Item | Value |
---|---|
geneid | 26511 |
ensemblid | ENSG00000109220.11 |
hgncid | 1935 |
symbol | CHIC2 |
name | cysteine rich hydrophobic domain 2 |
refseq_nuc | NM_012110.4 |
refseq_prot | NP_036242.1 |
ensembl_nuc | ENST00000263921.8 |
ensembl_prot | ENSP00000263921.3 |
mane_status | MANE Select |
chr | chr4 |
start | 54009789 |
end | 54064605 |
strand | - |
ver | v1.2 |
region | chr4:54009789-54064605 |
region5000 | chr4:54004789-54069605 |
regionname0 | CHIC2_chr4_54009789_54064605 |
regionname5000 | CHIC2_chr4_54004789_54069605 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 495 | 240 | 80 | 42 | 70 | 16 | 30 | CHIC2_chr4_54004789_54069605 | CHIC2 | ATGGC others(490): Show |
chr4 | 54004789 | 54069605 | ||
a0001c0002 | 0/0 | 495 | 4 | 4 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | ATGGC others(490): Show |
chr4 | 54004789 | 54069605 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1109 | 147 | 55 | 22 | 48 | 8 | 13 | CHIC2_chr4_54004789_54069605 | CHIC2 | GGTTT others(1104): Show |
chr4 | 54004789 | 54069605 |
a0001c0001t0002 | 0/0 | 1108 | 68 | 8 | 17 | 21 | 7 | 15 | CHIC2_chr4_54004789_54069605 | CHIC2 | GGTTT others(1103): Show |
chr4 | 54004789 | 54069605 |
a0001c0001t0003 | 0/0 | 1111 | 10 | 6 | 3 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | GGTTT others(1106): Show |
chr4 | 54004789 | 54069605 |
a0001c0001t0004 | 0/0 | 1110 | 5 | 4 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | GGTTT others(1105): Show |
chr4 | 54004789 | 54069605 |
a0001c0001t0005 | 0/0 | 1110 | 4 | 4 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | GGTTT others(1105): Show |
chr4 | 54004789 | 54069605 |
a0001c0001t0006 | 0/0 | 1108 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | GGTTT others(1103): Show |
chr4 | 54004789 | 54069605 |
a0001c0001t0007 | 0/0 | 1108 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | GGTTT others(1103): Show |
chr4 | 54004789 | 54069605 |
a0001c0001t0008 | 0/0 | 1109 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | GGTTT others(1104): Show |
chr4 | 54004789 | 54069605 |
a0001c0001t0009 | 0/0 | 1108 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | GGTTT others(1103): Show |
chr4 | 54004789 | 54069605 |
a0001c0001t0010 | 0/1 | 1109 | 1 | 0 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | GGTTT others(1104): Show |
chr4 | 54004789 | 54069605 |
a0001c0002t0001 | 0/0 | 1109 | 3 | 3 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | GGTTT others(1104): Show |
chr4 | 54004789 | 54069605 |
a0001c0002t0004 | 0/0 | 1110 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | GGTTT others(1105): Show |
chr4 | 54004789 | 54069605 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0002 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0010 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0016 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0008g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0009g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0001t0010g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
a0001c0002t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | GBR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0069 | EUR | GBR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0068 | EUR | GBR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | FIN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00323 | hp1 | a0001 | c0001 | t0008 | g0101 | EUR | FIN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0012 | EUR | FIN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | IBS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CDX | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0213 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02965 | hp2 | a0001 | c0002 | t0004 | g0209 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0214 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | ESN | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0124 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | STU | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | CHB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | LWK | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | LWK | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19065 | hp2 | a0001 | c0001 | t0009 | g0054 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ASW | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ASW | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0049 | EUR | TSI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | TSI | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | ACB | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | USA | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | USA | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | USA | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | USA | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
homoSapiens | chm13v2 | a0001 | c0001 | t0010 | g0198 | REF | REF | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0080 | REF | REF | CHIC2_chr4_54004789_54069605 | CHIC2 | chr4 | 54004789 | 54069605 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:54064249 | G | A | 1 | a0001c0002 | 4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
synonymous_variant | LOW | c.52C>T | p.Leu18Leu | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/6 | 357/1109 | 52/498 | 18/165 | chr4 | 54064249 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:54009875 | T | C | 1 | a0001c0001t0009 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*220A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 6/6 | 220 | chr4 | 54009875 | ||||||
chr4:54009924 | A | C | 1 | a0001c0001t0008 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*171T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 6/6 | 171 | chr4 | 54009924 | ||||||
chr4:54009951 | A | AT | 1 | a0001c0001t0005 | 4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*143dupA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 6/6 | 143 | chr4 | 54009951 | ||||||
chr4:54009954 | T | TA | 2 | a0001c0001t0004 a0001c0002t0004 |
6 | HG02647.hp1 HG02647.hp2 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*140dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 6/6 | 140 | chr4 | 54009954 | ||||||
chr4:54009954 | T | TAA | 1 | a0001c0001t0003 | 10 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*139_*140dupTT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 6/6 | 140 | chr4 | 54009954 | ||||||
chr4:54009964 | AC | A | 4 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(1): Show |
72 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*130delG | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 6/6 | 130 | chr4 | 54009964 | ||||||
chr4:54009965 | C | A | 7 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(4): Show |
165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*130G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 6/6 | 130 | chr4 | 54009965 | ||||||
chr4:54064347 | T | C | 1 | a0001c0001t0006 | 2 | HG02818.hp1 HG03195.hp1 |
5_prime_UTR_variant | MODIFIER | c.-47A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/6 | 47 | chr4 | 54064347 | ||||||
chr4:54064527 | C | T | 1 | a0001c0001t0007 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-227G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/6 | 227 | chr4 | 54064527 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:54010848 | C | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(19): Show |
24 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.448-703G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54010848 | |||||||
chr4:54010856 | C | T | 9 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0044 others(6): Show |
10 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.448-711G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54010856 | |||||||
chr4:54010954 | A | T | 1 | a0001c0001t0002g0136 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.448-809T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54010954 | |||||||
chr4:54011189 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.448-1044A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54011189 | |||||||
chr4:54011201 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.448-1056C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54011201 | |||||||
chr4:54011274 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.448-1129A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54011274 | |||||||
chr4:54011841 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.448-1696A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54011841 | |||||||
chr4:54012050 | C | CA | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+1786dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012050 | |||||||
chr4:54012123 | A | T | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(104): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.447+1714T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012123 | |||||||
chr4:54012183 | C | T | 6 | a0001c0001t0002g0012 a0001c0001t0002g0049 a0001c0001t0002g0055 others(3): Show |
7 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.447+1654G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012183 | |||||||
chr4:54012195 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.447+1642A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012195 | |||||||
chr4:54012294 | G | T | 1 | a0001c0001t0004g0122 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.447+1543C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012294 | |||||||
chr4:54012665 | G | C | 66 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(63): Show |
77 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.447+1172C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012665 | |||||||
chr4:54012732 | T | C | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+1105A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012732 | |||||||
chr4:54012745 | C | A | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(91): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.447+1092G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012745 | |||||||
chr4:54012998 | T | C | 1 | a0001c0001t0007g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.447+839A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54012998 | |||||||
chr4:54013011 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0185 |
2 | HG01258.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.447+826A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54013011 | |||||||
chr4:54013126 | T | C | 1 | a0001c0001t0004g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.447+711A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54013126 | |||||||
chr4:54013149 | A | T | 1 | a0001c0001t0002g0036 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.447+688T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54013149 | |||||||
chr4:54013450 | G | C | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.447+387C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54013450 | |||||||
chr4:54013521 | G | A | 1 | a0001c0001t0003g0015 | 2 | HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.447+316C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54013521 | |||||||
chr4:54013674 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.447+163G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 5/5 | chr4 | 54013674 | |||||||
chr4:54014238 | T | C | 2 | a0001c0001t0002g0055 a0001c0001t0002g0058 |
2 | HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.331-119A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54014238 | |||||||
chr4:54014450 | C | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(19): Show |
24 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.331-331G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54014450 | |||||||
chr4:54014539 | T | C | 3 | a0001c0001t0002g0008 a0001c0001t0002g0050 a0001c0001t0002g0063 |
4 | HG02683.hp1 HG02735.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-420A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54014539 | |||||||
chr4:54015192 | A | G | 1 | a0001c0001t0003g0015 | 2 | HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.331-1073T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54015192 | |||||||
chr4:54015259 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.331-1140C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54015259 | |||||||
chr4:54015363 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.331-1244G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54015363 | |||||||
chr4:54016084 | A | G | 1 | a0001c0001t0007g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.331-1965T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016084 | |||||||
chr4:54016123 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.331-2004C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016123 | |||||||
