Item | Value |
---|---|
geneid | 1105 |
ensemblid | ENSG00000153922.12 |
hgncid | 1915 |
symbol | CHD1 |
name | chromodomain helicase DNA binding protein 1 |
refseq_nuc | NM_001270.4 |
refseq_prot | NP_001261.2 |
ensembl_nuc | ENST00000614616.5 |
ensembl_prot | ENSP00000483667.1 |
mane_status | MANE Select |
chr | chr5 |
start | 98853985 |
end | 98929007 |
strand | - |
ver | v1.2 |
region | chr5:98853985-98929007 |
region5000 | chr5:98848985-98934007 |
regionname0 | CHD1_chr5_98853985_98929007 |
regionname5000 | CHD1_chr5_98848985_98934007 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1710 | 260 | 60 | 43 | 119 | 7 | 29 | 92 | CHD1_chr5_98848985_98934007 | CHD1 | MNGHS others(1705): Show |
chr5 | 98848985 | 98934007 |
a0002 | 0/0 | 1709 | 71 | 28 | 18 | 20 | 2 | 3 | 19 | CHD1_chr5_98848985_98934007 | CHD1 | MNGHS others(1704): Show |
chr5 | 98848985 | 98934007 |
a0003 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | MNGHS others(1705): Show |
chr5 | 98848985 | 98934007 |
a0004 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | MNGHS others(1705): Show |
chr5 | 98848985 | 98934007 |
a0005 | 0/0 | 1709 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | MNGHS others(1704): Show |
chr5 | 98848985 | 98934007 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 5130 | 215 | 24 | 40 | 117 | 6 | 26 | CHD1_chr5_98848985_98934007 | CHD1 | ATGAA others(5125): Show |
chr5 | 98848985 | 98934007 | ||
a0001c0003 | 0/0 | 5130 | 35 | 29 | 2 | 0 | 1 | 3 | CHD1_chr5_98848985_98934007 | CHD1 | ATGAA others(5125): Show |
chr5 | 98848985 | 98934007 | ||
a0001c0004 | 0/0 | 5130 | 6 | 6 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | ATGAA others(5125): Show |
chr5 | 98848985 | 98934007 | ||
a0001c0005 | 0/0 | 5130 | 2 | 1 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | ATGAA others(5125): Show |
chr5 | 98848985 | 98934007 | ||
a0001c0006 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | ATGAA others(5125): Show |
chr5 | 98848985 | 98934007 | ||
a0001c0008 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | ATGAA others(5125): Show |
chr5 | 98848985 | 98934007 | ||
a0002c0002 | 0/0 | 5127 | 71 | 28 | 18 | 20 | 2 | 3 | CHD1_chr5_98848985_98934007 | CHD1 | ATGAA others(5122): Show |
chr5 | 98848985 | 98934007 | ||
a0003c0010 | 0/0 | 5130 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | ATGAA others(5125): Show |
chr5 | 98848985 | 98934007 | ||
a0004c0007 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | ATGAA others(5125): Show |
chr5 | 98848985 | 98934007 | ||
a0005c0009 | 0/0 | 5127 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | ATGAA others(5122): Show |
chr5 | 98848985 | 98934007 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 8145 | 168 | 23 | 35 | 87 | 3 | 18 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0001t0003 | 0/0 | 8145 | 18 | 0 | 3 | 9 | 3 | 3 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0001t0004 | 0/0 | 8145 | 13 | 0 | 0 | 11 | 0 | 2 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0001t0008 | 0/0 | 8145 | 4 | 0 | 0 | 4 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0001t0014 | 0/0 | 8145 | 3 | 0 | 0 | 3 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0001t0015 | 0/0 | 8145 | 2 | 0 | 0 | 0 | 0 | 2 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0001t0019 | 0/0 | 8145 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0001t0021 | 0/0 | 8145 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0001t0023 | 0/0 | 8145 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0001t0026 | 0/0 | 8145 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0001t0027 | 0/0 | 8145 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0001t0029 | 0/0 | 8145 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0001t0030 | 0/0 | 8145 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0003t0002 | 0/0 | 8155 | 13 | 12 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8150): Show |
chr5 | 98848985 | 98934007 |
a0001c0003t0005 | 0/0 | 8152 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8147): Show |
chr5 | 98848985 | 98934007 |
a0001c0003t0006 | 0/0 | 8155 | 9 | 8 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8150): Show |
chr5 | 98848985 | 98934007 |
a0001c0003t0009 | 0/0 | 8150 | 4 | 0 | 0 | 0 | 1 | 3 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8145): Show |
chr5 | 98848985 | 98934007 |
a0001c0003t0012 | 0/0 | 8155 | 3 | 3 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8150): Show |
chr5 | 98848985 | 98934007 |
a0001c0003t0013 | 0/0 | 8155 | 3 | 3 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8150): Show |
chr5 | 98848985 | 98934007 |
a0001c0003t0020 | 0/0 | 8155 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8150): Show |
chr5 | 98848985 | 98934007 |
a0001c0003t0028 | 0/0 | 8155 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8150): Show |
chr5 | 98848985 | 98934007 |
a0001c0004t0001 | 0/0 | 8145 | 6 | 6 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0005t0001 | 0/0 | 8145 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0005t0022 | 0/0 | 8145 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0006t0001 | 0/0 | 8145 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0001c0008t0001 | 0/0 | 8145 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0002c0002t0002 | 0/0 | 8152 | 44 | 14 | 16 | 12 | 0 | 2 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8147): Show |
chr5 | 98848985 | 98934007 |
a0002c0002t0005 | 0/0 | 8149 | 9 | 9 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8144): Show |
chr5 | 98848985 | 98934007 |
a0002c0002t0007 | 0/0 | 8149 | 4 | 0 | 0 | 3 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8144): Show |
chr5 | 98848985 | 98934007 |
a0002c0002t0010 | 0/0 | 8152 | 4 | 0 | 0 | 4 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8147): Show |
chr5 | 98848985 | 98934007 |
a0002c0002t0011 | 0/0 | 8152 | 3 | 0 | 1 | 0 | 2 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8147): Show |
chr5 | 98848985 | 98934007 |
a0002c0002t0016 | 0/0 | 8152 | 2 | 2 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8147): Show |
chr5 | 98848985 | 98934007 |
a0002c0002t0017 | 0/0 | 8152 | 2 | 2 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8147): Show |
chr5 | 98848985 | 98934007 |
a0002c0002t0018 | 0/0 | 8149 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8144): Show |
chr5 | 98848985 | 98934007 |
a0002c0002t0024 | 0/0 | 8152 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8147): Show |
chr5 | 98848985 | 98934007 |
a0002c0002t0025 | 0/0 | 8152 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8147): Show |
chr5 | 98848985 | 98934007 |
a0003c0010t0001 | 0/0 | 8145 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0004c0007t0001 | 0/0 | 8145 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8140): Show |
chr5 | 98848985 | 98934007 |
a0005c0009t0002 | 0/0 | 8152 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | GCCTC others(8147): Show |
chr5 | 98848985 | 98934007 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0008g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0008g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0014g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0014g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0014g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0015g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0015g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0019g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0021g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0023g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0026g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0027g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0029g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0030g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0009g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0009g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0009g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0009g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0012g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0012g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0012g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0013g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0013g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0020g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0028g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0004t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0005t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0005t0022g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0006t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0008t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0007g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0007g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0007g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0010g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0010g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0010g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0011g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0011g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0011g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0016g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0017g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0017g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0018g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0024g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0025g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0003c0010t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0004c0007t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0005c0009t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0002 | c0002 | t0011 | g0082 | EUR | FIN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00323 | hp2 | a0001 | c0003 | t0009 | g0194 | EUR | FIN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00408 | hp1 | a0001 | c0001 | t0019 | g0019 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0113 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00741 | hp1 | a0001 | c0003 | t0002 | g0011 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0117 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0112 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0118 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01081 | hp1 | a0003 | c0010 | t0001 | g0251 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0114 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01109 | hp1 | a0001 | c0003 | t0006 | g0070 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0121 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0128 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0129 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0141 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0137 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01255 | hp1 | a0001 | c0005 | t0022 | g0049 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0105 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0104 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01358 | hp1 | a0002 | c0002 | t0011 | g0084 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01433 | hp1 | a0001 | c0001 | t0027 | g0142 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0116 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0199 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01496 | hp2 | a0002 | c0002 | t0025 | g0136 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01515 | hp1 | a0002 | c0002 | t0011 | g0085 | EUR | IBS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0297 | EUR | IBS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0299 | EUR | IBS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0298 | EUR | IBS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01884 | hp2 | a0001 | c0003 | t0006 | g0072 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01891 | hp2 | a0001 | c0003 | t0002 | g0062 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0303 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01981 | hp1 | a0001 | c0001 | t0021 | g0160 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0302 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02055 | hp2 | a0002 | c0002 | t0005 | g0020 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02258 | hp1 | a0001 | c0003 | t0006 | g0067 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02258 | hp2 | a0002 | c0002 | t0005 | g0021 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0301 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02572 | hp1 | a0002 | c0002 | t0002 | g0198 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02572 | hp2 | a0001 | c0003 | t0006 | g0069 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02622 | hp1 | a0001 | c0003 | t0005 | g0023 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02630 | hp1 | a0002 | c0002 | t0005 | g0026 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02647 | hp2 | a0001 | c0003 | t0006 | g0068 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0037 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0042 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02717 | hp1 | a0002 | c0002 | t0016 | g0007 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02717 | hp2 | a0001 | c0003 | t0006 | g0060 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02723 | hp1 | a0001 | c0004 | t0001 | g0133 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0135 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02818 | hp1 | a0002 | c0002 | t0005 | g0025 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02886 | hp1 | a0001 | c0003 | t0002 | g0063 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0287 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02895 | hp2 | a0001 | c0003 | t0012 | g0293 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02896 | hp2 | a0001 | c0003 | t0002 | g0056 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02897 | hp1 | a0001 | c0003 | t0002 | g0055 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02897 | hp2 | a0001 | c0003 | t0012 | g0294 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02922 | hp1 | a0002 | c0002 | t0005 | g0022 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02922 | hp2 | a0001 | c0003 | t0002 | g0054 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02965 | hp1 | a0001 | c0003 | t0020 | g0045 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0079 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02970 | hp2 | a0001 | c0003 | t0002 | g0004 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02976 | hp1 | a0001 | c0001 | t0026 | g0249 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02976 | hp2 | a0002 | c0002 | t0005 | g0027 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03041 | hp1 | a0001 | c0004 | t0001 | g0093 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0134 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03098 | hp1 | a0002 | c0002 | t0005 | g0028 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03098 | hp2 | a0001 | c0004 | t0001 | g0094 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03130 | hp1 | a0001 | c0003 | t0002 | g0066 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03130 | hp2 | a0001 | c0004 | t0001 | g0130 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03139 | hp1 | a0002 | c0002 | t0005 | g0024 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03139 | hp2 | a0001 | c0003 | t0002 | g0071 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0124 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0089 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03225 | hp1 | a0001 | c0003 | t0006 | g0061 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0092 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03453 | hp1 | a0001 | c0003 | t0006 | g0058 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03491 | hp1 | a0001 | c0003 | t0009 | g0193 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03492 | hp2 | a0001 | c0003 | t0009 | g0224 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03516 | hp1 | a0002 | c0002 | t0024 | g0051 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03516 | hp2 | a0002 | c0002 | t0002 | g0081 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03540 | hp1 | a0002 | c0002 | t0017 | g0139 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03540 | hp2 | a0002 | c0002 | t0016 | g0007 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03579 | hp1 | a0001 | c0003 | t0028 | g0057 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03688 | hp1 | a0001 | c0003 | t0009 | g0225 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0115 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03710 | hp2 | a0001 | c0001 | t0015 | g0046 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0307 | SAS | BEB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0311 | SAS | BEB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04184 | hp2 | a0001 | c0001 | t0015 | g0047 | SAS | BEB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04199 | hp1 | a0002 | c0002 | t0007 | g0015 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04204 | hp1 | a0001 | c0001 | t0030 | g0319 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0304 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0083 | AFR | YRI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | CHB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18906 | hp1 | a0001 | c0003 | t0002 | g0004 | AFR | YRI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18906 | hp2 | a0001 | c0005 | t0001 | g0048 | AFR | YRI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18947 | hp2 | a0002 | c0002 | t0007 | g0017 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18949 | hp2 | a0002 | c0002 | t0010 | g0123 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18950 | hp1 | a0002 | c0002 | t0018 | g0018 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18969 | hp1 | a0001 | c0001 | t0014 | g0315 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18970 | hp1 | a0002 | c0002 | t0007 | g0016 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18970 | hp2 | a0002 | c0002 | t0010 | g0006 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18972 | hp1 | a0001 | c0001 | t0023 | g0176 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18975 | hp2 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18977 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18983 | hp1 | a0001 | c0001 | t0014 | g0317 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18988 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18998 | hp1 | a0002 | c0002 | t0010 | g0122 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18998 | hp2 | a0001 | c0006 | t0001 | g0075 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19003 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19006 | hp1 | a0001 | c0001 | t0029 | g0318 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19006 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19009 | hp1 | a0001 | c0001 | t0008 | g0044 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19030 | hp1 | a0001 | c0004 | t0001 | g0091 | AFR | LWK | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19030 | hp2 | a0001 | c0003 | t0013 | g0295 | AFR | LWK | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0086 | AFR | LWK | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19043 | hp2 | a0001 | c0003 | t0002 | g0065 | AFR | LWK | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19057 | hp1 | a0001 | c0001 | t0008 | g0043 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19077 | hp2 | a0004 | c0007 | t0001 | g0186 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19088 | hp2 | a0001 | c0008 | t0001 | g0270 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19089 | hp2 | a0001 | c0001 | t0014 | g0316 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19091 | hp2 | a0002 | c0002 | t0010 | g0006 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19240 | hp1 | a0001 | c0003 | t0002 | g0064 | AFR | YRI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20129 | hp1 | a0001 | c0003 | t0013 | g0013 | AFR | ASW | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20129 | hp2 | a0001 | c0003 | t0002 | g0011 | AFR | ASW | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20752 | hp2 | a0005 | c0009 | t0002 | g0088 | EUR | TSI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | GIH | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | GIH | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0078 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02486 | hp1 | a0001 | c0003 | t0012 | g0296 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0087 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02559 | hp1 | a0001 | c0003 | t0006 | g0059 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03471 | hp1 | a0002 | c0002 | t0017 | g0226 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03471 | hp2 | a0002 | c0002 | t0005 | g0029 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG06807 | hp1 | a0001 | c0003 | t0013 | g0013 | AFR | USA | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | USA | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18955 | hp2 | a0002 | c0002 | t0007 | g0014 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0125 | AFR | USA | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | USA | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | LWK | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0080 | AFR | LWK | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0229 | REF | REF | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0165 | REF | REF | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:98856460 | AAGG | A | 2 | a0002 a0005 |
72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
conservative_inframe_deletion | MODERATE | c.5050_5052delCCT | p.Pro1684del | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 5669/8145 | 5050/5133 | 1684/1710 | chr5 | 98856460 | |||
chr5:98869828 | T | C | 1 | a0005 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.4033A>G | p.Ile1345Val | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/36 | 4650/8145 | 4033/5133 | 1345/1710 | chr5 | 98869828 | |||
chr5:98872160 | A | G | 1 | a0004 | 1 | NA19077.hp2 | missense_variant | MODERATE | c.3752T>C | p.Ile1251Thr | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/36 | 4369/8145 | 3752/5133 | 1251/1710 | chr5 | 98872160 | |||
chr5:98892699 | T | A | 1 | a0003 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.2006A>T | p.Glu669Val | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/36 | 2623/8145 | 2006/5133 | 669/1710 | chr5 | 98892699 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:98856658 | A | G | 1 | a0001c0004 | 6 | HG02723.hp1 HG03041.hp1 HG03098.hp2 others(3): Show |
synonymous_variant | LOW | c.4855T>C | p.Leu1619Leu | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 5472/8145 | 4855/5133 | 1619/1710 | chr5 | 98856658 | |||
chr5:98856707 | C | T | 1 | a0001c0008 | 1 | NA19088.hp2 | synonymous_variant | LOW | c.4806G>A | p.Glu1602Glu | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 5423/8145 | 4806/5133 | 1602/1710 | chr5 | 98856707 | |||
chr5:98863500 | C | T | 3 | a0001c0003 a0002c0002 a0005c0009 |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
synonymous_variant | LOW | c.4335G>A | p.Glu1445Glu | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/36 | 4952/8145 | 4335/5133 | 1445/1710 | chr5 | 98863500 | |||
chr5:98882064 | C | T | 1 | a0001c0006 | 1 | NA18998.hp2 | synonymous_variant | LOW | c.2778G>A | p.Ala926Ala | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/36 | 3395/8145 | 2778/5133 | 926/1710 | chr5 | 98882064 | |||
chr5:98897315 | T | C | 1 | a0001c0005 | 2 | HG01255.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.1371A>G | p.Leu457Leu | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/36 | 1988/8145 | 1371/5133 | 457/1710 | chr5 | 98897315 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:98853995 | A | T | 1 | a0001c0005t0022 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2385T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 2385 | chr5 | 98853995 | ||||||
chr5:98854071 | A | G | 1 | a0002c0002t0017 | 2 | HG03471.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2309T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 2309 | chr5 | 98854071 | ||||||
chr5:98854077 | G | A | 1 | a0001c0001t0023 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2303C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 2303 | chr5 | 98854077 | ||||||
chr5:98854175 | T | TCTTA | 19 | a0001c0003t0002 a0001c0003t0005 a0001c0003t0006 others(16): Show |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2204_*2205insTAAG | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 2204 | chr5 | 98854175 | ||||||
