||||||
chr9:126628056 | G | T | 2 | a0001c0002t0054g0146 a0001c0002t0055g0145 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.326+12487G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628056 | |||||||
chr9:126628080 | A | C | 2 | a0001c0007t0048g0318 a0001c0007t0048g0319 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.326+12511A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628080 | |||||||
chr9:126628170 | G | T | 1 | a0001c0003t0049g0150 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.326+12601G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628170 | |||||||
chr9:126628229 | G | C | 1 | a0001c0001t0148g0333 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.326+12660G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628229 | |||||||
chr9:126628492 | G | A | 1 | a0001c0001t0036g0003 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.326+12923G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628492 | |||||||
chr9:126628521 | C | T | 67 | a0001c0001t0025g0084 a0001c0001t0026g0100 a0001c0001t0026g0107 others(64): Show |
68 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.326+12952C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628521 | |||||||
chr9:126628627 | C | T | 1 | a0001c0001t0134g0066 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.326+13058C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628627 | |||||||
chr9:126628956 | C | T | 1 | a0001c0001t0164g0241 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.326+13387C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628956 | |||||||
chr9:126628993 | TA | T | 311 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(308): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.326+13437delA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126628993 | ||||||
chr9:126629086 | A | G | 1 | a0001c0001t0148g0333 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.326+13517A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126629086 | |||||||
chr9:126629259 | C | T | 29 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0052g0182 others(26): Show |
29 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.326+13690C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126629259 | |||||||
chr9:126629405 | G | A | 4 | a0001c0002t0100g0147 a0001c0002t0105g0166 a0001c0008t0034g0148 others(1): Show |
4 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+13836G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126629405 | |||||||
chr9:126629583 | A | ATG | 29 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0052g0182 others(26): Show |
29 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.326+14015_326+1401 others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126629583 | ||||||
chr9:126629589 | G | C | 5 | a0001c0002t0100g0147 a0001c0002t0105g0166 a0001c0003t0109g0136 others(2): Show |
5 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+14020G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126629589 | |||||||
chr9:126629692 | T | C | 2 | a0001c0001t0101g0170 a0001c0003t0049g0169 |
2 | HG00639.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.326+14123T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126629692 | |||||||
chr9:126629697 | G | A | 1 | a0001c0001t0124g0252 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.326+14128G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126629697 | |||||||
chr9:126629962 | G | A | 14 | a0001c0001t0101g0170 a0001c0002t0189g0172 a0001c0002t0192g0171 others(11): Show |
14 | HG00639.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.326+14393G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126629962 | |||||||
chr9:126630086 | C | T | 39 | a0001c0001t0026g0107 a0001c0001t0027g0072 a0001c0001t0027g0129 others(36): Show |
39 | HG00323.hp1 HG00621.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.326+14517C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126630086 | |||||||
chr9:126630161 | C | CA | 22 | a0001c0001t0011g0063 a0001c0001t0021g0255 a0001c0001t0021g0320 others(19): Show |
22 | HG00621.hp1 HG00639.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.326+14611dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126630161 | ||||||
chr9:126630161 | C | CAA | 100 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(97): Show |
101 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.326+14610_326+1461 others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126630161 | ||||||
chr9:126630286 | C | G | 1 | a0001c0012t0116g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326+14717C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126630286 | |||||||
chr9:126630512 | C | T | 1 | a0001c0002t0191g0192 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.326+14943C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126630512 | |||||||
chr9:126630636 | T | G | 1 | a0001c0002t0001g0064 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.326+15067T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126630636 | |||||||
chr9:126630901 | G | A | 1 | a0001c0002t0192g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.326+15332G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126630901 | |||||||
chr9:126631073 | G | A | 6 | a0001c0001t0179g0195 a0001c0003t0024g0163 a0001c0003t0024g0165 others(3): Show |
6 | HG01109.hp2 HG03041.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.326+15504G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631073 | |||||||
chr9:126631153 | C | T | 1 | a0001c0001t0004g0272 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.326+15584C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631153 | |||||||
chr9:126631224 | A | G | 14 | a0001c0001t0101g0170 a0001c0002t0189g0172 a0001c0002t0192g0171 others(11): Show |
14 | HG00639.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.326+15655A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631224 | |||||||
chr9:126631345 | G | A | 1 | a0001c0003t0109g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+15776G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631345 | |||||||
chr9:126631386 | G | A | 1 | a0001c0003t0109g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+15817G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631386 | |||||||
chr9:126631509 | G | A | 60 | a0001c0001t0007g0040 a0001c0001t0007g0051 a0001c0001t0008g0030 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+15940G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631509 | |||||||
chr9:126631509 | G | T | 1 | a0001c0003t0165g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+15940G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631509 | |||||||
chr9:126631510 | G | C | 1 | a0001c0003t0165g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+15941G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631510 | |||||||
chr9:126631512 | C | T | 1 | a0001c0003t0165g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+15943C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631512 | |||||||
chr9:126631516 | C | T | 60 | a0001c0001t0007g0040 a0001c0001t0007g0051 a0001c0001t0008g0030 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+15947C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631516 | |||||||
chr9:126631517 | G | A | 1 | a0001c0002t0013g0176 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.326+15948G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631517 | |||||||
chr9:126631518 | GGATGGGG others(1160): Show |
G | 1 | a0001c0002t0013g0176 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.326+15950_326+1711 others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631518 | |||||||
chr9:126631763 | A | C | 1 | a0001c0002t0107g0023 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.326+16194A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631763 | |||||||
chr9:126631772 | G | A | 60 | a0001c0001t0007g0040 a0001c0001t0007g0051 a0001c0001t0008g0030 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+16203G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631772 | |||||||
chr9:126632139 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.326+16570C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126632139 | |||||||
chr9:126632304 | G | A | 1 | a0001c0002t0191g0192 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.326+16735G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126632304 | |||||||
chr9:126632650 | G | A | 1 | a0001c0001t0194g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.326+17081G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126632650 | |||||||
chr9:126632687 | A | T | 1 | a0001c0002t0013g0176 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.326+17118A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126632687 | |||||||
chr9:126632691 | G | A | 1 | a0001c0002t0013g0176 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.326+17122G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126632691 | |||||||
chr9:126632721 | C | T | 1 | a0001c0003t0109g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+17152C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126632721 | |||||||
chr9:126632788 | G | T | 2 | a0001c0001t0008g0054 a0001c0002t0001g0055 |
2 | HG00597.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.326+17219G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126632788 | |||||||
chr9:126633067 | C | T | 216 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(213): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.326+17498C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633067 | |||||||
chr9:126633084 | C | G | 2 | a0001c0001t0058g0089 a0001c0001t0078g0090 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.326+17515C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633084 | |||||||
chr9:126633285 | T | C | 216 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(213): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.326+17716T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633285 | |||||||
chr9:126633374 | C | T | 1 | a0001c0001t0007g0317 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.326+17805C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633374 | |||||||
chr9:126633639 | A | G | 1 | a0001c0001t0039g0316 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.326+18070A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633639 | |||||||
chr9:126633758 | A | G | 216 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(213): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.326+18189A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633758 | |||||||
chr9:126633890 | C | T | 1 | a0001c0002t0013g0176 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.326+18321C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633890 | |||||||
chr9:126633913 | G | A | 1 | a0001c0002t0017g0014 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.326+18344G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633913 | |||||||
chr9:126633986 | C | G | 216 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(213): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.326+18417C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633986 | |||||||
chr9:126634062 | G | C | 3 | a0001c0001t0011g0321 a0001c0001t0020g0323 a0001c0001t0098g0322 |
3 | NA18984.hp2 NA19006.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.326+18493G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634062 | |||||||
chr9:126634129 | C | T | 216 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(213): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.326+18560C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634129 | |||||||
chr9:126634155 | G | A | 138 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(135): Show |
139 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.326+18586G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634155 | |||||||
chr9:126634184 | G | A | 1 | a0001c0001t0081g0102 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.326+18615G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634184 | |||||||
chr9:126634342 | C | T | 1 | a0001c0001t0008g0331 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.326+18773C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634342 | |||||||
chr9:126634444 | G | A | 1 | a0001c0001t0002g0248 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.326+18875G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634444 | |||||||
chr9:126634451 | C | T | 216 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(213): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.326+18882C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634451 | |||||||
chr9:126634453 | T | C | 1 | a0001c0002t0033g0012 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.326+18884T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634453 | |||||||
chr9:126634514 | C | T | 3 | a0001c0002t0054g0146 a0001c0002t0055g0145 a0001c0002t0189g0172 |
3 | HG02559.hp2 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.326+18945C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634514 | |||||||
chr9:126634546 | A | G | 1 | a0001c0012t0116g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326+18977A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634546 | |||||||
chr9:126634602 | A | AC | 65 | a0001c0001t0026g0100 a0001c0001t0026g0107 a0001c0001t0027g0072 others(62): Show |
66 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.326+19041dupC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126634602 | ||||||
chr9:126634603 | C | A | 8 | a0001c0001t0101g0170 a0001c0002t0192g0171 a0001c0003t0049g0169 others(5): Show |
8 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.326+19034C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634603 | |||||||
chr9:126634608 | C | A | 1 | a0001c0003t0114g0210 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.326+19039C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634608 | |||||||
chr9:126634610 | C | A | 3 | a0001c0001t0005g0280 a0001c0002t0001g0278 a0001c0002t0001g0279 |
3 | NA18942.hp1 NA18971.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.326+19041C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634610 | |||||||
chr9:126634735 | C | T | 78 | a0001c0001t0025g0084 a0001c0001t0026g0100 a0001c0001t0026g0107 others(75): Show |
79 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.326+19166C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634735 | |||||||
chr9:126634755 | C | T | 17 | a0001c0001t0010g0006 a0001c0001t0010g0007 a0001c0001t0010g0315 others(14): Show |
17 | HG00558.hp1 HG02027.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.326+19186C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634755 | |||||||
chr9:126634821 | G | A | 1 | a0001c0002t0087g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.326+19252G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634821 | |||||||
chr9:126635285 | G | A | 1 | a0001c0002t0055g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.326+19716G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635285 | |||||||
chr9:126635476 | G | A | 48 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(45): Show |
49 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.326+19907G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635476 | |||||||
chr9:126635525 | G | A | 1 | a0001c0002t0151g0026 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.326+19956G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635525 | |||||||
chr9:126635529 | G | A | 5 | a0001c0001t0101g0170 a0001c0002t0192g0171 a0001c0003t0049g0169 others(2): Show |
5 | HG00639.hp1 HG02145.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+19960G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635529 | |||||||
chr9:126635683 | G | A | 2 | a0001c0002t0046g0257 a0001c0004t0150g0067 |
2 | HG02886.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.326+20114G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635683 | |||||||
chr9:126635684 | C | G | 1 | a0001c0002t0046g0257 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.326+20115C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635684 | |||||||
chr9:126635824 | A | G | 60 | a0001c0001t0007g0040 a0001c0001t0007g0051 a0001c0001t0008g0030 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+20255A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635824 | |||||||
chr9:126635979 | A | T | 1 | a0001c0002t0015g0123 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.326+20410A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635979 | |||||||
chr9:126636057 | CT | C | 117 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(114): Show |
118 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.326+20489delT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636057 | |||||||
chr9:126636251 | A | G | 118 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(115): Show |
119 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.326+20682A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636251 | |||||||
chr9:126636280 | T | C | 5 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0039g0282 others(2): Show |
5 | HG00099.hp1 HG01168.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+20711T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636280 | |||||||
chr9:126636292 | C | T | 60 | a0001c0001t0007g0040 a0001c0001t0007g0051 a0001c0001t0008g0030 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+20723C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636292 | |||||||
chr9:126636406 | T | A | 1 | a0001c0002t0046g0257 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.326+20837T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636406 | |||||||
chr9:126636710 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.326+21141G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636710 | |||||||
chr9:126636772 | A | G | 1 | a0001c0002t0001g0065 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.326+21203A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636772 | |||||||
chr9:126636801 | G | A | 5 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0039g0282 others(2): Show |
5 | HG00099.hp1 HG01168.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+21232G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636801 | |||||||
chr9:126637065 | A | G | 1 | a0001c0001t0004g0240 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.326+21496A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637065 | |||||||
chr9:126637176 | G | GTGCTCTG others(5): Show |
1 | a0001c0001t0172g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.326+21607_326+2160 others(16): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637176 | |||||||
chr9:126637179 | A | C | 1 | a0001c0001t0172g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.326+21610A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637179 | |||||||
chr9:126637195 | G | A | 1 | a0001c0001t0041g0284 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.326+21626G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637195 | |||||||
chr9:126637283 | A | G | 121 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(118): Show |
122 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.326+21714A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637283 | |||||||
chr9:126637383 | G | A | 121 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(118): Show |
122 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.326+21814G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637383 | |||||||
chr9:126637575 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.326+22006G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637575 | |||||||
chr9:126637591 | A | G | 121 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(118): Show |
122 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.326+22022A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637591 | |||||||
chr9:126637598 | G | A | 1 | a0001c0002t0191g0192 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.326+22029G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637598 | |||||||
chr9:126637749 | T | C | 297 | a0001c0001t0002g0211 a0001c0001t0002g0246 a0001c0001t0002g0248 others(294): Show |
299 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.326+22180T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637749 | |||||||
chr9:126637763 | G | A | 3 | a0001c0001t0011g0321 a0001c0001t0020g0323 a0001c0001t0098g0322 |
3 | NA18984.hp2 NA19006.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.326+22194G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637763 | |||||||
chr9:126637822 | T | TC | 64 | a0001c0001t0002g0215 a0001c0001t0002g0219 a0001c0001t0005g0221 others(61): Show |
64 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.326+22264dupC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126637822 | ||||||
chr9:126637822 | TC | T | 120 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(117): Show |
121 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.326+22264delC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126637822 | ||||||
chr9:126637829 | C | G | 1 | a0001c0001t0125g0203 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.326+22260C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637829 | |||||||
chr9:126637916 | C | T | 1 | a0001c0001t0097g0325 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.326+22347C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637916 | |||||||
chr9:126637943 | C | A | 121 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(118): Show |
122 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.326+22374C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637943 | |||||||
chr9:126637970 | C | T | 6 | a0001c0003t0109g0136 a0001c0003t0165g0141 a0001c0005t0012g0137 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.326+22401C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637970 | |||||||
chr9:126637979 | G | T | 2 | a0001c0001t0058g0089 a0001c0001t0078g0090 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.326+22410G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637979 | |||||||
chr9:126638015 | C | T | 6 | a0001c0003t0109g0136 a0001c0003t0165g0141 a0001c0005t0012g0137 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.326+22446C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126638015 | |||||||
chr9:126638168 | G | A | 27 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0052g0201 others(24): Show |
27 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.326+22599G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126638168 | |||||||
chr9:126638209 | G | A | 2 | a0001c0002t0001g0064 a0001c0002t0001g0065 |