chr4:54016173 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.331-2054A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016173 | |||||||
chr4:54016289 | TATA | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(5): Show |
9 | HG02258.hp2 HG02622.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-2173_331-2171d others(5): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016289 | |||||||
chr4:54016358 | T | C | 4 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-2239A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016358 | |||||||
chr4:54016530 | T | G | 58 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(55): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.331-2411A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016530 | |||||||
chr4:54016594 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.331-2475G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016594 | |||||||
chr4:54016909 | GA | G | 32 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0100 others(29): Show |
36 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.331-2791delT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54016909 | |||||||
chr4:54017082 | T | C | 1 | a0001c0001t0002g0137 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.331-2963A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54017082 | |||||||
chr4:54017177 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.331-3058T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54017177 | |||||||
chr4:54017205 | C | CAAATCTA others(28): Show |
3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 |
3 | HG02145.hp2 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.331-3121_331-3087d others(37): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54017205 | |||||||
chr4:54017213 | A | C | 1 | a0001c0001t0004g0124 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.331-3094T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54017213 | |||||||
chr4:54017234 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.331-3115C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54017234 | |||||||
chr4:54017566 | G | A | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-3447C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54017566 | |||||||
chr4:54018040 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.331-3921C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54018040 | |||||||
chr4:54018112 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.331-3993G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54018112 | |||||||
chr4:54018292 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.331-4173G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54018292 | |||||||
chr4:54018575 | G | T | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | HG02602.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.331-4456C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54018575 | |||||||
chr4:54018727 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.331-4608A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54018727 | |||||||
chr4:54018813 | G | C | 9 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0044 others(6): Show |
10 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.331-4694C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54018813 | |||||||
chr4:54018911 | G | A | 1 | a0001c0001t0001g0018 | 2 | HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.331-4792C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54018911 | |||||||
chr4:54019244 | C | CA | 58 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(55): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.331-5126dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019244 | |||||||
chr4:54019424 | C | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-5305G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019424 | |||||||
chr4:54019424 | C | G | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-5305G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019424 | |||||||
chr4:54019572 | T | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(5): Show |
9 | HG02258.hp2 HG02622.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-5453A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019572 | |||||||
chr4:54019676 | T | G | 2 | a0001c0001t0002g0136 a0001c0001t0002g0142 |
2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.331-5557A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019676 | |||||||
chr4:54019777 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-5658C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019777 | |||||||
chr4:54019787 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.331-5668C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019787 | |||||||
chr4:54019796 | G | C | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-5677C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019796 | |||||||
chr4:54019895 | T | TA | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(89): Show |
108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.331-5777dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54019895 | |||||||
chr4:54020031 | G | A | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.331-5912C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020031 | |||||||
chr4:54020105 | C | A | 6 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-5986G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020105 | |||||||
chr4:54020356 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.331-6237G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020356 | |||||||
chr4:54020429 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.331-6310G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020429 | |||||||
chr4:54020437 | C | T | 1 | a0001c0001t0003g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.331-6318G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020437 | |||||||
chr4:54020621 | G | T | 1 | a0001c0001t0004g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331-6502C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020621 | |||||||
chr4:54020651 | G | A | 2 | a0001c0001t0002g0135 a0001c0001t0002g0143 |
2 | HG00642.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.331-6532C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020651 | |||||||
chr4:54020658 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-6539G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020658 | |||||||
chr4:54020829 | A | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.331-6710T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020829 | |||||||
chr4:54020867 | A | T | 88 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(85): Show |
104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.331-6748T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54020867 | |||||||
chr4:54021081 | CTTCTCCC others(3): Show |
C | 2 | a0001c0001t0003g0125 a0001c0001t0003g0126 |
2 | HG02109.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.331-6972_331-6963d others(12): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54021081 | |||||||
chr4:54021129 | C | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0208 |
2 | NA18950.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.331-7010G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54021129 | |||||||
chr4:54021193 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.331-7074G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54021193 | |||||||
chr4:54021753 | G | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-7634C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54021753 | |||||||
chr4:54022114 | C | A | 58 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(55): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.331-7995G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022114 | |||||||
chr4:54022137 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.331-8018A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022137 | |||||||
chr4:54022192 | C | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-8073G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022192 | |||||||
chr4:54022271 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.331-8152C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022271 | |||||||
chr4:54022281 | C | T | 1 | a0001c0001t0008g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.331-8162G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022281 | |||||||
chr4:54022325 | C | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(19): Show |
24 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.331-8206G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022325 | |||||||
chr4:54022640 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.331-8521A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022640 | |||||||
chr4:54022686 | C | A | 2 | a0001c0001t0002g0077 a0001c0001t0002g0127 |
2 | HG01255.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.331-8567G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022686 | |||||||
chr4:54022699 | G | C | 1 | a0001c0001t0002g0068 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.331-8580C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022699 | |||||||
chr4:54022702 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.331-8583G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022702 | |||||||
chr4:54022787 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.331-8668C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022787 | |||||||
chr4:54022849 | C | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(5): Show |
9 | HG02258.hp2 HG02622.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-8730G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022849 | |||||||
chr4:54022939 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.331-8820C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022939 | |||||||
chr4:54022973 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.331-8854C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54022973 | |||||||
chr4:54023102 | T | TA | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-8984dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023102 | |||||||
chr4:54023121 | T | C | 4 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-9002A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023121 | |||||||
chr4:54023129 | C | T | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(3): Show |
6 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-9010G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023129 | |||||||
chr4:54023193 | G | A | 8 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(5): Show |
8 | HG02145.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.331-9074C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023193 | |||||||
chr4:54023212 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0150 |
5 | HG02717.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-9093C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023212 | |||||||
chr4:54023217 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.331-9098C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023217 | |||||||
chr4:54023288 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.331-9169C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023288 | |||||||
chr4:54023305 | G | A | 1 | a0001c0001t0004g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331-9186C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023305 | |||||||
chr4:54023416 | T | C | 1 | a0001c0001t0001g0001 | 5 | NA18747.hp2 NA18960.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-9297A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023416 | |||||||
chr4:54023426 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.331-9307C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023426 | |||||||
chr4:54023453 | G | A | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(104): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.331-9334C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023453 | |||||||
chr4:54023540 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.331-9421C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023540 | |||||||
chr4:54023568 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0041 |
4 | HG02622.hp1 HG02809.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-9449A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023568 | |||||||
chr4:54023650 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.331-9531G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023650 | |||||||
chr4:54023719 | C | A | 1 | a0001c0001t0001g0070 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.331-9600G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023719 | |||||||
chr4:54023845 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.331-9726G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023845 | |||||||