chr5:98854187 | C | CA | 19 | a0001c0003t0002 a0001c0003t0005 a0001c0003t0006 others(16): Show |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2192dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 2192 | chr5 | 98854187 | ||||||
chr5:98854267 | G | A | 1 | a0001c0003t0028 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2113C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 2113 | chr5 | 98854267 | ||||||
chr5:98854349 | C | CAATAG | 18 | a0001c0003t0002 a0001c0003t0005 a0001c0003t0006 others(15): Show |
103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2030_*2031insCTAT others(1): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 2030 | chr5 | 98854349 | ||||||
chr5:98854754 | C | T | 1 | a0002c0002t0016 | 2 | HG02717.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1626G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1626 | chr5 | 98854754 | ||||||
chr5:98854868 | G | A | 1 | a0002c0002t0024 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1512C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1512 | chr5 | 98854868 | ||||||
chr5:98854908 | A | G | 1 | a0001c0003t0006 | 9 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1472T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1472 | chr5 | 98854908 | ||||||
chr5:98854986 | C | G | 1 | a0001c0001t0021 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1394G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1394 | chr5 | 98854986 | ||||||
chr5:98855035 | C | A | 1 | a0002c0002t0025 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1345G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1345 | chr5 | 98855035 | ||||||
chr5:98855095 | T | C | 1 | a0001c0001t0026 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1285A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1285 | chr5 | 98855095 | ||||||
chr5:98855097 | T | C | 1 | a0002c0002t0018 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1283A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1283 | chr5 | 98855097 | ||||||
chr5:98855138 | C | T | 1 | a0001c0003t0009 | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1242G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1242 | chr5 | 98855138 | ||||||
chr5:98855327 | T | A | 1 | a0001c0003t0028 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1053A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1053 | chr5 | 98855327 | ||||||
chr5:98855948 | G | C | 1 | a0001c0003t0013 | 3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*432C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 432 | chr5 | 98855948 | ||||||
chr5:98856013 | T | C | 1 | a0002c0002t0011 | 3 | HG00323.hp1 HG01358.hp1 HG01515.hp1 |
3_prime_UTR_variant | MODIFIER | c.*367A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 367 | chr5 | 98856013 | ||||||
chr5:98856032 | T | C | 1 | a0001c0001t0027 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*348A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 348 | chr5 | 98856032 | ||||||
chr5:98856045 | G | A | 1 | a0001c0003t0028 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*335C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 335 | chr5 | 98856045 | ||||||
chr5:98856327 | T | C | 1 | a0002c0002t0010 | 4 | NA18949.hp2 NA18970.hp2 NA18998.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*53A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 53 | chr5 | 98856327 | ||||||
chr5:98928589 | C | G | 1 | a0001c0001t0015 | 2 | HG03710.hp2 HG04184.hp2 |
5_prime_UTR_variant | MODIFIER | c.-199G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2203 | chr5 | 98928589 | ||||||
chr5:98928592 | G | A | 2 | a0001c0003t0012 a0001c0003t0013 |
6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-202C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2206 | chr5 | 98928592 | ||||||
chr5:98928631 | C | G | 1 | a0001c0003t0020 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-241G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2245 | chr5 | 98928631 | ||||||
chr5:98928691 | G | A | 1 | a0001c0001t0003 | 18 | HG00621.hp2 HG01515.hp2 HG01516.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-301C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2305 | chr5 | 98928691 | ||||||
chr5:98928702 | C | T | 1 | a0001c0001t0008 | 4 | NA18975.hp2 NA18977.hp1 NA19009.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-312G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2316 | chr5 | 98928702 | ||||||
chr5:98928708 | T | C | 1 | a0001c0001t0014 | 3 | NA18969.hp1 NA18983.hp1 NA19089.hp2 |
5_prime_UTR_variant | MODIFIER | c.-318A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2322 | chr5 | 98928708 | ||||||
chr5:98928709 | C | T | 1 | a0001c0001t0004 | 13 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-319G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2323 | chr5 | 98928709 | ||||||
chr5:98928806 | TCGC | T | 4 | a0001c0003t0005 a0002c0002t0005 a0002c0002t0007 others(1): Show |
15 | HG02055.hp2 HG02258.hp2 HG02622.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-419_-417delGCG | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2421 | chr5 | 98928806 | ||||||
chr5:98928834 | C | T | 1 | a0001c0001t0019 | 1 | HG00408.hp1 | 5_prime_UTR_variant | MODIFIER | c.-444G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2448 | chr5 | 98928834 | ||||||
chr5:98928849 | T | G | 1 | a0001c0001t0029 | 1 | NA19006.hp1 | 5_prime_UTR_variant | MODIFIER | c.-459A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2463 | chr5 | 98928849 | ||||||
chr5:98928962 | G | A | 1 | a0001c0001t0030 | 1 | HG04204.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-572C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | chr5 | 98928962 | |||||||
chr5:98928971 | G | T | 2 | a0002c0002t0007 a0002c0002t0018 |
5 | HG04199.hp1 NA18947.hp2 NA18950.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-581C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2585 | chr5 | 98928971 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:98856761 | T | C | 95 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(92): Show |
103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.4788-36A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856761 | |||||||
chr5:98856790 | T | C | 3 | a0001c0001t0001g0050 a0001c0001t0001g0240 a0001c0001t0001g0243 |
3 | HG01928.hp1 HG02273.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.4788-65A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856790 | |||||||
chr5:98856841 | T | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(217): Show |
231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.4788-116A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856841 | |||||||
chr5:98856859 | AACTT | A | 5 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0198 others(2): Show |
6 | HG01496.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.4788-138_4788-135d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856859 | |||||||
chr5:98856878 | A | T | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4788-153T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856878 | |||||||
chr5:98856880 | A | T | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4788-155T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856880 | |||||||
chr5:98856887 | G | A | 1 | a0001c0001t0004g0032 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.4788-162C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856887 | |||||||
chr5:98856938 | T | C | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4788-213A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856938 | |||||||
chr5:98857117 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4788-392T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857117 | |||||||
chr5:98857297 | TGA | T | 3 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0198 |
3 | HG02572.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4788-574_4788-573d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857297 | |||||||
chr5:98857365 | AAG | A | 8 | a0001c0003t0002g0004 a0001c0003t0002g0062 a0001c0003t0002g0063 others(5): Show |
9 | HG01891.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.4788-642_4788-641d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857365 | |||||||
chr5:98857460 | C | T | 95 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(92): Show |
103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.4787+720G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857460 | |||||||
chr5:98857604 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4787+576G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857604 | |||||||
chr5:98857605 | G | A | 1 | a0002c0002t0005g0020 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4787+575C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857605 | |||||||
chr5:98857766 | T | A | 1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4787+414A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857766 | |||||||
chr5:98857952 | A | G | 1 | a0001c0008t0001g0270 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4787+228T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857952 | |||||||
chr5:98858090 | T | C | 7 | a0001c0003t0002g0004 a0001c0003t0002g0062 a0001c0003t0002g0063 others(4): Show |
8 | HG01891.hp2 HG02886.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.4787+90A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98858090 | |||||||
chr5:98858163 | G | T | 18 | a0001c0001t0001g0156 a0001c0001t0001g0171 a0001c0001t0003g0297 others(15): Show |
18 | HG00621.hp2 HG01515.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.4787+17C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98858163 | |||||||
chr5:98858398 | A | G | 2 | a0002c0002t0002g0128 a0002c0002t0002g0129 |
2 | HG01168.hp1 HG01169.hp1 |
splice_region_variant&intron_variant | LOW | c.4577-8T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858398 | |||||||
chr5:98858472 | G | A | 4 | a0001c0001t0001g0222 a0001c0001t0001g0259 a0001c0001t0001g0260 others(1): Show |
4 | HG01928.hp2 NA18948.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.4577-82C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858472 | |||||||
chr5:98858482 | T | C | 5 | a0001c0003t0012g0293 a0001c0003t0012g0294 a0001c0003t0012g0296 others(2): Show |
6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4577-92A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858482 | |||||||
chr5:98858640 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.4577-250A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858640 | |||||||
chr5:98858758 | T | C | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4576+206A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858758 | |||||||
chr5:98858788 | G | T | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4576+176C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858788 | |||||||
chr5:98858885 | T | C | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4576+79A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858885 | |||||||
chr5:98858914 | T | A | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4576+50A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858914 | |||||||
chr5:98858915 | A | T | 1 | a0002c0002t0002g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4576+49T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858915 | |||||||
chr5:98858930 | T | A | 7 | a0002c0002t0002g0079 a0002c0002t0002g0080 a0002c0002t0002g0081 others(4): Show |
7 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.4576+34A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858930 | |||||||
chr5:98859077 | C | G | 101 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0003t0002g0004 others(98): Show |
109 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.4525-62G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859077 | |||||||
chr5:98859184 | C | T | 99 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(96): Show |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.4525-169G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859184 | |||||||
chr5:98859251 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.4525-236C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859251 | |||||||
chr5:98859277 | T | C | 4 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
4 | HG01099.hp1 HG01192.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.4525-262A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859277 | |||||||
chr5:98859298 | T | C | 1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4525-283A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859298 | |||||||
chr5:98859362 | T | C | 13 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(10): Show |
13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.4525-347A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859362 | |||||||
chr5:98859514 | G | A | 20 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0198 others(17): Show |
21 | HG01496.hp2 HG02055.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.4524+458C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859514 | |||||||
chr5:98859670 | T | C | 20 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0198 others(17): Show |
21 | HG01496.hp2 HG02055.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.4524+302A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859670 | |||||||
chr5:98859822 | G | A | 6 | a0001c0003t0006g0058 a0001c0003t0006g0061 a0001c0003t0006g0067 others(3): Show |
6 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4524+150C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859822 | |||||||
chr5:98859955 | TATG | T | 5 | a0002c0002t0002g0079 a0002c0002t0002g0080 a0002c0002t0002g0081 others(2): Show |
5 | HG02486.hp2 HG02965.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.4524+14_4524+16del others(3): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859955 | |||||||
chr5:98860114 | A | G | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4428-46T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98860114 | |||||||
chr5:98860478 | T | C | 15 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0004g0030 others(12): Show |
15 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(12): Show |
intron_variant | MODIFIER | c.4428-410A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98860478 | |||||||
chr5:98861120 | T | TA | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4428-1053dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98861120 | |||||||
chr5:98861179 | G | C | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4428-1111C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98861179 | |||||||
chr5:98861301 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.4428-1233C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98861301 | |||||||
chr5:98861777 | T | C | 1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4427+1631A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98861777 | |||||||
chr5:98861793 | T | A | 1 | a0002c0002t0007g0017 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4427+1615A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98861793 | |||||||
chr5:98861795 | C | T | 18 | a0001c0001t0001g0156 a0001c0001t0001g0171 a0001c0001t0003g0297 others(15): Show |
18 | HG00621.hp2 HG01515.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.4427+1613G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98861795 | |||||||
chr5:98862026 | G | A | 64 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0078 others(61): Show |
69 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.4427+1382C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98862026 | |||||||
chr5:98862353 | A | C | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4427+1055T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98862353 | |||||||
chr5:98862364 | C | A | 1 | a0001c0001t0001g0288 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4427+1044G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98862364 | |||||||
chr5:98862443 | G | C | 2 | a0001c0003t0013g0013 a0001c0003t0013g0295 |
3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4427+965C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98862443 | |||||||
chr5:98862854 | G | T | 1 | a0001c0001t0001g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4427+554C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98862854 | |||||||
chr5:98863344 | CA | C | 97 | a0001c0001t0004g0041 a0001c0001t0029g0318 a0001c0003t0002g0004 others(94): Show |
105 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.4427+63delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98863344 | |||||||
chr5:98863349 | A | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0210 |
2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.4427+59T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98863349 | |||||||
chr5:98863373 | T | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(116): Show |
122 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.4427+35A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98863373 | |||||||
chr5:98863690 | C | A | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4249-104G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98863690 | |||||||
chr5:98863719 | C | T | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.4249-133G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98863719 | |||||||
chr5:98864263 | G | A | 1 | a0002c0002t0002g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4249-677C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864263 | |||||||
chr5:98864433 | A | G | 1 | a0002c0002t0005g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4249-847T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864433 | |||||||
chr5:98864517 | C | CA | 36 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0074 others(33): Show |
37 | HG00621.hp1 HG01243.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.4249-932dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864517 | |||||||
chr5:98864517 | C | CAA | 20 | a0001c0001t0001g0077 a0001c0003t0002g0054 a0001c0003t0002g0055 others(17): Show |
21 | HG00323.hp1 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.4249-933_4249-932d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864517 | |||||||
chr5:98864517 | C | CAAA | 8 | a0001c0003t0002g0004 a0001c0003t0002g0063 a0001c0003t0002g0064 others(5): Show |
9 | HG02486.hp1 HG02572.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.4249-934_4249-932d others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864517 | |||||||
chr5:98864517 | CA | C | 9 | a0001c0001t0001g0191 a0001c0001t0001g0244 a0001c0001t0001g0292 others(6): Show |
12 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.4249-932delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864517 | |||||||
chr5:98864517 | CAA | C | 29 | a0002c0002t0002g0005 a0002c0002t0002g0104 a0002c0002t0002g0105 others(26): Show |
31 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.4249-933_4249-932d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864517 | |||||||
chr5:98864517 | CAAAAAAA others(3): Show |
C | 13 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0001g0097 others(10): Show |
13 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.4249-941_4249-932d others(12): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864517 | |||||||
chr5:98864517 | CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0001g0220 a0001c0001t0001g0262 a0001c0001t0001g0263 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.4249-943_4249-932d others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864517 | |||||||
chr5:98864977 | C | T | 3 | a0001c0003t0002g0054 a0001c0003t0002g0055 a0001c0003t0002g0056 |
3 | HG02896.hp2 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.4249-1391G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864977 | |||||||
chr5:98865157 | G | A | 1 | a0001c0006t0001g0075 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.4249-1571C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98865157 | |||||||
chr5:98865370 | A | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0103 |
2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.4249-1784T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98865370 | |||||||
chr5:98865397 | T | C | 1 | a0002c0002t0002g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4249-1811A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98865397 | |||||||
chr5:98865950 | TG | T | 220 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(217): Show |
231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.4249-2365delC | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98865950 | |||||||
chr5:98865964 | G | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(217): Show |
231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.4249-2378C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98865964 | |||||||
chr5:98866081 | CT | C | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4248+2413delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866081 | |||||||
chr5:98866107 | TAAAAAAC others(12): Show |
T | 1 | a0001c0001t0001g0161 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4248+2369_4248+238 others(23): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866107 | |||||||
chr5:98866145 | C | T | 1 | a0001c0001t0003g0307 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4248+2350G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866145 | |||||||
chr5:98866191 | CAG | C | 95 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(92): Show |
103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.4248+2302_4248+230 others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866191 | |||||||
chr5:98866198 | G | A | 2 | a0002c0002t0017g0139 a0002c0002t0017g0226 |
2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4248+2297C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866198 | |||||||
chr5:98866208 | A | T | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4248+2287T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866208 | |||||||
chr5:98866313 | A | C | 27 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(24): Show |
29 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.4248+2182T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866313 | |||||||
chr5:98866324 | G | A | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4248+2171C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866324 | |||||||
chr5:98866514 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4248+1981A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866514 | |||||||
chr5:98866614 | A | G | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4248+1881T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866614 | |||||||
chr5:98866659 | G | T | 13 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(10): Show |
13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.4248+1836C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866659 | |||||||
chr5:98866821 | A | C | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.4248+1674T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866821 | |||||||
chr5:98866863 | T | G | 1 | a0001c0001t0001g0245 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4248+1632A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866863 | |||||||
chr5:98867018 | A | G | 1 | a0001c0001t0004g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4248+1477T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867018 | |||||||
chr5:98867236 | A | T | 1 | a0001c0001t0001g0265 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4248+1259T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867236 | |||||||
chr5:98867558 | A | ATG | 17 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0001g0097 others(14): Show |
17 | HG00738.hp1 HG01192.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4248+935_4248+936d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867558 | |||||||
chr5:98867558 | A | ATGTG | 13 | a0001c0003t0002g0004 a0001c0003t0002g0062 a0001c0003t0002g0063 others(10): Show |
15 | HG01891.hp2 HG02486.hp1 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.4248+933_4248+936d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867558 | |||||||
chr5:98867558 | A | ATGTGTG | 12 | a0001c0003t0002g0054 a0001c0003t0002g0055 a0001c0003t0002g0056 others(9): Show |
12 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.4248+931_4248+936d others(8): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867558 | |||||||
chr5:98867568 | G | A | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4248+927C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867568 | |||||||
chr5:98867578 | A | T | 1 | a0001c0001t0001g0255 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4248+917T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867578 | |||||||
chr5:98867580 | A | G | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4248+915T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867580 | |||||||
chr5:98867795 | G | GT | 111 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
117 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.4248+699dupA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867795 | |||||||
