Item | Value |
---|---|
geneid | 9355 |
ensemblid | ENSG00000106689.11 |
hgncid | 6594 |
symbol | LHX2 |
name | LIM homeobox 2 |
refseq_nuc | NM_004789.4 |
refseq_prot | NP_004780.3 |
ensembl_nuc | ENST00000373615.9 |
ensembl_prot | ENSP00000362717.4 |
mane_status | MANE Select |
chr | chr9 |
start | 124011768 |
end | 124033301 |
strand | + |
ver | v1.2 |
region | chr9:124011768-124033301 |
region5000 | chr9:124006768-124038301 |
regionname0 | LHX2_chr9_124011768_124033301 |
regionname5000 | LHX2_chr9_124006768_124038301 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 406 | 398 | 100 | 70 | 174 | 12 | 40 | 127 | LHX2_chr9_124006768_124038301 | LHX2 | MLFHS others(401): Show |
chr9 | 124006768 | 124038301 |
a0002 | 0/0 | 406 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | LHX2_chr9_124006768_124038301 | LHX2 | MLFHS others(401): Show |
chr9 | 124006768 | 124038301 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1218 | 258 | 79 | 41 | 104 | 8 | 24 | LHX2_chr9_124006768_124038301 | LHX2 | ATGCT others(1213): Show |
chr9 | 124006768 | 124038301 | ||
a0001c0002 | 0/0 | 1218 | 120 | 20 | 26 | 56 | 3 | 15 | LHX2_chr9_124006768_124038301 | LHX2 | ATGCT others(1213): Show |
chr9 | 124006768 | 124038301 | ||
a0001c0003 | 0/0 | 1218 | 8 | 0 | 0 | 8 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | ATGCT others(1213): Show |
chr9 | 124006768 | 124038301 | ||
a0001c0004 | 0/0 | 1218 | 7 | 0 | 2 | 5 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | ATGCT others(1213): Show |
chr9 | 124006768 | 124038301 | ||
a0001c0006 | 0/0 | 1218 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | ATGCT others(1213): Show |
chr9 | 124006768 | 124038301 | ||
a0001c0007 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | ATGCT others(1213): Show |
chr9 | 124006768 | 124038301 | ||
a0001c0008 | 0/0 | 1218 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | ATGCT others(1213): Show |
chr9 | 124006768 | 124038301 | ||
a0001c0009 | 0/0 | 1218 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | ATGCT others(1213): Show |
chr9 | 124006768 | 124038301 | ||
a0001c0010 | 0/0 | 1218 | 1 | 0 | 0 | 0 | 1 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | ATGCT others(1213): Show |
chr9 | 124006768 | 124038301 | ||
a0002c0005 | 0/0 | 1218 | 4 | 0 | 0 | 4 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | ATGCT others(1213): Show |
chr9 | 124006768 | 124038301 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2396 | 146 | 56 | 17 | 51 | 4 | 16 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2391): Show |
chr9 | 124006768 | 124038301 |
a0001c0001t0002 | 0/0 | 2397 | 9 | 5 | 2 | 0 | 0 | 2 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2392): Show |
chr9 | 124006768 | 124038301 |
a0001c0001t0003 | 0/0 | 2397 | 52 | 1 | 11 | 36 | 2 | 2 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2392): Show |
chr9 | 124006768 | 124038301 |
a0001c0001t0004 | 0/0 | 2396 | 31 | 14 | 7 | 4 | 2 | 4 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2391): Show |
chr9 | 124006768 | 124038301 |
a0001c0001t0005 | 0/0 | 2395 | 8 | 3 | 0 | 5 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2390): Show |
chr9 | 124006768 | 124038301 |
a0001c0001t0006 | 0/0 | 2397 | 2 | 0 | 0 | 2 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2392): Show |
chr9 | 124006768 | 124038301 |
a0001c0001t0007 | 0/0 | 2397 | 2 | 0 | 0 | 2 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2392): Show |
chr9 | 124006768 | 124038301 |
a0001c0001t0008 | 0/0 | 2396 | 2 | 0 | 0 | 2 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2391): Show |
chr9 | 124006768 | 124038301 |
a0001c0001t0009 | 0/0 | 2396 | 2 | 0 | 2 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2391): Show |
chr9 | 124006768 | 124038301 |
a0001c0001t0010 | 0/0 | 2396 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2391): Show |
chr9 | 124006768 | 124038301 |
a0001c0001t0012 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2392): Show |
chr9 | 124006768 | 124038301 |
a0001c0001t0015 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2392): Show |
chr9 | 124006768 | 124038301 |
a0001c0001t0016 | 0/0 | 2396 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2391): Show |
chr9 | 124006768 | 124038301 |
a0001c0002t0001 | 0/0 | 2396 | 72 | 15 | 16 | 27 | 3 | 11 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2391): Show |
chr9 | 124006768 | 124038301 |
a0001c0002t0002 | 0/0 | 2397 | 42 | 0 | 10 | 29 | 0 | 3 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2392): Show |
chr9 | 124006768 | 124038301 |
a0001c0002t0003 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2392): Show |
chr9 | 124006768 | 124038301 |
a0001c0002t0005 | 0/0 | 2395 | 3 | 3 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2390): Show |
chr9 | 124006768 | 124038301 |
a0001c0002t0011 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2392): Show |
chr9 | 124006768 | 124038301 |
a0001c0002t0014 | 0/0 | 2396 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2391): Show |
chr9 | 124006768 | 124038301 |
a0001c0003t0002 | 0/0 | 2397 | 8 | 0 | 0 | 8 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2392): Show |
chr9 | 124006768 | 124038301 |
a0001c0004t0002 | 0/0 | 2397 | 7 | 0 | 2 | 5 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2392): Show |
chr9 | 124006768 | 124038301 |
a0001c0006t0013 | 0/0 | 2396 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2391): Show |
chr9 | 124006768 | 124038301 |
a0001c0007t0003 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2392): Show |
chr9 | 124006768 | 124038301 |
a0001c0008t0001 | 0/0 | 2396 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2391): Show |
chr9 | 124006768 | 124038301 |
a0001c0009t0003 | 0/0 | 2397 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2392): Show |
chr9 | 124006768 | 124038301 |
a0001c0010t0001 | 0/0 | 2396 | 1 | 0 | 0 | 0 | 1 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2391): Show |
chr9 | 124006768 | 124038301 |
a0002c0005t0001 | 0/0 | 2396 | 4 | 0 | 0 | 4 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | AATTC others(2391): Show |
chr9 | 124006768 | 124038301 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 36 | 7 | 1 | 20 | 2 | 6 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0011 | 1/1 | 4 | 0 | 2 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0001 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0005 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0004g0004 | 0/0 | 17 | 10 | 4 | 0 | 2 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0004g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0004g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0005g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0006g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0008g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0009g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0010g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0001t0016g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0002 | 0/0 | 33 | 7 | 7 | 12 | 0 | 7 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0039 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0002g0003 | 0/0 | 24 | 0 | 7 | 14 | 0 | 3 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0002g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0011g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0002t0014g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0003t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0003t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0004t0002g0003 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0006t0013g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0007t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0008t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0009t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0001c0010t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
a0002c0005t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0004 | g0004 | EUR | GBR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0131 | EUR | FIN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0136 | EUR | FIN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00408 | hp1 | a0002 | c0005 | t0001 | g0012 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00639 | hp2 | a0001 | c0001 | t0016 | g0169 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0156 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0160 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01167 | hp1 | a0001 | c0001 | t0010 | g0096 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0140 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01255 | hp2 | a0001 | c0009 | t0003 | g0005 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01257 | hp2 | a0001 | c0001 | t0009 | g0001 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01258 | hp1 | a0001 | c0001 | t0009 | g0001 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0123 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0145 | EUR | IBS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0135 | EUR | IBS | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01891 | hp2 | a0001 | c0002 | t0003 | g0059 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01928 | hp2 | a0001 | c0004 | t0002 | g0003 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0163 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0071 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02074 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02074 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | CDX | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02273 | hp2 | a0001 | c0004 | t0002 | g0003 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0124 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | KHV | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0068 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02630 | hp1 | a0001 | c0002 | t0005 | g0075 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02630 | hp2 | a0001 | c0002 | t0014 | g0154 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0045 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02735 | hp2 | a0001 | c0006 | t0013 | g0001 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02965 | hp2 | a0001 | c0002 | t0005 | g0027 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | MSL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0128 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03516 | hp2 | a0001 | c0002 | t0005 | g0047 | AFR | ESN | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | MSL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0164 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0045 | SAS | STU | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | STU | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03704 | hp2 | a0001 | c0002 | t0011 | g0076 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0087 | SAS | BEB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0133 | SAS | BEB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0116 | SAS | BEB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0103 | SAS | STU | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | STU | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | YRI | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | YRI | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | CHB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | CHB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | YRI | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18939 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18940 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18942 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18945 | hp1 | a0001 | c0001 | t0007 | g0161 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18948 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18952 | hp1 | a0001 | c0003 | t0002 | g0016 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18956 | hp2 | a0001 | c0001 | t0007 | g0159 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18957 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18962 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18964 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18966 | hp2 | a0001 | c0003 | t0002 | g0016 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18970 | hp2 | a0001 | c0003 | t0002 | g0019 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18971 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18971 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18974 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18984 | hp1 | a0001 | c0003 | t0002 | g0019 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18986 | hp1 | a0001 | c0003 | t0002 | g0019 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18986 | hp2 | a0002 | c0005 | t0001 | g0012 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18988 | hp2 | a0001 | c0003 | t0002 | g0016 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18989 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18990 | hp1 | a0002 | c0005 | t0001 | g0012 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19001 | hp2 | a0002 | c0005 | t0001 | g0012 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19006 | hp2 | a0001 | c0003 | t0002 | g0138 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | LWK | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19068 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19068 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19075 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19082 | hp1 | a0001 | c0003 | t0002 | g0016 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19084 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19085 | hp2 | a0001 | c0008 | t0001 | g0002 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ASW | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ASW | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA20752 | hp2 | a0001 | c0010 | t0001 | g0089 | EUR | TSI | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0004 | EUR | TSI | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | TSI | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0118 | AMR | CLM | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02109 | hp1 | a0001 | c0007 | t0003 | g0170 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | MSL | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | USA | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0060 | AFR | USA | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | USA | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | USA | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | LWK | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0011 | REF | REF | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0011 | REF | REF | LHX2_chr9_124006768_124038301 | LHX2 | chr9 | 124006768 | 124038301 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:124015447 | G | A | 1 | a0002 | 4 | HG00408.hp1 NA18986.hp2 NA18990.hp1 others(1): Show |
missense_variant | MODERATE | c.649G>A | p.Val217Met | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/5 | 1230/2396 | 649/1221 | 217/406 | chr9 | 124015447 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:124014023 | G | C | 1 | a0001c0006 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.183G>C | p.Ser61Ser | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/5 | 764/2396 | 183/1221 | 61/406 | chr9 | 124014023 | |||
chr9:124014131 | C | T | 1 | a0001c0010 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.291C>T | p.Asp97Asp | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/5 | 872/2396 | 291/1221 | 97/406 | chr9 | 124014131 | |||
chr9:124015182 | G | C | 1 | a0001c0007 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.384G>C | p.Val128Val | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/5 | 965/2396 | 384/1221 | 128/406 | chr9 | 124015182 | |||
chr9:124021136 | C | T | 1 | a0001c0004 | 7 | HG01928.hp2 HG02074.hp1 HG02273.hp2 others(4): Show |
synonymous_variant | LOW | c.765C>T | p.Asp255Asp | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/5 | 1346/2396 | 765/1221 | 255/406 | chr9 | 124021136 | |||
chr9:124021154 | G | C | 4 | a0001c0002 a0001c0003 a0001c0004 others(1): Show |
136 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
synonymous_variant | LOW | c.783G>C | p.Pro261Pro | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/5 | 1364/2396 | 783/1221 | 261/406 | chr9 | 124021154 | |||
chr9:124032503 | G | A | 1 | a0001c0008 | 1 | NA19085.hp2 | synonymous_variant | LOW | c.1017G>A | p.Ala339Ala | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 5/5 | 1598/2396 | 1017/1221 | 339/406 | chr9 | 124032503 | |||
chr9:124032533 | G | A | 2 | a0001c0003 a0001c0009 |
9 | HG01255.hp2 NA18952.hp1 NA18966.hp2 others(6): Show |
synonymous_variant | LOW | c.1047G>A | p.Pro349Pro | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 5/5 | 1628/2396 | 1047/1221 | 349/406 | chr9 | 124032533 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:124011819 | C | G | 1 | a0001c0001t0009 | 2 | HG01257.hp2 HG01258.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-530C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/5 | chr9 | 124011819 | |||||||
chr9:124012009 | G | T | 1 | a0001c0001t0008 | 2 | NA18962.hp1 NA18971.hp1 |
5_prime_UTR_variant | MODIFIER | c.-340G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/5 | 340 | chr9 | 124012009 | ||||||
chr9:124012070 | C | T | 1 | a0001c0001t0016 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-279C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/5 | 279 | chr9 | 124012070 | ||||||
chr9:124012236 | G | T | 2 | a0001c0001t0004 a0001c0001t0007 |
33 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-113G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/5 | 113 | chr9 | 124012236 | ||||||
chr9:124012255 | G | A | 1 | a0001c0001t0010 | 1 | HG01167.hp1 | 5_prime_UTR_variant | MODIFIER | c.-94G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/5 | 94 | chr9 | 124012255 | ||||||
chr9:124012261 | G | A | 1 | a0001c0002t0011 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-88G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/5 | 88 | chr9 | 124012261 | ||||||
chr9:124012270 | A | G | 1 | a0001c0001t0006 | 2 | NA18942.hp2 NA18948.hp1 |
5_prime_UTR_variant | MODIFIER | c.-79A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/5 | 79 | chr9 | 124012270 | ||||||
chr9:124012292 | G | T | 1 | a0001c0001t0015 | 1 | NA19068.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-57G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/5 | chr9 | 124012292 | |||||||
chr9:124012306 | C | G | 1 | a0001c0002t0014 | 1 | HG02630.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-43C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/5 | chr9 | 124012306 | |||||||
chr9:124012311 | G | T | 1 | a0001c0006t0013 | 1 | HG02735.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-38G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/5 | chr9 | 124012311 | |||||||
chr9:124032840 | T | TA | 7 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0012 others(4): Show |
59 | HG00423.hp2 HG00558.hp1 HG00673.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*141dupA | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 5/5 | 142 | INFO_REALIGN_3_PRIME | chr9 | 124032840 | |||||
chr9:124033116 | C | CA | 6 | a0001c0001t0002 a0001c0001t0007 a0001c0002t0002 others(3): Show |