2 | NA18946.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.326+22640G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126638209 | |||||||
chr9:126638335 | C | T | 1 | a0001c0002t0189g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.326+22766C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126638335 | |||||||
chr9:126638572 | T | C | 8 | a0001c0001t0004g0260 a0001c0001t0004g0261 a0001c0001t0004g0262 others(5): Show |
8 | NA18941.hp2 NA18943.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.326+23003T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126638572 | |||||||
chr9:126639184 | T | C | 1 | a0001c0001t0004g0240 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.326+23615T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639184 | |||||||
chr9:126639271 | C | T | 67 | a0001c0001t0002g0211 a0001c0001t0025g0084 a0001c0001t0026g0100 others(64): Show |
68 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.326+23702C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639271 | |||||||
chr9:126639290 | A | C | 124 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(121): Show |
126 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.326+23721A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639290 | |||||||
chr9:126639313 | C | T | 1 | a0001c0002t0151g0026 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.326+23744C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639313 | |||||||
chr9:126639465 | C | G | 1 | a0001c0001t0004g0271 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.326+23896C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639465 | |||||||
chr9:126639475 | G | A | 4 | a0001c0002t0100g0147 a0001c0002t0105g0166 a0001c0008t0034g0148 others(1): Show |
4 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+23906G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639475 | |||||||
chr9:126639620 | C | T | 1 | a0001c0002t0088g0122 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.326+24051C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639620 | |||||||
chr9:126639700 | G | T | 2 | a0001c0001t0121g0277 a0001c0001t0146g0254 |
2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.326+24131G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639700 | |||||||
chr9:126640064 | A | C | 1 | a0001c0001t0083g0131 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.326+24495A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640064 | |||||||
chr9:126640184 | C | T | 299 | a0001c0001t0002g0211 a0001c0001t0002g0246 a0001c0001t0002g0248 others(296): Show |
302 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.326+24615C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640184 | |||||||
chr9:126640288 | G | A | 117 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(114): Show |
119 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.326+24719G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640288 | |||||||
chr9:126640438 | A | T | 124 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(121): Show |
126 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.326+24869A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640438 | |||||||
chr9:126640615 | C | T | 1 | a0001c0001t0083g0131 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.326+25046C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640615 | |||||||
chr9:126640690 | G | A | 3 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0127g0209 |
3 | HG00099.hp2 HG01175.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.326+25121G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640690 | |||||||
chr9:126640694 | C | A | 1 | a0001c0001t0083g0131 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.326+25125C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640694 | |||||||
chr9:126640926 | A | C | 1 | a0001c0011t0085g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.326+25357A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640926 | |||||||
chr9:126640928 | G | A | 1 | a0001c0001t0052g0201 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.326+25359G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640928 | |||||||
chr9:126641162 | A | G | 1 | a0001c0001t0083g0131 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.326+25593A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641162 | |||||||
chr9:126641163 | G | A | 1 | a0001c0001t0083g0131 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.326+25594G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641163 | |||||||
chr9:126641180 | C | G | 1 | a0001c0003t0024g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.326+25611C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641180 | |||||||
chr9:126641260 | A | G | 1 | a0001c0004t0037g0227 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.326+25691A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641260 | |||||||
chr9:126641359 | A | G | 1 | a0001c0002t0189g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.326+25790A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641359 | |||||||
chr9:126641570 | C | G | 1 | a0001c0001t0029g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.326+26001C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641570 | |||||||
chr9:126641605 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.326+26036C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641605 | |||||||
chr9:126641817 | T | C | 1 | a0001c0001t0129g0220 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.326+26248T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641817 | |||||||
chr9:126641827 | C | T | 1 | a0001c0001t0025g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.326+26258C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641827 | |||||||
chr9:126641830 | G | A | 124 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(121): Show |
126 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.326+26261G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641830 | |||||||
chr9:126642003 | C | A | 6 | a0001c0001t0101g0170 a0001c0002t0192g0171 a0001c0003t0049g0169 others(3): Show |
6 | HG00639.hp1 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.326+26434C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642003 | |||||||
chr9:126642176 | C | T | 1 | a0001c0001t0125g0203 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.326+26607C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642176 | |||||||
chr9:126642246 | T | A | 336 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(333): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.326+26677T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642246 | |||||||
chr9:126642253 | G | A | 1 | a0001c0002t0014g0198 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.326+26684G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642253 | |||||||
chr9:126642254 | C | A | 1 | a0001c0002t0014g0198 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.326+26685C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642254 | |||||||
chr9:126642400 | C | T | 1 | a0001c0001t0040g0259 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.326+26831C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642400 | |||||||
chr9:126642401 | G | A | 2 | a0001c0001t0007g0040 a0001c0002t0003g0041 |
2 | NA18962.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.326+26832G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642401 | |||||||
chr9:126642417 | C | A | 2 | a0001c0009t0102g0167 a0001c0010t0193g0168 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.326+26848C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642417 | |||||||
chr9:126642543 | G | A | 3 | a0001c0004t0043g0213 a0001c0004t0043g0214 a0001c0004t0145g0222 |
3 | HG03225.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.326+26974G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642543 | |||||||
chr9:126642601 | T | G | 1 | a0001c0002t0188g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.326+27032T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642601 | |||||||
chr9:126642619 | G | A | 1 | a0001c0002t0014g0183 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.326+27050G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642619 | |||||||
chr9:126642657 | T | A | 1 | a0001c0001t0002g0231 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.326+27088T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642657 | |||||||
chr9:126642725 | T | C | 123 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(120): Show |
125 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.326+27156T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642725 | |||||||
chr9:126642911 | G | A | 1 | a0001c0001t0002g0215 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.326+27342G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642911 | |||||||
chr9:126642949 | C | G | 1 | a0001c0001t0123g0232 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.326+27380C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642949 | |||||||
chr9:126643326 | G | A | 1 | a0001c0012t0116g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326+27757G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643326 | |||||||
chr9:126643466 | G | A | 1 | a0001c0003t0165g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+27897G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643466 | |||||||
chr9:126643484 | G | A | 1 | a0001c0001t0194g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.326+27915G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643484 | |||||||
chr9:126643510 | A | G | 123 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(120): Show |
125 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.326+27941A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643510 | |||||||
chr9:126643584 | G | A | 1 | a0001c0001t0119g0217 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.326+28015G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643584 | |||||||
chr9:126643600 | C | A | 1 | a0001c0002t0006g0184 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.326+28031C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643600 | |||||||
chr9:126643805 | C | T | 3 | a0001c0002t0161g0068 a0001c0003t0112g0225 a0001c0004t0150g0067 |
3 | HG02615.hp1 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.326+28236C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643805 | |||||||
chr9:126643820 | T | C | 122 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(119): Show |
124 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.326+28251T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643820 | |||||||
chr9:126643885 | C | A | 1 | a0001c0001t0005g0275 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.326+28316C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643885 | |||||||
chr9:126643898 | C | T | 1 | a0001c0001t0173g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.326+28329C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643898 | |||||||
chr9:126644154 | C | T | 4 | a0001c0002t0014g0193 a0001c0002t0014g0194 a0001c0002t0045g0212 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+28585C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644154 | |||||||
chr9:126644365 | T | C | 41 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0052g0182 others(38): Show |
41 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.326+28796T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644365 | |||||||
chr9:126644591 | G | A | 1 | a0001c0002t0001g0009 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.326+29022G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644591 | |||||||
chr9:126644640 | G | C | 41 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0052g0182 others(38): Show |
41 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.326+29071G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644640 | |||||||
chr9:126644647 | T | G | 122 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(119): Show |
124 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.326+29078T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644647 | |||||||
chr9:126644670 | GCCGAGTG others(4): Show |
G | 1 | a0001c0003t0109g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+29103_326+2911 others(15): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126644670 | ||||||
chr9:126644710 | C | A | 122 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(119): Show |
124 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.326+29141C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644710 | |||||||
chr9:126644730 | G | T | 1 | a0001c0002t0189g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.326+29161G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644730 | |||||||
chr9:126644840 | C | A | 7 | a0001c0003t0109g0136 a0001c0003t0165g0141 a0001c0005t0012g0137 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.326+29271C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644840 | |||||||
chr9:126644988 | G | A | 5 | a0001c0001t0038g0004 a0001c0001t0038g0332 a0001c0001t0132g0004 others(2): Show |
5 | HG02074.hp1 NA18973.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+29419G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644988 | |||||||
chr9:126645014 | C | T | 55 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0001c0001t0002g0300 others(52): Show |
57 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.326+29445C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645014 | |||||||
chr9:126645221 | G | A | 14 | a0001c0001t0052g0182 a0001c0001t0101g0170 a0001c0001t0181g0143 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.326+29652G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645221 | |||||||
chr9:126645264 | G | A | 36 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0215 others(33): Show |
36 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.326+29695G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645264 | |||||||
chr9:126645292 | C | CA | 75 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0001c0001t0002g0300 others(72): Show |
77 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.326+29724dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126645292 | ||||||
chr9:126645560 | C | G | 1 | a0001c0003t0108g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.326+29991C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645560 | |||||||
chr9:126645657 | C | T | 1 | a0001c0001t0173g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.326+30088C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645657 | |||||||
chr9:126645801 | C | G | 13 | a0001c0001t0002g0324 a0001c0001t0007g0292 a0001c0001t0008g0331 others(10): Show |
13 | HG02071.hp2 HG03139.hp2 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.326+30232C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645801 | |||||||
chr9:126645801 | C | T | 1 | a0001c0003t0165g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+30232C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645801 | |||||||
chr9:126645887 | C | T | 1 | a0001c0002t0151g0026 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.326+30318C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645887 | |||||||
chr9:126645888 | G | A | 1 | a0001c0012t0116g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326+30319G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645888 | |||||||
chr9:126646011 | C | T | 175 | a0001c0001t0002g0211 a0001c0001t0002g0215 a0001c0001t0003g0243 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.326+30442C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646011 | |||||||
chr9:126646086 | G | A | 1 | a0001c0003t0109g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+30517G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646086 | |||||||
chr9:126646152 | C | T | 1 | a0001c0002t0009g0121 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.326+30583C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646152 | |||||||
chr9:126646166 | G | C | 301 | a0001c0001t0002g0211 a0001c0001t0002g0215 a0001c0001t0002g0246 others(298): Show |
304 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.326+30597G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646166 | |||||||
chr9:126646234 | G | A | 134 | a0001c0001t0002g0211 a0001c0001t0002g0215 a0001c0001t0007g0040 others(131): Show |
135 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.326+30665G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646234 | |||||||
chr9:126646317 | TATCCATC others(13): Show |
T | 126 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(123): Show |
128 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.326+30774_326+3079 others(24): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126646317 | ||||||
chr9:126646323 | T | C | 14 | a0001c0001t0052g0182 a0001c0001t0101g0170 a0001c0001t0181g0143 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.326+30754T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646323 | |||||||
chr9:126646373 | C | T | 112 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0273 others(109): Show |
114 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.326+30804C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646373 | |||||||
chr9:126646403 | C | CCCAT | 73 | a0001c0001t0002g0211 a0001c0001t0002g0215 a0001c0001t0011g0224 others(70): Show |
74 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.326+30854_326+3085 others(8): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126646403 | ||||||
chr9:126646712 | T | G | 4 | a0001c0002t0100g0147 a0001c0002t0105g0166 a0001c0008t0034g0148 others(1): Show |
4 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+31143T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646712 | |||||||
chr9:126646722 | A | G | 62 | a0001c0001t0007g0040 a0001c0001t0007g0051 a0001c0001t0008g0030 others(59): Show |
62 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.326+31153A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646722 | |||||||
chr9:126646783 | C | A | 63 | a0001c0001t0007g0040 a0001c0001t0007g0051 a0001c0001t0008g0030 others(60): Show |
63 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.326+31214C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646783 | |||||||
chr9:126646838 | G | A | 49 | a0001c0001t0002g0215 a0001c0001t0002g0231 a0001c0001t0011g0224 others(46): Show |
50 | HG00621.hp2 HG00642.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.326+31269G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646838 | |||||||
chr9:126646896 | A | AG | 24 | a0001c0001t0002g0231 a0001c0001t0027g0072 a0001c0001t0027g0129 others(21): Show |
25 | HG00621.hp2 HG01070.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.326+31332dupG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126646896 | ||||||
chr9:126646919 | T | C | 76 | a0001c0001t0002g0215 a0001c0001t0002g0231 a0001c0001t0002g0239 others(73): Show |
77 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.326+31350T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646919 | |||||||
chr9:126646919 | T | G | 1 | a0001c0001t0051g0153 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.326+31350T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646919 | |||||||
chr9:126646950 | G | A | 2 | a0001c0001t0066g0126 a0001c0001t0067g0073 |
2 | HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.326+31381G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646950 | |||||||
chr9:126647059 | A | G | 5 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+31490A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126647059 | |||||||
chr9:126647111 | C | A | 10 | a0001c0001t0025g0157 a0001c0001t0051g0153 a0001c0001t0051g0158 others(7): Show |
10 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.326+31542C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126647111 | |||||||
chr9:126647289 | C | A | 2 | a0001c0007t0048g0318 a0001c0007t0048g0319 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.326+31720C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126647289 | |||||||
chr9:126647418 | C | G | 2 | a0001c0001t0038g0332 a0001c0002t0003g0312 |
2 | NA18973.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.326+31849C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126647418 | |||||||
chr9:126647783 | A | C | 257 | a0001c0001t0002g0211 a0001c0001t0002g0215 a0001c0001t0002g0231 others(254): Show |
260 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.326+32214A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126647783 | |||||||
chr9:126648165 | C | G | 2 | a0001c0001t0027g0072 a0001c0001t0027g0129 |
2 | NA18953.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.326+32596C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648165 | |||||||
chr9:126648315 | C | T | 224 | a0001c0001t0002g0215 a0001c0001t0002g0231 a0001c0001t0002g0246 others(221): Show |
227 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.326+32746C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648315 | |||||||
chr9:126648328 | G | A | 1 | a0001c0001t0025g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.326+32759G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648328 | |||||||
chr9:126648573 | G | A | 114 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0001c0001t0002g0300 others(111): Show |
116 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.326+33004G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648573 | |||||||
chr9:126648639 | G | A | 26 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0178g0200 others(23): Show |
26 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.326+33070G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648639 | |||||||
chr9:126648811 | T | G | 2 | a0001c0001t0027g0072 a0001c0001t0027g0129 |
2 | NA18953.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.326+33242T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648811 | |||||||
chr9:126648963 | C | A | 26 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0178g0200 others(23): Show |
26 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.326+33394C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648963 | |||||||
chr9:126648985 | C | T | 1 | a0001c0001t0120g0238 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.326+33416C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648985 | |||||||
chr9:126649159 | C | T | 2 | a0001c0002t0054g0146 a0001c0002t0055g0145 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.326+33590C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649159 | |||||||
chr9:126649160 | G | A | 64 | a0001c0001t0002g0211 a0001c0001t0003g0243 a0001c0001t0025g0084 others(61): Show |
64 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.326+33591G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649160 | |||||||