chr5:98867795 | G | GTT | 10 | a0001c0001t0001g0076 a0001c0001t0001g0180 a0001c0001t0001g0195 others(7): Show |
10 | HG00738.hp2 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.4248+698_4248+699d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867795 | |||||||
chr5:98867795 | GT | G | 60 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(57): Show |
64 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.4248+699delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867795 | |||||||
chr5:98868016 | A | G | 99 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(96): Show |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.4248+479T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98868016 | |||||||
chr5:98868031 | C | T | 1 | a0001c0001t0014g0315 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.4248+464G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98868031 | |||||||
chr5:98868060 | A | T | 31 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(28): Show |
35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.4248+435T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98868060 | |||||||
chr5:98868114 | C | T | 15 | a0002c0002t0002g0287 a0002c0002t0005g0020 a0002c0002t0005g0021 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.4248+381G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98868114 | |||||||
chr5:98868266 | G | A | 13 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(10): Show |
13 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.4248+229C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98868266 | |||||||
chr5:98868331 | G | GA | 13 | a0001c0001t0001g0073 a0001c0001t0001g0189 a0001c0001t0001g0197 others(10): Show |
14 | HG00741.hp1 HG02886.hp2 HG02976.hp2 others(11): Show |
intron_variant | MODIFIER | c.4248+163dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98868331 | |||||||
chr5:98868331 | GA | G | 22 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0090 others(19): Show |
23 | HG01243.hp2 HG01496.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.4248+163delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98868331 | |||||||
chr5:98868753 | T | C | 4 | a0001c0001t0001g0050 a0001c0001t0001g0240 a0001c0001t0001g0243 others(1): Show |
4 | HG01928.hp1 HG02273.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.4108-118A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98868753 | |||||||
chr5:98868823 | T | A | 1 | a0001c0003t0028g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4108-188A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98868823 | |||||||
chr5:98868865 | C | T | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4108-230G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98868865 | |||||||
chr5:98868991 | A | AT | 34 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(31): Show |
35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.4108-357dupA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98868991 | |||||||
chr5:98868991 | AT | A | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4108-357delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98868991 | |||||||
chr5:98869326 | C | A | 69 | a0001c0003t0002g0011 a0001c0003t0005g0023 a0002c0002t0002g0001 others(66): Show |
75 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.4107+428G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869326 | |||||||
chr5:98869517 | C | T | 7 | a0002c0002t0005g0028 a0002c0002t0005g0029 a0002c0002t0007g0014 others(4): Show |
7 | HG03098.hp1 HG03471.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.4107+237G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869517 | |||||||
chr5:98869529 | G | C | 1 | a0002c0002t0005g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4107+225C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869529 | |||||||
chr5:98869606 | G | A | 1 | a0001c0003t0012g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4107+148C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869606 | |||||||
chr5:98869607 | T | C | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0131 |
3 | HG01192.hp2 HG02257.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.4107+147A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869607 | |||||||
chr5:98869615 | T | TGC | 5 | a0001c0001t0003g0311 a0001c0001t0004g0031 a0001c0001t0004g0032 others(2): Show |
5 | HG04184.hp1 NA18948.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.4107+137_4107+138d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869615 | |||||||
chr5:98869615 | TGCGC | T | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.4107+135_4107+138d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869615 | |||||||
chr5:98869618 | G | GCA | 5 | a0002c0002t0002g0198 a0002c0002t0002g0287 a0002c0002t0016g0007 others(2): Show |
6 | HG01496.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.4107+135_4107+136i others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869618 | |||||||
chr5:98869618 | G | GCACA | 3 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0005g0027 |
3 | HG02723.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4107+135_4107+136i others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869618 | |||||||
chr5:98869618 | G | GCACACA | 8 | a0002c0002t0002g0079 a0002c0002t0002g0080 a0002c0002t0002g0081 others(5): Show |
8 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.4107+135_4107+136i others(8): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869618 | |||||||
chr5:98869620 | G | A | 16 | a0002c0002t0002g0079 a0002c0002t0002g0080 a0002c0002t0002g0081 others(13): Show |
17 | HG01243.hp1 HG01496.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.4107+134C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869620 | |||||||
chr5:98869620 | G | GCA | 4 | a0002c0002t0011g0082 a0002c0002t0011g0084 a0002c0002t0011g0085 others(1): Show |
4 | HG00323.hp1 HG01358.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.4107+133_4107+134i others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869620 | |||||||
chr5:98869620 | GCGCACAC others(3): Show |
G | 13 | a0002c0002t0005g0020 a0002c0002t0005g0021 a0002c0002t0005g0022 others(10): Show |
13 | HG02055.hp2 HG02258.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.4107+124_4107+133d others(12): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869620 | |||||||
chr5:98869622 | G | A | 23 | a0001c0001t0001g0265 a0001c0003t0005g0023 a0002c0002t0002g0078 others(20): Show |
24 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.4107+132C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869622 | |||||||
chr5:98869622 | G | GCA | 95 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0090 others(92): Show |
95 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.4107+130_4107+131d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869622 | |||||||
chr5:98869622 | G | GCACA | 32 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0077 others(29): Show |
35 | HG00423.hp2 HG01099.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.4107+128_4107+131d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869622 | |||||||
chr5:98869622 | G | GCGCACAC others(1): Show |
3 | a0001c0001t0001g0103 a0001c0005t0001g0048 a0001c0005t0022g0049 |
3 | HG01255.hp1 HG02055.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4107+131_4107+132i others(10): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869622 | |||||||
chr5:98869622 | GCA | G | 12 | a0001c0001t0001g0143 a0001c0001t0001g0183 a0001c0001t0001g0215 others(9): Show |
12 | HG02698.hp2 HG03041.hp1 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.4107+130_4107+131d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869622 | |||||||
chr5:98869622 | GCACACAC others(3): Show |
G | 31 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(28): Show |
35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.4107+122_4107+131d others(12): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869622 | |||||||
chr5:98869624 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4107+130T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869624 | |||||||
chr5:98869685 | T | A | 1 | a0002c0002t0002g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4107+69A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869685 | |||||||
chr5:98869892 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3979-10T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98869892 | |||||||
chr5:98869917 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3979-35G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98869917 | |||||||
chr5:98869925 | A | T | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3979-43T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98869925 | |||||||
chr5:98870104 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3979-222T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98870104 | |||||||
chr5:98870318 | C | G | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.3978+369G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98870318 | |||||||
chr5:98870414 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0266 others(6): Show |
12 | HG00423.hp2 HG02015.hp2 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.3978+273G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98870414 | |||||||
chr5:98870419 | G | A | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.3978+268C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98870419 | |||||||
chr5:98870425 | C | T | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.3978+262G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98870425 | |||||||
chr5:98870493 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3978+194G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98870493 | |||||||
chr5:98870614 | T | C | 2 | a0002c0002t0005g0025 a0002c0002t0005g0026 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3978+73A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98870614 | |||||||
chr5:98871054 | C | CCT | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3862-252_3862-251i others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871054 | |||||||
chr5:98871055 | A | T | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3862-252T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871055 | |||||||
chr5:98871062 | T | A | 5 | a0001c0003t0012g0293 a0001c0003t0012g0294 a0001c0003t0012g0296 others(2): Show |
6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3862-259A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871062 | |||||||
chr5:98871116 | A | ATTTTTTT others(296): Show |
1 | a0002c0002t0017g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3862-314_3862-313i others(305): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871116 | |||||||
chr5:98871117 | T | C | 2 | a0002c0002t0002g0124 a0002c0002t0002g0125 |
2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3862-314A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871117 | |||||||
chr5:98871153 | G | A | 1 | a0002c0002t0002g0199 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3862-350C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871153 | |||||||
chr5:98871181 | C | T | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3862-378G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871181 | |||||||
chr5:98871369 | C | CA | 38 | a0001c0001t0001g0074 a0001c0001t0001g0155 a0001c0001t0001g0161 others(35): Show |
39 | HG01167.hp1 HG01433.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.3862-567dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | |||||||
chr5:98871369 | C | CAAAAAAA others(7): Show |
1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3862-580_3862-567d others(16): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | |||||||
chr5:98871369 | CA | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0090 others(91): Show |
98 | HG00423.hp1 HG00621.hp2 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.3862-567delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | |||||||
chr5:98871369 | CAA | C | 15 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0006g0059 others(12): Show |
16 | HG00323.hp1 HG01243.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.3862-568_3862-567d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | |||||||
chr5:98871369 | CAAAAAAA others(3): Show |
C | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.3862-576_3862-567d others(12): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | |||||||
chr5:98871369 | CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0010g0122 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3862-577_3862-567d others(13): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | |||||||
chr5:98871369 | CAAAAAAA others(5): Show |
C | 32 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(29): Show |
36 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.3862-578_3862-567d others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | |||||||
chr5:98871369 | CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0221 |
2 | NA18946.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3862-580_3862-567d others(16): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | |||||||
chr5:98871369 | CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3862-581_3862-567d others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | |||||||
chr5:98871369 | CAAAAAAA others(9): Show |
C | 1 | a0001c0003t0028g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3862-582_3862-567d others(18): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | |||||||
chr5:98871572 | G | A | 9 | a0002c0002t0002g0005 a0002c0002t0002g0106 a0002c0002t0002g0107 others(6): Show |
10 | NA18944.hp1 NA18946.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.3861+479C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871572 | |||||||
chr5:98871801 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3861+250A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871801 | |||||||
chr5:98871839 | A | G | 2 | a0001c0005t0001g0048 a0001c0005t0022g0049 |
2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3861+212T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871839 | |||||||
chr5:98872696 | T | C | 49 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0096 others(46): Show |
49 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.3572-141A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98872696 | |||||||
chr5:98872725 | A | T | 220 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(217): Show |
231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.3572-170T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98872725 | |||||||
chr5:98872860 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3572-305G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98872860 | |||||||
chr5:98872874 | G | A | 1 | a0001c0003t0002g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3572-319C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98872874 | |||||||
chr5:98872981 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3572-426G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98872981 | |||||||
chr5:98873054 | C | T | 1 | a0002c0002t0005g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3572-499G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98873054 | |||||||
chr5:98873057 | G | T | 2 | a0001c0003t0013g0013 a0001c0003t0013g0295 |
3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3572-502C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98873057 | |||||||
chr5:98873072 | C | G | 1 | a0001c0008t0001g0270 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3572-517G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98873072 | |||||||
chr5:98873293 | CTGTG | C | 2 | a0001c0001t0001g0184 a0001c0003t0002g0011 |
3 | HG00741.hp1 NA18978.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3571+296_3571+299d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98873293 | |||||||
chr5:98873419 | C | T | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.3571+174G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98873419 | |||||||
chr5:98874091 | G | GATA | 219 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(216): Show |
230 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.3441-371_3441-369d others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874091 | |||||||
chr5:98874092 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3441-369T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874092 | |||||||
chr5:98874096 | G | A | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3441-373C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874096 | |||||||
chr5:98874097 | A | T | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3441-374T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874097 | |||||||
chr5:98874102 | T | A | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3441-379A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874102 | |||||||
chr5:98874183 | C | G | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3441-460G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874183 | |||||||
chr5:98874249 | G | A | 1 | a0002c0002t0018g0018 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3441-526C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874249 | |||||||
chr5:98874323 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3441-600A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874323 | |||||||
chr5:98874396 | A | T | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3441-673T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874396 | |||||||
chr5:98874525 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3440+547G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874525 | |||||||
chr5:98874537 | T | TA | 11 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0190 others(8): Show |
11 | HG00621.hp1 HG00621.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.3440+534dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874537 | |||||||
chr5:98874537 | TA | T | 183 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(180): Show |
193 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.3440+534delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874537 | |||||||
chr5:98874585 | G | C | 1 | a0001c0003t0012g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3440+487C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874585 | |||||||
chr5:98874643 | T | C | 100 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(97): Show |
108 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.3440+429A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874643 | |||||||
chr5:98874692 | A | G | 1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3440+380T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874692 | |||||||
chr5:98874716 | G | GA | 9 | a0001c0003t0006g0058 a0001c0003t0006g0059 a0001c0003t0006g0060 others(6): Show |
9 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3440+355dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874716 | |||||||
chr5:98874953 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3440+119C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874953 | |||||||
chr5:98874986 | A | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(115): Show |
121 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.3440+86T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874986 | |||||||
chr5:98875164 | T | A | 100 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(97): Show |
108 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.3399-51A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98875164 | |||||||
chr5:98875361 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3399-248T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98875361 | |||||||
chr5:98875501 | A | G | 100 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(97): Show |
108 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.3399-388T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98875501 | |||||||
chr5:98875635 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0216 |
2 | HG01346.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3399-522C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98875635 | |||||||
chr5:98875934 | A | G | 1 | a0002c0002t0002g0106 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3398+464T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98875934 | |||||||
chr5:98876011 | C | T | 1 | a0002c0002t0002g0120 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3398+387G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98876011 | |||||||
chr5:98876036 | C | T | 1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3398+362G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98876036 | |||||||
chr5:98876155 | T | TA | 7 | a0001c0003t0006g0058 a0001c0003t0006g0061 a0001c0003t0006g0067 others(4): Show |
7 | HG01109.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3398+242dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98876155 | |||||||
chr5:98876186 | C | T | 13 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(10): Show |
13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.3398+212G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98876186 | |||||||
chr5:98876227 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3398+171A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98876227 | |||||||
chr5:98876329 | G | A | 14 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00738.hp1 HG01192.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.3398+69C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98876329 | |||||||
chr5:98876690 | T | A | 1 | a0001c0001t0030g0319 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3238-132A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876690 | |||||||
chr5:98876811 | C | A | 8 | a0002c0002t0002g0001 a0002c0002t0002g0112 a0002c0002t0002g0113 others(5): Show |
10 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.3238-253G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876811 | |||||||
chr5:98876825 | A | C | 1 | a0001c0001t0001g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3238-267T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876825 | |||||||
chr5:98876826 | G | T | 1 | a0001c0001t0001g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3238-268C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876826 | |||||||
chr5:98876831 | G | T | 1 | a0001c0001t0001g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3238-273C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876831 | |||||||
chr5:98876840 | A | T | 1 | a0001c0001t0001g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3238-282T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876840 | |||||||
chr5:98876847 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3238-289A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876847 | |||||||
chr5:98876867 | C | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(65): Show |
71 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.3238-309G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876867 | |||||||
chr5:98876932 | G | A | 1 | a0001c0003t0009g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3238-374C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876932 | |||||||
chr5:98877269 | A | C | 4 | a0001c0001t0001g0175 a0001c0001t0001g0201 a0001c0001t0001g0212 others(1): Show |
4 | HG01167.hp1 HG01168.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.3238-711T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98877269 | |||||||
chr5:98877374 | G | T | 13 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(10): Show |
13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.3238-816C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98877374 | |||||||
chr5:98877441 | C | T | 3 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | NA18947.hp1 NA18991.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.3238-883G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98877441 | |||||||
chr5:98877623 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0276 |
2 | HG04199.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.3238-1065C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98877623 | |||||||
chr5:98877655 | A | G | 4 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0198 others(1): Show |
4 | HG01496.hp2 HG02572.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3238-1097T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98877655 | |||||||
chr5:98877944 | C | T | 1 | a0001c0003t0006g0072 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3238-1386G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98877944 | |||||||
chr5:98877959 | C | T | 3 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0198 |
3 | HG02572.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3238-1401G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98877959 | |||||||
chr5:98878287 | T | C | 34 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(31): Show |