69 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*417dupA | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 5/5 | 418 | INFO_REALIGN_3_PRIME | chr9 | 124033116 | |||||
chr9:124033125 | C | A | 1 | a0001c0001t0012 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*418C>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 5/5 | 418 | chr9 | 124033125 | ||||||
chr9:124033126 | A | C | 1 | a0001c0001t0012 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*419A>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 5/5 | 419 | chr9 | 124033126 | ||||||
chr9:124033171 | GA | G | 2 | a0001c0001t0005 a0001c0002t0005 |
11 | HG02055.hp2 HG02071.hp1 HG02074.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*476delA | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 5/5 | 476 | INFO_REALIGN_3_PRIME | chr9 | 124033171 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:124012581 | C | T | 2 | a0001c0001t0003g0171 a0001c0007t0003g0170 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.120+113C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124012581 | |||||||
chr9:124012700 | A | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0016g0169 others(1): Show |
8 | HG00639.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.120+232A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124012700 | |||||||
chr9:124012827 | G | T | 1 | a0001c0001t0016g0169 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.120+359G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124012827 | |||||||
chr9:124012845 | G | A | 1 | a0001c0002t0005g0047 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.120+377G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124012845 | |||||||
chr9:124012868 | T | C | 1 | a0001c0002t0002g0048 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.120+400T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124012868 | |||||||
chr9:124013209 | G | A | 2 | a0001c0002t0002g0049 a0001c0002t0002g0050 |
2 | NA18978.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.120+741G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124013209 | |||||||
chr9:124013275 | G | A | 3 | a0001c0001t0003g0171 a0001c0002t0001g0051 a0001c0007t0003g0170 |
3 | HG02109.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.121-686G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124013275 | |||||||
chr9:124013276 | A | G | 1 | a0001c0002t0002g0167 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.121-685A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124013276 | |||||||
chr9:124013357 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.121-604C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124013357 | |||||||
chr9:124013602 | G | T | 3 | a0001c0001t0003g0171 a0001c0002t0001g0051 a0001c0007t0003g0170 |
3 | HG02109.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.121-359G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124013602 | |||||||
chr9:124013663 | G | A | 2 | a0001c0001t0016g0169 a0001c0002t0001g0020 |
4 | HG00639.hp2 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-298G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124013663 | |||||||
chr9:124013743 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.121-218G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124013743 | |||||||
chr9:124013790 | A | AT | 1 | a0001c0002t0001g0020 | 3 | HG02559.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.121-170dupT | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 124013790 | ||||||
chr9:124013821 | C | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0016g0169 others(1): Show |
8 | HG00639.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.121-140C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124013821 | |||||||
chr9:124013821 | C | T | 3 | a0001c0001t0003g0171 a0001c0002t0001g0051 a0001c0007t0003g0170 |
3 | HG02109.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.121-140C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124013821 | |||||||
chr9:124013822 | G | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
19 | HG00735.hp2 HG01168.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.121-139G>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124013822 | |||||||
chr9:124013844 | C | T | 16 | a0001c0001t0004g0004 a0001c0001t0004g0045 a0001c0001t0004g0046 others(13): Show |
34 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.121-117C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124013844 | |||||||
chr9:124013866 | G | T | 3 | a0001c0001t0003g0171 a0001c0002t0001g0051 a0001c0007t0003g0170 |
3 | HG02109.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.121-95G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 1/4 | chr9 | 124013866 | |||||||
chr9:124014174 | C | G | 1 | a0001c0002t0001g0044 | 2 | HG00423.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.323+11C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014174 | |||||||
chr9:124014218 | G | A | 8 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0002g0062 others(5): Show |
12 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.323+55G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014218 | |||||||
chr9:124014283 | C | G | 1 | a0001c0001t0004g0165 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.323+120C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014283 | |||||||
chr9:124014293 | C | T | 1 | a0001c0002t0001g0043 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.323+130C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014293 | |||||||
chr9:124014294 | C | G | 2 | a0001c0002t0002g0048 a0001c0002t0002g0152 |
2 | HG00544.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.323+131C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014294 | |||||||
chr9:124014318 | T | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0016g0169 others(1): Show |
8 | HG00639.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+155T>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014318 | |||||||
chr9:124014357 | T | C | 1 | a0001c0002t0001g0020 | 3 | HG02559.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.323+194T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014357 | |||||||
chr9:124014446 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.323+283G>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014446 | |||||||
chr9:124014528 | A | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0016g0169 others(1): Show |
8 | HG00639.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+365A>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014528 | |||||||
chr9:124014597 | T | C | 1 | a0001c0001t0002g0062 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.323+434T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014597 | |||||||
chr9:124014675 | T | C | 3 | a0001c0001t0003g0171 a0001c0002t0001g0051 a0001c0007t0003g0170 |
3 | HG02109.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.324-447T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014675 | |||||||
chr9:124014686 | G | A | 1 | a0001c0001t0003g0025 | 2 | HG01123.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.324-436G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014686 | |||||||
chr9:124014815 | G | C | 1 | a0001c0001t0003g0064 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.324-307G>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014815 | |||||||
chr9:124014927 | A | G | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | HG01884.hp2 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.324-195A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014927 | |||||||
chr9:124014931 | G | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0002g0066 |
4 | HG02145.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-191G>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014931 | |||||||
chr9:124014985 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.324-137C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014985 | |||||||
chr9:124014989 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0016g0169 others(1): Show |
8 | HG00639.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.324-133T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014989 | |||||||
chr9:124014991 | C | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0147 |
3 | HG01168.hp1 HG01169.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.324-131C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124014991 | |||||||
chr9:124015038 | C | G | 1 | a0001c0001t0001g0041 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.324-84C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 2/4 | chr9 | 124015038 | |||||||
chr9:124015551 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.727+26C>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124015551 | |||||||
chr9:124015645 | G | A | 1 | a0001c0001t0005g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.727+120G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124015645 | |||||||
chr9:124015668 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.727+143C>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124015668 | |||||||
chr9:124015675 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.727+150G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124015675 | |||||||
chr9:124015727 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.727+202C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124015727 | |||||||
chr9:124015789 | G | T | 2 | a0001c0002t0002g0167 a0001c0003t0002g0016 |
5 | NA18952.hp1 NA18966.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.727+264G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124015789 | |||||||
chr9:124015856 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.727+331A>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124015856 | |||||||