chr9:126649282 | T | A | 1 | a0001c0001t0143g0285 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.326+33713T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649282 | |||||||
chr9:126649362 | A | G | 1 | a0001c0002t0001g0289 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.326+33793A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649362 | |||||||
chr9:126649787 | T | C | 1 | a0001c0001t0060g0106 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.326+34218T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649787 | |||||||
chr9:126649824 | C | T | 1 | a0001c0003t0109g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+34255C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649824 | |||||||
chr9:126649854 | C | T | 219 | a0001c0001t0002g0215 a0001c0001t0002g0231 a0001c0001t0002g0246 others(216): Show |
222 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.326+34285C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649854 | |||||||
chr9:126649958 | T | G | 1 | a0001c0001t0060g0106 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.326+34389T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649958 | |||||||
chr9:126649960 | T | C | 10 | a0001c0001t0025g0157 a0001c0001t0051g0153 a0001c0001t0051g0158 others(7): Show |
10 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.326+34391T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649960 | |||||||
chr9:126649997 | A | G | 1 | a0001c0002t0023g0052 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.326+34428A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649997 | |||||||
chr9:126650100 | A | C | 9 | a0001c0002t0189g0172 a0001c0003t0165g0141 a0001c0005t0012g0137 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.326+34531A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650100 | |||||||
chr9:126650252 | A | G | 1 | a0001c0002t0001g0025 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.326+34683A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650252 | |||||||
chr9:126650267 | C | T | 104 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0001c0001t0002g0300 others(101): Show |
106 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.326+34698C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650267 | |||||||
chr9:126650351 | C | T | 45 | a0001c0001t0002g0215 a0001c0001t0002g0231 a0001c0001t0002g0246 others(42): Show |
46 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.326+34782C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650351 | |||||||
chr9:126650598 | C | T | 1 | a0001c0001t0130g0237 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.326+35029C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650598 | |||||||
chr9:126650631 | C | T | 2 | a0001c0001t0002g0219 a0001c0001t0106g0218 |
2 | HG02647.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.326+35062C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650631 | |||||||
chr9:126650643 | C | G | 1 | a0001c0003t0165g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+35074C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650643 | |||||||
chr9:126650659 | A | G | 222 | a0001c0001t0002g0211 a0001c0001t0002g0273 a0001c0001t0002g0274 others(219): Show |
224 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.326+35090A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650659 | |||||||
chr9:126650703 | G | A | 1 | a0001c0001t0081g0102 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.326+35134G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650703 | |||||||
chr9:126650734 | C | T | 1 | a0001c0002t0189g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.326+35165C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650734 | |||||||
chr9:126650798 | C | T | 1 | a0001c0012t0116g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326+35229C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650798 | |||||||
chr9:126650930 | G | A | 30 | a0001c0001t0003g0243 a0001c0001t0101g0170 a0001c0001t0178g0200 others(27): Show |
30 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.326+35361G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650930 | |||||||
chr9:126651019 | C | T | 157 | a0001c0001t0002g0211 a0001c0001t0002g0215 a0001c0001t0002g0231 others(154): Show |
159 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.326+35450C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651019 | |||||||
chr9:126651203 | C | T | 2 | a0001c0002t0003g0244 a0001c0002t0003g0287 |
2 | NA18975.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.326+35634C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651203 | |||||||
chr9:126651211 | C | T | 266 | a0001c0001t0002g0211 a0001c0001t0002g0215 a0001c0001t0002g0231 others(263): Show |
269 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.326+35642C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651211 | |||||||
chr9:126651296 | C | CT | 17 | a0001c0001t0003g0243 a0001c0001t0178g0200 a0001c0002t0006g0184 others(14): Show |
17 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.326+35728dupT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126651296 | ||||||
chr9:126651299 | G | T | 9 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0053g0177 others(6): Show |
9 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.326+35730G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651299 | |||||||
chr9:126651317 | T | G | 2 | a0001c0001t0079g0104 a0001c0002t0088g0122 |
2 | HG01106.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.326+35748T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651317 | |||||||
chr9:126651399 | A | G | 236 | a0001c0001t0002g0211 a0001c0001t0002g0215 a0001c0001t0002g0231 others(233): Show |
239 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.326+35830A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651399 | |||||||
chr9:126651417 | G | A | 37 | a0001c0001t0002g0231 a0001c0001t0002g0246 a0001c0001t0002g0248 others(34): Show |
38 | HG00621.hp2 HG00738.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.326+35848G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651417 | |||||||
chr9:126651496 | T | C | 2 | a0001c0002t0001g0249 a0001c0002t0001g0250 |
2 | NA18966.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.326+35927T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651496 | |||||||
chr9:126651647 | G | A | 2 | a0001c0002t0001g0249 a0001c0002t0001g0250 |
2 | NA18966.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.326+36078G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651647 | |||||||
chr9:126651718 | C | T | 2 | a0001c0004t0184g0086 a0001c0004t0185g0088 |
2 | HG01243.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.326+36149C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651718 | |||||||
chr9:126651854 | G | A | 2 | a0001c0005t0012g0137 a0001c0005t0012g0138 |
2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.326+36285G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651854 | |||||||
chr9:126651890 | G | T | 249 | a0001c0001t0002g0211 a0001c0001t0002g0215 a0001c0001t0002g0219 others(246): Show |
252 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.326+36321G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651890 | |||||||
chr9:126652000 | T | TG | 168 | a0001c0001t0002g0211 a0001c0001t0002g0215 a0001c0001t0002g0219 others(165): Show |
171 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.326+36440dupG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126652000 | ||||||
chr9:126652009 | G | T | 1 | a0001c0005t0167g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.326+36440G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652009 | |||||||
chr9:126652024 | G | T | 8 | a0001c0002t0006g0184 a0001c0002t0006g0186 a0001c0002t0006g0187 others(5): Show |
8 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.326+36455G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652024 | |||||||
chr9:126652045 | C | T | 180 | a0001c0001t0002g0215 a0001c0001t0002g0219 a0001c0001t0002g0231 others(177): Show |
183 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.326+36476C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652045 | |||||||
chr9:126652164 | A | G | 1 | a0001c0002t0090g0099 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.326+36595A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652164 | |||||||
chr9:126652230 | C | T | 1 | a0001c0001t0042g0309 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.326+36661C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652230 | |||||||
chr9:126652231 | G | A | 31 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0007g0040 others(28): Show |
32 | HG00621.hp2 HG01070.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.326+36662G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652231 | |||||||
chr9:126652296 | A | AGG | 123 | a0001c0001t0002g0211 a0001c0001t0002g0215 a0001c0001t0002g0219 others(120): Show |
124 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.326+36736_326+3673 others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126652296 | ||||||
chr9:126652298 | G | T | 1 | a0001c0002t0001g0050 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.326+36729G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652298 | |||||||
chr9:126652304 | G | C | 2 | a0001c0003t0049g0150 a0001c0003t0049g0169 |
2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.326+36735G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652304 | |||||||
chr9:126652304 | G | T | 2 | a0001c0001t0118g0297 a0001c0001t0143g0285 |
2 | HG02083.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.326+36735G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652304 | |||||||
chr9:126652391 | G | T | 4 | a0001c0001t0002g0211 a0001c0001t0144g0205 a0001c0001t0170g0155 others(1): Show |
4 | HG01496.hp2 HG02818.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.326+36822G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652391 | |||||||
chr9:126652453 | G | A | 50 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0028g0076 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.326+36884G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652453 | |||||||
chr9:126652534 | T | C | 9 | a0001c0002t0186g0133 a0001c0003t0057g0134 a0001c0003t0076g0132 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.326+36965T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652534 | |||||||
chr9:126652650 | G | A | 71 | a0001c0001t0008g0030 a0001c0001t0008g0054 a0001c0001t0011g0063 others(68): Show |
71 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.326+37081G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652650 | |||||||
chr9:126652659 | G | A | 50 | a0001c0001t0025g0191 a0001c0001t0028g0076 a0001c0001t0065g0119 others(47): Show |
50 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.326+37090G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652659 | |||||||
chr9:126652780 | G | A | 2 | a0001c0001t0178g0200 a0001c0002t0103g0196 |
2 | HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.326+37211G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652780 | |||||||
chr9:126652790 | G | A | 1 | a0001c0010t0193g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.326+37221G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652790 | |||||||
chr9:126652868 | A | G | 1 | a0001c0002t0055g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.326+37299A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652868 | |||||||
chr9:126652873 | G | A | 1 | a0001c0003t0108g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.326+37304G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652873 | |||||||
chr9:126652888 | C | T | 3 | a0001c0004t0043g0213 a0001c0004t0043g0214 a0001c0004t0145g0222 |
3 | HG03225.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.326+37319C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652888 | |||||||
chr9:126652889 | G | A | 1 | a0001c0002t0158g0291 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.326+37320G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652889 | |||||||
chr9:126653088 | C | T | 1 | a0001c0001t0007g0330 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.326+37519C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653088 | |||||||
chr9:126653142 | C | CT | 37 | a0001c0001t0002g0239 a0001c0001t0002g0273 a0001c0001t0002g0300 others(34): Show |
37 | HG00597.hp1 HG00621.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.326+37601dupT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126653142 | ||||||
chr9:126653142 | CT | C | 46 | a0001c0001t0004g0262 a0001c0001t0004g0271 a0001c0001t0005g0280 others(43): Show |
46 | HG00280.hp1 HG00609.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.326+37601delT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126653142 | ||||||
chr9:126653142 | CTT | C | 93 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0007g0040 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.326+37600_326+3760 others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126653142 | ||||||
chr9:126653142 | CTTT | C | 14 | a0001c0001t0068g0078 a0001c0001t0080g0080 a0001c0001t0142g0281 others(11): Show |
14 | HG00280.hp2 HG00323.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.326+37599_326+3760 others(7): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126653142 | ||||||
chr9:126653142 | CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0055g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.326+37592_326+3760 others(14): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126653142 | ||||||
chr9:126653142 | CTTTTTTT others(5): Show |
C | 1 | a0001c0002t0189g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.326+37590_326+3760 others(16): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126653142 | ||||||
chr9:126653143 | T | C | 1 | a0001c0001t0148g0333 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.326+37574T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653143 | |||||||
chr9:126653155 | T | C | 1 | a0001c0002t0189g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.326+37586T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653155 | |||||||
chr9:126653195 | C | T | 34 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0007g0040 others(31): Show |
35 | HG00621.hp2 HG01070.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.326+37626C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653195 | |||||||
chr9:126653198 | G | A | 1 | a0001c0012t0116g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326+37629G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653198 | |||||||
chr9:126653198 | G | C | 1 | a0001c0010t0193g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.326+37629G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653198 | |||||||
chr9:126653255 | C | T | 1 | a0001c0002t0071g0092 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.327-37581C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653255 | |||||||
chr9:126653280 | G | A | 35 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0007g0040 others(32): Show |
36 | HG00621.hp2 HG01070.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.327-37556G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653280 | |||||||
chr9:126653397 | C | T | 65 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0028g0076 others(62): Show |
65 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.327-37439C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653397 | |||||||
chr9:126653491 | G | A | 1 | a0001c0010t0193g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327-37345G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653491 | |||||||
chr9:126653496 | A | G | 69 | a0001c0001t0008g0030 a0001c0001t0008g0054 a0001c0001t0011g0063 others(66): Show |
69 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.327-37340A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653496 | |||||||
chr9:126653524 | A | C | 4 | a0001c0002t0003g0244 a0001c0002t0003g0287 a0001c0002t0003g0296 others(1): Show |
4 | NA18960.hp1 NA18975.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-37312A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653524 | |||||||
chr9:126653642 | G | A | 2 | a0001c0002t0023g0028 a0001c0002t0023g0052 |
2 | NA18954.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.327-37194G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653642 | |||||||
chr9:126653742 | C | T | 1 | a0001c0001t0119g0217 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.327-37094C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653742 | |||||||
chr9:126653747 | C | G | 1 | a0001c0001t0119g0217 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.327-37089C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653747 | |||||||
chr9:126653934 | T | C | 66 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0028g0076 others(63): Show |
66 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.327-36902T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653934 | |||||||
chr9:126654038 | C | T | 27 | a0001c0001t0003g0243 a0001c0001t0101g0170 a0001c0001t0178g0200 others(24): Show |
27 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.327-36798C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126654038 | |||||||
chr9:126654294 | C | G | 1 | a0001c0003t0108g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.327-36542C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126654294 | |||||||
chr9:126654415 | T | C | 1 | a0001c0002t0032g0002 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.327-36421T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126654415 | |||||||
chr9:126654571 | A | G | 65 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0028g0076 others(62): Show |
65 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.327-36265A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126654571 | |||||||
chr9:126654700 | C | G | 1 | a0001c0012t0116g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.327-36136C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126654700 | |||||||
chr9:126655159 | T | C | 1 | a0001c0005t0168g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.327-35677T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655159 | |||||||
chr9:126655243 | A | G | 66 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0028g0076 others(63): Show |
66 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.327-35593A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655243 | |||||||
chr9:126655272 | C | T | 1 | a0001c0010t0193g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327-35564C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655272 | |||||||
chr9:126655302 | C | T | 1 | a0001c0003t0109g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.327-35534C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655302 | |||||||
chr9:126655367 | A | G | 66 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0028g0076 others(63): Show |
66 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.327-35469A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655367 | |||||||
chr9:126655375 | TG | T | 22 | a0001c0001t0025g0191 a0001c0001t0028g0076 a0001c0001t0065g0119 others(19): Show |
22 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.327-35456delG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126655375 | ||||||
chr9:126655452 | T | G | 77 | a0001c0001t0003g0243 a0001c0001t0007g0040 a0001c0001t0025g0191 others(74): Show |
77 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.327-35384T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655452 | |||||||
chr9:126655494 | G | A | 1 | a0001c0004t0180g0083 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.327-35342G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655494 | |||||||
chr9:126655530 | G | C | 65 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0028g0076 others(62): Show |
65 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.327-35306G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655530 | |||||||
chr9:126655745 | T | C | 5 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.327-35091T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655745 | |||||||
chr9:126655770 | T | C | 182 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0003g0243 others(179): Show |
183 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.327-35066T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655770 | |||||||
chr9:126655877 | G | A | 65 | a0001c0001t0003g0243 a0001c0001t0025g0191 a0001c0001t0028g0076 others(62): Show |
65 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.327-34959G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655877 | |||||||
chr9:126656000 | G | A | 1 | a0001c0012t0116g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.327-34836G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656000 | |||||||
chr9:126656074 | A | G | 1 | a0001c0002t0055g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-34762A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656074 | |||||||
chr9:126656081 | G | A | 64 | a0001c0001t0003g0243 a0001c0001t0028g0076 a0001c0001t0065g0119 others(61): Show |
64 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.327-34755G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656081 | |||||||
chr9:126656124 | A | G | 1 | a0001c0010t0193g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327-34712A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656124 | |||||||
chr9:126656146 | A | T | 2 | a0001c0001t0172g0160 a0001c0001t0173g0159 |
2 | HG02280.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.327-34690A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656146 | |||||||
chr9:126656169 | A | G | 16 | a0001c0001t0003g0243 a0001c0001t0178g0200 a0001c0002t0006g0184 others(13): Show |
16 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.327-34667A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656169 | |||||||
chr9:126656178 | A | AT | 4 | a0001c0002t0100g0147 a0001c0002t0166g0181 a0001c0008t0034g0148 others(1): Show |
4 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-34652dupT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656178 | ||||||
chr9:126656271 | C | T | 36 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0011g0328 others(33): Show |
37 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.327-34565C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656271 | |||||||
chr9:126656381 | CT | C | 3 | a0001c0001t0004g0263 a0001c0001t0008g0331 a0001c0001t0083g0131 |
3 | NA18941.hp1 NA18970.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.327-34452delT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656381 | ||||||