35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.3237+1265A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878287 | |||||||
chr5:98878301 | C | T | 220 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(217): Show |
231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.3237+1251G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878301 | |||||||
chr5:98878416 | C | G | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | NA18948.hp1 NA18987.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.3237+1136G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878416 | |||||||
chr5:98878428 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3237+1124G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878428 | |||||||
chr5:98878449 | A | C | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3237+1103T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878449 | |||||||
chr5:98878449 | A | T | 3 | a0001c0003t0002g0054 a0001c0003t0002g0055 a0001c0003t0002g0056 |
3 | HG02896.hp2 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3237+1103T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878449 | |||||||
chr5:98878469 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3237+1083A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878469 | |||||||
chr5:98878483 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3237+1069G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878483 | |||||||
chr5:98878556 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3237+996C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878556 | |||||||
chr5:98878734 | C | T | 2 | a0001c0005t0001g0048 a0001c0005t0022g0049 |
2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3237+818G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878734 | |||||||
chr5:98878801 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3237+751A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878801 | |||||||
chr5:98878886 | G | A | 1 | a0002c0002t0002g0120 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3237+666C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878886 | |||||||
chr5:98878969 | G | A | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3237+583C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878969 | |||||||
chr5:98879343 | A | C | 13 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(10): Show |
13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.3237+209T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98879343 | |||||||
chr5:98879523 | T | C | 2 | a0001c0005t0001g0048 a0001c0005t0022g0049 |
2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3237+29A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98879523 | |||||||
chr5:98879765 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3061-37C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98879765 | |||||||
chr5:98879780 | A | G | 1 | a0001c0001t0003g0306 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3061-52T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98879780 | |||||||
chr5:98879813 | T | C | 2 | a0001c0001t0001g0217 a0001c0001t0029g0318 |
2 | NA18991.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.3061-85A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98879813 | |||||||
chr5:98879915 | T | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0132 |
3 | HG00738.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3061-187A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98879915 | |||||||
chr5:98880004 | C | T | 31 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(28): Show |
35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.3061-276G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98880004 | |||||||
chr5:98880052 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3061-324G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98880052 | |||||||
chr5:98880149 | G | A | 1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3061-421C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98880149 | |||||||
chr5:98880224 | T | C | 3 | a0001c0001t0001g0242 a0001c0001t0001g0244 a0003c0010t0001g0251 |
3 | HG01081.hp1 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.3061-496A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98880224 | |||||||
chr5:98880313 | T | C | 5 | a0001c0003t0012g0293 a0001c0003t0012g0294 a0001c0003t0012g0296 others(2): Show |
6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3061-585A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98880313 | |||||||
chr5:98880827 | C | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG01256.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3060+249G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98880827 | |||||||
chr5:98881252 | C | CT | 22 | a0001c0001t0001g0209 a0001c0001t0001g0219 a0001c0001t0001g0273 others(19): Show |
22 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.2964+26dupA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 21/35 | chr5 | 98881252 | |||||||
chr5:98881252 | CT | C | 20 | a0001c0001t0001g0179 a0001c0001t0001g0218 a0001c0001t0001g0222 others(17): Show |
21 | HG01070.hp2 HG01169.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.2964+26delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 21/35 | chr5 | 98881252 | |||||||
chr5:98881252 | CTTTTTTT | C | 9 | a0001c0003t0006g0058 a0001c0003t0006g0059 a0001c0003t0006g0060 others(6): Show |
9 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2964+20_2964+26del others(7): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 21/35 | chr5 | 98881252 | |||||||
chr5:98881276 | T | A | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
splice_region_variant&intron_variant | LOW | c.2964+3A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 21/35 | chr5 | 98881276 | |||||||
chr5:98881411 | A | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0221 |
2 | NA18946.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2868-36T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881411 | |||||||
chr5:98881411 | A | T | 1 | a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2868-36T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881411 | |||||||
chr5:98881499 | A | C | 1 | a0001c0001t0003g0307 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2868-124T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881499 | |||||||
chr5:98881510 | T | A | 1 | a0001c0004t0001g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2868-135A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881510 | |||||||
chr5:98881512 | CT | C | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.2868-138delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881512 | |||||||
chr5:98881513 | T | C | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.2868-138A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881513 | |||||||
chr5:98881579 | A | G | 1 | a0002c0002t0016g0007 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2868-204T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881579 | |||||||
chr5:98881626 | C | T | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2868-251G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881626 | |||||||
chr5:98882137 | CAT | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0132 |
3 | HG00738.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2719-16_2719-15del others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882137 | |||||||
chr5:98882237 | T | C | 1 | a0001c0001t0004g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2719-114A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882237 | |||||||
chr5:98882341 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2719-218C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882341 | |||||||
chr5:98882418 | TG | T | 65 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0230 others(62): Show |
69 | HG00323.hp1 HG00741.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.2719-296delC | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882418 | |||||||
chr5:98882460 | G | C | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2719-337C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882460 | |||||||
chr5:98882503 | T | C | 1 | a0001c0003t0006g0072 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2719-380A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882503 | |||||||
chr5:98882782 | A | C | 8 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG00738.hp1 HG01192.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2718+306T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882782 | |||||||
chr5:98882793 | G | A | 1 | a0002c0002t0005g0020 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2718+295C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882793 | |||||||
chr5:98882961 | C | G | 1 | a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2718+127G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882961 | |||||||
chr5:98883386 | T | C | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.2569-149A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883386 | |||||||
chr5:98883468 | T | C | 1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2569-231A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883468 | |||||||
chr5:98883498 | A | C | 1 | a0001c0001t0003g0307 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2569-261T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883498 | |||||||
chr5:98883600 | A | G | 4 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG02071.hp1 HG02080.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.2569-363T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883600 | |||||||
chr5:98883629 | G | T | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2569-392C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883629 | |||||||
chr5:98883824 | TAA | T | 3 | a0001c0001t0001g0211 a0001c0001t0001g0227 a0001c0001t0019g0019 |
3 | HG00408.hp1 HG00408.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.2569-589_2569-588d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883824 | |||||||
chr5:98883826 | A | AATAT | 3 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0001t0003g0307 |
3 | HG01515.hp2 HG01517.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2569-593_2569-590d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | |||||||
chr5:98883826 | A | AATATAT | 3 | a0001c0001t0001g0171 a0001c0001t0001g0274 a0001c0008t0001g0270 |
3 | HG02970.hp1 NA18956.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2569-595_2569-590d others(8): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | |||||||
chr5:98883826 | A | AATATATA others(7): Show |
1 | a0001c0001t0026g0249 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2569-603_2569-590d others(16): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | |||||||
chr5:98883826 | A | AATATATA others(9): Show |
2 | a0001c0001t0001g0173 a0001c0003t0002g0011 |
2 | NA18973.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2569-605_2569-590d others(18): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | |||||||
chr5:98883826 | AAT | A | 9 | a0001c0001t0001g0050 a0001c0001t0001g0077 a0001c0001t0001g0223 others(6): Show |
9 | HG01243.hp2 HG01928.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.2569-591_2569-590d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | |||||||
chr5:98883826 | AATAT | A | 8 | a0001c0001t0001g0167 a0001c0001t0001g0172 a0001c0001t0001g0177 others(5): Show |
8 | HG02027.hp1 HG02523.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.2569-593_2569-590d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | |||||||
chr5:98883826 | AATATATA others(3): Show |
A | 5 | a0001c0003t0006g0058 a0001c0003t0006g0061 a0001c0003t0006g0067 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2569-599_2569-590d others(12): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | |||||||
chr5:98883826 | AATATATA others(5): Show |
A | 9 | a0001c0003t0002g0004 a0001c0003t0002g0062 a0001c0003t0002g0063 others(6): Show |
10 | HG01891.hp2 HG02886.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2569-601_2569-590d others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | |||||||
chr5:98883826 | AATATATA others(7): Show |
A | 2 | a0001c0003t0002g0054 a0001c0003t0009g0224 |
2 | HG02922.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2569-603_2569-590d others(16): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | |||||||
chr5:98883826 | AATATATA others(11): Show |
A | 1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2569-607_2569-590d others(20): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | |||||||
chr5:98883826 | AATATATA others(13): Show |
A | 1 | a0002c0002t0011g0082 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2569-609_2569-590d others(22): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | |||||||
chr5:98883842 | TATATATA others(12): Show |
T | 15 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(12): Show |
16 | HG00642.hp1 HG01243.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.2569-624_2569-606d others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883842 | |||||||
chr5:98883843 | ATATATAT others(12): Show |
A | 28 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(25): Show |
30 | HG00741.hp2 HG01069.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2569-625_2569-607d others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883843 | |||||||
chr5:98883843 | ATATATAT others(13): Show |
A | 2 | a0002c0002t0002g0109 a0002c0002t0002g0128 |
2 | HG01168.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.2569-626_2569-607d others(22): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883843 | |||||||
chr5:98883844 | TATATATA others(8): Show |
T | 1 | a0001c0003t0009g0193 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2569-622_2569-608d others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883844 | |||||||
chr5:98883844 | TATATATA others(10): Show |
T | 1 | a0002c0002t0002g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2569-624_2569-608d others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883844 | |||||||
chr5:98883845 | ATATATAT others(10): Show |
A | 1 | a0002c0002t0016g0007 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2569-625_2569-609d others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883845 | |||||||
chr5:98883845 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0221 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2569-627_2569-609d others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883845 | |||||||
chr5:98883847 | ATATATAT others(8): Show |
A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0170 |
2 | HG01255.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2569-625_2569-611d others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883847 | |||||||
chr5:98883847 | ATATATAT others(9): Show |
A | 2 | a0001c0003t0002g0055 a0001c0003t0002g0056 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2569-626_2569-611d others(18): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883847 | |||||||
chr5:98883847 | ATATATAT others(11): Show |
A | 5 | a0001c0003t0012g0293 a0001c0003t0012g0294 a0002c0002t0002g0001 others(2): Show |
5 | HG00735.hp1 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2569-628_2569-611d others(20): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883847 | |||||||
chr5:98883849 | ATATATAT others(6): Show |
A | 1 | a0001c0003t0006g0072 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2569-625_2569-613d others(15): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883849 | |||||||
chr5:98883849 | ATATATAT others(8): Show |
A | 2 | a0002c0002t0002g0198 a0002c0002t0005g0027 |
2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2569-627_2569-613d others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883849 | |||||||
chr5:98883849 | ATATATAT others(10): Show |
A | 1 | a0002c0002t0025g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2569-629_2569-613d others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883849 | |||||||
chr5:98883849 | ATATATAT others(11): Show |
A | 1 | a0001c0003t0012g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2569-630_2569-613d others(20): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883849 | |||||||
chr5:98883849 | ATATATAT others(12): Show |
A | 2 | a0001c0003t0013g0013 a0001c0003t0013g0295 |
3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2569-631_2569-613d others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883849 | |||||||
chr5:98883850 | TATATATA others(4): Show |
T | 1 | a0001c0003t0006g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2569-624_2569-614d others(13): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883850 | |||||||
chr5:98883851 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0004g0039 a0001c0003t0006g0060 |
2 | HG00544.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2569-625_2569-615d others(13): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883851 | |||||||
chr5:98883851 | ATATATAT others(5): Show |
A | 3 | a0001c0001t0001g0164 a0002c0002t0005g0025 a0002c0002t0005g0026 |
3 | HG02630.hp1 HG02818.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.2569-626_2569-615d others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883851 | |||||||
chr5:98883851 | ATATATAT others(7): Show |
A | 8 | a0002c0002t0005g0021 a0002c0002t0005g0024 a0002c0002t0005g0028 others(5): Show |
8 | HG02258.hp2 HG03098.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.2569-628_2569-615d others(16): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883851 | |||||||
chr5:98883853 | ATATATAT others(5): Show |
A | 2 | a0002c0002t0005g0020 a0002c0002t0005g0022 |
2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2569-628_2569-617d others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883853 | |||||||
chr5:98883855 | ATATATAT others(5): Show |
A | 1 | a0002c0002t0007g0017 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2569-630_2569-619d others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883855 | |||||||
chr5:98883856 | TATATA | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG01099.hp2 HG02074.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2569-624_2569-620d others(7): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883856 | |||||||
chr5:98883857 | ATATAT | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0053 a0001c0001t0001g0143 others(35): Show |
40 | HG00423.hp1 HG00621.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.2569-625_2569-621d others(7): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883857 | |||||||
chr5:98883857 | ATATATT | A | 7 | a0001c0001t0001g0052 a0001c0001t0001g0126 a0001c0001t0001g0148 others(4): Show |
7 | HG01516.hp1 NA18957.hp2 NA19058.hp1 others(4): Show |
intron_variant | MODIFIER | c.2569-626_2569-621d others(8): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883857 | |||||||
chr5:98883858 | TATA | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0076 a0001c0001t0001g0201 others(7): Show |
10 | HG00438.hp1 HG01099.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2569-624_2569-622d others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883858 | |||||||
chr5:98883859 | A | T | 2 | a0001c0001t0029g0318 a0001c0003t0009g0224 |
2 | HG03492.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.2569-622T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883859 | |||||||
chr5:98883859 | ATAT | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(35): Show |
40 | HG00423.hp2 HG00642.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.2569-625_2569-623d others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883859 | |||||||
chr5:98883859 | ATATT | A | 6 | a0001c0001t0001g0154 a0001c0001t0001g0169 a0001c0001t0001g0209 others(3): Show |
6 | HG00438.hp2 HG00544.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.2569-626_2569-623d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883859 | |||||||
chr5:98883859 | ATATTT | A | 7 | a0001c0001t0001g0096 a0001c0001t0001g0156 a0001c0001t0001g0175 others(4): Show |
7 | HG01167.hp1 HG02109.hp2 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.2569-627_2569-623d others(7): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883859 | |||||||
chr5:98883861 | A | ATATATAT others(14): Show |
1 | a0001c0003t0002g0011 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2569-625_2569-624i others(23): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883861 | |||||||
chr5:98883861 | A | T | 18 | a0001c0001t0001g0181 a0001c0001t0001g0206 a0001c0001t0001g0223 others(15): Show |
18 | HG01109.hp1 HG01358.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2569-624T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883861 | |||||||
chr5:98883861 | AT | A | 15 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0132 others(12): Show |
15 | HG00738.hp1 HG01070.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.2569-625delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883861 | |||||||
chr5:98883861 | ATT | A | 8 | a0001c0001t0001g0166 a0001c0001t0001g0242 a0001c0001t0001g0264 others(5): Show |
8 | HG01255.hp1 HG01516.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.2569-626_2569-625d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883861 | |||||||
chr5:98883861 | ATTT | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0073 a0001c0001t0001g0090 others(9): Show |
12 | HG00323.hp2 HG01192.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2569-627_2569-625d others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883861 | |||||||
chr5:98883862 | T | TA | 9 | a0001c0001t0001g0149 a0001c0001t0001g0174 a0001c0001t0001g0204 others(6): Show |
9 | HG00621.hp2 HG01517.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.2569-626_2569-625i others(3): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883862 | |||||||
chr5:98883862 | T | TATATATA others(6): Show |
1 | a0001c0001t0001g0246 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2569-626_2569-625i others(15): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883862 | |||||||
chr5:98883862 | T | TATATATA others(8): Show |
1 | a0001c0001t0001g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2569-626_2569-625i others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883862 | |||||||
chr5:98883863 | T | A | 18 | a0001c0001t0001g0074 a0001c0001t0001g0171 a0001c0001t0001g0173 others(15): Show |
18 | HG01515.hp2 HG01517.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2569-626A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883863 | |||||||
chr5:98883864 | T | A | 12 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0132 others(9): Show |
12 | HG00738.hp1 HG01517.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2569-627A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883864 | |||||||
chr5:98883865 | T | A | 9 | a0001c0001t0001g0074 a0001c0001t0003g0297 a0001c0001t0003g0298 others(6): Show |
9 | HG01255.hp1 HG01515.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2569-628A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883865 | |||||||
chr5:98883866 | T | A | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0131 others(4): Show |
7 | HG00323.hp2 HG01192.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.2569-629A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883866 | |||||||
chr5:98883867 | T | A | 4 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0001t0003g0299 others(1): Show |
4 | HG01255.hp1 HG01515.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2569-630A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883867 | |||||||
chr5:98883868 | T | A | 2 | a0001c0001t0001g0149 a0001c0003t0009g0194 |
2 | HG00323.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2569-631A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883868 | |||||||
chr5:98883870 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2569-633A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883870 | |||||||
chr5:98883926 | C | CCACCT | 95 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(92): Show |
103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.2569-694_2569-690d others(7): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883926 | |||||||
chr5:98884078 | G | GT | 20 | a0001c0001t0001g0159 a0001c0001t0001g0204 a0001c0001t0004g0040 others(17): Show |
20 | HG00438.hp1 HG01496.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.2569-842dupA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884078 | |||||||
chr5:98884097 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2569-860C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884097 | |||||||
chr5:98884142 | C | T | 67 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0078 others(64): Show |
72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.2569-905G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884142 | |||||||
chr5:98884328 | C | A | 1 | a0001c0001t0001g0231 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2569-1091G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884328 | |||||||
chr5:98884509 | G | GA | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.2568+1068dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884509 | |||||||