chr4:54023985 | G | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0150 |
5 | HG02717.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-9866C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54023985 | |||||||
chr4:54024001 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.331-9882C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024001 | |||||||
chr4:54024049 | G | A | 1 | a0001c0001t0002g0105 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.331-9930C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024049 | |||||||
chr4:54024065 | C | T | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-9946G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024065 | |||||||
chr4:54024222 | T | A | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-10103A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024222 | |||||||
chr4:54024437 | T | TA | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0004g0154 |
3 | HG02257.hp1 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.331-10319dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024437 | |||||||
chr4:54024568 | G | A | 4 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-10449C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024568 | |||||||
chr4:54024639 | G | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-10520C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024639 | |||||||
chr4:54024887 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.331-10768T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54024887 | |||||||
chr4:54025018 | A | G | 1 | a0001c0001t0005g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.331-10899T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54025018 | |||||||
chr4:54025072 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-10953T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54025072 | |||||||
chr4:54025766 | G | A | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.331-11647C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54025766 | |||||||
chr4:54025854 | C | CA | 14 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0002g0128 others(11): Show |
15 | HG00639.hp1 HG00642.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.331-11736dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54025854 | |||||||
chr4:54025854 | C | CAA | 53 | a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0005 others(50): Show |
65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.331-11737_331-1173 others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54025854 | |||||||
chr4:54025854 | CA | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0159 a0001c0001t0005g0025 others(3): Show |
6 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.331-11736delT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54025854 | |||||||
chr4:54025923 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.331-11804C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54025923 | |||||||
chr4:54026034 | T | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG02615.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.331-11915A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026034 | |||||||
chr4:54026040 | C | A | 1 | a0001c0001t0002g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.331-11921G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026040 | |||||||
chr4:54026229 | C | A | 1 | a0001c0001t0002g0134 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.331-12110G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026229 | |||||||
chr4:54026230 | A | C | 1 | a0001c0001t0002g0134 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.331-12111T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026230 | |||||||
chr4:54026232 | T | A | 1 | a0001c0001t0002g0134 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.331-12113A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026232 | |||||||
chr4:54026452 | G | GGGGTTGC others(9): Show |
1 | a0001c0001t0001g0082 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.331-12334_331-1233 others(20): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026452 | |||||||
chr4:54026456 | G | T | 1 | a0001c0001t0001g0082 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.331-12337C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026456 | |||||||
chr4:54026457 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.331-12338A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026457 | |||||||
chr4:54026856 | T | C | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-12737A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026856 | |||||||
chr4:54026974 | A | C | 1 | a0001c0001t0001g0171 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.331-12855T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54026974 | |||||||
chr4:54027112 | A | G | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(91): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.331-12993T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54027112 | |||||||
chr4:54027167 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.331-13048T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54027167 | |||||||
chr4:54027218 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0073 |
2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.331-13099T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54027218 | |||||||
chr4:54027448 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.331-13329C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54027448 | |||||||
chr4:54027655 | A | G | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-13536T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54027655 | |||||||
chr4:54027764 | A | G | 1 | a0001c0001t0006g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.331-13645T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54027764 | |||||||
chr4:54028079 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.331-13960A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54028079 | |||||||
chr4:54028146 | T | C | 4 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-14027A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54028146 | |||||||
chr4:54028531 | A | C | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(104): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.331-14412T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54028531 | |||||||
chr4:54028737 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.331-14618A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54028737 | |||||||
chr4:54028830 | A | G | 6 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
6 | HG02647.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-14711T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54028830 | |||||||
chr4:54028855 | C | T | 58 | a0001c0001t0001g0158 a0001c0001t0002g0002 a0001c0001t0002g0005 others(55): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.331-14736G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54028855 | |||||||
chr4:54028967 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.331-14848G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54028967 | |||||||
chr4:54029049 | G | A | 1 | a0001c0001t0006g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.331-14930C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029049 | |||||||
chr4:54029113 | C | G | 2 | a0001c0001t0003g0125 a0001c0001t0003g0126 |
2 | HG02109.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.331-14994G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029113 | |||||||
chr4:54029126 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.331-15007T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029126 | |||||||
chr4:54029135 | A | C | 1 | a0001c0001t0001g0088 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.331-15016T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029135 | |||||||
chr4:54029202 | T | C | 23 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(20): Show |
25 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.331-15083A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029202 | |||||||
chr4:54029305 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.331-15186C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029305 | |||||||
chr4:54029340 | G | A | 1 | a0001c0001t0003g0015 | 2 | HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.331-15221C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029340 | |||||||
chr4:54029478 | T | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-15359A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029478 | |||||||
chr4:54029598 | A | C | 1 | a0001c0002t0004g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.331-15479T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029598 | |||||||
chr4:54029635 | T | A | 19 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(16): Show |
21 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.331-15516A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029635 | |||||||
chr4:54029647 | A | G | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-15528T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54029647 | |||||||
chr4:54030214 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG03704.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.331-16095A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030214 | |||||||
chr4:54030305 | C | T | 1 | a0001c0001t0002g0134 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.331-16186G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030305 | |||||||
chr4:54030460 | C | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-16341G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030460 | |||||||
chr4:54030467 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.331-16348C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030467 | |||||||
chr4:54030523 | GA | G | 21 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(18): Show |
22 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.331-16405delT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030523 | |||||||
chr4:54030523 | GAA | G | 70 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(67): Show |
85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.331-16406_331-1640 others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030523 | |||||||
chr4:54030533 | A | T | 1 | a0001c0001t0003g0047 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.331-16414T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030533 | |||||||
chr4:54030535 | A | T | 73 | a0001c0001t0001g0017 a0001c0001t0001g0071 a0001c0001t0001g0072 others(70): Show |
86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.331-16416T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030535 | |||||||
chr4:54030537 | A | T | 96 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(93): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.331-16418T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030537 | |||||||
chr4:54030539 | T | A | 2 | a0001c0001t0001g0121 a0001c0001t0002g0081 |
2 | HG01255.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.331-16420A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030539 | |||||||
chr4:54030561 | C | CACACACA others(3): Show |
107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(104): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.331-16443_331-1644 others(14): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030561 | |||||||
chr4:54030618 | A | G | 1 | a0001c0001t0002g0002 | 4 | HG00733.hp1 HG01070.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-16499T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030618 | |||||||
chr4:54030637 | T | C | 1 | a0001c0001t0004g0122 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.331-16518A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030637 | |||||||
chr4:54030643 | T | C | 6 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-16524A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030643 | |||||||
chr4:54030666 | A | AT | 14 | a0001c0001t0001g0108 a0001c0001t0001g0113 a0001c0001t0001g0148 others(11): Show |
14 | HG00597.hp1 HG00597.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.331-16548dupA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030666 | |||||||
chr4:54030666 | AT | A | 16 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(13): Show |
18 | HG00099.hp2 HG00642.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.331-16548delA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030666 | |||||||
chr4:54030731 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.331-16612C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030731 | |||||||
chr4:54030757 | T | A | 1 | a0001c0001t0001g0018 | 2 | HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.331-16638A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030757 | |||||||
chr4:54030878 | A | AT | 5 | a0001c0001t0001g0084 a0001c0001t0002g0130 a0001c0001t0002g0140 others(2): Show |