chr9:126656383 | T | TTAGA | 46 | a0001c0001t0002g0273 a0001c0001t0005g0288 a0001c0001t0005g0304 others(43): Show |
46 | HG00738.hp2 HG01074.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.327-34401_327-3439 others(8): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656383 | ||||||
chr9:126656383 | T | TTAGATAG others(1): Show |
12 | a0001c0001t0036g0003 a0001c0001t0039g0282 a0001c0001t0058g0089 others(9): Show |
13 | HG00099.hp1 HG00609.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.327-34405_327-3439 others(12): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656383 | ||||||
chr9:126656383 | TTAGA | T | 86 | a0001c0001t0002g0208 a0001c0001t0002g0211 a0001c0001t0002g0239 others(83): Show |
86 | HG00323.hp1 HG00558.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.327-34401_327-3439 others(8): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656383 | ||||||
chr9:126656383 | TTAGATAG others(1): Show |
T | 29 | a0001c0001t0002g0324 a0001c0001t0004g0261 a0001c0001t0007g0292 others(26): Show |
29 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.327-34405_327-3439 others(12): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656383 | ||||||
chr9:126656383 | TTAGATAG others(5): Show |
T | 13 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0026g0100 others(10): Show |
13 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.327-34409_327-3439 others(16): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656383 | ||||||
chr9:126656383 | TTAGATAG others(9): Show |
T | 13 | a0001c0001t0002g0274 a0001c0001t0003g0243 a0001c0001t0030g0117 others(10): Show |
13 | HG00438.hp1 HG00609.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.327-34413_327-3439 others(20): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656383 | ||||||
chr9:126656383 | TTAGATAG others(13): Show |
T | 6 | a0001c0001t0007g0051 a0001c0001t0021g0255 a0001c0001t0026g0107 others(3): Show |
6 | HG00558.hp2 HG02071.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-34417_327-3439 others(24): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656383 | ||||||
chr9:126656474 | C | G | 1 | a0001c0010t0193g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327-34362C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656474 | |||||||
chr9:126656688 | C | T | 1 | a0001c0006t0115g0235 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.327-34148C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656688 | |||||||
chr9:126656746 | G | A | 69 | a0001c0001t0008g0030 a0001c0001t0008g0054 a0001c0001t0011g0063 others(66): Show |
69 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.327-34090G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656746 | |||||||
chr9:126656778 | C | CCTAT | 4 | a0001c0001t0003g0243 a0001c0002t0013g0176 a0001c0002t0013g0178 others(1): Show |
4 | HG00738.hp1 HG00741.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-34057_327-3405 others(8): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656778 | ||||||
chr9:126656851 | C | T | 1 | a0001c0001t0173g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.327-33985C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656851 | |||||||
chr9:126657011 | T | C | 100 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0003g0243 others(97): Show |
101 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.327-33825T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657011 | |||||||
chr9:126657126 | C | A | 1 | a0001c0012t0116g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.327-33710C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657126 | |||||||
chr9:126657144 | T | C | 1 | a0001c0001t0002g0329 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.327-33692T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657144 | |||||||
chr9:126657145 | G | T | 1 | a0001c0001t0004g0261 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.327-33691G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657145 | |||||||
chr9:126657146 | A | G | 1 | a0001c0001t0004g0261 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.327-33690A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657146 | |||||||
chr9:126657244 | G | A | 37 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0005g0304 others(34): Show |
38 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.327-33592G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657244 | |||||||
chr9:126657445 | C | T | 1 | a0001c0002t0009g0109 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.327-33391C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657445 | |||||||
chr9:126657530 | G | T | 27 | a0001c0001t0003g0243 a0001c0001t0101g0170 a0001c0001t0178g0200 others(24): Show |
27 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.327-33306G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657530 | |||||||
chr9:126657683 | C | T | 1 | a0001c0001t0051g0153 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.327-33153C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657683 | |||||||
chr9:126657711 | A | G | 109 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0003g0243 others(106): Show |
110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.327-33125A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657711 | |||||||
chr9:126657746 | C | T | 69 | a0001c0001t0008g0030 a0001c0001t0008g0054 a0001c0001t0011g0063 others(66): Show |
69 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.327-33090C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657746 | |||||||
chr9:126657956 | C | T | 2 | a0001c0001t0095g0247 a0001c0001t0117g0245 |
2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.327-32880C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657956 | |||||||
chr9:126657962 | A | C | 67 | a0001c0001t0003g0243 a0001c0001t0028g0076 a0001c0001t0065g0119 others(64): Show |
67 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.327-32874A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657962 | |||||||
chr9:126657962 | A | T | 4 | a0001c0002t0186g0133 a0001c0003t0057g0134 a0001c0003t0076g0132 others(1): Show |
4 | HG02109.hp1 HG02647.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-32874A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657962 | |||||||
chr9:126657976 | G | A | 1 | a0001c0010t0193g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327-32860G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657976 | |||||||
chr9:126658037 | G | A | 1 | a0001c0001t0064g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.327-32799G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658037 | |||||||
chr9:126658055 | T | C | 72 | a0001c0001t0003g0243 a0001c0001t0028g0076 a0001c0001t0065g0119 others(69): Show |
72 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.327-32781T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658055 | |||||||
chr9:126658219 | G | C | 3 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0127g0209 |
3 | HG00099.hp2 HG01175.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.327-32617G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658219 | |||||||
chr9:126658357 | G | A | 81 | a0001c0001t0003g0243 a0001c0001t0028g0076 a0001c0001t0028g0081 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.327-32479G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658357 | |||||||
chr9:126658380 | C | T | 1 | a0001c0001t0011g0328 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.327-32456C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658380 | |||||||
chr9:126658381 | C | T | 1 | a0001c0001t0011g0328 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.327-32455C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658381 | |||||||
chr9:126658390 | C | T | 5 | a0001c0002t0100g0147 a0001c0002t0166g0181 a0001c0008t0034g0148 others(2): Show |
5 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.327-32446C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658390 | |||||||
chr9:126658396 | C | CG | 54 | a0001c0001t0008g0054 a0001c0001t0035g0020 a0001c0001t0035g0062 others(51): Show |
54 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.327-32437dupG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126658396 | ||||||
chr9:126658407 | G | C | 47 | a0001c0001t0008g0054 a0001c0001t0035g0020 a0001c0001t0035g0062 others(44): Show |
47 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.327-32429G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658407 | |||||||
chr9:126658452 | C | G | 6 | a0001c0001t0025g0157 a0001c0001t0051g0153 a0001c0001t0051g0158 others(3): Show |
6 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.327-32384C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658452 | |||||||
chr9:126658513 | T | G | 2 | a0001c0003t0165g0141 a0001c0012t0116g0142 |
2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.327-32323T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658513 | |||||||
chr9:126658570 | C | T | 68 | a0001c0001t0008g0030 a0001c0001t0008g0054 a0001c0001t0011g0063 others(65): Show |
68 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.327-32266C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658570 | |||||||
chr9:126658869 | A | G | 75 | a0001c0001t0003g0243 a0001c0001t0028g0076 a0001c0001t0058g0089 others(72): Show |
75 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.327-31967A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658869 | |||||||
chr9:126658873 | G | C | 4 | a0001c0002t0186g0133 a0001c0003t0057g0134 a0001c0003t0076g0132 others(1): Show |
4 | HG02109.hp1 HG02647.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-31963G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658873 | |||||||
chr9:126659025 | C | T | 1 | a0001c0002t0017g0014 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.327-31811C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659025 | |||||||
chr9:126659052 | C | T | 1 | a0001c0002t0054g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.327-31784C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659052 | |||||||
chr9:126659053 | G | A | 1 | a0001c0001t0127g0209 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.327-31783G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659053 | |||||||
chr9:126659105 | G | T | 69 | a0001c0001t0008g0030 a0001c0001t0008g0054 a0001c0001t0011g0063 others(66): Show |
69 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.327-31731G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659105 | |||||||
chr9:126659302 | A | G | 70 | a0001c0001t0008g0030 a0001c0001t0008g0054 a0001c0001t0011g0063 others(67): Show |
70 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.327-31534A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659302 | |||||||
chr9:126659434 | T | C | 83 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0004g0240 others(80): Show |
84 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.327-31402T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659434 | |||||||
chr9:126659459 | G | A | 1 | a0001c0002t0055g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-31377G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659459 | |||||||
chr9:126659651 | G | C | 9 | a0001c0001t0068g0078 a0001c0002t0013g0128 a0001c0004t0062g0085 others(6): Show |
9 | HG00280.hp2 HG01243.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-31185G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659651 | |||||||
chr9:126659744 | G | A | 82 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0004g0240 others(79): Show |
83 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.327-31092G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659744 | |||||||
chr9:126659820 | A | G | 4 | a0001c0002t0186g0133 a0001c0003t0057g0134 a0001c0003t0076g0132 others(1): Show |
4 | HG02109.hp1 HG02647.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-31016A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659820 | |||||||
chr9:126659933 | A | AGCCTTAG others(65): Show |
82 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0004g0240 others(79): Show |
83 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.327-30879_327-3087 others(76): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126659933 | ||||||
chr9:126659953 | G | A | 1 | a0001c0002t0055g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-30883G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659953 | |||||||
chr9:126659963 | C | A | 1 | a0001c0001t0140g0269 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.327-30873C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659963 | |||||||
chr9:126660019 | C | CTGTGTGG others(178): Show |
79 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0004g0240 others(76): Show |
80 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.327-30807_327-3080 others(189): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126660019 | ||||||
chr9:126660019 | C | CTGTGTGG others(178): Show |
2 | a0001c0001t0079g0104 a0001c0002t0088g0122 |
2 | HG01106.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.327-30807_327-3080 others(189): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126660019 | ||||||
chr9:126660022 | T | TGTGGGGG others(215): Show |
1 | a0001c0002t0054g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.327-30807_327-3080 others(226): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126660022 | ||||||
chr9:126660104 | T | C | 1 | a0001c0002t0153g0303 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.327-30732T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660104 | |||||||
chr9:126660172 | T | TGGGGGTA others(178): Show |
79 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0004g0240 others(76): Show |
80 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.327-30630_327-3062 others(189): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126660172 | ||||||
chr9:126660172 | T | TGGGGGTA others(179): Show |
1 | a0001c0002t0071g0092 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.327-30630_327-3062 others(190): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126660172 | ||||||
chr9:126660207 | T | A | 2 | a0001c0003t0057g0134 a0001c0003t0076g0132 |
2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.327-30629T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660207 | |||||||
chr9:126660213 | G | A | 80 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0004g0240 others(77): Show |
81 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.327-30623G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660213 | |||||||
chr9:126660227 | C | CTTCAGAG others(177): Show |
2 | a0001c0003t0057g0134 a0001c0003t0076g0132 |
2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.327-30609_327-3060 others(188): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660227 | |||||||
chr9:126660235 | A | G | 2 | a0001c0003t0057g0134 a0001c0003t0076g0132 |
2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.327-30601A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660235 | |||||||
chr9:126660240 | T | C | 2 | a0001c0003t0057g0134 a0001c0003t0076g0132 |
2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.327-30596T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660240 | |||||||
chr9:126660271 | G | C | 25 | a0001c0001t0003g0243 a0001c0001t0058g0089 a0001c0001t0078g0090 others(22): Show |
25 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.327-30565G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660271 | |||||||
chr9:126660479 | G | A | 1 | a0001c0001t0068g0078 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.327-30357G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660479 | |||||||
chr9:126660485 | A | G | 1 | a0001c0001t0020g0266 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.327-30351A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660485 | |||||||
chr9:126660504 | G | A | 82 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0004g0240 others(79): Show |
83 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.327-30332G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660504 | |||||||
chr9:126660513 | T | G | 1 | a0001c0001t0084g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.327-30323T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660513 | |||||||
chr9:126660676 | A | G | 1 | a0001c0002t0017g0014 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.327-30160A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660676 | |||||||
chr9:126660950 | G | C | 1 | a0001c0001t0133g0018 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.327-29886G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660950 | |||||||
chr9:126661099 | A | G | 178 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0324 others(175): Show |
179 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.327-29737A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661099 | |||||||
chr9:126661130 | T | C | 86 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0004g0240 others(83): Show |
87 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.327-29706T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661130 | |||||||
chr9:126661174 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.327-29662G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661174 | |||||||
chr9:126661199 | A | ACCCCACG others(29): Show |
1 | a0001c0001t0002g0274 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.327-29618_327-2961 others(40): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126661199 | ||||||
chr9:126661199 | A | ACCCCACG others(29): Show |
44 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0004g0240 others(41): Show |
45 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.327-29617_327-2958 others(40): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126661199 | ||||||
chr9:126661199 | A | ACCCCACG others(65): Show |
1 | a0001c0002t0003g0287 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.327-29582_327-2958 others(76): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126661199 | ||||||
chr9:126661200 | C | G | 1 | a0001c0001t0149g0283 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.327-29636C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661200 | |||||||
chr9:126661219 | T | C | 29 | a0001c0001t0003g0243 a0001c0001t0038g0332 a0001c0001t0058g0089 others(26): Show |
29 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-29617T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661219 | |||||||
chr9:126661219 | TCAGGCCA others(29): Show |
T | 66 | a0001c0001t0002g0324 a0001c0001t0008g0030 a0001c0001t0008g0054 others(63): Show |
66 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.327-29581_327-2954 others(40): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126661219 | ||||||
chr9:126661255 | C | CCAGGCCA others(29): Show |
26 | a0001c0001t0003g0243 a0001c0001t0064g0091 a0001c0001t0068g0078 others(23): Show |
26 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.327-29562_327-2952 others(40): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126661255 | ||||||
chr9:126661255 | C | T | 77 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0004g0240 others(74): Show |
78 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.327-29581C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661255 | |||||||
chr9:126661336 | G | A | 3 | a0001c0001t0058g0089 a0001c0001t0078g0090 a0001c0001t0146g0254 |
3 | HG02965.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.327-29500G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661336 | |||||||
chr9:126661392 | T | A | 47 | a0001c0001t0002g0211 a0001c0001t0002g0226 a0001c0001t0025g0157 others(44): Show |
47 | HG00099.hp1 HG00735.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.327-29444T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661392 | |||||||
chr9:126661416 | G | A | 1 | a0001c0002t0001g0242 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.327-29420G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661416 | |||||||
chr9:126661483 | A | G | 2 | a0001c0002t0001g0064 a0001c0002t0001g0065 |
2 | NA18946.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.327-29353A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661483 | |||||||
chr9:126661489 | G | A | 14 | a0001c0001t0106g0218 a0001c0001t0172g0160 a0001c0001t0178g0200 others(11): Show |
14 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.327-29347G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661489 | |||||||
chr9:126661535 | C | T | 1 | a0001c0001t0175g0125 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.327-29301C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661535 | |||||||
chr9:126661651 | T | A | 1 | a0001c0001t0003g0243 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.327-29185T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661651 | |||||||
chr9:126661701 | G | A | 1 | a0001c0001t0131g0305 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.327-29135G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661701 | |||||||
chr9:126661800 | G | C | 9 | a0001c0001t0101g0170 a0001c0005t0012g0137 a0001c0005t0012g0138 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-29036G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661800 | |||||||
chr9:126661808 | G | A | 1 | a0001c0003t0165g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.327-29028G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661808 | |||||||
chr9:126661823 | G | A | 10 | a0001c0001t0068g0078 a0001c0001t0181g0143 a0001c0002t0013g0128 others(7): Show |
10 | HG00280.hp2 HG01243.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.327-29013G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661823 | |||||||
chr9:126661869 | G | A | 42 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0004g0240 others(39): Show |
43 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.327-28967G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661869 | |||||||
chr9:126661970 | C | T | 1 | a0001c0002t0001g0311 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.327-28866C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661970 | |||||||
chr9:126661971 | G | A | 1 | a0001c0003t0111g0233 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.327-28865G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661971 | |||||||
chr9:126662002 | T | G | 3 | a0001c0001t0003g0243 a0001c0002t0013g0176 a0001c0002t0013g0178 |
3 | HG00738.hp1 HG02602.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.327-28834T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662002 | |||||||
chr9:126662429 | T | C | 1 | a0001c0012t0116g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.327-28407T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662429 | |||||||