chr9:124015893 | G | A | 1 | a0001c0001t0005g0071 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.727+368G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124015893 | |||||||
chr9:124015897 | A | G | 1 | a0001c0001t0003g0145 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.727+372A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124015897 | |||||||
chr9:124016012 | A | C | 1 | a0001c0001t0001g0061 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.727+487A>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124016012 | |||||||
chr9:124016020 | AGGCTTGG others(8): Show |
A | 1 | a0001c0001t0016g0169 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.727+510_727+524del others(15): Show |
LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 124016020 | ||||||
chr9:124016053 | A | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
7 | HG02723.hp1 HG02896.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.727+528A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124016053 | |||||||
chr9:124016054 | A | G | 1 | a0001c0001t0016g0169 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.727+529A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124016054 | |||||||
chr9:124016086 | G | A | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.727+561G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124016086 | |||||||
chr9:124016180 | A | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0003g0171 others(4): Show |
11 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.727+655A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124016180 | |||||||
chr9:124016217 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.727+692C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124016217 | |||||||
chr9:124016294 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.727+769A>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124016294 | |||||||
chr9:124016397 | G | C | 1 | a0001c0001t0003g0017 | 3 | NA18962.hp2 NA19010.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.727+872G>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124016397 | |||||||
chr9:124016427 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0168 |
4 | HG02258.hp1 HG02486.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+902G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124016427 | |||||||
chr9:124016542 | A | G | 47 | a0001c0001t0001g0037 a0001c0002t0001g0002 a0001c0002t0001g0003 others(44): Show |
130 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.727+1017A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124016542 | |||||||
chr9:124016583 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.727+1058T>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124016583 | |||||||
chr9:124016966 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.727+1441G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124016966 | |||||||
chr9:124017096 | G | C | 2 | a0001c0001t0016g0169 a0001c0002t0014g0154 |
2 | HG00639.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.727+1571G>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124017096 | |||||||
chr9:124017167 | G | A | 1 | a0001c0002t0001g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.727+1642G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124017167 | |||||||
chr9:124017189 | C | T | 1 | a0001c0002t0002g0140 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.727+1664C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124017189 | |||||||
chr9:124017215 | T | C | 76 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0022 others(73): Show |
168 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.727+1690T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124017215 | |||||||
chr9:124017354 | C | G | 2 | a0001c0001t0016g0169 a0001c0002t0011g0076 |
2 | HG00639.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.727+1829C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124017354 | |||||||
chr9:124017438 | G | T | 1 | a0001c0001t0016g0169 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.727+1913G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124017438 | |||||||
chr9:124017467 | C | A | 2 | a0001c0001t0002g0062 a0001c0001t0016g0169 |
2 | HG00639.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.727+1942C>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124017467 | |||||||
chr9:124017536 | C | T | 1 | a0001c0002t0011g0076 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.727+2011C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124017536 | |||||||
chr9:124017590 | C | T | 1 | a0001c0002t0001g0139 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.727+2065C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124017590 | |||||||
chr9:124017668 | C | T | 2 | a0001c0001t0003g0171 a0001c0007t0003g0170 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.727+2143C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124017668 | |||||||
chr9:124017769 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.727+2244T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124017769 | |||||||
chr9:124017888 | C | T | 44 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0014 others(41): Show |
123 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.727+2363C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124017888 | |||||||
chr9:124017895 | A | C | 4 | a0001c0001t0003g0171 a0001c0002t0001g0051 a0001c0002t0003g0059 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+2370A>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124017895 | |||||||
chr9:124018009 | C | T | 1 | a0001c0001t0016g0169 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.727+2484C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124018009 | |||||||
chr9:124018272 | G | GA | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0073 others(3): Show |
8 | HG02258.hp1 HG02647.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.727+2761dupA | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 124018272 | ||||||
chr9:124018272 | GA | G | 78 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0037 others(75): Show |
182 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.727+2761delA | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 124018272 | ||||||
chr9:124018286 | AG | A | 11 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
17 | HG00735.hp2 HG01168.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.727+2763delG | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 124018286 | ||||||
chr9:124018435 | TC | T | 5 | a0001c0001t0001g0112 a0001c0002t0002g0167 a0001c0003t0002g0016 others(2): Show |
10 | NA18952.hp1 NA18966.hp2 NA18970.hp2 others(7): Show |
intron_variant | MODIFIER | c.728-2659delC | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 124018435 | ||||||
chr9:124018441 | G | T | 4 | a0001c0002t0002g0167 a0001c0003t0002g0016 a0001c0003t0002g0019 others(1): Show |
9 | NA18952.hp1 NA18966.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.728-2658G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124018441 | |||||||
chr9:124018456 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.728-2643C>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124018456 | |||||||
chr9:124018548 | C | T | 1 | a0001c0002t0003g0059 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.728-2551C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124018548 | |||||||
chr9:124018553 | A | G | 19 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0002g0114 others(16): Show |
37 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.728-2546A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124018553 | |||||||
chr9:124018574 | T | A | 1 | a0001c0001t0003g0030 | 2 | HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.728-2525T>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124018574 | |||||||
chr9:124018598 | G | A | 1 | a0001c0002t0003g0059 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.728-2501G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124018598 | |||||||
chr9:124018633 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
5 | HG00735.hp2 HG01168.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.728-2466G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124018633 | |||||||
chr9:124018645 | G | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0146 a0001c0001t0002g0110 |
8 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.728-2454G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124018645 | |||||||
chr9:124018877 | C | T | 1 | a0001c0003t0002g0138 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.728-2222C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124018877 | |||||||
chr9:124018923 | C | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0002g0066 |
4 | HG02145.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-2176C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124018923 | |||||||
chr9:124019052 | G | A | 2 | a0001c0002t0001g0020 a0001c0002t0014g0154 |
4 | HG02559.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-2047G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124019052 | |||||||
chr9:124019102 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0056 |
6 | NA18965.hp2 NA18967.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.728-1997G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124019102 | |||||||
chr9:124019242 | A | G | 3 | a0001c0002t0001g0051 a0001c0002t0003g0059 a0001c0002t0011g0076 |
3 | HG01891.hp2 HG02615.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.728-1857A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124019242 | |||||||
chr9:124019485 | A | G | 2 | a0001c0001t0003g0171 a0001c0007t0003g0170 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.728-1614A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124019485 | |||||||