5 | HG02257.hp2 HG03098.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-16760dupA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030878 | |||||||
chr4:54030878 | AT | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0150 others(1): Show |
6 | HG02717.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-16760delA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030878 | |||||||
chr4:54030898 | C | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-16779G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030898 | |||||||
chr4:54030952 | C | T | 57 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(54): Show |
69 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.331-16833G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54030952 | |||||||
chr4:54031178 | G | GA | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(91): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.331-17060dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031178 | |||||||
chr4:54031220 | C | A | 1 | a0001c0001t0001g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.331-17101G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031220 | |||||||
chr4:54031344 | A | G | 1 | a0001c0001t0004g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331-17225T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031344 | |||||||
chr4:54031347 | T | A | 1 | a0001c0001t0001g0001 | 5 | NA18747.hp2 NA18960.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-17228A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031347 | |||||||
chr4:54031611 | C | CT | 57 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(54): Show |
58 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.330+17343dupA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031611 | |||||||
chr4:54031611 | CT | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0002g0076 others(1): Show |
5 | HG02809.hp1 HG02896.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+17343delA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031611 | |||||||
chr4:54031641 | CAG | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+17312_330+1731 others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031641 | |||||||
chr4:54031676 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.330+17279C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031676 | |||||||
chr4:54031902 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+17053C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031902 | |||||||
chr4:54031916 | A | G | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(104): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.330+17039T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54031916 | |||||||
chr4:54032260 | T | TCCCTCC | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+16689_330+1669 others(10): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032260 | |||||||
chr4:54032286 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.330+16669A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032286 | |||||||
chr4:54032330 | G | C | 1 | a0001c0001t0002g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.330+16625C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032330 | |||||||
chr4:54032380 | C | CG | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+16574_330+1657 others(5): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032380 | |||||||
chr4:54032381 | T | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+16574A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032381 | |||||||
chr4:54032382 | C | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+16573G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032382 | |||||||
chr4:54032383 | A | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+16572T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032383 | |||||||
chr4:54032389 | C | A | 4 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+16566G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032389 | |||||||
chr4:54032415 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+16540C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032415 | |||||||
chr4:54032471 | T | G | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.330+16484A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032471 | |||||||
chr4:54032555 | T | C | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(91): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.330+16400A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032555 | |||||||
chr4:54032607 | A | G | 2 | a0001c0001t0002g0009 a0001c0001t0009g0054 |
3 | NA18966.hp2 NA19065.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.330+16348T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032607 | |||||||
chr4:54032643 | AATTAC | A | 4 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+16307_330+1631 others(9): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032643 | |||||||
chr4:54032715 | C | A | 1 | a0001c0001t0004g0124 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.330+16240G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032715 | |||||||
chr4:54032804 | C | T | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(91): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.330+16151G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032804 | |||||||
chr4:54032848 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0002g0136 a0001c0001t0002g0142 |
3 | HG00639.hp1 HG01109.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.330+16107G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54032848 | |||||||
chr4:54033059 | G | A | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(3): Show |
6 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+15896C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54033059 | |||||||
chr4:54033162 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.330+15793A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54033162 | |||||||
chr4:54033512 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.330+15443C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54033512 | |||||||
chr4:54033637 | TAG | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0196 a0001c0001t0001g0197 |
4 | HG00741.hp2 HG01346.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+15316_330+1531 others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54033637 | |||||||
chr4:54033697 | A | C | 1 | a0001c0001t0001g0176 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.330+15258T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54033697 | |||||||
chr4:54033722 | A | T | 1 | a0001c0001t0004g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.330+15233T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54033722 | |||||||
chr4:54034046 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.330+14909G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034046 | |||||||
chr4:54034100 | T | C | 7 | a0001c0001t0002g0129 a0001c0001t0002g0130 a0001c0001t0002g0131 others(4): Show |
8 | HG00544.hp1 HG00642.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+14855A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034100 | |||||||
chr4:54034120 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.330+14835G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034120 | |||||||
chr4:54034124 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.330+14831C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034124 | |||||||
chr4:54034196 | G | C | 4 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+14759C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034196 | |||||||
chr4:54034202 | C | T | 4 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+14753G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034202 | |||||||
chr4:54034318 | C | T | 58 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(55): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.330+14637G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034318 | |||||||
chr4:54034339 | A | G | 86 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(83): Show |
102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.330+14616T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034339 | |||||||
chr4:54034404 | CA | C | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(106): Show |
126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.330+14550delT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034404 | |||||||
chr4:54034437 | A | T | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(104): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.330+14518T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034437 | |||||||
chr4:54034462 | T | C | 1 | a0001c0001t0001g0018 | 2 | HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.330+14493A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034462 | |||||||
chr4:54034573 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.330+14382T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034573 | |||||||
chr4:54034576 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.330+14379C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034576 | |||||||
chr4:54034577 | T | TATTTTTT others(8): Show |
1 | a0001c0001t0001g0087 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.330+14377_330+1437 others(19): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034577 | |||||||
chr4:54034582 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.330+14373G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034582 | |||||||
chr4:54034585 | T | G | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+14370A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034585 | |||||||
chr4:54034636 | T | C | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.330+14319A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034636 | |||||||
chr4:54034720 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.330+14235G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034720 | |||||||
chr4:54034724 | A | G | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0103 |
3 | HG02615.hp2 HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.330+14231T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034724 | |||||||
chr4:54034849 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.330+14106A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54034849 | |||||||
chr4:54035165 | A | G | 1 | a0001c0001t0004g0122 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.330+13790T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035165 | |||||||
chr4:54035242 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.330+13713C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035242 | |||||||
chr4:54035309 | T | C | 55 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(52): Show |
67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.330+13646A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035309 | |||||||
chr4:54035317 | A | G | 7 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.330+13638T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035317 | |||||||
chr4:54035503 | T | C | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+13452A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035503 | |||||||
chr4:54035634 | C | T | 58 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(55): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.330+13321G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035634 | |||||||
chr4:54035645 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.330+13310A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035645 | |||||||
chr4:54035684 | T | C | 1 | a0001c0001t0002g0077 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.330+13271A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035684 | |||||||
chr4:54035737 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.330+13218G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035737 | |||||||
chr4:54035795 | G | A | 58 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(55): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.330+13160C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035795 | |||||||
chr4:54035931 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.330+13024A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035931 | |||||||
chr4:54035971 | C | T | 4 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+12984G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54035971 | |||||||
chr4:54036138 | G | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG02615.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.330+12817C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036138 | |||||||
chr4:54036391 | G | A | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+12564C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036391 | |||||||