chr5:98884520 | A | AG | 5 | a0001c0001t0001g0152 a0001c0001t0001g0269 a0001c0003t0013g0295 others(2): Show |
5 | HG01099.hp1 HG01496.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2568+1057dupC | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884520 | |||||||
chr5:98884550 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2568+1028C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884550 | |||||||
chr5:98884785 | T | C | 4 | a0001c0001t0001g0143 a0001c0001t0001g0172 a0001c0001t0001g0183 others(1): Show |
4 | NA18953.hp1 NA18974.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2568+793A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884785 | |||||||
chr5:98884792 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2568+786G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884792 | |||||||
chr5:98884861 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(64): Show |
70 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.2568+717C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884861 | |||||||
chr5:98884927 | T | A | 1 | a0001c0001t0027g0142 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2568+651A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884927 | |||||||
chr5:98885196 | G | A | 99 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(96): Show |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.2568+382C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98885196 | |||||||
chr5:98885283 | T | C | 33 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(30): Show |
34 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.2568+295A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98885283 | |||||||
chr5:98885679 | A | AT | 99 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(96): Show |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.2497-31_2497-30ins others(1): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98885679 | |||||||
chr5:98886015 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2497-366A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886015 | |||||||
chr5:98886029 | C | A | 1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2497-380G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886029 | |||||||
chr5:98886077 | G | C | 13 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0266 others(10): Show |
16 | HG00423.hp2 HG02015.hp2 NA18951.hp1 others(13): Show |
intron_variant | MODIFIER | c.2497-428C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886077 | |||||||
chr5:98886117 | C | A | 1 | a0001c0003t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2497-468G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886117 | |||||||
chr5:98886558 | G | A | 8 | a0001c0003t0002g0004 a0001c0003t0002g0062 a0001c0003t0002g0063 others(5): Show |
9 | HG01891.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2497-909C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886558 | |||||||
chr5:98886697 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2497-1048G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886697 | |||||||
chr5:98886896 | A | G | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2496+1192T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886896 | |||||||
chr5:98886939 | G | C | 2 | a0001c0003t0002g0055 a0001c0003t0002g0056 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2496+1149C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886939 | |||||||
chr5:98886957 | TA | T | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(3): Show |
6 | NA18947.hp1 NA18991.hp2 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.2496+1130delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886957 | |||||||
chr5:98887108 | C | T | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.2496+980G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887108 | |||||||
chr5:98887129 | T | A | 2 | a0001c0003t0009g0193 a0001c0003t0009g0224 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2496+959A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887129 | |||||||
chr5:98887199 | C | T | 11 | a0001c0001t0001g0164 a0001c0001t0001g0180 a0001c0001t0001g0187 others(8): Show |
11 | HG00544.hp2 HG01981.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.2496+889G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887199 | |||||||
chr5:98887279 | C | G | 2 | a0002c0002t0007g0014 a0002c0002t0007g0016 |
2 | NA18955.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2496+809G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887279 | |||||||
chr5:98887322 | T | G | 1 | a0001c0003t0012g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2496+766A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887322 | |||||||
chr5:98887427 | T | C | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2496+661A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887427 | |||||||
chr5:98887546 | T | C | 1 | a0002c0002t0007g0015 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2496+542A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887546 | |||||||
chr5:98887602 | A | T | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2496+486T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887602 | |||||||
chr5:98887603 | G | T | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2496+485C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887603 | |||||||
chr5:98887604 | A | T | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2496+484T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887604 | |||||||
chr5:98887766 | G | C | 6 | a0002c0002t0002g0005 a0002c0002t0002g0107 a0002c0002t0002g0108 others(3): Show |
7 | NA18944.hp1 NA18946.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.2496+322C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887766 | |||||||
chr5:98887929 | G | A | 1 | a0002c0002t0005g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2496+159C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887929 | |||||||
chr5:98888297 | C | T | 1 | a0001c0001t0004g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2344-57G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 16/35 | chr5 | 98888297 | |||||||
chr5:98888298 | G | A | 1 | a0002c0002t0002g0119 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2344-58C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 16/35 | chr5 | 98888298 | |||||||
chr5:98888678 | C | T | 5 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0198 others(2): Show |
6 | HG01496.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2343+398G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 16/35 | chr5 | 98888678 | |||||||
chr5:98889010 | C | T | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2343+66G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 16/35 | chr5 | 98889010 | |||||||
chr5:98889271 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2181-33C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98889271 | |||||||
chr5:98889516 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2181-278C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98889516 | |||||||
chr5:98889582 | AT | A | 99 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(96): Show |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.2181-345delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98889582 | |||||||
chr5:98889659 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2181-421T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98889659 | |||||||
chr5:98890053 | G | T | 95 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(92): Show |
103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.2181-815C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890053 | |||||||
chr5:98890062 | A | T | 1 | a0001c0001t0001g0219 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2181-824T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890062 | |||||||
chr5:98890177 | T | C | 1 | a0001c0001t0003g0299 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2181-939A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890177 | |||||||
chr5:98890455 | A | G | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.2181-1217T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890455 | |||||||
chr5:98890733 | T | C | 3 | a0001c0003t0006g0059 a0001c0003t0006g0060 a0001c0003t0006g0068 |
3 | HG02559.hp1 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2181-1495A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890733 | |||||||
chr5:98890762 | T | C | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.2181-1524A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890762 | |||||||
chr5:98890775 | G | C | 1 | a0001c0003t0028g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2181-1537C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890775 | |||||||
chr5:98890859 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2181-1621G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890859 | |||||||
chr5:98890958 | G | A | 3 | a0001c0003t0002g0054 a0001c0003t0002g0055 a0001c0003t0002g0056 |
3 | HG02896.hp2 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2180+1567C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890958 | |||||||
chr5:98891399 | A | G | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2180+1126T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98891399 | |||||||
chr5:98891661 | A | G | 1 | a0001c0003t0006g0067 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2180+864T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98891661 | |||||||
chr5:98891798 | G | C | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2180+727C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98891798 | |||||||
chr5:98891808 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2180+717G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98891808 | |||||||
chr5:98891846 | A | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2180+679T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98891846 | |||||||
chr5:98891932 | T | C | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2180+593A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98891932 | |||||||
chr5:98891982 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2180+543T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98891982 | |||||||
chr5:98892108 | C | T | 1 | a0002c0002t0002g0116 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2180+417G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98892108 | |||||||
chr5:98892164 | C | G | 5 | a0001c0003t0002g0004 a0001c0003t0002g0062 a0001c0003t0002g0063 others(2): Show |
6 | HG01891.hp2 HG02886.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2180+361G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98892164 | |||||||
chr5:98892181 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2180+344C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98892181 | |||||||
chr5:98892837 | T | A | 1 | a0001c0003t0009g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1992-124A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 14/35 | chr5 | 98892837 | |||||||
chr5:98893074 | T | C | 4 | a0001c0001t0001g0126 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | NA19005.hp2 NA19058.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.1991+342A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 14/35 | chr5 | 98893074 | |||||||
chr5:98893235 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1991+181T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 14/35 | chr5 | 98893235 | |||||||
chr5:98893255 | T | C | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.1991+161A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 14/35 | chr5 | 98893255 | |||||||
chr5:98893265 | C | A | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.1991+151G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 14/35 | chr5 | 98893265 | |||||||
chr5:98893285 | T | A | 9 | a0001c0003t0006g0058 a0001c0003t0006g0059 a0001c0003t0006g0060 others(6): Show |
9 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1991+131A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 14/35 | chr5 | 98893285 | |||||||
chr5:98893400 | T | C | 34 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(31): Show |
35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.1991+16A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 14/35 | chr5 | 98893400 | |||||||
chr5:98893645 | G | A | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1801-39C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98893645 | |||||||
chr5:98893682 | A | T | 1 | a0001c0001t0001g0264 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1801-76T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98893682 | |||||||
chr5:98893824 | C | A | 1 | a0001c0001t0004g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1801-218G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98893824 | |||||||
chr5:98893836 | T | C | 2 | a0002c0002t0002g0124 a0002c0002t0002g0125 |
2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1801-230A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98893836 | |||||||
chr5:98893859 | C | T | 1 | a0001c0003t0020g0045 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1801-253G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98893859 | |||||||
chr5:98893911 | A | T | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1801-305T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98893911 | |||||||
chr5:98893926 | C | T | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1801-320G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98893926 | |||||||
chr5:98894010 | C | T | 20 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0198 others(17): Show |
21 | HG01496.hp2 HG02055.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1801-404G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98894010 | |||||||
chr5:98894116 | C | CT | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | NA18948.hp1 NA18987.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1800+480dupA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98894116 | |||||||
chr5:98894313 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1800+284G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98894313 | |||||||
chr5:98894473 | A | G | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1800+124T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98894473 | |||||||
chr5:98894517 | T | C | 50 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0096 others(47): Show |
50 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1800+80A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98894517 | |||||||
chr5:98894567 | G | C | 1 | a0002c0002t0007g0017 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1800+30C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98894567 | |||||||
chr5:98894752 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1711-66T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98894752 | |||||||
chr5:98894826 | G | T | 1 | a0001c0001t0003g0308 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1711-140C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98894826 | |||||||
chr5:98894844 | A | T | 1 | a0001c0003t0028g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1711-158T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98894844 | |||||||
chr5:98894914 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1711-228G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98894914 | |||||||
chr5:98895010 | A | T | 1 | a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1711-324T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895010 | |||||||
chr5:98895026 | G | C | 1 | a0001c0001t0001g0189 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1711-340C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895026 | |||||||
chr5:98895262 | TAA | T | 28 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(25): Show |
31 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1711-578_1711-577d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895262 | |||||||
chr5:98895291 | G | C | 1 | a0002c0002t0005g0020 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1711-605C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895291 | |||||||
chr5:98895450 | T | G | 1 | a0001c0001t0004g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1711-764A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895450 | |||||||
chr5:98895523 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1710+703G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895523 | |||||||
chr5:98895745 | C | CA | 14 | a0001c0001t0001g0245 a0001c0001t0001g0265 a0001c0001t0001g0276 others(11): Show |
14 | HG00323.hp2 HG01109.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1710+480dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895745 | |||||||
chr5:98895745 | CA | C | 8 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0250 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1710+480delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895745 | |||||||
chr5:98895759 | C | A | 8 | a0002c0002t0002g0079 a0002c0002t0002g0080 a0002c0002t0002g0081 others(5): Show |
8 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1710+467G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895759 | |||||||
chr5:98896006 | C | T | 3 | a0001c0001t0001g0235 a0001c0001t0001g0247 a0001c0001t0001g0265 |
3 | NA19011.hp1 NA19075.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1710+220G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98896006 | |||||||
chr5:98896073 | C | T | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1710+153G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98896073 | |||||||
chr5:98896111 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1710+115A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98896111 | |||||||
chr5:98896451 | T | A | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1494-9A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896451 | |||||||
chr5:98896540 | A | T | 3 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0198 |
3 | HG02572.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1494-98T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896540 | |||||||
chr5:98896569 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1494-127G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896569 | |||||||
chr5:98896595 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1494-153A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896595 | |||||||
chr5:98896655 | C | T | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1494-213G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896655 | |||||||
chr5:98896775 | T | C | 1 | a0001c0001t0003g0300 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1494-333A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896775 | |||||||
chr5:98896791 | T | TA | 315 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(312): Show |
330 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.1494-350dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896791 | |||||||
chr5:98896850 | T | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(64): Show |
70 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.1493+343A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896850 | |||||||
chr5:98897020 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1493+173C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98897020 | |||||||
chr5:98897069 | A | G | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | HG02818.hp2 HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1493+124T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98897069 | |||||||
chr5:98897105 | T | C | 101 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0003t0002g0004 others(98): Show |
109 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.1493+88A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98897105 | |||||||
chr5:98897364 | A | G | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1366-44T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 10/35 | chr5 | 98897364 | |||||||
chr5:98897435 | T | A | 2 | a0001c0003t0009g0193 a0001c0003t0009g0224 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1366-115A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 10/35 | chr5 | 98897435 | |||||||
chr5:98898019 | T | C | 21 | a0001c0001t0008g0044 a0002c0002t0002g0134 a0002c0002t0002g0135 others(18): Show |
22 | HG01496.hp2 HG02055.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1365+237A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 10/35 | chr5 | 98898019 | |||||||
chr5:98898023 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1365+233G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 10/35 | chr5 | 98898023 | |||||||
chr5:98898047 | T | TAA | 99 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(96): Show |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.1365+207_1365+208d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 10/35 | chr5 | 98898047 | |||||||
chr5:98898215 | A | G | 10 | a0001c0001t0001g0164 a0001c0001t0001g0180 a0001c0001t0001g0187 others(7): Show |
10 | HG00544.hp2 HG01981.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1365+41T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 10/35 | chr5 | 98898215 | |||||||
chr5:98898228 | A | G | 9 | a0001c0003t0006g0058 a0001c0003t0006g0059 a0001c0003t0006g0060 others(6): Show |
9 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1365+28T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 10/35 | chr5 | 98898228 | |||||||
chr5:98898556 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1186+108A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 9/35 | chr5 | 98898556 | |||||||
chr5:98899097 | C | G | 1 | a0001c0001t0001g0266 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1086-333G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 8/35 | chr5 | 98899097 | |||||||
chr5:98899228 | C | T | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085+252G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 8/35 | chr5 | 98899228 | |||||||
chr5:98899309 | G | T | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085+171C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 8/35 | chr5 | 98899309 | |||||||
chr5:98899397 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1085+83A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 8/35 | chr5 | 98899397 | |||||||
chr5:98899751 | T | C | 2 | a0002c0002t0017g0139 a0002c0002t0017g0226 |
2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.860-46A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98899751 | |||||||
chr5:98899879 | G | A | 2 | a0002c0002t0002g0287 a0002c0002t0005g0027 |
2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.860-174C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98899879 | |||||||
chr5:98899909 | G | A | 1 | a0002c0002t0002g0117 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.860-204C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98899909 | |||||||
chr5:98900007 | G | A | 1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.860-302C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900007 | |||||||
chr5:98900192 | G | A | 4 | a0001c0004t0001g0092 a0001c0004t0001g0093 a0001c0004t0001g0094 others(1): Show |
4 | HG03041.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-487C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900192 | |||||||
chr5:98900259 | A | G | 99 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(96): Show |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.859+552T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900259 | |||||||
chr5:98900281 | CA | C | 93 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(90): Show |
100 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.859+529delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900281 | |||||||
chr5:98900441 | CT | C | 15 | a0001c0001t0001g0101 a0001c0001t0003g0312 a0002c0002t0005g0020 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.859+369delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900441 | |||||||
chr5:98900471 | G | A | 2 | a0002c0002t0002g0124 a0002c0002t0002g0125 |
2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.859+340C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900471 | |||||||
chr5:98900586 | C | T | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.859+225G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900586 | |||||||
chr5:98900697 | C | T | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.859+114G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900697 | |||||||
chr5:98900703 | C | T | 6 | a0001c0001t0001g0095 a0001c0001t0001g0103 a0001c0001t0001g0233 others(3): Show |
6 | HG00642.hp2 HG01070.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.859+108G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900703 | |||||||
chr5:98900705 | G | GC | 13 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(10): Show |
13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.859+105dupG | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900705 | |||||||