chr9:126662440 | A | G | 171 | a0001c0001t0002g0239 a0001c0001t0002g0324 a0001c0001t0003g0243 others(168): Show |
172 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.327-28396A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662440 | |||||||
chr9:126662691 | C | A | 1 | a0001c0001t0002g0231 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.327-28145C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662691 | |||||||
chr9:126662751 | G | A | 13 | a0001c0001t0005g0221 a0001c0001t0005g0275 a0001c0001t0005g0280 others(10): Show |
13 | HG00621.hp1 HG00642.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.327-28085G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662751 | |||||||
chr9:126662918 | G | A | 1 | a0001c0001t0125g0203 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.327-27918G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662918 | |||||||
chr9:126662922 | A | G | 14 | a0001c0002t0053g0177 a0001c0002t0053g0180 a0001c0002t0054g0146 others(11): Show |
14 | HG00639.hp1 HG01109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.327-27914A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662922 | |||||||
chr9:126662926 | G | A | 14 | a0001c0002t0053g0177 a0001c0002t0053g0180 a0001c0002t0054g0146 others(11): Show |
14 | HG00639.hp1 HG01109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.327-27910G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662926 | |||||||
chr9:126663190 | GTTGAGGC others(11): Show |
G | 30 | a0001c0001t0003g0243 a0001c0001t0101g0170 a0001c0001t0146g0254 others(27): Show |
30 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.327-27639_327-2762 others(22): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126663190 | ||||||
chr9:126663423 | C | CA | 10 | a0001c0001t0175g0125 a0001c0001t0181g0143 a0001c0002t0001g0035 others(7): Show |
10 | HG01243.hp2 HG01496.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.327-27398dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126663423 | ||||||
chr9:126663423 | CA | C | 26 | a0001c0001t0035g0062 a0001c0001t0064g0091 a0001c0001t0137g0307 others(23): Show |
26 | HG00639.hp1 HG01109.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.327-27398delA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126663423 | ||||||
chr9:126663423 | CAAAAAAA others(3): Show |
C | 52 | a0001c0001t0003g0243 a0001c0001t0004g0240 a0001c0001t0178g0200 others(49): Show |
53 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.327-27407_327-2739 others(14): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126663423 | ||||||
chr9:126663466 | G | A | 16 | a0001c0001t0041g0314 a0001c0001t0065g0119 a0001c0001t0067g0073 others(13): Show |
16 | HG00280.hp2 HG00738.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.327-27370G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126663466 | |||||||
chr9:126663567 | G | A | 35 | a0001c0001t0101g0170 a0001c0001t0146g0254 a0001c0002t0053g0177 others(32): Show |
35 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.327-27269G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126663567 | |||||||
chr9:126663631 | C | T | 1 | a0001c0005t0168g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.327-27205C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126663631 | |||||||
chr9:126663643 | A | G | 1 | a0001c0001t0149g0283 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.327-27193A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126663643 | |||||||
chr9:126663927 | G | C | 17 | a0001c0002t0053g0177 a0001c0002t0053g0180 a0001c0002t0054g0146 others(14): Show |
17 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.327-26909G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126663927 | |||||||
chr9:126664190 | G | T | 85 | a0001c0001t0008g0054 a0001c0001t0019g0031 a0001c0001t0066g0126 others(82): Show |
85 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.327-26646G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664190 | |||||||
chr9:126664247 | C | T | 1 | a0001c0001t0008g0331 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.327-26589C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664247 | |||||||
chr9:126664248 | G | A | 1 | a0001c0012t0116g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.327-26588G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664248 | |||||||
chr9:126664360 | G | A | 1 | a0001c0001t0007g0330 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.327-26476G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664360 | |||||||
chr9:126664371 | C | T | 9 | a0001c0001t0101g0170 a0001c0005t0012g0137 a0001c0005t0012g0138 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-26465C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664371 | |||||||
chr9:126664410 | G | A | 1 | a0001c0003t0109g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.327-26426G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664410 | |||||||
chr9:126664428 | C | T | 1 | a0001c0002t0191g0192 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.327-26408C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664428 | |||||||
chr9:126664474 | A | G | 4 | a0001c0001t0146g0254 a0001c0002t0055g0145 a0001c0008t0034g0148 others(1): Show |
4 | HG02559.hp2 HG02717.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-26362A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664474 | |||||||
chr9:126664527 | G | A | 1 | a0001c0001t0002g0208 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.327-26309G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664527 | |||||||
chr9:126664624 | C | T | 36 | a0001c0001t0004g0240 a0001c0002t0003g0041 a0001c0002t0003g0228 others(33): Show |
37 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.327-26212C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664624 | |||||||
chr9:126664645 | G | T | 9 | a0001c0001t0101g0170 a0001c0005t0012g0137 a0001c0005t0012g0138 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-26191G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664645 | |||||||
chr9:126664745 | C | T | 3 | a0001c0002t0003g0268 a0001c0002t0009g0109 a0001c0002t0077g0075 |
3 | HG02132.hp1 NA18747.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.327-26091C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664745 | |||||||
chr9:126664811 | G | A | 1 | a0001c0003t0165g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.327-26025G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664811 | |||||||
chr9:126664831 | C | T | 1 | a0001c0002t0001g0058 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.327-26005C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664831 | |||||||
chr9:126664837 | C | T | 336 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(333): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.327-25999C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664837 | |||||||
chr9:126664895 | C | G | 1 | a0001c0002t0055g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-25941C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664895 | |||||||
chr9:126665096 | A | G | 12 | a0001c0001t0027g0072 a0001c0001t0027g0129 a0001c0001t0181g0143 others(9): Show |
12 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-25740A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126665096 | |||||||
chr9:126665235 | C | G | 1 | a0001c0002t0055g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-25601C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126665235 | |||||||
chr9:126665593 | T | A | 1 | a0001c0002t0001g0035 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.327-25243T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126665593 | |||||||
chr9:126665745 | T | C | 1 | a0001c0002t0001g0035 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.327-25091T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126665745 | |||||||
chr9:126665746 | G | T | 1 | a0001c0002t0001g0035 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.327-25090G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126665746 | |||||||
chr9:126665747 | C | G | 1 | a0001c0002t0001g0035 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.327-25089C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126665747 | |||||||
chr9:126666003 | C | G | 9 | a0001c0001t0181g0143 a0001c0004t0062g0085 a0001c0004t0063g0087 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.327-24833C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666003 | |||||||
chr9:126666089 | T | G | 9 | a0001c0001t0181g0143 a0001c0004t0062g0085 a0001c0004t0063g0087 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.327-24747T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666089 | |||||||
chr9:126666099 | G | A | 1 | a0001c0004t0037g0227 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.327-24737G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666099 | |||||||
chr9:126666143 | G | T | 3 | a0001c0001t0146g0254 a0001c0008t0034g0148 a0001c0008t0034g0149 |
3 | HG02717.hp2 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.327-24693G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666143 | |||||||
chr9:126666168 | A | G | 1 | a0001c0001t0064g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.327-24668A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666168 | |||||||
chr9:126666265 | C | T | 7 | a0001c0001t0101g0170 a0001c0005t0012g0137 a0001c0005t0012g0138 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.327-24571C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666265 | |||||||
chr9:126666349 | G | T | 1 | a0001c0004t0037g0227 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.327-24487G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666349 | |||||||
chr9:126666398 | A | G | 167 | a0001c0001t0004g0240 a0001c0001t0019g0031 a0001c0001t0066g0126 others(164): Show |
168 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.327-24438A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666398 | |||||||
chr9:126666486 | A | G | 2 | a0001c0004t0184g0086 a0001c0004t0185g0088 |
2 | HG01243.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.327-24350A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666486 | |||||||
chr9:126666568 | T | TTAAAA | 165 | a0001c0001t0004g0240 a0001c0001t0019g0031 a0001c0001t0066g0126 others(162): Show |
166 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.327-24265_327-2426 others(9): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126666568 | ||||||
chr9:126666675 | G | A | 1 | a0001c0002t0161g0068 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.327-24161G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666675 | |||||||
chr9:126666748 | T | C | 1 | a0001c0002t0189g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.327-24088T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666748 | |||||||
chr9:126666812 | A | G | 98 | a0001c0001t0066g0126 a0001c0001t0101g0170 a0001c0001t0146g0254 others(95): Show |
98 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.327-24024A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666812 | |||||||
chr9:126667010 | T | A | 1 | a0001c0005t0012g0137 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.327-23826T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667010 | |||||||
chr9:126667038 | C | T | 1 | a0001c0001t0096g0230 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.327-23798C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667038 | |||||||
chr9:126667137 | C | G | 335 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(332): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.327-23699C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667137 | |||||||
chr9:126667296 | G | A | 1 | a0001c0001t0140g0269 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.327-23540G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667296 | |||||||
chr9:126667425 | C | T | 12 | a0001c0001t0178g0200 a0001c0002t0006g0184 a0001c0002t0006g0186 others(9): Show |
12 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.327-23411C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667425 | |||||||
chr9:126667475 | C | T | 66 | a0001c0001t0066g0126 a0001c0002t0001g0009 a0001c0002t0001g0015 others(63): Show |
66 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.327-23361C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667475 | |||||||
chr9:126667502 | C | T | 2 | a0001c0001t0011g0224 a0001c0001t0060g0106 |
2 | HG01361.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.327-23334C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667502 | |||||||
chr9:126667901 | G | A | 1 | a0001c0001t0004g0271 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.327-22935G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667901 | |||||||
chr9:126668059 | G | A | 54 | a0001c0001t0101g0170 a0001c0001t0178g0200 a0001c0001t0181g0143 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.327-22777G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668059 | |||||||
chr9:126668158 | G | A | 28 | a0001c0001t0181g0143 a0001c0002t0054g0146 a0001c0002t0100g0147 others(25): Show |
28 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.327-22678G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668158 | |||||||
chr9:126668191 | G | A | 1 | a0001c0001t0007g0317 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.327-22645G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668191 | |||||||
chr9:126668291 | C | T | 54 | a0001c0001t0101g0170 a0001c0001t0178g0200 a0001c0001t0181g0143 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.327-22545C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668291 | |||||||
chr9:126668443 | T | TTTA | 3 | a0001c0001t0038g0004 a0001c0001t0038g0332 a0001c0001t0132g0004 |
3 | NA18973.hp2 NA19005.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.327-22369_327-2236 others(7): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | ||||||
chr9:126668443 | T | TTTATTA | 59 | a0001c0001t0066g0126 a0001c0002t0001g0009 a0001c0002t0001g0015 others(56): Show |
59 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.327-22372_327-2236 others(10): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | ||||||
chr9:126668443 | T | TTTATTAT others(2): Show |
55 | a0001c0001t0004g0240 a0001c0001t0011g0224 a0001c0001t0060g0106 others(52): Show |
56 | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.327-22375_327-2236 others(13): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | ||||||
chr9:126668443 | T | TTTATTAT others(5): Show |
15 | a0001c0002t0001g0279 a0001c0002t0003g0046 a0001c0002t0003g0049 others(12): Show |
15 | HG02055.hp1 HG02129.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.327-22378_327-2236 others(16): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | ||||||
chr9:126668443 | T | TTTATTAT others(8): Show |
11 | a0001c0002t0186g0133 a0001c0002t0189g0172 a0001c0003t0049g0150 others(8): Show |
11 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.327-22381_327-2236 others(19): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | ||||||
chr9:126668443 | T | TTTATTAT others(11): Show |
2 | a0001c0002t0054g0146 a0001c0003t0112g0225 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.327-22384_327-2236 others(22): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | ||||||
chr9:126668443 | T | TTTATTAT others(14): Show |
13 | a0001c0001t0178g0200 a0001c0001t0181g0143 a0001c0002t0006g0184 others(10): Show |
13 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.327-22387_327-2236 others(25): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | ||||||
chr9:126668443 | T | TTTATTAT others(17): Show |
10 | a0001c0002t0006g0189 a0001c0002t0013g0185 a0001c0002t0100g0147 others(7): Show |
10 | HG00609.hp1 HG02055.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.327-22390_327-2236 others(28): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | ||||||
chr9:126668443 | T | TTTATTAT others(20): Show |
3 | a0001c0002t0006g0190 a0001c0004t0063g0087 a0001c0004t0183g0101 |
3 | HG01346.hp2 HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.327-22367_327-2236 others(31): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | ||||||
chr9:126668443 | T | TTTATTAT others(23): Show |
2 | a0001c0001t0101g0170 a0001c0002t0103g0196 |
2 | HG01192.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.327-22367_327-2236 others(34): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | ||||||
chr9:126668492 | C | T | 116 | a0001c0001t0004g0240 a0001c0001t0011g0224 a0001c0001t0060g0106 others(113): Show |
117 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.327-22344C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668492 | |||||||
chr9:126668502 | G | T | 8 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(5): Show |
8 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.327-22334G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668502 | |||||||
chr9:126668598 | C | T | 2 | a0001c0002t0003g0228 a0001c0002t0013g0128 |
2 | HG01257.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.327-22238C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668598 | |||||||
chr9:126668618 | T | A | 1 | a0001c0001t0018g0290 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.327-22218T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668618 | |||||||
chr9:126668934 | C | T | 172 | a0001c0001t0004g0240 a0001c0001t0011g0224 a0001c0001t0060g0106 others(169): Show |
173 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.327-21902C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668934 | |||||||
chr9:126669085 | C | T | 2 | a0001c0002t0001g0042 a0001c0002t0001g0242 |
2 | NA19003.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.327-21751C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669085 | |||||||
chr9:126669117 | G | A | 1 | a0001c0002t0001g0036 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.327-21719G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669117 | |||||||
chr9:126669139 | A | T | 29 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0054g0146 others(26): Show |
29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-21697A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669139 | |||||||
chr9:126669177 | G | A | 2 | a0001c0004t0184g0086 a0001c0004t0185g0088 |
2 | HG01243.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.327-21659G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669177 | |||||||
chr9:126669241 | CGAG | C | 172 | a0001c0001t0004g0240 a0001c0001t0011g0224 a0001c0001t0060g0106 others(169): Show |
173 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.327-21590_327-2158 others(7): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126669241 | ||||||
chr9:126669245 | G | A | 2 | a0001c0002t0053g0177 a0001c0002t0053g0180 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.327-21591G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669245 | |||||||
chr9:126669356 | A | G | 7 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.327-21480A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669356 | |||||||
chr9:126669380 | C | G | 1 | a0001c0002t0188g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.327-21456C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669380 | |||||||
chr9:126669670 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.327-21166G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669670 | |||||||
chr9:126669765 | T | G | 336 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(333): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.327-21071T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669765 | |||||||
chr9:126669956 | C | T | 23 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0043 others(20): Show |
23 | HG00408.hp2 HG02027.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.327-20880C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669956 | |||||||
chr9:126669957 | G | A | 1 | a0001c0002t0022g0011 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.327-20879G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669957 | |||||||
chr9:126670451 | T | G | 2 | a0001c0010t0193g0168 a0001c0012t0116g0142 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.327-20385T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670451 | |||||||
chr9:126670455 | G | T | 4 | a0001c0004t0150g0067 a0001c0004t0182g0154 a0001c0004t0184g0086 others(1): Show |
4 | HG01243.hp2 HG02886.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-20381G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670455 | |||||||
chr9:126670460 | G | A | 6 | a0001c0002t0053g0177 a0001c0002t0053g0180 a0001c0002t0105g0166 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-20376G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670460 | |||||||
chr9:126670462 | T | C | 29 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0054g0146 others(26): Show |
29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-20374T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670462 | |||||||
chr9:126670473 | G | A | 1 | a0001c0002t0016g0019 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.327-20363G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670473 | |||||||
chr9:126670483 | G | A | 14 | a0001c0001t0178g0200 a0001c0002t0006g0184 a0001c0002t0006g0186 others(11): Show |
14 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.327-20353G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670483 | |||||||
chr9:126670514 | G | A | 28 | a0001c0001t0178g0200 a0001c0002t0006g0184 a0001c0002t0006g0186 others(25): Show |
28 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.327-20322G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670514 | |||||||
chr9:126670519 | G | A | 2 | a0001c0001t0028g0081 a0001c0001t0059g0120 |
2 | HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.327-20317G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670519 | |||||||
chr9:126670572 | G | A | 1 | a0001c0004t0037g0227 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.327-20264G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670572 | |||||||
chr9:126670589 | A | G | 2 | a0001c0002t0001g0059 a0001c0002t0156g0053 |
2 | NA18985.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.327-20247A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670589 | |||||||
chr9:126670662 | C | G | 17 | a0001c0001t0101g0170 a0001c0002t0054g0146 a0001c0002t0100g0147 others(14): Show |
17 | HG00639.hp1 HG01109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.327-20174C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670662 | |||||||
chr9:126670770 | C | T | 12 | a0001c0001t0181g0143 a0001c0004t0043g0213 a0001c0004t0043g0214 others(9): Show |
12 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-20066C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670770 | |||||||