chr4:54036403 | T | G | 58 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(55): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.330+12552A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036403 | |||||||
chr4:54036487 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.330+12468C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036487 | |||||||
chr4:54036558 | T | A | 1 | a0001c0001t0002g0135 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.330+12397A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036558 | |||||||
chr4:54036577 | G | A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG02615.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.330+12378C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036577 | |||||||
chr4:54036701 | C | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.330+12254G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036701 | |||||||
chr4:54036791 | C | CA | 58 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(55): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.330+12163dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036791 | |||||||
chr4:54036826 | C | CA | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(104): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.330+12128_330+1212 others(5): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036826 | |||||||
chr4:54036962 | T | C | 3 | a0001c0001t0001g0093 a0001c0001t0002g0132 a0001c0001t0003g0126 |
3 | HG02109.hp1 HG02132.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.330+11993A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036962 | |||||||
chr4:54036997 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.330+11958T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54036997 | |||||||
chr4:54037168 | A | G | 1 | a0001c0001t0003g0015 | 2 | HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.330+11787T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037168 | |||||||
chr4:54037209 | A | C | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(104): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.330+11746T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037209 | |||||||
chr4:54037381 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+11574C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037381 | |||||||
chr4:54037497 | T | C | 58 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(55): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.330+11458A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037497 | |||||||
chr4:54037657 | T | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.330+11298A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037657 | |||||||
chr4:54037700 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.330+11255G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037700 | |||||||
chr4:54037839 | G | C | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+11116C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037839 | |||||||
chr4:54037866 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+11089A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54037866 | |||||||
chr4:54038289 | G | A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0090 a0001c0001t0001g0092 others(2): Show |
5 | HG01074.hp2 HG01167.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+10666C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54038289 | |||||||
chr4:54038399 | T | C | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+10556A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54038399 | |||||||
chr4:54038432 | T | C | 1 | a0001c0002t0004g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.330+10523A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54038432 | |||||||
chr4:54038462 | C | CA | 6 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+10492dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54038462 | |||||||
chr4:54038609 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0150 |
5 | HG02717.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+10346A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54038609 | |||||||
chr4:54039013 | G | A | 9 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0044 others(6): Show |
10 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.330+9942C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039013 | |||||||
chr4:54039132 | C | T | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+9823G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039132 | |||||||
chr4:54039169 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.330+9786A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039169 | |||||||
chr4:54039255 | C | T | 2 | a0001c0001t0002g0052 a0001c0001t0002g0053 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.330+9700G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039255 | |||||||
chr4:54039268 | G | A | 1 | a0001c0001t0006g0213 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.330+9687C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039268 | |||||||
chr4:54039325 | T | A | 56 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(53): Show |
68 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.330+9630A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039325 | |||||||
chr4:54039331 | C | T | 1 | a0001c0001t0008g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.330+9624G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039331 | |||||||
chr4:54039572 | C | T | 5 | a0001c0001t0001g0086 a0001c0001t0001g0090 a0001c0001t0001g0092 others(2): Show |
5 | HG01074.hp2 HG01167.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+9383G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039572 | |||||||
chr4:54039746 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.330+9209A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039746 | |||||||
chr4:54039785 | G | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.330+9170C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039785 | |||||||
chr4:54039807 | T | C | 1 | a0001c0001t0001g0041 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.330+9148A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039807 | |||||||
chr4:54039881 | TAAAAG | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.330+9069_330+9073d others(7): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54039881 | |||||||
chr4:54040041 | C | A | 1 | a0001c0001t0004g0122 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.330+8914G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040041 | |||||||
chr4:54040194 | T | C | 34 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0099 others(31): Show |
38 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.330+8761A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040194 | |||||||
chr4:54040293 | G | A | 1 | a0001c0001t0003g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.330+8662C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040293 | |||||||
chr4:54040372 | G | C | 1 | a0001c0001t0002g0060 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.330+8583C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040372 | |||||||
chr4:54040396 | G | A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG02615.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.330+8559C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040396 | |||||||
chr4:54040471 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.330+8484G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040471 | |||||||
chr4:54040665 | T | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0204 |
2 | HG01070.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.330+8290A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040665 | |||||||
chr4:54040703 | C | CA | 38 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0020 others(35): Show |
44 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.330+8251dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040703 | |||||||
chr4:54040703 | C | CAA | 11 | a0001c0001t0001g0075 a0001c0001t0001g0083 a0001c0001t0001g0092 others(8): Show |
11 | HG00323.hp1 HG00438.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.330+8250_330+8251d others(4): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040703 | |||||||
chr4:54040703 | CA | C | 30 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0033 others(27): Show |
33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.330+8251delT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040703 | |||||||
chr4:54040703 | CAA | C | 53 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(50): Show |
65 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.330+8250_330+8251d others(4): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040703 | |||||||
chr4:54040703 | CAAA | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(4): Show |
9 | HG01255.hp1 HG02717.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.330+8249_330+8251d others(5): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040703 | |||||||
chr4:54040800 | C | A | 56 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(53): Show |
68 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.330+8155G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040800 | |||||||
chr4:54040973 | AT | A | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(5): Show |
8 | HG01070.hp1 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+7981delA | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54040973 | |||||||
chr4:54041020 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.330+7935C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54041020 | |||||||
chr4:54041070 | C | A | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+7885G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54041070 | |||||||
chr4:54041311 | A | C | 1 | a0001c0001t0002g0138 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.330+7644T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54041311 | |||||||
chr4:54041361 | C | T | 1 | a0001c0001t0006g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.330+7594G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54041361 | |||||||
chr4:54041384 | T | C | 3 | a0001c0001t0002g0077 a0001c0001t0002g0127 a0001c0001t0004g0122 |
3 | HG01255.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.330+7571A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54041384 | |||||||
chr4:54041391 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.330+7564G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54041391 | |||||||
chr4:54042103 | T | C | 1 | a0001c0002t0004g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.330+6852A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042103 | |||||||
chr4:54042106 | A | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.330+6849T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042106 | |||||||
chr4:54042218 | T | C | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0110 others(1): Show |
4 | HG02559.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+6737A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042218 | |||||||
chr4:54042314 | C | T | 4 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+6641G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042314 | |||||||
chr4:54042316 | T | C | 2 | a0001c0001t0002g0077 a0001c0001t0002g0127 |
2 | HG01255.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.330+6639A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042316 | |||||||
chr4:54042339 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.330+6616C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042339 | |||||||
chr4:54042397 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.330+6558T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042397 | |||||||
chr4:54042460 | G | A | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+6495C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042460 | |||||||
chr4:54042524 | A | T | 1 | a0001c0002t0001g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.330+6431T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042524 | |||||||
chr4:54042587 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.330+6368C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042587 | |||||||
chr4:54042716 | C | T | 2 | a0001c0001t0003g0125 a0001c0001t0003g0126 |
2 | HG02109.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.330+6239G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042716 | |||||||
chr4:54042923 | G | T | 2 | a0001c0001t0002g0008 a0001c0001t0002g0050 |
3 | HG02683.hp1 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.330+6032C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042923 | |||||||
chr4:54042953 | C | T | 3 | a0001c0001t0002g0012 a0001c0001t0002g0060 a0001c0001t0002g0069 |
4 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+6002G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54042953 | |||||||
chr4:54043100 | C | A | 1 | a0001c0001t0001g0184 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.330+5855G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043100 | |||||||