chr9:124019557 | T | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0003g0010 others(2): Show |
9 | HG02027.hp2 HG02071.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.728-1542T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124019557 | |||||||
chr9:124019593 | A | G | 1 | a0001c0002t0011g0076 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.728-1506A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124019593 | |||||||
chr9:124019657 | A | G | 3 | a0001c0001t0002g0062 a0001c0001t0003g0171 a0001c0007t0003g0170 |
3 | HG02109.hp1 HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.728-1442A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124019657 | |||||||
chr9:124019735 | C | T | 2 | a0001c0002t0001g0051 a0001c0002t0003g0059 |
2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.728-1364C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124019735 | |||||||
chr9:124019851 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.728-1248G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124019851 | |||||||
chr9:124019882 | C | A | 2 | a0001c0002t0001g0020 a0001c0002t0014g0154 |
4 | HG02559.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-1217C>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124019882 | |||||||
chr9:124020024 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.728-1075C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124020024 | |||||||
chr9:124020033 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0002g0066 |
4 | HG02145.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-1066G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124020033 | |||||||
chr9:124020258 | T | C | 1 | a0001c0001t0016g0169 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.728-841T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124020258 | |||||||
chr9:124020394 | G | T | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728-705G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124020394 | |||||||
chr9:124020563 | C | G | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | HG01884.hp2 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.728-536C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124020563 | |||||||
chr9:124020569 | G | A | 1 | a0001c0002t0003g0059 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.728-530G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124020569 | |||||||
chr9:124020606 | C | T | 1 | a0001c0002t0003g0059 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.728-493C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124020606 | |||||||
chr9:124020739 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.728-360C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124020739 | |||||||
chr9:124020793 | T | TTGC | 5 | a0001c0001t0001g0080 a0001c0001t0002g0062 a0001c0001t0003g0171 others(2): Show |
5 | HG00639.hp2 HG02109.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-286_728-284dup others(3): Show |
LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 124020793 | ||||||
chr9:124020816 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.728-283A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124020816 | |||||||
chr9:124020825 | C | T | 99 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0021 others(96): Show |
211 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.728-274C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124020825 | |||||||
chr9:124021091 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA19058.hp2 | splice_region_variant&intron_variant | LOW | c.728-8C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 3/4 | chr9 | 124021091 | |||||||
chr9:124021358 | A | G | 1 | a0001c0002t0001g0136 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.933+54A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124021358 | |||||||
chr9:124021541 | C | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
21 | HG00735.hp2 HG01168.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.933+237C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124021541 | |||||||
chr9:124021557 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.933+253C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124021557 | |||||||
chr9:124021568 | C | T | 45 | a0001c0001t0002g0114 a0001c0002t0001g0002 a0001c0002t0001g0003 others(42): Show |
124 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.933+264C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124021568 | |||||||
chr9:124021573 | G | A | 1 | a0001c0002t0001g0038 | 2 | HG02523.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.933+269G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124021573 | |||||||
chr9:124021708 | C | T | 1 | a0001c0002t0005g0075 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.933+404C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124021708 | |||||||
chr9:124021886 | G | A | 1 | a0001c0002t0001g0020 | 3 | HG02559.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.933+582G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124021886 | |||||||
chr9:124022008 | T | A | 60 | a0001c0001t0001g0037 a0001c0001t0001g0149 a0001c0001t0001g0150 others(57): Show |
143 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.933+704T>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124022008 | |||||||
chr9:124022186 | G | A | 2 | a0001c0002t0001g0020 a0001c0002t0014g0154 |
4 | HG02559.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+882G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124022186 | |||||||
chr9:124022215 | T | G | 16 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(13): Show |
23 | HG00735.hp2 HG01168.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.933+911T>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124022215 | |||||||
chr9:124022256 | T | A | 1 | a0001c0001t0001g0082 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.933+952T>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124022256 | |||||||
chr9:124022284 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0168 |
4 | HG02258.hp1 HG02486.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.933+980C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124022284 | |||||||
chr9:124022316 | T | C | 1 | a0001c0001t0001g0037 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.933+1012T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124022316 | |||||||
chr9:124022415 | T | C | 1 | a0001c0002t0001g0117 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.933+1111T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124022415 | |||||||
chr9:124022462 | A | G | 1 | a0001c0002t0001g0135 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.933+1158A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124022462 | |||||||
chr9:124022879 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.933+1575G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124022879 | |||||||
chr9:124023009 | A | G | 82 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(79): Show |
174 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.933+1705A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124023009 | |||||||
chr9:124023012 | G | T | 82 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(79): Show |
174 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.933+1708G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124023012 | |||||||
chr9:124023058 | C | T | 1 | a0001c0001t0002g0062 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.933+1754C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124023058 | |||||||
chr9:124023246 | T | C | 17 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(14): Show |
27 | HG00639.hp2 HG00735.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.933+1942T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124023246 | |||||||
chr9:124023248 | GGAA | G | 2 | a0001c0002t0001g0020 a0001c0002t0014g0154 |
4 | HG02559.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+1954_933+1956d others(5): Show |
LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124023248 | ||||||
chr9:124023314 | A | AAAT | 6 | a0001c0001t0001g0037 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
7 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.933+2029_933+2031d others(5): Show |
LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124023314 | ||||||
chr9:124023379 | C | G | 6 | a0001c0001t0001g0037 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
7 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.933+2075C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124023379 | |||||||
chr9:124023564 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0084 |
2 | NA18965.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.933+2260G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124023564 | |||||||
chr9:124023596 | T | A | 2 | a0001c0002t0001g0020 a0001c0002t0014g0154 |
4 | HG02559.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+2292T>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124023596 | |||||||
chr9:124023747 | C | T | 1 | a0001c0002t0001g0134 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.933+2443C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124023747 | |||||||
chr9:124023835 | G | A | 1 | a0001c0002t0002g0118 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.933+2531G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124023835 | |||||||
chr9:124023851 | C | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0065 |
3 | HG02145.hp1 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.933+2547C>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124023851 | |||||||
chr9:124023879 | G | A | 1 | a0001c0002t0002g0119 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.933+2575G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124023879 | |||||||