chr9:126670859 | C | T | 29 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0054g0146 others(26): Show |
29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-19977C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670859 | |||||||
chr9:126670926 | G | A | 3 | a0001c0001t0028g0076 a0001c0001t0095g0247 a0001c0001t0117g0245 |
3 | HG01175.hp2 HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.327-19910G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670926 | |||||||
chr9:126670978 | C | T | 1 | a0001c0002t0001g0057 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.327-19858C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670978 | |||||||
chr9:126671001 | G | C | 14 | a0001c0001t0178g0200 a0001c0002t0006g0184 a0001c0002t0006g0186 others(11): Show |
14 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.327-19835G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671001 | |||||||
chr9:126671152 | G | A | 29 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0054g0146 others(26): Show |
29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-19684G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671152 | |||||||
chr9:126671163 | T | C | 2 | a0001c0001t0040g0039 a0001c0001t0040g0259 |
2 | HG00597.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.327-19673T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671163 | |||||||
chr9:126671250 | T | C | 8 | a0001c0001t0002g0273 a0001c0001t0002g0300 a0001c0001t0002g0301 others(5): Show |
8 | HG01081.hp1 HG01106.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.327-19586T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671250 | |||||||
chr9:126671306 | T | C | 29 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0054g0146 others(26): Show |
29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-19530T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671306 | |||||||
chr9:126671514 | A | C | 14 | a0001c0001t0178g0200 a0001c0002t0006g0184 a0001c0002t0006g0186 others(11): Show |
14 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.327-19322A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671514 | |||||||
chr9:126671650 | A | G | 281 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(278): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.327-19186A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671650 | |||||||
chr9:126671691 | G | A | 5 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.327-19145G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671691 | |||||||
chr9:126671832 | G | A | 2 | a0001c0007t0048g0318 a0001c0007t0048g0319 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.327-19004G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671832 | |||||||
chr9:126671860 | A | G | 12 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0239 others(9): Show |
12 | HG00099.hp2 HG00642.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.327-18976A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671860 | |||||||
chr9:126672231 | G | A | 20 | a0001c0001t0178g0200 a0001c0002t0006g0184 a0001c0002t0006g0186 others(17): Show |
20 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.327-18605G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672231 | |||||||
chr9:126672308 | G | A | 5 | a0001c0003t0108g0253 a0001c0003t0109g0136 a0001c0010t0193g0168 others(2): Show |
5 | HG01884.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.327-18528G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672308 | |||||||
chr9:126672371 | G | A | 1 | a0001c0001t0142g0281 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.327-18465G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672371 | |||||||
chr9:126672521 | C | T | 5 | a0001c0003t0108g0253 a0001c0003t0109g0136 a0001c0010t0193g0168 others(2): Show |
5 | HG01884.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.327-18315C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672521 | |||||||
chr9:126672551 | TAAATTGG others(132): Show |
T | 1 | a0001c0002t0001g0057 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.327-18283_327-1814 others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126672551 | ||||||
chr9:126672701 | G | A | 2 | a0001c0004t0184g0086 a0001c0004t0185g0088 |
2 | HG01243.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.327-18135G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672701 | |||||||
chr9:126672742 | C | T | 55 | a0001c0001t0101g0170 a0001c0001t0178g0200 a0001c0001t0181g0143 others(52): Show |
55 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.327-18094C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672742 | |||||||
chr9:126672766 | G | A | 1 | a0001c0011t0085g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.327-18070G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672766 | |||||||
chr9:126672824 | C | T | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-18012C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672824 | |||||||
chr9:126672875 | G | A | 3 | a0001c0001t0002g0324 a0001c0002t0046g0256 a0001c0002t0046g0257 |
3 | NA18953.hp2 NA18993.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.327-17961G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672875 | |||||||
chr9:126672997 | C | T | 5 | a0001c0001t0025g0157 a0001c0001t0051g0153 a0001c0001t0051g0158 others(2): Show |
5 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.327-17839C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672997 | |||||||
chr9:126673177 | G | C | 1 | a0001c0001t0002g0329 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.327-17659G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673177 | |||||||
chr9:126673481 | A | G | 1 | a0001c0002t0001g0057 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.327-17355A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673481 | |||||||
chr9:126673494 | G | A | 2 | a0001c0001t0027g0072 a0001c0001t0027g0129 |
2 | NA18953.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.327-17342G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673494 | |||||||
chr9:126673562 | C | G | 63 | a0001c0001t0011g0224 a0001c0001t0060g0106 a0001c0001t0101g0170 others(60): Show |
63 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.327-17274C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673562 | |||||||
chr9:126673613 | G | A | 2 | a0001c0001t0002g0219 a0001c0001t0174g0156 |
2 | HG02897.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.327-17223G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673613 | |||||||
chr9:126673653 | G | A | 1 | a0001c0004t0180g0083 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.327-17183G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673653 | |||||||
chr9:126673774 | G | T | 1 | a0001c0002t0001g0057 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.327-17062G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673774 | |||||||
chr9:126673790 | C | G | 1 | a0001c0002t0001g0057 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.327-17046C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673790 | |||||||
chr9:126673801 | G | T | 1 | a0001c0001t0008g0331 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.327-17035G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673801 | |||||||
chr9:126673826 | G | A | 1 | a0001c0002t0055g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-17010G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673826 | |||||||
chr9:126673993 | C | T | 63 | a0001c0001t0066g0126 a0001c0002t0001g0009 a0001c0002t0001g0015 others(60): Show |
63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.327-16843C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673993 | |||||||
chr9:126674097 | C | T | 11 | a0001c0001t0178g0200 a0001c0002t0006g0184 a0001c0002t0006g0186 others(8): Show |
11 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.327-16739C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674097 | |||||||
chr9:126674136 | G | A | 2 | a0001c0003t0057g0134 a0001c0003t0076g0132 |
2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.327-16700G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674136 | |||||||
chr9:126674246 | G | A | 11 | a0001c0001t0178g0200 a0001c0002t0006g0186 a0001c0002t0006g0187 others(8): Show |
11 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.327-16590G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674246 | |||||||
chr9:126674283 | C | G | 3 | a0001c0003t0057g0134 a0001c0003t0076g0132 a0001c0003t0110g0069 |
3 | HG02109.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.327-16553C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674283 | |||||||
chr9:126674389 | T | TG | 25 | a0001c0001t0178g0200 a0001c0002t0006g0184 a0001c0002t0006g0186 others(22): Show |
25 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.327-16440dupG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126674389 | ||||||
chr9:126674517 | T | G | 1 | a0001c0002t0001g0057 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.327-16319T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674517 | |||||||
chr9:126674614 | A | C | 3 | a0001c0001t0025g0084 a0001c0001t0125g0203 a0001c0001t0170g0155 |
3 | HG01099.hp2 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.327-16222A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674614 | |||||||
chr9:126674683 | C | T | 6 | a0001c0002t0055g0145 a0001c0003t0108g0253 a0001c0003t0109g0136 others(3): Show |
6 | HG01884.hp1 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-16153C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674683 | |||||||
chr9:126674840 | C | A | 1 | a0001c0001t0106g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.327-15996C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674840 | |||||||
chr9:126674860 | A | G | 6 | a0001c0002t0055g0145 a0001c0003t0108g0253 a0001c0003t0109g0136 others(3): Show |
6 | HG01884.hp1 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-15976A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674860 | |||||||
chr9:126674961 | G | T | 13 | a0001c0001t0178g0200 a0001c0002t0006g0184 a0001c0002t0006g0186 others(10): Show |
13 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.327-15875G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674961 | |||||||
chr9:126674981 | G | A | 1 | a0001c0011t0085g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.327-15855G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674981 | |||||||
chr9:126675056 | A | G | 35 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0054g0146 others(32): Show |
35 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.327-15780A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675056 | |||||||
chr9:126675175 | AC | A | 60 | a0001c0001t0101g0170 a0001c0001t0178g0200 a0001c0001t0181g0143 others(57): Show |
60 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.327-15654delC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126675175 | ||||||
chr9:126675395 | G | T | 1 | a0001c0001t0029g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.327-15441G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675395 | |||||||
chr9:126675554 | G | A | 2 | a0001c0008t0034g0148 a0001c0008t0034g0149 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.327-15282G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675554 | |||||||
chr9:126675595 | C | T | 3 | a0001c0001t0025g0084 a0001c0001t0125g0203 a0001c0001t0170g0155 |
3 | HG01099.hp2 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.327-15241C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675595 | |||||||
chr9:126675657 | A | C | 2 | a0001c0010t0193g0168 a0001c0012t0116g0142 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.327-15179A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675657 | |||||||
chr9:126675735 | T | TA | 30 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0001g0057 others(27): Show |
30 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.327-15087dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126675735 | ||||||
chr9:126675735 | TA | T | 8 | a0001c0001t0010g0007 a0001c0001t0018g0007 a0001c0002t0001g0035 others(5): Show |
8 | HG01975.hp1 HG02922.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.327-15087delA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126675735 | ||||||
chr9:126675736 | A | T | 24 | a0001c0001t0178g0200 a0001c0002t0006g0184 a0001c0002t0006g0186 others(21): Show |
24 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.327-15100A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675736 | |||||||
chr9:126675737 | A | T | 1 | a0001c0002t0053g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.327-15099A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675737 | |||||||
chr9:126675772 | G | A | 2 | a0001c0002t0016g0013 a0001c0002t0016g0019 |
2 | HG02015.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.327-15064G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675772 | |||||||
chr9:126675816 | G | C | 2 | a0001c0003t0108g0253 a0001c0003t0109g0136 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.327-15020G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675816 | |||||||
chr9:126675831 | C | T | 6 | a0001c0002t0053g0177 a0001c0002t0053g0180 a0001c0002t0105g0166 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-15005C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675831 | |||||||
chr9:126675906 | G | A | 2 | a0001c0002t0100g0147 a0001c0002t0166g0181 |
2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.327-14930G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675906 | |||||||
chr9:126675909 | C | T | 2 | a0001c0002t0100g0147 a0001c0002t0166g0181 |
2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.327-14927C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675909 | |||||||
chr9:126675915 | A | G | 2 | a0001c0002t0100g0147 a0001c0002t0166g0181 |
2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.327-14921A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675915 | |||||||
chr9:126675942 | G | A | 1 | a0001c0002t0103g0196 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.327-14894G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675942 | |||||||
chr9:126675945 | A | T | 24 | a0001c0001t0002g0231 a0001c0001t0002g0273 a0001c0001t0002g0300 others(21): Show |
24 | HG00639.hp2 HG00735.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.327-14891A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675945 | |||||||
chr9:126676048 | C | CA | 20 | a0001c0001t0002g0211 a0001c0001t0002g0215 a0001c0001t0004g0264 others(17): Show |
20 | HG00741.hp1 HG01099.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.327-14770dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126676048 | ||||||
chr9:126676048 | CA | C | 35 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0031g0096 others(32): Show |
35 | HG00639.hp1 HG01070.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.327-14770delA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126676048 | ||||||
chr9:126676158 | G | A | 2 | a0001c0003t0108g0253 a0001c0003t0109g0136 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.327-14678G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676158 | |||||||
chr9:126676310 | T | C | 2 | a0001c0002t0070g0105 a0001c0002t0089g0111 |
2 | NA18945.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.327-14526T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676310 | |||||||
chr9:126676312 | C | A | 37 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0054g0146 others(34): Show |
37 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.327-14524C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676312 | |||||||
chr9:126676454 | T | G | 1 | a0001c0002t0189g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.327-14382T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676454 | |||||||
chr9:126676510 | G | A | 1 | a0001c0002t0091g0135 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.327-14326G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676510 | |||||||
chr9:126676582 | A | G | 335 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(332): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.327-14254A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676582 | |||||||
chr9:126676593 | A | G | 62 | a0001c0001t0101g0170 a0001c0001t0178g0200 a0001c0001t0181g0143 others(59): Show |
62 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.327-14243A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676593 | |||||||
chr9:126676771 | C | T | 2 | a0001c0002t0001g0036 a0001c0002t0055g0145 |
2 | HG02559.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.327-14065C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676771 | |||||||
chr9:126676947 | T | C | 1 | a0001c0001t0134g0066 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.327-13889T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676947 | |||||||
chr9:126676996 | C | T | 12 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0239 others(9): Show |
12 | HG00099.hp2 HG00642.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.327-13840C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676996 | |||||||
chr9:126676997 | G | A | 1 | a0001c0001t0084g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.327-13839G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676997 | |||||||
chr9:126677095 | C | T | 3 | a0001c0003t0057g0134 a0001c0003t0076g0132 a0001c0003t0110g0069 |
3 | HG02109.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.327-13741C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126677095 | |||||||
chr9:126677184 | C | T | 29 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0054g0146 others(26): Show |
29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-13652C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126677184 | |||||||
chr9:126677286 | C | T | 2 | a0001c0002t0006g0186 a0001c0002t0006g0188 |
2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.327-13550C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126677286 | |||||||
chr9:126677681 | C | A | 1 | a0001c0001t0029g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.327-13155C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126677681 | |||||||
chr9:126677977 | T | G | 3 | a0001c0002t0015g0110 a0001c0002t0015g0112 a0001c0002t0015g0123 |
3 | NA18984.hp1 NA19054.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.327-12859T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126677977 | |||||||
chr9:126678178 | C | T | 1 | a0001c0001t0101g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.327-12658C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678178 | |||||||
chr9:126678309 | C | CA | 9 | a0001c0001t0002g0329 a0001c0001t0007g0330 a0001c0001t0061g0077 others(6): Show |
9 | HG00735.hp1 HG01175.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-12515dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126678309 | ||||||
chr9:126678311 | AAAAAAAA others(11): Show |
A | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-12514_327-1249 others(22): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126678311 | ||||||
chr9:126678314 | A | G | 1 | a0001c0001t0052g0201 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.327-12522A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678314 | |||||||
chr9:126678321 | AC | A | 4 | a0001c0001t0178g0200 a0001c0004t0182g0154 a0001c0004t0184g0086 others(1): Show |
4 | HG01243.hp2 HG03195.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-12514delC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678321 | |||||||
chr9:126678322 | C | A | 55 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0006g0184 others(52): Show |
55 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.327-12514C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678322 | |||||||
chr9:126678325 | A | C | 28 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0054g0146 others(25): Show |
28 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.327-12511A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678325 | |||||||
chr9:126678326 | A | C | 1 | a0001c0003t0108g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.327-12510A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678326 | |||||||
chr9:126678329 | C | A | 58 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0006g0184 others(55): Show |
58 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.327-12507C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678329 | |||||||
chr9:126678329 | C | CA | 8 | a0001c0001t0002g0239 a0001c0001t0003g0243 a0001c0001t0005g0304 others(5): Show |
8 | HG01243.hp1 HG01981.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.327-12495dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126678329 | ||||||
chr9:126678332 | A | C | 1 | a0001c0001t0068g0078 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.327-12504A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678332 | |||||||
chr9:126678335 | A | AC | 9 | a0001c0001t0178g0200 a0001c0002t0053g0177 a0001c0002t0053g0180 others(6): Show |
9 | HG00741.hp1 HG02280.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-12501_327-1250 others(5): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678335 | |||||||
chr9:126678335 | A | C | 43 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0006g0184 others(40): Show |
43 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.327-12501A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678335 | |||||||
chr9:126678342 | C | A | 9 | a0001c0003t0057g0134 a0001c0003t0076g0132 a0001c0003t0110g0069 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-12494C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678342 | |||||||
chr9:126678561 | A | C | 54 | a0001c0001t0101g0170 a0001c0001t0178g0200 a0001c0001t0181g0143 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.327-12275A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678561 | |||||||
chr9:126678612 | G | C | 2 | a0001c0008t0034g0148 a0001c0008t0034g0149 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.327-12224G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678612 | |||||||
chr9:126678637 | C | G | 1 | a0001c0001t0081g0102 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.327-12199C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678637 | |||||||
chr9:126678712 | C | G | 3 | a0001c0003t0057g0134 a0001c0003t0076g0132 a0001c0003t0110g0069 |
3 | HG02109.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.327-12124C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678712 | |||||||
chr9:126678765 | A | C | 1 | a0001c0001t0142g0281 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.327-12071A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678765 | |||||||