chr4:54043139 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0197 |
2 | HG01123.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.330+5816G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043139 | |||||||
chr4:54043144 | A | G | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(102): Show |
122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.330+5811T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043144 | |||||||
chr4:54043160 | G | A | 2 | a0001c0001t0002g0011 a0001c0001t0002g0059 |
3 | HG02074.hp1 NA18977.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.330+5795C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043160 | |||||||
chr4:54043174 | C | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG02559.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.330+5781G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043174 | |||||||
chr4:54043255 | A | C | 1 | a0001c0001t0002g0145 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.330+5700T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043255 | |||||||
chr4:54043410 | G | A | 1 | a0001c0001t0003g0046 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.330+5545C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043410 | |||||||
chr4:54043420 | C | CA | 13 | a0001c0001t0001g0017 a0001c0001t0001g0095 a0001c0001t0001g0110 others(10): Show |
14 | HG02145.hp2 HG02559.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.330+5534dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043420 | |||||||
chr4:54043420 | CA | C | 6 | a0001c0001t0001g0114 a0001c0001t0001g0162 a0001c0001t0001g0169 others(3): Show |
6 | HG01943.hp1 HG02109.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.330+5534delT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043420 | |||||||
chr4:54043531 | C | G | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
5 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+5424G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043531 | |||||||
chr4:54043538 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.330+5417T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043538 | |||||||
chr4:54043645 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.330+5310G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54043645 | |||||||
chr4:54044041 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.330+4914A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044041 | |||||||
chr4:54044118 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+4837G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044118 | |||||||
chr4:54044399 | C | A | 1 | a0001c0001t0003g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.330+4556G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044399 | |||||||
chr4:54044504 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+4451A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044504 | |||||||
chr4:54044586 | C | T | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(102): Show |
122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.330+4369G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044586 | |||||||
chr4:54044648 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0189 |
2 | HG00280.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.330+4307C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044648 | |||||||
chr4:54044648 | G | C | 1 | a0001c0001t0001g0191 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.330+4307C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044648 | |||||||
chr4:54044704 | T | C | 1 | a0001c0001t0002g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.330+4251A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044704 | |||||||
chr4:54044896 | C | T | 4 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+4059G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044896 | |||||||
chr4:54044911 | TAAAG | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+4040_330+4043d others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044911 | |||||||
chr4:54044976 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.330+3979C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044976 | |||||||
chr4:54044993 | A | G | 2 | a0001c0001t0002g0005 a0001c0001t0002g0137 |
4 | NA18975.hp2 NA18998.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+3962T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044993 | |||||||
chr4:54044998 | C | A | 1 | a0001c0001t0002g0005 | 3 | NA18975.hp2 NA18998.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.330+3957G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54044998 | |||||||
chr4:54045027 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.330+3928C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045027 | |||||||
chr4:54045046 | C | G | 1 | a0001c0001t0001g0197 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.330+3909G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045046 | |||||||
chr4:54045129 | A | G | 1 | a0001c0001t0004g0122 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.330+3826T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045129 | |||||||
chr4:54045217 | G | A | 1 | a0001c0001t0003g0015 | 2 | HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.330+3738C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045217 | |||||||
chr4:54045223 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.330+3732T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045223 | |||||||
chr4:54045261 | T | A | 1 | a0001c0001t0004g0124 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.330+3694A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045261 | |||||||
chr4:54045309 | A | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0070 others(9): Show |
17 | HG00438.hp2 HG00597.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+3646T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045309 | |||||||
chr4:54045310 | T | G | 1 | a0001c0001t0002g0051 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.330+3645A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045310 | |||||||
chr4:54045314 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0070 others(9): Show |
17 | HG00438.hp2 HG00597.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+3641G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045314 | |||||||
chr4:54045318 | A | C | 6 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+3637T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045318 | |||||||
chr4:54045344 | A | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0070 others(9): Show |
17 | HG00438.hp2 HG00597.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+3611T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045344 | |||||||
chr4:54045395 | T | G | 106 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(103): Show |
123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.330+3560A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045395 | |||||||
chr4:54045643 | C | T | 1 | a0001c0001t0004g0122 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.330+3312G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045643 | |||||||
chr4:54045644 | A | G | 1 | a0001c0001t0004g0122 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.330+3311T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045644 | |||||||
chr4:54045648 | C | T | 1 | a0001c0001t0004g0122 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.330+3307G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045648 | |||||||
chr4:54045733 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.330+3222G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045733 | |||||||
chr4:54045741 | A | C | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 |
3 | HG02145.hp2 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.330+3214T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045741 | |||||||
chr4:54045752 | C | T | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+3203G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045752 | |||||||
chr4:54045768 | A | C | 1 | a0001c0001t0003g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.330+3187T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045768 | |||||||
chr4:54045770 | A | G | 1 | a0001c0001t0003g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.330+3185T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045770 | |||||||
chr4:54045883 | T | C | 1 | a0001c0001t0007g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.330+3072A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045883 | |||||||
chr4:54045905 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | NA18978.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.330+3050G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045905 | |||||||
chr4:54045971 | G | T | 1 | a0001c0001t0002g0081 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.330+2984C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54045971 | |||||||
chr4:54046071 | T | G | 1 | a0001c0002t0004g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.330+2884A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046071 | |||||||
chr4:54046139 | G | T | 88 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(85): Show |
104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.330+2816C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046139 | |||||||
chr4:54046201 | A | G | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | NA18747.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.330+2754T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046201 | |||||||
chr4:54046381 | C | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(19): Show |
24 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.330+2574G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046381 | |||||||
chr4:54046584 | C | T | 7 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.330+2371G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046584 | |||||||
chr4:54046601 | C | G | 1 | a0001c0001t0003g0046 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.330+2354G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046601 | |||||||
chr4:54046678 | C | G | 1 | a0001c0001t0002g0051 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.330+2277G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046678 | |||||||
chr4:54046739 | G | A | 1 | a0001c0001t0002g0077 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.330+2216C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046739 | |||||||
chr4:54046773 | G | C | 99 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(96): Show |
116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.330+2182C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54046773 | |||||||
chr4:54047051 | C | T | 3 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 |
3 | HG01243.hp1 HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.330+1904G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047051 | |||||||
chr4:54047095 | A | T | 2 | a0001c0001t0003g0125 a0001c0001t0003g0126 |
2 | HG02109.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.330+1860T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047095 | |||||||
chr4:54047102 | C | T | 7 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0044 others(4): Show |
8 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+1853G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047102 | |||||||
chr4:54047150 | C | A | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+1805G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047150 | |||||||
chr4:54047177 | A | G | 58 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(55): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.330+1778T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047177 | |||||||
chr4:54047285 | A | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(19): Show |
24 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.330+1670T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047285 | |||||||
chr4:54047410 | C | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(19): Show |
24 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.330+1545G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047410 | |||||||
chr4:54047422 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.330+1533C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047422 | |||||||
chr4:54047543 | G | A | 2 | a0001c0001t0003g0125 a0001c0001t0003g0126 |
2 | HG02109.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.330+1412C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047543 | |||||||
chr4:54047591 | T | C | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+1364A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047591 | |||||||
chr4:54047632 | C | T | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+1323G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047632 | |||||||