chr5:98900708 | C | A | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.859+103G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900708 | |||||||
chr5:98901127 | T | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(65): Show |
71 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.588-45A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 6/35 | chr5 | 98901127 | |||||||
chr5:98901479 | A | G | 2 | a0001c0001t0001g0241 a0001c0001t0001g0276 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.438-144T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901479 | |||||||
chr5:98901551 | A | G | 1 | a0001c0001t0030g0319 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.438-216T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901551 | |||||||
chr5:98901654 | T | C | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.438-319A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901654 | |||||||
chr5:98901694 | C | A | 1 | a0002c0002t0005g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.438-359G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901694 | |||||||
chr5:98901749 | T | TA | 71 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0003t0009g0193 others(68): Show |
76 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.438-415dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901749 | |||||||
chr5:98901749 | TA | T | 19 | a0001c0001t0001g0197 a0001c0001t0001g0273 a0001c0003t0002g0054 others(16): Show |
20 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.438-415delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901749 | |||||||
chr5:98901780 | A | G | 1 | a0002c0002t0002g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.438-445T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901780 | |||||||
chr5:98901884 | T | C | 1 | a0001c0003t0009g0194 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.438-549A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901884 | |||||||
chr5:98901898 | G | T | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.438-563C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901898 | |||||||
chr5:98902104 | C | T | 1 | a0001c0004t0001g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.438-769G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98902104 | |||||||
chr5:98902372 | A | C | 12 | a0001c0003t0002g0054 a0001c0003t0002g0055 a0001c0003t0002g0056 others(9): Show |
12 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.437+528T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98902372 | |||||||
chr5:98902430 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG00738.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.437+470C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98902430 | |||||||
chr5:98902499 | C | A | 4 | a0002c0002t0002g0079 a0002c0002t0002g0081 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02965.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+401G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98902499 | |||||||
chr5:98902672 | G | T | 5 | a0001c0003t0012g0293 a0001c0003t0012g0294 a0001c0003t0012g0296 others(2): Show |
6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.437+228C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98902672 | |||||||
chr5:98902979 | T | G | 1 | a0001c0001t0001g0162 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.373-15A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98902979 | |||||||
chr5:98902989 | A | T | 1 | a0002c0002t0017g0226 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.373-25T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98902989 | |||||||
chr5:98903136 | T | C | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.373-172A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903136 | |||||||
chr5:98903225 | A | T | 18 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0001t0003g0299 others(15): Show |
18 | HG00621.hp2 HG01515.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.373-261T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903225 | |||||||
chr5:98903308 | TTGTTA | T | 5 | a0002c0002t0007g0014 a0002c0002t0007g0015 a0002c0002t0007g0016 others(2): Show |
5 | HG04199.hp1 NA18947.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-349_373-345del others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903308 | |||||||
chr5:98903325 | G | A | 2 | a0001c0003t0013g0013 a0001c0003t0013g0295 |
3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.373-361C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903325 | |||||||
chr5:98903438 | TTTCGTAC others(27): Show |
T | 14 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00738.hp1 HG01192.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.372+320_372+353del others(34): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903438 | |||||||
chr5:98903442 | G | A | 1 | a0001c0005t0001g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.372+350C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903442 | |||||||
chr5:98903566 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.372+226C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903566 | |||||||
chr5:98903686 | C | T | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+106G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903686 | |||||||
chr5:98904096 | A | G | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.256-188T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904096 | |||||||
chr5:98904190 | G | A | 2 | a0002c0002t0002g0121 a0002c0002t0002g0141 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.256-282C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904190 | |||||||
chr5:98904318 | T | G | 95 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(92): Show |
103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.256-410A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904318 | |||||||
chr5:98904348 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.256-440T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904348 | |||||||
chr5:98904387 | C | A | 34 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(31): Show |
35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.256-479G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904387 | |||||||
chr5:98904460 | C | G | 6 | a0001c0001t0003g0306 a0001c0001t0003g0308 a0001c0001t0003g0309 others(3): Show |
6 | HG00621.hp2 HG02027.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+437G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904460 | |||||||
chr5:98904579 | T | C | 1 | a0001c0001t0019g0019 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.255+318A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904579 | |||||||
chr5:98904769 | A | G | 1 | a0002c0002t0017g0226 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.255+128T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904769 | |||||||
chr5:98905343 | A | G | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-245T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98905343 | |||||||
chr5:98905361 | A | G | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.54-263T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98905361 | |||||||
chr5:98905524 | TA | T | 67 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0078 others(64): Show |
72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.54-427delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98905524 | |||||||
chr5:98905733 | T | C | 1 | a0002c0002t0002g0113 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.54-635A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98905733 | |||||||
chr5:98905785 | G | A | 95 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(92): Show |
103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.54-687C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98905785 | |||||||
chr5:98906014 | A | G | 17 | a0001c0003t0002g0054 a0001c0003t0002g0055 a0001c0003t0002g0056 others(14): Show |
18 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.54-916T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98906014 | |||||||
chr5:98906045 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0132 |
3 | HG00738.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.54-947G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98906045 | |||||||
chr5:98906095 | CTT | C | 13 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(10): Show |
13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-999_54-998delAA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98906095 | |||||||
chr5:98906478 | G | A | 5 | a0001c0003t0012g0293 a0001c0003t0012g0294 a0001c0003t0012g0296 others(2): Show |
6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.54-1380C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98906478 | |||||||
chr5:98906499 | T | C | 99 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(96): Show |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.54-1401A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98906499 | |||||||
chr5:98907418 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.54-2320C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907418 | |||||||
chr5:98907471 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.54-2373G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907471 | |||||||
chr5:98907531 | T | C | 1 | a0001c0001t0003g0305 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.54-2433A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907531 | |||||||
chr5:98907588 | C | CA | 157 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(154): Show |
167 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.54-2491dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907588 | |||||||
chr5:98907588 | C | CAA | 11 | a0001c0001t0001g0228 a0002c0002t0002g0081 a0002c0002t0002g0104 others(8): Show |
11 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.54-2492_54-2491dup others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907588 | |||||||
chr5:98907663 | T | G | 1 | a0001c0001t0001g0090 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.54-2565A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907663 | |||||||
chr5:98907672 | A | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0006t0001g0075 |
3 | HG02083.hp2 NA18998.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.54-2574T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907672 | |||||||
chr5:98907698 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.54-2600A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907698 | |||||||
chr5:98907707 | C | T | 8 | a0001c0003t0002g0004 a0001c0003t0002g0062 a0001c0003t0002g0063 others(5): Show |
9 | HG01891.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.54-2609G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907707 | |||||||
chr5:98907836 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.54-2738T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907836 | |||||||
chr5:98908115 | T | G | 1 | a0001c0001t0015g0047 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.54-3017A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98908115 | |||||||
chr5:98908136 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.54-3038A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98908136 | |||||||
chr5:98908236 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.54-3138G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98908236 | |||||||
chr5:98908760 | C | T | 3 | a0002c0002t0002g0106 a0002c0002t0002g0119 a0002c0002t0002g0138 |
3 | NA18965.hp2 NA18981.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.54-3662G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98908760 | |||||||
chr5:98908800 | G | GAATA | 220 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(217): Show |
231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.54-3706_54-3703dup others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98908800 | |||||||
chr5:98908883 | T | C | 5 | a0001c0003t0012g0293 a0001c0003t0012g0294 a0001c0003t0012g0296 others(2): Show |
6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.54-3785A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98908883 | |||||||
chr5:98909014 | C | CATGAA | 20 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0198 others(17): Show |
21 | HG01496.hp2 HG02055.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.54-3921_54-3917dup others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909014 | |||||||
chr5:98909054 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.54-3956G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909054 | |||||||
chr5:98909193 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.54-4095C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909193 | |||||||
chr5:98909318 | T | C | 1 | a0001c0001t0003g0307 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.54-4220A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909318 | |||||||
chr5:98909413 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.54-4315A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909413 | |||||||
chr5:98909538 | T | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(65): Show |
71 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.54-4440A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909538 | |||||||
chr5:98909555 | A | G | 1 | a0001c0003t0028g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54-4457T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909555 | |||||||
chr5:98909577 | C | T | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.54-4479G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909577 | |||||||
chr5:98909608 | C | T | 6 | a0001c0003t0006g0058 a0001c0003t0006g0061 a0001c0003t0006g0067 others(3): Show |
6 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.54-4510G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909608 | |||||||
chr5:98909750 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.54-4652A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909750 | |||||||
chr5:98909802 | T | G | 95 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(92): Show |
103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.54-4704A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909802 | |||||||
chr5:98909848 | C | T | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.54-4750G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909848 | |||||||
chr5:98910073 | T | C | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.54-4975A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98910073 | |||||||
chr5:98910129 | G | A | 2 | a0002c0002t0017g0139 a0002c0002t0017g0226 |
2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.54-5031C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98910129 | |||||||
chr5:98910208 | T | C | 13 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(10): Show |
13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-5110A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98910208 | |||||||
chr5:98910462 | G | C | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.54-5364C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98910462 | |||||||
chr5:98910494 | G | T | 1 | a0001c0003t0028g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54-5396C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98910494 | |||||||
chr5:98910858 | C | A | 1 | a0001c0003t0028g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54-5760G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98910858 | |||||||
chr5:98910930 | T | C | 34 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(31): Show |
35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.54-5832A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98910930 | |||||||
chr5:98911130 | G | GA | 16 | a0001c0001t0001g0102 a0001c0001t0001g0132 a0001c0001t0003g0303 others(13): Show |
16 | HG00738.hp1 HG01975.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.54-6033dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911130 | |||||||
chr5:98911130 | G | GAA | 9 | a0002c0002t0002g0112 a0002c0002t0002g0113 a0002c0002t0002g0114 others(6): Show |
9 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.54-6034_54-6033dup others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911130 | |||||||
chr5:98911130 | GA | G | 17 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0097 others(14): Show |
19 | HG00544.hp2 HG00621.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.54-6033delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911130 | |||||||
chr5:98911130 | GAA | G | 42 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0096 others(39): Show |
43 | HG00408.hp1 HG00438.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.54-6034_54-6033del others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911130 | |||||||
chr5:98911142 | A | AATATATA others(11): Show |
1 | a0001c0001t0001g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.54-6045_54-6044ins others(18): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911142 | |||||||
chr5:98911142 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0246 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.54-6045_54-6044ins others(11): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911142 | |||||||
chr5:98911142 | A | ATATATAT others(10): Show |
1 | a0001c0001t0015g0046 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.54-6045_54-6044ins others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911142 | |||||||
chr5:98911142 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0228 a0001c0001t0001g0230 |
2 | HG01192.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.54-6045_54-6044ins others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911142 | |||||||
chr5:98911144 | A | AATATATA others(13): Show |
2 | a0001c0001t0001g0258 a0001c0001t0001g0266 |
2 | HG01070.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.54-6047_54-6046ins others(20): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | |||||||
chr5:98911144 | A | AATATATA others(15): Show |
1 | a0001c0001t0015g0047 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.54-6047_54-6046ins others(22): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | |||||||
chr5:98911144 | A | AT | 3 | a0001c0001t0001g0184 a0001c0001t0001g0269 a0001c0001t0004g0039 |
3 | HG00544.hp1 HG01099.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.54-6047_54-6046ins others(1): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | |||||||
chr5:98911144 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0261 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.54-6047_54-6046ins others(26): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | |||||||
chr5:98911144 | A | ATATATAT others(6): Show |
3 | a0001c0001t0001g0242 a0001c0001t0001g0244 a0003c0010t0001g0251 |
3 | HG01081.hp1 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.54-6047_54-6046ins others(13): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | |||||||
chr5:98911144 | A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0232 a0001c0001t0001g0280 |
3 | HG01358.hp2 HG04228.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.54-6047_54-6046ins others(15): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | |||||||
chr5:98911144 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0290 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.54-6047_54-6046ins others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | |||||||
chr5:98911144 | A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0257 a0001c0001t0001g0289 a0001c0001t0001g0291 others(1): Show |
4 | HG02071.hp1 HG02080.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-6047_54-6046ins others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | |||||||
chr5:98911144 | A | ATATATAT others(12): Show |
4 | a0001c0001t0001g0240 a0001c0001t0001g0247 a0001c0001t0001g0292 others(1): Show |
4 | HG02273.hp1 HG02922.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-6047_54-6046ins others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | |||||||
chr5:98911144 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0260 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.54-6047_54-6046ins others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | |||||||
chr5:98911144 | A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0235 a0001c0001t0001g0255 |
2 | HG01256.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.54-6047_54-6046ins others(23): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | |||||||
chr5:98911144 | A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0236 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.54-6047_54-6046ins others(25): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | |||||||
chr5:98911144 | A | T | 13 | a0001c0001t0001g0175 a0001c0001t0001g0220 a0001c0001t0001g0228 others(10): Show |
13 | HG01167.hp1 HG01192.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.54-6046T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | |||||||
chr5:98911144 | AAAATATA others(3): Show |
A | 1 | a0001c0001t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.54-6056_54-6047del others(10): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | |||||||
chr5:98911146 | A | AAAAAAAA others(9): Show |
1 | a0002c0002t0002g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(16): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAAAAAAA others(19): Show |
1 | a0002c0002t0002g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(26): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAAAAAAA others(11): Show |
1 | a0002c0002t0002g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(18): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAAAAAAA others(19): Show |
1 | a0002c0002t0011g0085 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(26): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAAAAAAA others(23): Show |
1 | a0002c0002t0025g0136 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(30): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAAAAAAT others(12): Show |
1 | a0002c0002t0002g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAAAAAAT others(26): Show |
1 | a0002c0002t0011g0084 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(33): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAAAATAT others(28): Show |
1 | a0002c0002t0011g0082 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(35): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAAATATA others(3): Show |
1 | a0001c0003t0006g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(10): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAAATATA others(15): Show |
2 | a0001c0003t0006g0061 a0001c0003t0006g0069 |
2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(22): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAAATATA others(17): Show |
2 | a0001c0003t0006g0067 a0002c0002t0002g0080 |
2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(24): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAAATATA others(23): Show |
2 | a0002c0002t0002g0081 a0002c0002t0002g0087 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(30): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAAATATA others(27): Show |
3 | a0001c0003t0009g0193 a0001c0003t0009g0224 a0002c0002t0002g0089 |
3 | HG03209.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(34): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAAATATA others(68): Show |
1 | a0002c0002t0002g0083 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(75): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAATATAT others(4): Show |
2 | a0001c0001t0026g0249 a0002c0002t0016g0007 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(11): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAATATAT others(8): Show |
1 | a0002c0002t0005g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(15): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAATATAT others(10): Show |
2 | a0001c0001t0001g0002 a0002c0002t0016g0007 |
2 | HG03540.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAATATAT others(12): Show |
1 | a0001c0001t0001g0237 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAATATAT others(14): Show |
1 | a0001c0001t0001g0281 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAATATAT others(16): Show |
1 | a0002c0002t0005g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(23): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AAT | 10 | a0001c0001t0001g0201 a0001c0001t0004g0040 a0002c0002t0002g0001 others(7): Show |
12 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.54-6050_54-6049dup others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AATAT | 7 | a0001c0001t0004g0031 a0002c0002t0002g0005 a0002c0002t0002g0104 others(4): Show |
8 | HG01257.hp1 NA18944.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-6052_54-6049dup others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AATATATA others(3): Show |
1 | a0001c0003t0006g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.54-6058_54-6049dup others(10): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AATATATA others(5): Show |