chr9:124023884 | G | A | 1 | a0001c0001t0001g0022 | 2 | NA18968.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.933+2580G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124023884 | |||||||
chr9:124023937 | G | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0144 others(5): Show |
11 | HG01891.hp2 HG02630.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.933+2633G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124023937 | |||||||
chr9:124024213 | T | A | 1 | a0001c0001t0001g0085 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.933+2909T>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124024213 | |||||||
chr9:124024221 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.933+2917G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124024221 | |||||||
chr9:124024427 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.933+3123G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124024427 | |||||||
chr9:124024454 | C | G | 56 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0144 others(53): Show |
141 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.933+3150C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124024454 | |||||||
chr9:124024561 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.933+3257G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124024561 | |||||||
chr9:124024562 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.933+3258G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124024562 | |||||||
chr9:124024602 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.933+3298A>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124024602 | |||||||
chr9:124024639 | A | C | 52 | a0001c0001t0001g0015 a0001c0001t0001g0144 a0001c0001t0002g0066 others(49): Show |
137 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.933+3335A>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124024639 | |||||||
chr9:124024640 | G | A | 1 | a0001c0002t0001g0120 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.933+3336G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124024640 | |||||||
chr9:124024727 | A | G | 54 | a0001c0001t0001g0015 a0001c0001t0001g0144 a0001c0001t0002g0062 others(51): Show |
139 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.933+3423A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124024727 | |||||||
chr9:124024788 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(186): Show |
398 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(395): Show |
intron_variant | MODIFIER | c.933+3484A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124024788 | |||||||
chr9:124024899 | C | T | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | HG01884.hp2 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.933+3595C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124024899 | |||||||
chr9:124024952 | A | G | 3 | a0001c0001t0002g0062 a0001c0001t0003g0171 a0001c0007t0003g0170 |
3 | HG02109.hp1 HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.933+3648A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124024952 | |||||||
chr9:124024996 | G | A | 1 | a0001c0001t0003g0088 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.933+3692G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124024996 | |||||||
chr9:124025164 | C | T | 2 | a0001c0002t0001g0020 a0001c0002t0014g0154 |
4 | HG02559.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+3860C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124025164 | |||||||
chr9:124025177 | G | A | 11 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
17 | HG00639.hp2 HG00735.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.933+3873G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124025177 | |||||||
chr9:124025203 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0005g0060 |
2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.933+3899C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124025203 | |||||||
chr9:124025218 | G | A | 1 | a0001c0010t0001g0089 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.933+3914G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124025218 | |||||||
chr9:124025311 | T | G | 4 | a0001c0002t0001g0027 a0001c0002t0005g0027 a0001c0002t0005g0047 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.933+4007T>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124025311 | |||||||
chr9:124025358 | G | A | 1 | a0001c0001t0003g0090 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.933+4054G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124025358 | |||||||
chr9:124025379 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.933+4075T>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124025379 | |||||||
chr9:124025385 | G | C | 51 | a0001c0001t0001g0015 a0001c0001t0001g0144 a0001c0001t0002g0114 others(48): Show |
136 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.933+4081G>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124025385 | |||||||
chr9:124025390 | A | G | 1 | a0001c0001t0003g0107 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.933+4086A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124025390 | |||||||
chr9:124025427 | T | C | 91 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0021 others(88): Show |
199 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.933+4123T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124025427 | |||||||
chr9:124025440 | C | CA | 16 | a0001c0001t0001g0031 a0001c0001t0001g0053 a0001c0001t0001g0054 others(13): Show |
16 | HG00642.hp2 HG01168.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.933+4159dupA | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124025440 | ||||||
chr9:124025440 | CA | C | 10 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0001g0080 others(7): Show |
13 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.933+4159delA | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124025440 | ||||||
chr9:124025440 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0002g0114 a0001c0002t0001g0135 |
2 | HG01516.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.933+4149_933+4159d others(13): Show |
LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124025440 | ||||||
chr9:124025440 | CAAAAAAA others(5): Show |
C | 51 | a0001c0001t0001g0058 a0001c0001t0004g0164 a0001c0002t0001g0002 others(48): Show |
131 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.933+4148_933+4159d others(14): Show |
LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124025440 | ||||||
chr9:124025519 | T | C | 1 | a0001c0002t0001g0121 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.933+4215T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124025519 | |||||||
chr9:124025860 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0106 |
2 | NA18967.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.933+4556C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124025860 | |||||||
chr9:124025871 | G | C | 1 | a0001c0002t0001g0122 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.933+4567G>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124025871 | |||||||
chr9:124026014 | G | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0168 |
4 | HG02258.hp1 HG02486.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.933+4710G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026014 | |||||||
chr9:124026015 | G | A | 53 | a0001c0001t0001g0058 a0001c0001t0002g0114 a0001c0001t0004g0164 others(50): Show |
133 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.933+4711G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026015 | |||||||
chr9:124026033 | C | T | 92 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0021 others(89): Show |
200 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.933+4729C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026033 | |||||||
chr9:124026122 | G | A | 6 | a0001c0001t0001g0058 a0001c0002t0001g0027 a0001c0002t0003g0059 others(3): Show |
6 | HG01891.hp2 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.933+4818G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026122 | |||||||
chr9:124026190 | G | A | 53 | a0001c0001t0001g0058 a0001c0001t0002g0114 a0001c0001t0004g0164 others(50): Show |
133 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.933+4886G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026190 | |||||||
chr9:124026223 | C | T | 9 | a0001c0001t0003g0005 a0001c0001t0003g0025 a0001c0001t0003g0032 others(6): Show |
22 | HG00408.hp1 HG01123.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.933+4919C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026223 | |||||||
chr9:124026284 | C | A | 1 | a0001c0001t0004g0156 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.933+4980C>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026284 | |||||||
chr9:124026460 | C | CA | 6 | a0001c0001t0001g0015 a0001c0001t0001g0112 a0001c0001t0001g0144 others(3): Show |
12 | HG02559.hp1 HG02630.hp2 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.933+5172dupA | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124026460 | ||||||
chr9:124026530 | G | A | 3 | a0001c0001t0002g0062 a0001c0001t0003g0171 a0001c0007t0003g0170 |
3 | HG02109.hp1 HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.933+5226G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026530 | |||||||
chr9:124026557 | C | T | 60 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0144 others(57): Show |
145 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.933+5253C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026557 | |||||||
chr9:124026597 | C | A | 53 | a0001c0001t0001g0058 a0001c0001t0002g0114 a0001c0001t0004g0164 others(50): Show |