chr9:126678773 | T | G | 1 | a0001c0001t0131g0305 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.327-12063T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678773 | |||||||
chr9:126679157 | C | T | 2 | a0001c0001t0011g0224 a0001c0001t0060g0106 |
2 | HG01361.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.327-11679C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126679157 | |||||||
chr9:126679235 | C | CTA | 29 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0054g0146 others(26): Show |
29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-11600_327-1159 others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126679235 | ||||||
chr9:126679280 | C | T | 6 | a0001c0002t0001g0034 a0001c0002t0001g0037 a0001c0002t0001g0048 others(3): Show |
6 | HG02155.hp1 NA18950.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-11556C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126679280 | |||||||
chr9:126679422 | G | A | 2 | a0001c0010t0193g0168 a0001c0012t0116g0142 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.327-11414G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126679422 | |||||||
chr9:126679437 | G | A | 2 | a0001c0001t0002g0211 a0001c0001t0144g0205 |
2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.327-11399G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126679437 | |||||||
chr9:126679475 | G | C | 55 | a0001c0001t0004g0240 a0001c0001t0178g0200 a0001c0002t0003g0029 others(52): Show |
56 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.327-11361G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126679475 | |||||||
chr9:126679518 | A | G | 97 | a0001c0001t0004g0240 a0001c0001t0101g0170 a0001c0001t0178g0200 others(94): Show |
98 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.327-11318A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126679518 | |||||||
chr9:126679568 | A | T | 29 | a0001c0001t0101g0170 a0001c0001t0181g0143 a0001c0002t0054g0146 others(26): Show |
29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-11268A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126679568 | |||||||
chr9:126679597 | T | TG | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-11237dupG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126679597 | ||||||
chr9:126680040 | G | T | 1 | a0001c0002t0054g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.327-10796G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680040 | |||||||
chr9:126680067 | G | A | 1 | a0001c0001t0148g0333 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.327-10769G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680067 | |||||||
chr9:126680104 | G | A | 1 | a0001c0002t0188g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.327-10732G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680104 | |||||||
chr9:126680104 | G | T | 64 | a0001c0001t0066g0126 a0001c0002t0001g0009 a0001c0002t0001g0015 others(61): Show |
64 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.327-10732G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680104 | |||||||
chr9:126680314 | G | C | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-10522G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680314 | |||||||
chr9:126680378 | G | T | 2 | a0001c0002t0003g0046 a0001c0002t0003g0049 |
2 | NA18999.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.327-10458G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680378 | |||||||
chr9:126680402 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.327-10434A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680402 | |||||||
chr9:126680451 | C | T | 1 | a0001c0001t0040g0259 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.327-10385C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680451 | |||||||
chr9:126680600 | A | G | 1 | a0001c0002t0013g0178 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.327-10236A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680600 | |||||||
chr9:126680780 | G | A | 3 | a0001c0003t0057g0134 a0001c0003t0076g0132 a0001c0003t0110g0069 |
3 | HG02109.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.327-10056G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680780 | |||||||
chr9:126680784 | A | G | 2 | a0001c0002t0053g0177 a0001c0002t0053g0180 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.327-10052A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680784 | |||||||
chr9:126680835 | C | A | 2 | a0001c0001t0002g0274 a0001c0001t0011g0328 |
2 | HG00558.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.327-10001C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680835 | |||||||
chr9:126681037 | G | A | 1 | a0001c0001t0169g0152 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.327-9799G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681037 | |||||||
chr9:126681041 | C | T | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-9795C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681041 | |||||||
chr9:126681055 | A | G | 17 | a0001c0001t0101g0170 a0001c0002t0054g0146 a0001c0002t0100g0147 others(14): Show |
17 | HG00639.hp1 HG01109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.327-9781A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681055 | |||||||
chr9:126681221 | A | G | 2 | a0001c0002t0016g0024 a0001c0002t0191g0192 |
2 | HG00609.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.327-9615A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681221 | |||||||
chr9:126681255 | A | G | 1 | a0001c0001t0042g0309 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.327-9581A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681255 | |||||||
chr9:126681371 | G | T | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-9465G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681371 | |||||||
chr9:126681467 | G | GC | 173 | a0001c0001t0004g0240 a0001c0001t0066g0126 a0001c0001t0101g0170 others(170): Show |
174 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.327-9366dupC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126681467 | ||||||
chr9:126681573 | G | GC | 62 | a0001c0001t0004g0240 a0001c0001t0178g0200 a0001c0002t0003g0029 others(59): Show |
63 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.327-9256dupC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126681573 | ||||||
chr9:126681579 | C | G | 1 | a0001c0001t0137g0307 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.327-9257C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681579 | |||||||
chr9:126681616 | C | A | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-9220C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681616 | |||||||
chr9:126681770 | G | A | 2 | a0001c0003t0108g0253 a0001c0003t0109g0136 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.327-9066G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681770 | |||||||
chr9:126681799 | G | T | 6 | a0001c0002t0055g0145 a0001c0008t0034g0148 a0001c0008t0034g0149 others(3): Show |
6 | HG01884.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-9037G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681799 | |||||||
chr9:126681887 | T | C | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-8949T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681887 | |||||||
chr9:126681900 | C | CA | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-8924dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126681900 | ||||||
chr9:126681907 | A | AAT | 12 | a0001c0001t0181g0143 a0001c0004t0043g0213 a0001c0004t0043g0214 others(9): Show |
12 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-8928_327-8927i others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126681907 | ||||||
chr9:126681910 | A | T | 88 | a0001c0001t0002g0239 a0001c0001t0004g0240 a0001c0001t0029g0094 others(85): Show |
89 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.327-8926A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681910 | |||||||
chr9:126681913 | T | A | 8 | a0001c0001t0010g0006 a0001c0001t0010g0007 a0001c0001t0010g0315 others(5): Show |
8 | HG02165.hp1 NA18959.hp2 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.327-8923T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681913 | |||||||
chr9:126681965 | G | A | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-8871G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681965 | |||||||
chr9:126682081 | G | GCC | 11 | a0001c0001t0066g0126 a0001c0002t0001g0034 a0001c0002t0001g0035 others(8): Show |
11 | HG02027.hp2 HG02074.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.327-8755_327-8754i others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | |||||||
chr9:126682081 | G | GCCTTTTT | 9 | a0001c0001t0101g0170 a0001c0002t0003g0041 a0001c0002t0009g0121 others(6): Show |
9 | HG00621.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-8755_327-8754i others(9): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | |||||||
chr9:126682081 | G | GCCTTTTT others(1): Show |
33 | a0001c0001t0178g0200 a0001c0002t0003g0029 a0001c0002t0003g0049 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.327-8755_327-8754i others(10): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | |||||||
chr9:126682081 | G | GCCTTTTT others(2): Show |
23 | a0001c0001t0004g0240 a0001c0001t0029g0127 a0001c0002t0003g0046 others(20): Show |
23 | HG00609.hp1 HG01074.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.327-8755_327-8754i others(11): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | |||||||
chr9:126682081 | G | GCCTTTTT others(3): Show |
13 | a0001c0002t0006g0187 a0001c0002t0013g0178 a0001c0002t0053g0177 others(10): Show |
13 | HG01884.hp2 HG01978.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.327-8755_327-8754i others(12): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | |||||||
chr9:126682081 | G | GCCTTTTT others(4): Show |
8 | a0001c0002t0006g0189 a0001c0002t0087g0103 a0001c0002t0089g0111 others(5): Show |
8 | HG00741.hp1 HG00741.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.327-8755_327-8754i others(13): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | |||||||
chr9:126682081 | G | GCCTTTTT others(5): Show |
3 | a0001c0002t0013g0176 a0001c0002t0192g0171 a0001c0005t0168g0164 |
3 | HG00738.hp1 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.327-8755_327-8754i others(14): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | |||||||
chr9:126682081 | GT | G | 4 | a0001c0002t0055g0145 a0001c0004t0037g0227 a0001c0008t0034g0148 others(1): Show |
4 | HG01167.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-8754delT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | |||||||
chr9:126682082 | T | C | 69 | a0001c0001t0181g0143 a0001c0002t0001g0009 a0001c0002t0001g0015 others(66): Show |
69 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.327-8754T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682082 | |||||||
chr9:126682083 | C | CT | 64 | a0001c0001t0007g0330 a0001c0001t0008g0331 a0001c0001t0019g0335 others(61): Show |
64 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.327-8728dupT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126682083 | ||||||
chr9:126682083 | C | T | 101 | a0001c0001t0004g0240 a0001c0001t0029g0127 a0001c0001t0066g0126 others(98): Show |
102 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.327-8753C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682083 | |||||||
chr9:126682084 | T | C | 4 | a0001c0002t0055g0145 a0001c0004t0037g0227 a0001c0008t0034g0148 others(1): Show |
4 | HG01167.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-8752T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682084 | |||||||
chr9:126682108 | T | TTTTTTTT others(6): Show |
5 | a0001c0001t0181g0143 a0001c0004t0043g0213 a0001c0004t0063g0087 others(2): Show |
5 | HG01496.hp2 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.327-8728_327-8727i others(15): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682108 | |||||||
chr9:126682108 | T | TTTTTTTT others(7): Show |
5 | a0001c0004t0043g0214 a0001c0004t0180g0083 a0001c0004t0182g0154 others(2): Show |
5 | HG02055.hp2 HG03195.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.327-8728_327-8727i others(16): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682108 | |||||||
chr9:126682108 | T | TTTTTTTT others(8): Show |
1 | a0001c0004t0185g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.327-8728_327-8727i others(17): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682108 | |||||||
chr9:126682308 | G | T | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-8528G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682308 | |||||||
chr9:126682342 | G | A | 6 | a0001c0002t0055g0145 a0001c0008t0034g0148 a0001c0008t0034g0149 others(3): Show |
6 | HG01884.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-8494G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682342 | |||||||
chr9:126682500 | A | G | 1 | a0001c0001t0008g0331 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.327-8336A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682500 | |||||||
chr9:126682763 | C | A | 1 | a0001c0001t0002g0273 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.327-8073C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682763 | |||||||
chr9:126682812 | T | C | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-8024T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682812 | |||||||
chr9:126682820 | A | G | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-8016A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682820 | |||||||
chr9:126682861 | C | G | 1 | a0001c0001t0194g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.327-7975C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682861 | |||||||
chr9:126682877 | A | G | 1 | a0001c0001t0021g0270 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.327-7959A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682877 | |||||||
chr9:126682894 | G | GA | 59 | a0001c0001t0002g0301 a0001c0001t0005g0221 a0001c0001t0007g0317 others(56): Show |
59 | HG00408.hp2 HG00609.hp2 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.327-7921dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126682894 | ||||||
chr9:126682894 | G | GAA | 19 | a0001c0002t0001g0009 a0001c0002t0001g0043 a0001c0002t0001g0279 others(16): Show |
19 | HG01069.hp1 HG01070.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.327-7922_327-7921d others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126682894 | ||||||
chr9:126682894 | G | GAAA | 19 | a0001c0001t0101g0170 a0001c0002t0001g0017 a0001c0002t0009g0109 others(16): Show |
19 | HG00438.hp1 HG00639.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.327-7923_327-7921d others(5): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126682894 | ||||||
chr9:126682894 | G | GAAAA | 55 | a0001c0001t0004g0240 a0001c0001t0080g0080 a0001c0001t0178g0200 others(52): Show |
56 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.327-7924_327-7921d others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126682894 | ||||||
chr9:126682894 | GA | G | 8 | a0001c0001t0005g0288 a0001c0001t0007g0330 a0001c0001t0010g0315 others(5): Show |
8 | HG01069.hp2 HG01167.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.327-7921delA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126682894 | ||||||
chr9:126682894 | GAA | G | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-7922_327-7921d others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126682894 | ||||||
chr9:126682912 | A | G | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-7924A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682912 | |||||||
chr9:126683096 | G | A | 1 | a0001c0010t0193g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327-7740G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683096 | |||||||
chr9:126683138 | G | A | 1 | a0001c0002t0088g0122 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.327-7698G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683138 | |||||||
chr9:126683157 | C | T | 79 | a0001c0001t0004g0240 a0001c0001t0101g0170 a0001c0001t0178g0200 others(76): Show |
80 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.327-7679C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683157 | |||||||
chr9:126683183 | G | A | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-7653G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683183 | |||||||
chr9:126683441 | G | A | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-7395G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683441 | |||||||
chr9:126683835 | G | A | 1 | a0001c0002t0055g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-7001G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683835 | |||||||
chr9:126683972 | C | T | 2 | a0001c0001t0025g0084 a0001c0001t0170g0155 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.327-6864C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683972 | |||||||
chr9:126683999 | C | T | 16 | a0001c0001t0002g0231 a0001c0001t0002g0324 a0001c0001t0010g0006 others(13): Show |
16 | HG00639.hp2 HG00735.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.327-6837C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683999 | |||||||
chr9:126684102 | A | G | 1 | a0001c0002t0192g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.327-6734A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684102 | |||||||
chr9:126684171 | G | C | 12 | a0001c0002t0053g0177 a0001c0002t0053g0180 a0001c0002t0105g0166 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-6665G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684171 | |||||||
chr9:126684180 | T | C | 12 | a0001c0002t0053g0177 a0001c0002t0053g0180 a0001c0002t0105g0166 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-6656T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684180 | |||||||
chr9:126684187 | G | A | 1 | a0001c0008t0034g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.327-6649G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684187 | |||||||
chr9:126684237 | T | C | 1 | a0001c0001t0133g0018 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.327-6599T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684237 | |||||||
chr9:126684312 | A | G | 57 | a0001c0001t0004g0240 a0001c0001t0178g0200 a0001c0002t0003g0029 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.327-6524A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684312 | |||||||
chr9:126684369 | G | C | 1 | a0001c0002t0055g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-6467G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684369 | |||||||
chr9:126684713 | C | A | 3 | a0001c0004t0043g0213 a0001c0004t0043g0214 a0001c0004t0145g0222 |
3 | HG03225.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.327-6123C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684713 | |||||||
chr9:126684746 | A | AC | 13 | a0001c0002t0053g0177 a0001c0002t0053g0180 a0001c0002t0105g0166 others(10): Show |
13 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.327-6084dupC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126684746 | ||||||
chr9:126684753 | G | A | 171 | a0001c0001t0004g0240 a0001c0001t0101g0170 a0001c0001t0178g0200 others(168): Show |
172 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.327-6083G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684753 | |||||||
chr9:126685060 | C | T | 63 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(60): Show |
63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.327-5776C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685060 | |||||||
chr9:126685284 | G | T | 2 | a0001c0001t0095g0247 a0001c0001t0117g0245 |
2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.327-5552G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685284 | |||||||
chr9:126685328 | C | T | 2 | a0001c0010t0193g0168 a0001c0011t0085g0082 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.327-5508C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685328 | |||||||
chr9:126685334 | G | A | 1 | a0001c0001t0181g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.327-5502G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685334 | |||||||
chr9:126685358 | G | A | 2 | a0001c0001t0002g0246 a0001c0001t0002g0248 |
2 | HG03834.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.327-5478G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685358 | |||||||
chr9:126685363 | C | T | 1 | a0001c0001t0181g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.327-5473C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685363 | |||||||
chr9:126685461 | G | A | 63 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(60): Show |
63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.327-5375G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685461 | |||||||
chr9:126685507 | G | A | 1 | a0001c0006t0050g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.327-5329G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685507 | |||||||
chr9:126685679 | G | A | 2 | a0001c0003t0049g0150 a0001c0003t0049g0169 |
2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.327-5157G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685679 | |||||||
chr9:126685795 | G | A | 12 | a0001c0001t0181g0143 a0001c0004t0043g0213 a0001c0004t0043g0214 others(9): Show |
12 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-5041G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685795 | |||||||
chr9:126685841 | T | C | 33 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0239 others(30): Show |
33 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.327-4995T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685841 | |||||||
chr9:126685852 | T | G | 172 | a0001c0001t0004g0240 a0001c0001t0101g0170 a0001c0001t0178g0200 others(169): Show |
173 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.327-4984T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685852 | |||||||
chr9:126685863 | T | C | 2 | a0001c0002t0003g0228 a0001c0002t0013g0128 |
2 | HG01257.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.327-4973T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685863 | |||||||
chr9:126685914 | G | A | 5 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.327-4922G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685914 | |||||||
chr9:126686136 | C | T | 16 | a0001c0001t0181g0143 a0001c0003t0057g0134 a0001c0003t0076g0132 others(13): Show |
16 | HG01167.hp2 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.327-4700C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686136 | |||||||
chr9:126686235 | A | G | 173 | a0001c0001t0004g0240 a0001c0001t0101g0170 a0001c0001t0178g0200 others(170): Show |
174 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.327-4601A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686235 | |||||||