chr4:54047663 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.330+1292C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047663 | |||||||
chr4:54047745 | C | T | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG00639.hp2 HG01070.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+1210G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047745 | |||||||
chr4:54047787 | T | C | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(104): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.330+1168A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047787 | |||||||
chr4:54047917 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.330+1038C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047917 | |||||||
chr4:54047970 | C | G | 1 | a0001c0002t0004g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.330+985G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54047970 | |||||||
chr4:54048008 | G | A | 1 | a0001c0001t0002g0077 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.330+947C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048008 | |||||||
chr4:54048146 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0002g0128 |
2 | HG00280.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.330+809C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048146 | |||||||
chr4:54048156 | T | C | 3 | a0001c0001t0002g0012 a0001c0001t0002g0060 a0001c0001t0002g0069 |
4 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+799A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048156 | |||||||
chr4:54048191 | T | C | 1 | a0001c0001t0002g0077 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.330+764A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048191 | |||||||
chr4:54048544 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.330+411G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048544 | |||||||
chr4:54048646 | G | A | 6 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.330+309C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048646 | |||||||
chr4:54048698 | T | C | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(176): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.330+257A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048698 | |||||||
chr4:54048835 | T | C | 5 | a0001c0001t0004g0122 a0001c0001t0005g0025 a0001c0001t0005g0026 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+120A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 3/5 | chr4 | 54048835 | |||||||
chr4:54049360 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0187 |
2 | HG00099.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.120-55A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54049360 | |||||||
chr4:54049893 | C | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.120-588G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54049893 | |||||||
chr4:54050024 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.120-719T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050024 | |||||||
chr4:54050156 | T | C | 86 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(83): Show |
102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.120-851A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050156 | |||||||
chr4:54050461 | T | C | 1 | a0001c0002t0004g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.120-1156A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050461 | |||||||
chr4:54050543 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.120-1238G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050543 | |||||||
chr4:54050552 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.120-1247T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050552 | |||||||
chr4:54050644 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.120-1339A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050644 | |||||||
chr4:54050758 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.120-1453C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050758 | |||||||
chr4:54050783 | T | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.120-1478A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54050783 | |||||||
chr4:54051200 | A | C | 58 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(55): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.120-1895T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051200 | |||||||
chr4:54051229 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.120-1924T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051229 | |||||||
chr4:54051317 | C | T | 86 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(83): Show |
102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.120-2012G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051317 | |||||||
chr4:54051517 | C | T | 1 | a0001c0001t0006g0213 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.120-2212G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051517 | |||||||
chr4:54051651 | C | G | 2 | a0001c0001t0002g0136 a0001c0001t0002g0142 |
2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.120-2346G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051651 | |||||||
chr4:54051770 | C | T | 21 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0016 others(18): Show |
27 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.120-2465G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051770 | |||||||
chr4:54051801 | A | T | 1 | a0001c0001t0003g0015 | 2 | HG00642.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.120-2496T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051801 | |||||||
chr4:54051864 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.120-2559C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051864 | |||||||
chr4:54051900 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.120-2595A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051900 | |||||||
chr4:54051915 | T | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG02615.hp1 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.120-2610A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54051915 | |||||||
chr4:54052068 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.120-2763A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54052068 | |||||||
chr4:54052123 | C | CCTT | 93 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(90): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.120-2821_120-2819d others(5): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54052123 | |||||||
chr4:54052228 | T | G | 1 | a0001c0001t0001g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.120-2923A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54052228 | |||||||
chr4:54052460 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.120-3155C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54052460 | |||||||
chr4:54052476 | T | C | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(104): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.120-3171A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54052476 | |||||||
chr4:54052731 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0189 |
2 | HG00280.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.120-3426C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54052731 | |||||||
chr4:54052976 | ATTATC | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.120-3676_120-3672d others(7): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54052976 | |||||||
chr4:54053044 | A | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(77): Show |
96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.120-3739T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053044 | |||||||
chr4:54053164 | C | G | 1 | a0001c0001t0002g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.120-3859G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053164 | |||||||
chr4:54053368 | C | A | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.120-4063G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053368 | |||||||
chr4:54053530 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.120-4225C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053530 | |||||||
chr4:54053551 | A | G | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.120-4246T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053551 | |||||||
chr4:54053556 | C | CA | 15 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(12): Show |
16 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.120-4252dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053556 | |||||||
chr4:54053556 | CA | C | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(81): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.120-4252delT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053556 | |||||||
chr4:54053556 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0002g0135 a0001c0001t0002g0143 |
2 | HG00642.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.120-4261_120-4252d others(12): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053556 | |||||||
chr4:54053838 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.120-4533A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54053838 | |||||||
chr4:54054054 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.120-4749A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54054054 | |||||||
chr4:54054878 | T | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.120-5573A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54054878 | |||||||
chr4:54054904 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.120-5599A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54054904 | |||||||
chr4:54055032 | G | A | 1 | a0001c0001t0003g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.120-5727C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54055032 | |||||||
chr4:54055042 | A | T | 1 | a0001c0001t0002g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.120-5737T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54055042 | |||||||
chr4:54055326 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.120-6021G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54055326 | |||||||
chr4:54055327 | G | A | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.120-6022C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54055327 | |||||||
chr4:54055578 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.120-6273G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54055578 | |||||||
chr4:54055735 | T | C | 7 | a0001c0001t0001g0114 a0001c0001t0003g0043 a0001c0001t0003g0044 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.120-6430A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54055735 | |||||||
chr4:54055919 | G | A | 6 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
6 | HG02647.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.120-6614C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54055919 | |||||||
chr4:54056315 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.120-7010A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54056315 | |||||||
chr4:54056521 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.120-7216C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54056521 | |||||||
chr4:54056560 | T | G | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.120-7255A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54056560 | |||||||
chr4:54056980 | C | T | 1 | a0001c0001t0004g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.119+7202G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54056980 | |||||||
chr4:54057015 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.119+7167T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54057015 | |||||||
chr4:54057038 | G | C | 1 | a0001c0001t0003g0048 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.119+7144C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54057038 | |||||||
chr4:54057159 | C | T | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+7023G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54057159 | |||||||
chr4:54057725 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.119+6457G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54057725 | |||||||
chr4:54057725 | C | T | 1 | a0001c0001t0002g0129 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.119+6457G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54057725 | |||||||
chr4:54057780 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.119+6402A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54057780 | |||||||
chr4:54058021 | T | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0194 a0001c0001t0001g0195 others(2): Show |
6 | HG00741.hp2 HG01346.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.119+6161A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058021 | |||||||
chr4:54058041 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.119+6141G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058041 | |||||||
