Item | Value |
---|---|
geneid | 10042 |
ensemblid | ENSG00000100281.14 |
hgncid | 5003 |
symbol | HMGXB4 |
name | HMG-box containing 4 |
refseq_nuc | NM_001003681.3 |
refseq_prot | NP_001003681.1 |
ensembl_nuc | ENST00000216106.6 |
ensembl_prot | ENSP00000216106.5 |
mane_status | MANE Select |
chr | chr22 |
start | 35257493 |
end | 35295807 |
strand | + |
ver | v1.2 |
region | chr22:35257493-35295807 |
region5000 | chr22:35252493-35300807 |
regionname0 | HMGXB4_chr22_35257493_35295807 |
regionname5000 | HMGXB4_chr22_35252493_35300807 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 601 | 209 | 63 | 27 | 97 | 5 | 16 | 75 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | MAYDD others(596): Show |
chr22 | 35252493 | 35300807 |
a0002 | 0/1 | 601 | 132 | 10 | 25 | 69 | 5 | 22 | 53 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | MAYDD others(596): Show |
chr22 | 35252493 | 35300807 |
a0003 | 0/0 | 601 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | MAYDD others(596): Show |
chr22 | 35252493 | 35300807 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1803 | 209 | 63 | 27 | 97 | 5 | 16 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | ATGGC others(1798): Show |
chr22 | 35252493 | 35300807 | ||
a0002c0002 | 0/1 | 1803 | 132 | 10 | 25 | 69 | 5 | 22 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | ATGGC others(1798): Show |
chr22 | 35252493 | 35300807 | ||
a0003c0003 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | ATGGC others(1798): Show |
chr22 | 35252493 | 35300807 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4095 | 141 | 49 | 21 | 56 | 5 | 9 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4090): Show |
chr22 | 35252493 | 35300807 |
a0001c0001t0002 | 0/0 | 4094 | 2 | 1 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4089): Show |
chr22 | 35252493 | 35300807 |
a0001c0001t0003 | 0/0 | 4090 | 42 | 0 | 0 | 39 | 0 | 3 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4085): Show |
chr22 | 35252493 | 35300807 |
a0001c0001t0004 | 0/0 | 4095 | 10 | 8 | 2 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4090): Show |
chr22 | 35252493 | 35300807 |
a0001c0001t0006 | 0/0 | 4095 | 4 | 2 | 2 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4090): Show |
chr22 | 35252493 | 35300807 |
a0001c0001t0007 | 0/0 | 4095 | 4 | 0 | 1 | 0 | 0 | 3 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4090): Show |
chr22 | 35252493 | 35300807 |
a0001c0001t0008 | 0/0 | 4095 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4090): Show |
chr22 | 35252493 | 35300807 |
a0001c0001t0009 | 0/0 | 4095 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4090): Show |
chr22 | 35252493 | 35300807 |
a0001c0001t0010 | 0/0 | 4094 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4089): Show |
chr22 | 35252493 | 35300807 |
a0001c0001t0014 | 0/0 | 4094 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4089): Show |
chr22 | 35252493 | 35300807 |
a0001c0001t0018 | 0/0 | 4095 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTT others(4090): Show |
chr22 | 35252493 | 35300807 |
a0002c0002t0002 | 0/1 | 4094 | 119 | 10 | 24 | 58 | 5 | 21 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4089): Show |
chr22 | 35252493 | 35300807 |
a0002c0002t0005 | 0/0 | 4094 | 7 | 0 | 0 | 7 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4089): Show |
chr22 | 35252493 | 35300807 |
a0002c0002t0011 | 0/0 | 4094 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4089): Show |
chr22 | 35252493 | 35300807 |
a0002c0002t0012 | 0/0 | 4094 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4089): Show |
chr22 | 35252493 | 35300807 |
a0002c0002t0013 | 0/0 | 4094 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4089): Show |
chr22 | 35252493 | 35300807 |
a0002c0002t0015 | 0/0 | 4094 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4089): Show |
chr22 | 35252493 | 35300807 |
a0002c0002t0016 | 0/0 | 4094 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4089): Show |
chr22 | 35252493 | 35300807 |
a0002c0002t0017 | 0/0 | 4094 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4089): Show |
chr22 | 35252493 | 35300807 |
a0003c0003t0001 | 0/0 | 4095 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | CTCTC others(4090): Show |
chr22 | 35252493 | 35300807 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 10 | 2 | 0 | 7 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0004 | 0/0 | 8 | 6 | 1 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0017 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0001 | 0/0 | 14 | 0 | 0 | 13 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0004g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0006g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0006g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0007g0018 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0007g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0008g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0009g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0010g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0014g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0001c0001t0018g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0002 | 0/0 | 12 | 1 | 4 | 4 | 1 | 2 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0005 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0008 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0011 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0005g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0005g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0011g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0012g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0013g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0015g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0016g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0002c0002t0017g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