3 | a0001c0001t0001g0250 a0001c0001t0001g0253 a0001c0003t0006g0059 |
3 | HG01891.hp1 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.54-6060_54-6049dup others(12): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AATATATA others(21): Show |
2 | a0002c0002t0002g0079 a0002c0002t0005g0029 |
2 | HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.54-6076_54-6049dup others(28): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | AT | 4 | a0001c0001t0001g0169 a0001c0001t0003g0298 a0002c0002t0002g0001 others(1): Show |
4 | HG01069.hp1 HG01169.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(1): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATAT | 9 | a0001c0001t0003g0306 a0001c0001t0003g0307 a0001c0001t0003g0308 others(6): Show |
9 | HG00621.hp2 HG02027.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(3): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATATAT | 6 | a0001c0001t0001g0245 a0001c0001t0001g0254 a0001c0001t0003g0299 others(3): Show |
6 | HG01109.hp2 HG01516.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATATATAT others(4): Show |
5 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0267 others(2): Show |
5 | HG00423.hp2 HG02015.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(11): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0233 a0001c0001t0001g0248 |
2 | HG01257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(13): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATATATAT others(8): Show |
6 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0277 others(3): Show |
6 | HG01928.hp1 HG03139.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(15): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATATATAT others(10): Show |
5 | a0001c0001t0001g0231 a0001c0001t0001g0256 a0001c0001t0001g0282 others(2): Show |
5 | HG00642.hp2 HG03490.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0234 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0283 a0001c0003t0009g0194 |
2 | HG00323.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0243 a0001c0001t0001g0268 |
2 | NA19005.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(23): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATATATAT others(18): Show |
2 | a0001c0001t0001g0278 a0001c0003t0006g0070 |
2 | HG01109.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(25): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0241 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(27): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0276 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(29): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATATATAT others(24): Show |
1 | a0001c0003t0006g0058 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(31): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATCTATAT others(16): Show |
1 | a0002c0002t0007g0015 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(23): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATCTATAT others(18): Show |
3 | a0002c0002t0007g0016 a0002c0002t0007g0017 a0002c0002t0018g0018 |
3 | NA18947.hp2 NA18950.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(25): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | ATCTATAT others(32): Show |
1 | a0002c0002t0007g0014 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(39): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | A | T | 71 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0053 others(68): Show |
71 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.54-6048T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | AAT | A | 20 | a0001c0001t0001g0010 a0001c0001t0001g0095 a0001c0001t0001g0103 others(17): Show |
20 | HG00408.hp2 HG01346.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.54-6050_54-6049del others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911146 | AATAT | A | 7 | a0001c0003t0002g0004 a0001c0003t0002g0062 a0001c0003t0002g0063 others(4): Show |
8 | HG01891.hp2 HG02886.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-6052_54-6049del others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | |||||||
chr5:98911147 | AT | A | 7 | a0001c0001t0001g0127 a0001c0001t0001g0170 a0001c0001t0004g0030 others(4): Show |
7 | HG01243.hp1 HG01255.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-6050delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911147 | |||||||
chr5:98911148 | T | A | 10 | a0001c0001t0003g0305 a0001c0004t0001g0092 a0001c0004t0001g0094 others(7): Show |
10 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.54-6050A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911148 | |||||||
chr5:98911150 | T | A | 4 | a0001c0001t0001g0178 a0001c0001t0001g0185 a0001c0001t0001g0216 others(1): Show |
4 | HG01346.hp2 HG02257.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-6052A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911150 | |||||||
chr5:98911152 | T | A | 2 | a0001c0005t0001g0048 a0005c0009t0002g0088 |
2 | NA18906.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.54-6054A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911152 | |||||||
chr5:98911154 | T | A | 2 | a0001c0005t0001g0048 a0005c0009t0002g0088 |
2 | NA18906.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.54-6056A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911154 | |||||||
chr5:98911168 | T | C | 2 | a0002c0002t0005g0020 a0002c0002t0005g0021 |
2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.54-6070A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911168 | |||||||
chr5:98911176 | T | G | 1 | a0001c0003t0028g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54-6078A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911176 | |||||||
chr5:98911219 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.54-6121T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911219 | |||||||
chr5:98911287 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.54-6189A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911287 | |||||||
chr5:98911337 | A | T | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.54-6239T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911337 | |||||||
chr5:98911484 | T | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(65): Show |
71 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.54-6386A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911484 | |||||||
chr5:98911518 | G | A | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.54-6420C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911518 | |||||||
chr5:98911725 | G | T | 1 | a0001c0001t0003g0307 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.54-6627C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911725 | |||||||
chr5:98911983 | C | A | 1 | a0001c0001t0001g0177 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.54-6885G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911983 | |||||||
chr5:98912340 | A | T | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.54-7242T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98912340 | |||||||
chr5:98912548 | G | A | 67 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0078 others(64): Show |
72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.54-7450C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98912548 | |||||||
chr5:98912578 | C | T | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.54-7480G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98912578 | |||||||
chr5:98912649 | C | T | 1 | a0001c0001t0003g0307 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.54-7551G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98912649 | |||||||
chr5:98912680 | A | G | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-7582T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98912680 | |||||||
chr5:98912730 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.54-7632G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98912730 | |||||||
chr5:98913201 | T | C | 13 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(10): Show |
13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-8103A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913201 | |||||||
chr5:98913680 | T | C | 3 | a0001c0003t0009g0193 a0001c0003t0009g0224 a0002c0002t0005g0027 |
3 | HG02976.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.54-8582A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913680 | |||||||
chr5:98913717 | A | G | 95 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(92): Show |
103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.54-8619T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913717 | |||||||
chr5:98913740 | G | T | 8 | a0002c0002t0002g0001 a0002c0002t0002g0112 a0002c0002t0002g0113 others(5): Show |
10 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.54-8642C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913740 | |||||||
chr5:98913780 | TAATACA | T | 34 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(31): Show |
35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.54-8688_54-8683del others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913780 | |||||||
chr5:98913851 | G | A | 101 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0003t0002g0004 others(98): Show |
109 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.54-8753C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913851 | |||||||
chr5:98913909 | T | C | 99 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(96): Show |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.54-8811A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913909 | |||||||
chr5:98913933 | T | A | 18 | a0001c0001t0001g0145 a0001c0001t0001g0202 a0001c0001t0001g0203 others(15): Show |
18 | HG00741.hp2 HG01099.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.54-8835A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913933 | |||||||
chr5:98913934 | A | T | 10 | a0001c0001t0001g0150 a0001c0003t0002g0004 a0001c0003t0002g0062 others(7): Show |
11 | HG00323.hp1 HG01891.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-8836T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913934 | |||||||
chr5:98914029 | G | A | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.54-8931C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98914029 | |||||||
chr5:98914244 | G | C | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-9146C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98914244 | |||||||
chr5:98914305 | G | T | 2 | a0002c0002t0017g0139 a0002c0002t0017g0226 |
2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.54-9207C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98914305 | |||||||
chr5:98914517 | G | GA | 34 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(31): Show |
38 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.54-9420dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98914517 | |||||||
chr5:98914649 | C | T | 1 | a0001c0003t0006g0067 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.54-9551G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98914649 | |||||||
chr5:98914838 | C | G | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.54-9740G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98914838 | |||||||
chr5:98914887 | A | ATC | 99 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(96): Show |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.54-9791_54-9790dup others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98914887 | |||||||
chr5:98915101 | C | T | 49 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0096 others(46): Show |
49 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.54-10003G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98915101 | |||||||
chr5:98915154 | T | C | 33 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(30): Show |
34 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.54-10056A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98915154 | |||||||
chr5:98915406 | A | AGGAAGAG others(334): Show |
1 | a0001c0003t0028g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54-10309_54-10308i others(343): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98915406 | |||||||
chr5:98915496 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.54-10398A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98915496 | |||||||
chr5:98915601 | A | G | 13 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(10): Show |
13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-10503T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98915601 | |||||||
chr5:98915870 | A | G | 4 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0198 others(1): Show |
4 | HG01496.hp2 HG02572.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+10464T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98915870 | |||||||
chr5:98916035 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.53+10299T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916035 | |||||||
chr5:98916073 | T | C | 3 | a0002c0002t0002g0112 a0002c0002t0002g0113 a0002c0002t0002g0118 |
3 | HG00642.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.53+10261A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916073 | |||||||
chr5:98916106 | C | T | 3 | a0002c0002t0002g0106 a0002c0002t0002g0119 a0002c0002t0002g0138 |
3 | NA18965.hp2 NA18981.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.53+10228G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916106 | |||||||
chr5:98916284 | A | G | 102 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0003g0299 others(99): Show |
110 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.53+10050T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916284 | |||||||
chr5:98916344 | G | A | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0260 others(1): Show |
4 | HG01243.hp2 NA18987.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.53+9990C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916344 | |||||||
chr5:98916442 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0214 |
3 | HG01943.hp2 NA19056.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.53+9892C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916442 | |||||||
chr5:98916470 | G | A | 1 | a0001c0003t0028g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.53+9864C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916470 | |||||||
chr5:98916491 | G | C | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+9843C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916491 | |||||||
chr5:98916545 | C | CA | 42 | a0001c0001t0001g0143 a0001c0001t0001g0180 a0001c0001t0001g0181 others(39): Show |
42 | HG00423.hp2 HG01109.hp2 HG01257.hp2 others(39): Show |
intron_variant | MODIFIER | c.53+9788dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916545 | |||||||
chr5:98916545 | CA | C | 12 | a0001c0001t0001g0090 a0001c0001t0001g0147 a0001c0001t0001g0200 others(9): Show |
12 | HG00323.hp2 HG00642.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.53+9788delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916545 | |||||||
chr5:98916545 | CAA | C | 25 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(22): Show |
27 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.53+9787_53+9788del others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916545 | |||||||
chr5:98916571 | G | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(65): Show |
71 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.53+9763C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916571 | |||||||
chr5:98916784 | T | C | 31 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(28): Show |
35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.53+9550A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916784 | |||||||
chr5:98916791 | T | C | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.53+9543A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916791 | |||||||
chr5:98916928 | C | CAT | 68 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(65): Show |
71 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.53+9405_53+9406ins others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916928 | |||||||
chr5:98916929 | G | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(217): Show |
231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.53+9405C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916929 | |||||||
chr5:98917202 | T | C | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+9132A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917202 | |||||||
chr5:98917299 | C | CAAAAAAA others(6): Show |
5 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0280 others(2): Show |
5 | HG01884.hp1 HG02074.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(13): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CAAAAAAA others(7): Show |
89 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(86): Show |
92 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CAAAAAAA others(8): Show |
22 | a0001c0001t0001g0103 a0001c0001t0001g0232 a0001c0001t0001g0246 others(19): Show |
22 | HG00423.hp1 HG01081.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(15): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53+9034_53+9035ins others(16): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA | 28 | a0002c0002t0002g0079 a0002c0002t0002g0080 a0002c0002t0002g0081 others(25): Show |
29 | HG00323.hp1 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(7): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(1): Show |
28 | a0002c0002t0002g0001 a0002c0002t0002g0104 a0002c0002t0002g0105 others(25): Show |
31 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(8): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(3): Show |
8 | a0002c0002t0002g0005 a0002c0002t0002g0106 a0002c0002t0002g0107 others(5): Show |
9 | NA18944.hp1 NA18946.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(10): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(4): Show |
1 | a0002c0002t0002g0111 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.53+9034_53+9035ins others(11): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(5): Show |
3 | a0001c0003t0005g0023 a0001c0003t0009g0193 a0001c0003t0009g0224 |
3 | HG02622.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(12): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(6): Show |
2 | a0001c0003t0009g0194 a0001c0003t0009g0225 |
2 | HG00323.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(13): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(7): Show |
3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0003t0002g0011 |
4 | HG00741.hp1 HG01243.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(10): Show |
2 | a0001c0003t0002g0062 a0001c0003t0002g0063 |
2 | HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(12): Show |
1 | a0001c0003t0028g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.53+9034_53+9035ins others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(13): Show |
5 | a0001c0003t0006g0058 a0001c0003t0006g0059 a0001c0003t0006g0060 others(2): Show |
5 | HG02258.hp1 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(20): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(14): Show |
2 | a0001c0003t0006g0069 a0001c0003t0006g0070 |
2 | HG01109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(15): Show |
2 | a0001c0003t0006g0061 a0001c0003t0006g0072 |
2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(22): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(18): Show |
1 | a0001c0003t0002g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.53+9034_53+9035ins others(25): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(19): Show |
1 | a0001c0003t0020g0045 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.53+9034_53+9035ins others(26): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(20): Show |
4 | a0001c0003t0002g0064 a0001c0003t0002g0065 a0001c0003t0013g0013 others(1): Show |
5 | HG06807.hp1 NA19030.hp2 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(27): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(21): Show |
5 | a0001c0003t0002g0004 a0001c0003t0002g0071 a0001c0003t0012g0293 others(2): Show |
6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(28): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917299 | C | CCAAAAAA others(22): Show |
3 | a0001c0003t0002g0055 a0001c0003t0002g0056 a0001c0003t0002g0066 |
3 | HG02896.hp2 HG02897.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(29): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | |||||||
chr5:98917312 | C | A | 5 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(2): Show |
5 | HG00323.hp2 HG02886.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+9022G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917312 | |||||||
chr5:98917313 | A | C | 67 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0078 others(64): Show |
72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.53+9021T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917313 | |||||||
chr5:98917372 | T | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.53+8962A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917372 | |||||||
chr5:98917377 | T | C | 2 | a0001c0005t0001g0048 a0001c0005t0022g0049 |
2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.53+8957A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917377 | |||||||
chr5:98917451 | A | G | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+8883T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917451 | |||||||
chr5:98917498 | C | T | 2 | a0001c0003t0013g0013 a0001c0003t0013g0295 |
3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.53+8836G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917498 | |||||||
chr5:98917816 | A | G | 1 | a0002c0002t0002g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.53+8518T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917816 | |||||||
chr5:98917937 | T | C | 13 | a0002c0002t0005g0020 a0002c0002t0005g0021 a0002c0002t0005g0022 others(10): Show |
13 | HG02055.hp2 HG02258.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.53+8397A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917937 | |||||||
chr5:98918060 | CT | C | 101 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0232 others(98): Show |
109 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.53+8273delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918060 | |||||||
chr5:98918127 | G | A | 2 | a0002c0002t0005g0028 a0002c0002t0005g0029 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.53+8207C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918127 | |||||||
chr5:98918136 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0205 |
2 | NA19058.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.53+8198G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918136 | |||||||
chr5:98918206 | C | T | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+8128G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918206 | |||||||
chr5:98918438 | C | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0200 a0001c0001t0003g0304 |
3 | HG02004.hp2 HG02273.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.53+7896G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918438 | |||||||
chr5:98918460 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.53+7874C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918460 | |||||||
chr5:98918536 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.53+7798T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918536 | |||||||
chr5:98918540 | C | T | 99 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(96): Show |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.53+7794G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918540 | |||||||
chr5:98918604 | C | G | 2 | a0001c0001t0001g0204 a0001c0001t0019g0019 |
2 | HG00408.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.53+7730G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918604 | |||||||
chr5:98918673 | C | G | 5 | a0001c0003t0012g0293 a0001c0003t0012g0294 a0001c0003t0012g0296 others(2): Show |
6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+7661G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918673 | |||||||
chr5:98918693 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.53+7641C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918693 | |||||||
chr5:98918767 | AAC | A | 6 | a0001c0003t0002g0011 a0001c0003t0005g0023 a0001c0003t0009g0193 others(3): Show |
7 | HG00323.hp2 HG00741.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.53+7565_53+7566del others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918767 | |||||||
chr5:98918769 | C | A | 32 | a0001c0001t0015g0046 a0001c0003t0002g0004 a0001c0003t0002g0054 others(29): Show |
34 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.53+7565G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918769 | |||||||
chr5:98918769 | CA | C | 61 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0078 others(58): Show |
66 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.53+7564delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918769 | |||||||
chr5:98918770 | A | C | 35 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(32): Show |