133 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.933+5293C>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026597 | |||||||
chr9:124026631 | G | A | 89 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0022 others(86): Show |
195 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.933+5327G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026631 | |||||||
chr9:124026656 | A | G | 54 | a0001c0001t0001g0015 a0001c0001t0001g0144 a0001c0001t0002g0062 others(51): Show |
139 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.933+5352A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026656 | |||||||
chr9:124026721 | C | T | 58 | a0001c0001t0001g0058 a0001c0001t0001g0072 a0001c0001t0002g0062 others(55): Show |
138 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.933+5417C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026721 | |||||||
chr9:124026739 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0144 |
5 | HG02723.hp1 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.933+5435A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026739 | |||||||
chr9:124026862 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.933+5558C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026862 | |||||||
chr9:124026929 | C | T | 56 | a0001c0001t0001g0058 a0001c0001t0002g0062 a0001c0001t0002g0114 others(53): Show |
136 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.934-5491C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124026929 | |||||||
chr9:124027121 | G | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0002g0066 |
4 | HG02145.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-5299G>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124027121 | |||||||
chr9:124027227 | A | G | 58 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0144 others(55): Show |
141 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.934-5193A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124027227 | |||||||
chr9:124027247 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.934-5173G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124027247 | |||||||
chr9:124027290 | G | T | 74 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0022 others(71): Show |
166 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.934-5130G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124027290 | |||||||
chr9:124027398 | T | G | 60 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0144 others(57): Show |
145 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.934-5022T>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124027398 | |||||||
chr9:124027399 | T | C | 60 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0144 others(57): Show |
145 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.934-5021T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124027399 | |||||||
chr9:124027412 | G | A | 1 | a0001c0001t0010g0096 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.934-5008G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124027412 | |||||||
chr9:124027536 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.934-4884T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124027536 | |||||||
chr9:124027696 | T | C | 1 | a0001c0002t0002g0049 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.934-4724T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124027696 | |||||||
chr9:124027831 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0005g0036 a0001c0001t0010g0096 |
3 | HG01167.hp1 HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.934-4589C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124027831 | |||||||
chr9:124027885 | C | T | 3 | a0001c0001t0002g0062 a0001c0001t0003g0171 a0001c0007t0003g0170 |
3 | HG02109.hp1 HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.934-4535C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124027885 | |||||||
chr9:124027902 | G | GT | 48 | a0001c0001t0001g0058 a0001c0001t0002g0114 a0001c0001t0004g0164 others(45): Show |
128 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.934-4509dupT | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124027902 | ||||||
chr9:124027902 | GT | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0144 |
5 | HG02723.hp1 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.934-4509delT | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124027902 | ||||||
chr9:124027922 | T | C | 47 | a0001c0001t0002g0114 a0001c0001t0004g0164 a0001c0002t0001g0002 others(44): Show |
127 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.934-4498T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124027922 | |||||||
chr9:124028281 | C | T | 12 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0025 others(9): Show |
26 | HG00408.hp1 HG01081.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.934-4139C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124028281 | |||||||
chr9:124028302 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.934-4118G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124028302 | |||||||
chr9:124028318 | T | C | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | HG01884.hp2 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.934-4102T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124028318 | |||||||
chr9:124028328 | A | C | 60 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0144 others(57): Show |
145 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.934-4092A>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124028328 | |||||||
chr9:124028387 | T | C | 60 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0144 others(57): Show |
145 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.934-4033T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124028387 | |||||||
chr9:124028452 | T | C | 1 | a0001c0001t0003g0092 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.934-3968T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124028452 | |||||||
chr9:124028607 | C | G | 2 | a0001c0001t0001g0072 a0001c0001t0005g0060 |
2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.934-3813C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124028607 | |||||||
chr9:124028619 | C | G | 1 | a0001c0001t0004g0163 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.934-3801C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124028619 | |||||||
chr9:124028699 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.934-3721G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124028699 | |||||||
chr9:124028723 | G | C | 1 | a0001c0001t0001g0097 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.934-3697G>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124028723 | |||||||
chr9:124028734 | C | G | 12 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
18 | HG00639.hp2 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.934-3686C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124028734 | |||||||
chr9:124028880 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.934-3540G>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124028880 | |||||||
chr9:124028882 | C | T | 5 | a0001c0002t0001g0027 a0001c0002t0003g0059 a0001c0002t0005g0027 others(2): Show |
5 | HG01891.hp2 HG02630.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.934-3538C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124028882 | |||||||
chr9:124028960 | A | G | 2 | a0001c0001t0003g0171 a0001c0007t0003g0170 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.934-3460A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124028960 | |||||||
chr9:124029009 | T | C | 90 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0022 others(87): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.934-3411T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124029009 | |||||||
chr9:124029011 | G | A | 2 | a0001c0002t0001g0020 a0001c0002t0014g0154 |
4 | HG02559.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.934-3409G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124029011 | |||||||
chr9:124029020 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.934-3400G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124029020 | |||||||
chr9:124029115 | A | AAAT | 5 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0065 others(2): Show |
7 | HG01099.hp1 HG02145.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.934-3285_934-3283d others(5): Show |
LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124029115 | ||||||
chr9:124029115 | A | AAATAAT | 2 | a0001c0001t0001g0015 a0001c0001t0001g0144 |
5 | HG02723.hp1 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.934-3288_934-3283d others(8): Show |
LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124029115 | ||||||
chr9:124029134 | A | AATG | 2 | a0001c0002t0001g0020 a0001c0002t0014g0154 |
4 | HG02559.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.934-3284_934-3283i others(5): Show |
LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124029134 | ||||||
chr9:124029138 | G | T | 2 | a0001c0001t0001g0072 a0001c0001t0005g0060 |
2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.934-3282G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124029138 | |||||||
chr9:124029450 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0168 |
4 | HG02258.hp1 HG02486.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-2970C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124029450 | |||||||
chr9:124029461 | C | A | 1 | a0001c0002t0001g0123 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.934-2959C>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124029461 | |||||||
chr9:124029466 | A | G | 1 | a0001c0002t0001g0133 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.934-2954A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124029466 | |||||||
chr9:124029628 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0036 others(6): Show |