chr4:54058068 | G | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0194 a0001c0001t0001g0195 others(2): Show |
6 | HG00741.hp2 HG01346.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.119+6114C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058068 | |||||||
chr4:54058423 | G | A | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+5759C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058423 | |||||||
chr4:54058447 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0071 others(3): Show |
8 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.119+5735A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058447 | |||||||
chr4:54058536 | T | TCACATAC others(1): Show |
2 | a0001c0001t0002g0013 a0001c0001t0002g0062 |
3 | HG01175.hp1 HG01192.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.119+5638_119+5645d others(10): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058536 | |||||||
chr4:54058549 | T | TACACACA others(3): Show |
2 | a0001c0001t0002g0063 a0001c0001t0002g0064 |
2 | HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.119+5632_119+5633i others(12): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058549 | |||||||
chr4:54058549 | TAC | T | 9 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0127 others(6): Show |
11 | HG00544.hp1 HG01255.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.119+5631_119+5632d others(4): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058549 | |||||||
chr4:54058551 | C | CACACAT | 16 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(13): Show |
18 | HG00099.hp1 HG00323.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.119+5630_119+5631i others(8): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058551 | |||||||
chr4:54058553 | C | CACAT | 10 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 others(7): Show |
10 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.119+5628_119+5629i others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058553 | |||||||
chr4:54058553 | CACACAT | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(10): Show |
17 | HG02258.hp2 HG02622.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.119+5623_119+5628d others(8): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058553 | |||||||
chr4:54058555 | C | CAT | 10 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0011 others(7): Show |
12 | HG02572.hp2 HG02683.hp1 HG03927.hp1 others(9): Show |
intron_variant | MODIFIER | c.119+5626_119+5627i others(4): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058555 | |||||||
chr4:54058555 | CACAT | C | 11 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.119+5623_119+5626d others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058555 | |||||||
chr4:54058557 | C | T | 11 | a0001c0001t0002g0002 a0001c0001t0002g0016 a0001c0001t0002g0056 others(8): Show |
15 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.119+5625G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058557 | |||||||
chr4:54058559 | T | C | 51 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(48): Show |
61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.119+5623A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058559 | |||||||
chr4:54058559 | T | TAC | 9 | a0001c0001t0001g0001 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG00639.hp2 HG01081.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.119+5621_119+5622d others(4): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058559 | |||||||
chr4:54058559 | T | TACAC | 6 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.119+5619_119+5622d others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058559 | |||||||
chr4:54058559 | TAC | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(41): Show |
49 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.119+5621_119+5622d others(4): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058559 | |||||||
chr4:54058559 | TACAC | T | 12 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 others(9): Show |
12 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.119+5619_119+5622d others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058559 | |||||||
chr4:54058561 | C | T | 11 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.119+5621G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058561 | |||||||
chr4:54058563 | C | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(10): Show |
17 | HG02258.hp2 HG02622.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.119+5619G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54058563 | |||||||
chr4:54059027 | A | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(19): Show |
24 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.119+5155T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059027 | |||||||
chr4:54059184 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.119+4998T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059184 | |||||||
chr4:54059251 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0208 |
2 | NA18950.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.119+4931C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059251 | |||||||
chr4:54059369 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.119+4813G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059369 | |||||||
chr4:54059386 | T | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0123 a0001c0001t0001g0155 others(2): Show |
5 | HG02257.hp1 HG02523.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.119+4796A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059386 | |||||||
chr4:54059444 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.119+4738T>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059444 | |||||||
chr4:54059585 | T | TA | 10 | a0001c0001t0003g0015 a0001c0001t0003g0043 a0001c0001t0003g0044 others(7): Show |
11 | HG00642.hp2 HG01167.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.119+4596dupT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059585 | |||||||
chr4:54059970 | T | C | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+4212A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059970 | |||||||
chr4:54059978 | T | A | 1 | a0001c0001t0002g0127 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.119+4204A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059978 | |||||||
chr4:54059997 | G | C | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+4185C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54059997 | |||||||
chr4:54060019 | T | C | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG00639.hp2 HG01070.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.119+4163A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060019 | |||||||
chr4:54060040 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.119+4142C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060040 | |||||||
chr4:54060073 | G | A | 1 | a0001c0001t0002g0005 | 3 | NA18975.hp2 NA18998.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.119+4109C>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060073 | |||||||
chr4:54060207 | ATCC | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG02145.hp1 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.119+3972_119+3974d others(5): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060207 | |||||||
chr4:54060208 | TCCC | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(12): Show |
17 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.119+3971_119+3973d others(5): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060208 | |||||||
chr4:54060302 | C | T | 50 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(47): Show |
62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.119+3880G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060302 | |||||||
chr4:54060311 | T | C | 4 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+3871A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060311 | |||||||
chr4:54060506 | G | C | 19 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0016 others(16): Show |
25 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.119+3676C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060506 | |||||||
chr4:54060744 | T | G | 1 | a0001c0001t0001g0018 | 2 | HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.119+3438A>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060744 | |||||||
chr4:54060747 | T | A | 1 | a0001c0001t0001g0206 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.119+3435A>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54060747 | |||||||
chr4:54061344 | G | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0150 |
5 | HG02717.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.119+2838C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54061344 | |||||||
chr4:54061441 | C | G | 1 | a0001c0001t0003g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.119+2741G>C | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54061441 | |||||||
chr4:54061867 | G | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0042 |
4 | HG02622.hp2 HG02809.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+2315C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54061867 | |||||||
chr4:54061867 | G | T | 1 | a0001c0001t0001g0029 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.119+2315C>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54061867 | |||||||
chr4:54062151 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.119+2031A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062151 | |||||||
chr4:54062159 | A | C | 6 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.119+2023T>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062159 | |||||||
chr4:54062302 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.119+1880C>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062302 | |||||||
chr4:54062329 | T | TTTTA | 10 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0208 others(7): Show |
12 | HG02145.hp2 HG02559.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.119+1849_119+1852d others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062329 | |||||||
chr4:54062329 | T | TTTTATTT others(1): Show |
3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02630.hp1 HG02717.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.119+1845_119+1852d others(10): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062329 | |||||||
chr4:54062329 | T | TTTTATTT others(5): Show |
2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.119+1841_119+1852d others(14): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062329 | |||||||
chr4:54062329 | T | TTTTATTT others(9): Show |
4 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG02257.hp1 HG02486.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.119+1837_119+1852d others(18): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062329 | |||||||
chr4:54062329 | TTTTA | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(15): Show |
20 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.119+1849_119+1852d others(6): Show |
CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062329 | |||||||
chr4:54062522 | C | T | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 |
3 | HG02145.hp2 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.119+1660G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062522 | |||||||
chr4:54062812 | A | T | 8 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(5): Show |
8 | HG02145.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.119+1370T>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54062812 | |||||||
chr4:54063458 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.119+724A>G | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54063458 | |||||||
chr4:54064008 | TC | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 |
4 | HG02922.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.119+173delG | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54064008 | |||||||
chr4:54064009 | C | A | 1 | a0001c0001t0001g0175 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.119+173G>T | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54064009 | |||||||
chr4:54064050 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.119+132G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54064050 | |||||||
chr4:54064102 | CAG | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(51): Show |
60 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.119+78_119+79delCT | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54064102 | |||||||
chr4:54064103 | AG | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0100 others(2): Show |
5 | HG00597.hp2 HG01258.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.119+78delC | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54064103 | |||||||
chr4:54064172 | C | T | 1 | a0001c0002t0004g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.119+10G>A | CHIC2 | ENSG00000109220.11 | transcript | ENST00000263921.8 | protein_coding | 1/5 | chr4 | 54064172 |