38 | HG00323.hp2 HG00741.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.53+7564T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918770 | |||||||
chr5:98918850 | A | G | 3 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0198 |
3 | HG02572.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.53+7484T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918850 | |||||||
chr5:98919096 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.53+7238A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919096 | |||||||
chr5:98919202 | G | C | 8 | a0001c0003t0002g0004 a0001c0003t0002g0062 a0001c0003t0002g0063 others(5): Show |
9 | HG01891.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+7132C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919202 | |||||||
chr5:98919225 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.53+7109C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919225 | |||||||
chr5:98919490 | T | G | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(2): Show |
5 | HG01981.hp2 NA18949.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+6844A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919490 | |||||||
chr5:98919709 | C | G | 3 | a0001c0001t0003g0301 a0001c0001t0003g0302 a0001c0001t0003g0303 |
3 | HG01975.hp1 HG01993.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.53+6625G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919709 | |||||||
chr5:98919751 | A | G | 5 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0198 others(2): Show |
6 | HG01496.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.53+6583T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919751 | |||||||
chr5:98919781 | G | A | 1 | a0001c0001t0030g0319 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.53+6553C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919781 | |||||||
chr5:98919865 | A | G | 1 | a0002c0002t0002g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.53+6469T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919865 | |||||||
chr5:98919906 | T | C | 1 | a0002c0002t0005g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.53+6428A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919906 | |||||||
chr5:98919922 | A | G | 1 | a0001c0001t0001g0262 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.53+6412T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919922 | |||||||
chr5:98920111 | A | G | 2 | a0001c0001t0003g0313 a0001c0001t0014g0316 |
2 | HG02027.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.53+6223T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920111 | |||||||
chr5:98920142 | G | A | 3 | a0002c0002t0010g0006 a0002c0002t0010g0122 a0002c0002t0010g0123 |
4 | NA18949.hp2 NA18970.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.53+6192C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920142 | |||||||
chr5:98920175 | C | T | 9 | a0002c0002t0002g0005 a0002c0002t0002g0106 a0002c0002t0002g0107 others(6): Show |
10 | NA18944.hp1 NA18946.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.53+6159G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920175 | |||||||
chr5:98920273 | C | A | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+6061G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920273 | |||||||
chr5:98920392 | A | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG01099.hp2 HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.53+5942T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920392 | |||||||
chr5:98920433 | G | T | 67 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0078 others(64): Show |
72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.53+5901C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920433 | |||||||
chr5:98920535 | A | G | 1 | a0002c0002t0002g0106 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.53+5799T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920535 | |||||||
chr5:98920586 | C | T | 2 | a0001c0003t0009g0193 a0001c0003t0009g0224 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.53+5748G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920586 | |||||||
chr5:98920675 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG01256.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.53+5659A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920675 | |||||||
chr5:98920752 | G | A | 8 | a0001c0003t0002g0004 a0001c0003t0002g0062 a0001c0003t0002g0063 others(5): Show |
9 | HG01891.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+5582C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920752 | |||||||
chr5:98920789 | G | A | 6 | a0001c0004t0001g0091 a0001c0004t0001g0092 a0001c0004t0001g0093 others(3): Show |
6 | HG02723.hp1 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+5545C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920789 | |||||||
chr5:98920792 | G | A | 1 | a0001c0001t0004g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.53+5542C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920792 | |||||||
chr5:98920796 | C | CA | 12 | a0001c0001t0001g0190 a0001c0001t0001g0261 a0001c0001t0001g0276 others(9): Show |
13 | HG00741.hp1 HG01496.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.53+5537dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920796 | |||||||
chr5:98920796 | CA | C | 14 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0259 others(11): Show |
14 | HG01109.hp1 HG01168.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+5537delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920796 | |||||||
chr5:98920812 | A | G | 34 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(31): Show |
35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.53+5522T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920812 | |||||||
chr5:98920820 | T | A | 1 | a0001c0003t0005g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.53+5514A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920820 | |||||||
chr5:98920833 | A | G | 99 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(96): Show |
107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.53+5501T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920833 | |||||||
chr5:98921028 | G | A | 1 | a0002c0002t0002g0120 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.53+5306C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921028 | |||||||
chr5:98921084 | CTT | C | 12 | a0001c0003t0002g0054 a0001c0003t0002g0055 a0001c0003t0002g0056 others(9): Show |
12 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.53+5248_53+5249del others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921084 | |||||||
chr5:98921126 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.53+5208G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921126 | |||||||
chr5:98921171 | G | A | 34 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(31): Show |
35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.53+5163C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921171 | |||||||
chr5:98921201 | T | C | 95 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(92): Show |
103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.53+5133A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921201 | |||||||
chr5:98921252 | G | A | 8 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(5): Show |
8 | HG00642.hp2 HG01070.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.53+5082C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921252 | |||||||
chr5:98921462 | C | T | 3 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0001t0003g0299 |
3 | HG01515.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.53+4872G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921462 | |||||||
chr5:98921492 | T | A | 1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.53+4842A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921492 | |||||||
chr5:98921665 | A | C | 95 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(92): Show |
103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.53+4669T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921665 | |||||||
chr5:98921670 | G | A | 1 | a0001c0001t0004g0038 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.53+4664C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921670 | |||||||
chr5:98921737 | C | T | 34 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(31): Show |
35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.53+4597G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921737 | |||||||
chr5:98921812 | T | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0221 |
2 | NA18946.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.53+4522A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921812 | |||||||
chr5:98921907 | T | C | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.53+4427A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921907 | |||||||
chr5:98921979 | C | G | 5 | a0001c0004t0001g0091 a0001c0004t0001g0092 a0001c0004t0001g0093 others(2): Show |
5 | HG03041.hp1 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.53+4355G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921979 | |||||||
chr5:98922017 | G | C | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | NA18948.hp1 NA18987.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.53+4317C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922017 | |||||||
chr5:98922071 | G | T | 1 | a0002c0002t0005g0020 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53+4263C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922071 | |||||||
chr5:98922146 | T | C | 33 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(30): Show |
34 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.53+4188A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922146 | |||||||
chr5:98922214 | T | C | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.53+4120A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922214 | |||||||
chr5:98922295 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.53+4039T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922295 | |||||||
chr5:98922331 | T | C | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | HG02818.hp2 HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.53+4003A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922331 | |||||||
chr5:98922407 | A | C | 1 | a0001c0001t0001g0233 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.53+3927T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922407 | |||||||
chr5:98922475 | T | C | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+3859A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922475 | |||||||
chr5:98922481 | A | T | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.53+3853T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922481 | |||||||
chr5:98922783 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.53+3551C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922783 | |||||||
chr5:98922811 | A | G | 1 | a0001c0003t0028g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.53+3523T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922811 | |||||||
chr5:98922844 | C | G | 2 | a0002c0002t0007g0014 a0002c0002t0007g0016 |
2 | NA18955.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.53+3490G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922844 | |||||||
chr5:98922920 | C | T | 1 | a0001c0001t0004g0030 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.53+3414G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922920 | |||||||
chr5:98922976 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.53+3358T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922976 | |||||||
chr5:98922996 | AG | A | 34 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(31): Show |
35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.53+3337delC | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922996 | |||||||
chr5:98923032 | T | C | 1 | a0002c0002t0002g0140 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.53+3302A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923032 | |||||||
chr5:98923039 | T | G | 2 | a0002c0002t0002g0121 a0002c0002t0002g0141 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.53+3295A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923039 | |||||||
chr5:98923042 | A | G | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+3292T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923042 | |||||||
chr5:98923070 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.53+3264G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923070 | |||||||
chr5:98923229 | G | A | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.53+3105C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923229 | |||||||
chr5:98923234 | C | G | 1 | a0001c0005t0001g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.53+3100G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923234 | |||||||
chr5:98923380 | T | C | 3 | a0002c0002t0010g0006 a0002c0002t0010g0122 a0002c0002t0010g0123 |
4 | NA18949.hp2 NA18970.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.53+2954A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923380 | |||||||
chr5:98923408 | G | A | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+2926C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923408 | |||||||
chr5:98923418 | AT | A | 8 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0265 others(5): Show |
8 | HG00323.hp2 HG01243.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.53+2915delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923418 | |||||||
chr5:98923418 | ATT | A | 94 | a0001c0003t0002g0004 a0001c0003t0002g0011 a0001c0003t0002g0054 others(91): Show |
102 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(99): Show |
intron_variant | MODIFIER | c.53+2914_53+2915del others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923418 | |||||||
chr5:98923451 | T | C | 2 | a0001c0005t0001g0048 a0001c0005t0022g0049 |
2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.53+2883A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923451 | |||||||
chr5:98923480 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.53+2854T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923480 | |||||||
chr5:98923543 | C | T | 1 | a0002c0002t0002g0104 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.53+2791G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923543 | |||||||
chr5:98923693 | G | A | 67 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0078 others(64): Show |
72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.53+2641C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923693 | |||||||
chr5:98923909 | T | C | 7 | a0001c0003t0002g0004 a0001c0003t0002g0062 a0001c0003t0002g0063 others(4): Show |
8 | HG01891.hp2 HG02886.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.53+2425A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923909 | |||||||
chr5:98923969 | T | G | 8 | a0001c0003t0002g0004 a0001c0003t0002g0062 a0001c0003t0002g0063 others(5): Show |
9 | HG01891.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+2365A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923969 | |||||||
chr5:98924090 | T | C | 4 | a0001c0003t0002g0011 a0001c0003t0005g0023 a0001c0005t0001g0048 others(1): Show |
5 | HG00741.hp1 HG01255.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+2244A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924090 | |||||||
chr5:98924118 | T | C | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.53+2216A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924118 | |||||||
chr5:98924143 | G | C | 2 | a0002c0002t0002g0124 a0002c0002t0002g0125 |
2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.53+2191C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924143 | |||||||
chr5:98924254 | A | T | 1 | a0001c0001t0001g0143 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.53+2080T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924254 | |||||||
chr5:98924383 | C | G | 1 | a0002c0002t0007g0014 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.53+1951G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924383 | |||||||
chr5:98924533 | G | A | 67 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0078 others(64): Show |
72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.53+1801C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924533 | |||||||
chr5:98924578 | C | G | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+1756G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924578 | |||||||
chr5:98924588 | C | T | 1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.53+1746G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924588 | |||||||
chr5:98924774 | G | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0266 others(10): Show |
16 | HG00423.hp2 HG02015.hp2 NA18951.hp1 others(13): Show |
intron_variant | MODIFIER | c.53+1560C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924774 | |||||||
chr5:98924823 | C | G | 3 | a0001c0003t0012g0293 a0001c0003t0012g0294 a0001c0003t0012g0296 |
3 | HG02486.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.53+1511G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924823 | |||||||
chr5:98924851 | G | A | 1 | a0001c0003t0002g0011 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+1483C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924851 | |||||||
chr5:98924851 | G | C | 1 | a0002c0002t0005g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.53+1483C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924851 | |||||||
chr5:98924871 | C | T | 1 | a0001c0001t0027g0142 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.53+1463G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924871 | |||||||
chr5:98924872 | G | A | 2 | a0001c0003t0002g0011 a0001c0003t0005g0023 |
3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+1462C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924872 | |||||||
chr5:98924885 | G | A | 1 | a0001c0001t0004g0039 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.53+1449C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924885 | |||||||
chr5:98924945 | T | A | 1 | a0001c0001t0003g0313 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.53+1389A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924945 | |||||||
chr5:98924947 | C | T | 4 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
4 | HG01099.hp1 HG01192.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+1387G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924947 | |||||||
chr5:98925017 | C | A | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.53+1317G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98925017 | |||||||
chr5:98925258 | T | C | 2 | a0001c0001t0014g0316 a0001c0001t0014g0317 |
2 | NA18983.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.53+1076A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98925258 | |||||||
chr5:98925281 | C | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(217): Show |
231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.53+1053G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98925281 | |||||||
chr5:98925327 | G | C | 2 | a0002c0002t0002g0128 a0002c0002t0002g0129 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.53+1007C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98925327 | |||||||
chr5:98925687 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.53+647G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98925687 | |||||||
chr5:98925705 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.53+629T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98925705 | |||||||
chr5:98925782 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.53+552A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98925782 | |||||||
chr5:98926104 | T | G | 1 | a0001c0001t0001g0223 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.53+230A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98926104 | |||||||
chr5:98926108 | T | C | 4 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0224 others(1): Show |
4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+226A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98926108 | |||||||
chr5:98926187 | T | C | 33 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0104 others(30): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.53+147A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98926187 | |||||||
chr5:98926596 | T | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG00738.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-148-62A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98926596 | |||||||
chr5:98926918 | T | TG | 58 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0053 others(55): Show |
59 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-148-385dupC | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98926918 | |||||||
chr5:98926918 | T | TGG | 18 | a0001c0001t0001g0227 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
19 | HG00423.hp2 HG00741.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.-148-386_-148-385d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98926918 | |||||||
chr5:98926918 | TG | T | 75 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0090 others(72): Show |
79 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.-148-385delC | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98926918 | |||||||
chr5:98926943 | C | CCTT | 3 | a0001c0003t0002g0054 a0001c0003t0002g0055 a0001c0003t0002g0056 |
3 | HG02896.hp2 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-148-412_-148-410d others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98926943 | |||||||
chr5:98926989 | G | A | 1 | a0001c0001t0004g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-148-455C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98926989 | |||||||
chr5:98927105 | T | C | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-148-571A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927105 | |||||||
chr5:98927212 | C | T | 12 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0080 others(9): Show |
12 | HG00323.hp1 HG01358.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.-148-678G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927212 | |||||||
chr5:98927333 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-148-799G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927333 | |||||||
chr5:98927409 | T | A | 1 | a0001c0001t0001g0286 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-148-875A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927409 | |||||||
chr5:98927595 | T | A | 1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-149+944A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927595 | |||||||
chr5:98927629 | A | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-149+910T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927629 | |||||||
chr5:98927725 | TA | T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0006t0001g0075 |
3 | HG02083.hp2 NA18998.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-149+813delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927725 | |||||||
chr5:98927865 | T | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0050 others(65): Show |
71 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.-149+674A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927865 | |||||||
chr5:98927901 | C | T | 26 | a0001c0003t0002g0004 a0001c0003t0002g0054 a0001c0003t0002g0055 others(23): Show |
28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-149+638G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927901 | |||||||
chr5:98927982 | G | C | 2 | a0002c0002t0002g0287 a0002c0002t0005g0027 |
2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-149+557C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927982 | |||||||
chr5:98928034 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-149+505A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98928034 | |||||||
chr5:98928084 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | NA18969.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.-149+455G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98928084 | |||||||
chr5:98928200 | C | G | 1 | a0002c0002t0024g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-149+339G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98928200 | |||||||
chr5:98928201 | C | G | 1 | a0001c0001t0001g0050 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-149+338G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98928201 | |||||||
chr5:98928291 | A | T | 2 | a0001c0005t0001g0048 a0001c0005t0022g0049 |
2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-149+248T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98928291 | |||||||
chr5:98928325 | G | A | 2 | a0002c0002t0005g0028 a0002c0002t0005g0029 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-149+214C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98928325 | |||||||
chr5:98928399 | G | A | 4 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG02071.hp1 HG02080.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.-149+140C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98928399 |