17 | HG01167.hp1 HG01433.hp2 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.934-2792C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124029628 | |||||||
chr9:124029718 | C | A | 3 | a0001c0001t0004g0046 a0001c0001t0004g0157 a0001c0001t0004g0165 |
4 | HG00609.hp2 NA19066.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.934-2702C>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124029718 | |||||||
chr9:124029726 | A | G | 63 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0035 others(60): Show |
147 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.934-2694A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124029726 | |||||||
chr9:124029779 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.934-2641C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124029779 | |||||||
chr9:124029807 | A | G | 58 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0144 others(55): Show |
140 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.934-2613A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124029807 | |||||||
chr9:124029823 | C | T | 1 | a0001c0002t0001g0020 | 3 | HG02559.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.934-2597C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124029823 | |||||||
chr9:124030036 | A | C | 1 | a0001c0002t0002g0132 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.934-2384A>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030036 | |||||||
chr9:124030209 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0168 |
4 | HG02258.hp1 HG02486.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-2211G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030209 | |||||||
chr9:124030236 | C | G | 61 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0058 others(58): Show |
143 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.934-2184C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030236 | |||||||
chr9:124030270 | C | T | 5 | a0001c0002t0001g0043 a0001c0002t0001g0116 a0001c0002t0001g0130 others(2): Show |
6 | HG00280.hp1 HG01074.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.934-2150C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030270 | |||||||
chr9:124030398 | T | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0002g0024 others(1): Show |
6 | HG02145.hp1 HG02615.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.934-2022T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030398 | |||||||
chr9:124030489 | C | G | 1 | a0001c0001t0003g0032 | 2 | NA18747.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.934-1931C>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030489 | |||||||
chr9:124030512 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.934-1908G>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030512 | |||||||
chr9:124030627 | C | CT | 18 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0042 others(15): Show |
35 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.934-1771dupT | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124030627 | ||||||
chr9:124030627 | C | T | 1 | a0001c0001t0003g0001 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.934-1793C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030627 | |||||||
chr9:124030627 | CT | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(72): Show |
169 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.934-1771delT | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124030627 | ||||||
chr9:124030627 | CTT | C | 17 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0058 others(14): Show |
21 | HG00280.hp1 HG01891.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.934-1772_934-1771d others(4): Show |
LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124030627 | ||||||
chr9:124030630 | T | TTC | 3 | a0001c0002t0002g0007 a0001c0002t0002g0127 a0001c0002t0002g0132 |
9 | HG00408.hp2 HG00673.hp1 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.934-1789_934-1788i others(4): Show |
LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124030630 | ||||||
chr9:124030632 | T | C | 17 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0022 others(14): Show |
28 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.934-1788T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030632 | |||||||
chr9:124030633 | T | C | 44 | a0001c0001t0001g0013 a0001c0001t0001g0085 a0001c0001t0001g0093 others(41): Show |
117 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.934-1787T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030633 | |||||||
chr9:124030634 | T | C | 3 | a0001c0001t0001g0074 a0001c0002t0001g0126 a0001c0002t0001g0131 |
3 | HG00280.hp1 HG03471.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.934-1786T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030634 | |||||||
chr9:124030654 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.934-1766T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030654 | |||||||
chr9:124030690 | G | T | 1 | a0001c0002t0003g0059 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.934-1730G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030690 | |||||||
chr9:124030724 | C | T | 1 | a0001c0001t0003g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.934-1696C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030724 | |||||||
chr9:124030756 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.934-1664C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030756 | |||||||
chr9:124030771 | A | G | 1 | a0001c0002t0001g0020 | 3 | HG02559.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.934-1649A>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030771 | |||||||
chr9:124030779 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.934-1641G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030779 | |||||||
chr9:124030821 | T | C | 1 | a0001c0001t0003g0064 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.934-1599T>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030821 | |||||||
chr9:124030914 | T | G | 8 | a0001c0001t0003g0005 a0001c0001t0003g0025 a0001c0001t0003g0032 others(5): Show |
18 | HG01123.hp1 HG01255.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.934-1506T>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030914 | |||||||
chr9:124030929 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.934-1491G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124030929 | |||||||
chr9:124031001 | G | A | 1 | a0001c0002t0002g0127 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.934-1419G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124031001 | |||||||
chr9:124031093 | C | T | 1 | a0001c0002t0001g0020 | 3 | HG02559.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.934-1327C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124031093 | |||||||
chr9:124031094 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.934-1326G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124031094 | |||||||
chr9:124031115 | G | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0168 |
4 | HG02258.hp1 HG02486.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-1305G>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124031115 | |||||||
chr9:124031137 | G | A | 1 | a0001c0002t0001g0020 | 3 | HG02559.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.934-1283G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124031137 | |||||||
chr9:124031305 | C | A | 2 | a0001c0001t0003g0171 a0001c0007t0003g0170 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.934-1115C>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124031305 | |||||||
chr9:124031305 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.934-1115C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124031305 | |||||||
chr9:124031455 | GA | G | 9 | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0002t0001g0027 others(6): Show |
9 | HG01891.hp2 HG02630.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.934-953delA | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124031455 | ||||||
chr9:124031851 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.934-569G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124031851 | |||||||
chr9:124031894 | G | A | 49 | a0001c0001t0001g0013 a0001c0001t0001g0093 a0001c0001t0001g0148 others(46): Show |
129 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.934-526G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124031894 | |||||||
chr9:124032046 | T | G | 79 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0026 others(76): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.934-374T>G | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124032046 | |||||||
chr9:124032094 | C | T | 1 | a0001c0002t0002g0048 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.934-326C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124032094 | |||||||
chr9:124032317 | C | T | 12 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0065 others(9): Show |
18 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.934-103C>T | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124032317 | |||||||
chr9:124032351 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.934-69G>C | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124032351 | |||||||
chr9:124032363 | C | CG | 52 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0021 others(49): Show |
108 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.934-51dupG | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 124032363 | ||||||
chr9:124032369 | G | A | 28 | a0001c0001t0001g0013 a0001c0001t0001g0093 a0001c0001t0001g0148 others(25): Show |
68 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.934-51G>A | LHX2 | ENSG00000106689.11 | transcript | ENST00000373615.9 | protein_coding | 4/4 | chr9 | 124032369 |