chr9:126686279 | C | CA | 16 | a0001c0001t0008g0030 a0001c0001t0030g0118 a0001c0001t0081g0102 others(13): Show |
16 | HG00438.hp2 HG01884.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.327-4540dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126686279 | ||||||
chr9:126686279 | C | CAA | 88 | a0001c0001t0101g0170 a0001c0002t0001g0009 a0001c0002t0001g0015 others(85): Show |
88 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.327-4541_327-4540d others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126686279 | ||||||
chr9:126686279 | C | CAAA | 47 | a0001c0001t0004g0240 a0001c0001t0178g0200 a0001c0002t0003g0041 others(44): Show |
48 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.327-4542_327-4540d others(5): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126686279 | ||||||
chr9:126686348 | T | G | 1 | a0001c0004t0043g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.327-4488T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686348 | |||||||
chr9:126686511 | A | G | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-4325A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686511 | |||||||
chr9:126686521 | G | A | 63 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(60): Show |
63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.327-4315G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686521 | |||||||
chr9:126686581 | C | T | 1 | a0001c0001t0175g0125 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.327-4255C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686581 | |||||||
chr9:126686641 | C | T | 3 | a0001c0002t0055g0145 a0001c0008t0034g0148 a0001c0008t0034g0149 |
3 | HG02559.hp2 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.327-4195C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686641 | |||||||
chr9:126686677 | G | T | 2 | a0001c0010t0193g0168 a0001c0011t0085g0082 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.327-4159G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686677 | |||||||
chr9:126686720 | G | A | 1 | a0001c0002t0160g0033 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.327-4116G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686720 | |||||||
chr9:126686973 | G | A | 1 | a0001c0001t0040g0259 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.327-3863G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686973 | |||||||
chr9:126687030 | G | A | 1 | a0001c0001t0067g0073 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.327-3806G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126687030 | |||||||
chr9:126687214 | T | C | 2 | a0001c0001t0011g0063 a0001c0001t0134g0066 |
2 | NA18942.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.327-3622T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126687214 | |||||||
chr9:126687217 | C | CT | 171 | a0001c0001t0004g0240 a0001c0001t0027g0129 a0001c0001t0101g0170 others(168): Show |
172 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.327-3608dupT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126687217 | ||||||
chr9:126687217 | C | T | 1 | a0001c0001t0130g0237 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.327-3619C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126687217 | |||||||
chr9:126687371 | G | C | 3 | a0001c0002t0055g0145 a0001c0008t0034g0148 a0001c0008t0034g0149 |
3 | HG02559.hp2 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.327-3465G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126687371 | |||||||
chr9:126687476 | C | T | 1 | a0001c0001t0021g0255 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.327-3360C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126687476 | |||||||
chr9:126687626 | G | T | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-3210G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126687626 | |||||||
chr9:126687952 | G | A | 6 | a0001c0002t0053g0177 a0001c0002t0053g0180 a0001c0002t0105g0166 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-2884G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126687952 | |||||||
chr9:126688058 | C | T | 1 | a0001c0002t0100g0147 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.327-2778C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688058 | |||||||
chr9:126688065 | C | T | 1 | a0001c0001t0173g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.327-2771C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688065 | |||||||
chr9:126688128 | C | A | 1 | a0001c0001t0130g0237 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.327-2708C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688128 | |||||||
chr9:126688160 | T | C | 172 | a0001c0001t0004g0240 a0001c0001t0178g0200 a0001c0001t0181g0143 others(169): Show |
173 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.327-2676T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688160 | |||||||
chr9:126688262 | G | A | 1 | a0001c0002t0162g0327 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.327-2574G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688262 | |||||||
chr9:126688315 | C | T | 1 | a0001c0001t0140g0269 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.327-2521C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688315 | |||||||
chr9:126688379 | A | C | 2 | a0001c0010t0193g0168 a0001c0011t0085g0082 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.327-2457A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688379 | |||||||
chr9:126688425 | G | A | 6 | a0001c0002t0053g0177 a0001c0002t0053g0180 a0001c0002t0105g0166 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-2411G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688425 | |||||||
chr9:126688598 | C | T | 1 | a0001c0003t0112g0225 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.327-2238C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688598 | |||||||
chr9:126688641 | G | C | 2 | a0001c0001t0011g0321 a0001c0001t0097g0325 |
2 | HG02523.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.327-2195G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688641 | |||||||
chr9:126688781 | A | G | 1 | a0001c0004t0037g0227 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.327-2055A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688781 | |||||||
chr9:126688848 | G | A | 4 | a0001c0002t0053g0177 a0001c0002t0053g0180 a0001c0002t0105g0166 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-1988G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688848 | |||||||
chr9:126688988 | C | G | 1 | a0001c0001t0040g0259 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.327-1848C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688988 | |||||||
chr9:126688988 | C | T | 1 | a0001c0001t0064g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.327-1848C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688988 | |||||||
chr9:126689333 | G | A | 16 | a0001c0001t0181g0143 a0001c0003t0057g0134 a0001c0003t0076g0132 others(13): Show |
16 | HG01167.hp2 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.327-1503G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689333 | |||||||
chr9:126689442 | G | A | 2 | a0001c0001t0078g0090 a0001c0001t0171g0151 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.327-1394G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689442 | |||||||
chr9:126689479 | G | A | 1 | a0001c0001t0175g0125 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.327-1357G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689479 | |||||||
chr9:126689552 | G | A | 1 | a0001c0001t0040g0039 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.327-1284G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689552 | |||||||
chr9:126689721 | TGATGGGA | T | 63 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(60): Show |
63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.327-1102_327-1096d others(9): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126689721 | ||||||
chr9:126689774 | C | T | 63 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(60): Show |
63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.327-1062C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689774 | |||||||
chr9:126689901 | G | C | 1 | a0001c0010t0193g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327-935G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689901 | |||||||
chr9:126689925 | T | C | 63 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(60): Show |
63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.327-911T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689925 | |||||||
chr9:126689994 | G | A | 2 | a0001c0001t0002g0231 a0001c0001t0096g0230 |
2 | HG02080.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.327-842G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689994 | |||||||
chr9:126690110 | CT | C | 64 | a0001c0001t0002g0324 a0001c0002t0001g0009 a0001c0002t0001g0015 others(61): Show |
64 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.327-725delT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126690110 | |||||||
chr9:126690498 | A | G | 69 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(66): Show |
69 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.327-338A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126690498 | |||||||
chr9:126690508 | C | G | 1 | a0001c0002t0001g0311 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.327-328C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126690508 | |||||||
chr9:126690518 | A | G | 173 | a0001c0001t0041g0284 a0001c0001t0178g0200 a0001c0002t0001g0009 others(170): Show |
174 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.327-318A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126690518 | |||||||
chr9:126690553 | T | A | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-283T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126690553 | |||||||
chr9:126690563 | G | A | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-273G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126690563 | |||||||
chr9:126690730 | C | T | 3 | a0001c0001t0026g0100 a0001c0001t0079g0104 a0001c0001t0126g0276 |
3 | HG00642.hp2 HG01106.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.327-106C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126690730 | |||||||
chr9:126691088 | G | A | 9 | a0001c0004t0037g0227 a0001c0005t0012g0137 a0001c0005t0012g0138 others(6): Show |
9 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.559+20G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691088 | |||||||
chr9:126691518 | G | A | 3 | a0001c0004t0037g0227 a0001c0007t0048g0318 a0001c0007t0048g0319 |
3 | HG01167.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.559+450G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691518 | |||||||
chr9:126691528 | C | G | 1 | a0001c0002t0053g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.559+460C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691528 | |||||||
chr9:126691537 | T | C | 1 | a0001c0001t0041g0284 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.559+469T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691537 | |||||||
chr9:126691612 | C | T | 21 | a0001c0002t0054g0146 a0001c0002t0100g0147 a0001c0002t0166g0181 others(18): Show |
21 | HG00639.hp1 HG01109.hp2 HG02717.hp2 others(18): Show |
intron_variant | MODIFIER | c.559+544C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691612 | |||||||
chr9:126691638 | G | T | 1 | a0001c0002t0001g0015 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.559+570G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691638 | |||||||
chr9:126691649 | A | G | 1 | a0001c0012t0116g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.559+581A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691649 | |||||||
chr9:126691743 | C | T | 3 | a0001c0001t0026g0100 a0001c0001t0079g0104 a0001c0001t0126g0276 |
3 | HG00642.hp2 HG01106.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.559+675C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691743 | |||||||
chr9:126691807 | G | A | 2 | a0001c0002t0003g0244 a0001c0002t0003g0287 |
2 | NA18975.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.559+739G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691807 | |||||||
chr9:126691809 | A | G | 2 | a0001c0007t0048g0318 a0001c0007t0048g0319 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.559+741A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691809 | |||||||
chr9:126691822 | G | A | 70 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(67): Show |
70 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.559+754G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691822 | |||||||
chr9:126691917 | C | G | 1 | a0001c0001t0080g0080 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.559+849C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691917 | |||||||
chr9:126692261 | C | A | 8 | a0001c0001t0037g0234 a0001c0001t0078g0090 a0001c0001t0120g0238 others(5): Show |
8 | HG00735.hp1 HG02886.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.560-881C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692261 | |||||||
chr9:126692435 | G | T | 57 | a0001c0002t0003g0029 a0001c0002t0003g0041 a0001c0002t0003g0046 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.560-707G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692435 | |||||||
chr9:126692483 | C | T | 1 | a0001c0001t0028g0076 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.560-659C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692483 | |||||||
chr9:126692484 | G | A | 1 | a0001c0002t0093g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.560-658G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692484 | |||||||
chr9:126692602 | G | A | 2 | a0001c0008t0034g0148 a0001c0008t0034g0149 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.560-540G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692602 | |||||||
chr9:126692653 | G | A | 2 | a0001c0007t0048g0318 a0001c0007t0048g0319 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.560-489G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692653 | |||||||
chr9:126692690 | T | C | 2 | a0001c0007t0048g0318 a0001c0007t0048g0319 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.560-452T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692690 | |||||||
chr9:126692745 | G | A | 3 | a0001c0002t0001g0035 a0001c0004t0182g0154 a0001c0012t0116g0142 |
3 | HG03195.hp1 NA19009.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.560-397G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692745 | |||||||
chr9:126692749 | G | A | 2 | a0001c0008t0034g0148 a0001c0008t0034g0149 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.560-393G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692749 | |||||||
chr9:126692809 | T | G | 1 | a0001c0001t0025g0157 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.560-333T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692809 | |||||||
chr9:126692928 | G | A | 2 | a0001c0001t0002g0211 a0001c0001t0106g0218 |
2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.560-214G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692928 | |||||||
chr9:126692967 | T | C | 2 | a0001c0007t0048g0318 a0001c0007t0048g0319 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.560-175T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692967 | |||||||
chr9:126693055 | A | G | 2 | a0001c0007t0048g0318 a0001c0007t0048g0319 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.560-87A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126693055 | |||||||
chr9:126693093 | C | T | 70 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(67): Show |
70 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.560-49C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126693093 | |||||||
chr9:126693114 | A | C | 3 | a0001c0007t0048g0318 a0001c0007t0048g0319 a0001c0010t0193g0168 |
3 | HG02895.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.560-28A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126693114 | |||||||
chr9:126693123 | C | T | 2 | a0001c0007t0048g0318 a0001c0007t0048g0319 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.560-19C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126693123 | |||||||
chr9:126693333 | G | A | 1 | a0001c0002t0032g0002 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.741+10G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 4/7 | chr9 | 126693333 | |||||||
chr9:126693337 | G | T | 1 | a0001c0001t0008g0005 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.741+14G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 4/7 | chr9 | 126693337 | |||||||
chr9:126693416 | C | T | 1 | a0001c0011t0085g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.741+93C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 4/7 | chr9 | 126693416 | |||||||
chr9:126693477 | G | A | 1 | a0001c0012t0116g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.742-47G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 4/7 | chr9 | 126693477 | |||||||
chr9:126693654 | G | A | 1 | a0001c0010t0193g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.819+53G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 5/7 | chr9 | 126693654 | |||||||
chr9:126693830 | C | T | 1 | a0001c0004t0062g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.886+18C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126693830 | |||||||
chr9:126693850 | G | A | 1 | a0001c0001t0131g0305 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.886+38G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126693850 | |||||||
chr9:126693937 | G | A | 1 | a0001c0001t0124g0252 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.886+125G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126693937 | |||||||
chr9:126694249 | G | C | 2 | a0001c0007t0048g0318 a0001c0007t0048g0319 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.886+437G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694249 | |||||||
chr9:126694251 | G | A | 102 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(99): Show |
102 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.886+439G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694251 | |||||||
chr9:126694302 | G | A | 4 | a0001c0001t0005g0221 a0001c0001t0005g0288 a0001c0001t0005g0304 others(1): Show |
4 | HG01934.hp2 HG01993.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.886+490G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694302 | |||||||
chr9:126694356 | A | G | 3 | a0001c0001t0011g0224 a0001c0001t0060g0106 a0001c0001t0084g0071 |
3 | HG01361.hp1 HG03239.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.886+544A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694356 | |||||||
chr9:126694401 | T | C | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.886+589T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694401 | |||||||
chr9:126694496 | C | A | 1 | a0001c0001t0081g0102 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.886+684C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694496 | |||||||
chr9:126694556 | C | T | 1 | a0001c0001t0028g0076 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.886+744C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694556 | |||||||
chr9:126694590 | C | T | 1 | a0001c0001t0080g0080 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.886+778C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694590 | |||||||
chr9:126694739 | G | T | 6 | a0001c0005t0012g0137 a0001c0005t0012g0138 a0001c0005t0012g0139 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.886+927G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694739 | |||||||
chr9:126694782 | C | T | 1 | a0001c0001t0137g0307 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.886+970C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694782 | |||||||
chr9:126694933 | G | A | 3 | a0001c0001t0002g0324 a0001c0001t0082g0124 a0001c0001t0124g0252 |
3 | HG02027.hp1 NA19004.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.887-906G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694933 | |||||||
chr9:126694933 | G | T | 7 | a0001c0003t0057g0134 a0001c0003t0076g0132 a0001c0003t0108g0253 others(4): Show |
7 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.887-906G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694933 | |||||||
chr9:126694996 | C | T | 3 | a0001c0001t0007g0040 a0001c0001t0007g0051 a0001c0001t0118g0297 |
3 | HG02083.hp2 NA19068.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.887-843C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694996 | |||||||
chr9:126695203 | C | T | 5 | a0001c0003t0057g0134 a0001c0003t0076g0132 a0001c0003t0108g0253 others(2): Show |
5 | HG02109.hp1 HG02647.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.887-636C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126695203 | |||||||
chr9:126695320 | G | A | 98 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(95): Show |
98 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.887-519G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126695320 | |||||||
chr9:126695368 | C | T | 58 | a0001c0001t0003g0243 a0001c0002t0003g0029 a0001c0002t0003g0041 others(55): Show |
59 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.887-471C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126695368 | |||||||
chr9:126695469 | CG | C | 58 | a0001c0001t0003g0243 a0001c0002t0003g0029 a0001c0002t0003g0041 others(55): Show |
59 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.887-365delG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 126695469 | ||||||
chr9:126695473 | G | C | 58 | a0001c0001t0003g0243 a0001c0002t0003g0029 a0001c0002t0003g0041 others(55): Show |
59 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.887-366G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126695473 | |||||||
chr9:126695675 | C | G | 1 | a0001c0002t0001g0057 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.887-164C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126695675 | |||||||
chr9:126695762 | T | A | 2 | a0001c0001t0179g0195 a0001c0001t0194g0216 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.887-77T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126695762 | |||||||
chr9:126695813 | G | T | 102 | a0001c0002t0001g0009 a0001c0002t0001g0015 a0001c0002t0001g0017 others(99): Show |
102 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.887-26G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126695813 | |||||||
chr9:126696095 | C | A | 1 | a0001c0010t0193g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1051+92C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 7/7 | chr9 | 126696095 | |||||||
chr9:126696097 | C | G | 1 | a0001c0001t0002g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1051+94C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 7/7 | chr9 | 126696097 |