a0003c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | GBR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00642 | hp1 | a0001 | c0001 | t0007 | g0018 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0119 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | CHS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0052 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0061 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0089 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0091 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0114 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0025 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0112 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01099 | hp1 | a0002 | c0002 | t0016 | g0095 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0062 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0242 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0121 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0243 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0086 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0126 | AMR | CLM | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0064 | AMR | CLM | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0122 | AMR | CLM | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0100 | AMR | CLM | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0085 | AMR | CLM | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0084 | EUR | IBS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0120 | EUR | IBS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | PEL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0025 | AMR | PEL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | KHV | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | KHV | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02055 | hp1 | a0001 | c0001 | t0010 | g0131 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | KHV | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02080 | hp2 | a0002 | c0002 | t0011 | g0080 | EAS | KHV | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02132 | hp2 | a0002 | c0002 | t0013 | g0113 | EAS | KHV | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CDX | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | CDX | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0063 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | KHV | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | KHV | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0115 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0087 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0129 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02723 | hp2 | a0001 | c0001 | t0018 | g0036 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0106 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02735 | hp2 | a0001 | c0001 | t0007 | g0018 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0096 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0094 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0245 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0167 | AFR | ESN | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0246 | AFR | ESN | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0210 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | MSL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | ESN | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0082 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | MSL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0065 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0011 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0060 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03688 | hp1 | a0002 | c0002 | t0015 | g0083 | SAS | STU | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0213 | SAS | STU | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0008 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0124 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03710 | hp2 | a0001 | c0001 | t0007 | g0018 | SAS | PJL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0066 | SAS | BEB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03927 | hp1 | a0001 | c0001 | t0014 | g0247 | SAS | BEB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0116 | SAS | BEB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0027 | SAS | BEB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0008 | SAS | STU | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0237 | SAS | STU | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0059 | SAS | STU | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | CHB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18943 | hp1 | a0002 | c0002 | t0005 | g0022 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18945 | hp1 | a0002 | c0002 | t0005 | g0057 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18950 | hp2 | a0001 | c0001 | t0008 | g0169 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18954 | hp2 | a0001 | c0001 | t0008 | g0170 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18984 | hp1 | a0002 | c0002 | t0017 | g0103 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18988 | hp2 | a0002 | c0002 | t0005 | g0021 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18989 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18998 | hp2 | a0002 | c0002 | t0005 | g0021 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19002 | hp1 | a0002 | c0002 | t0005 | g0055 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19006 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | LWK | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19063 | hp1 | a0002 | c0002 | t0005 | g0022 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19075 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19077 | hp2 | a0002 | c0002 | t0012 | g0005 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19087 | hp1 | a0002 | c0002 | t0005 | g0056 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | YRI | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ASW | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ASW | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0011 | EUR | TSI | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | TSI | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0011 | EUR | TSI | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | TSI | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0008 | SAS | GIH | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02486 | hp2 | a0003 | c0003 | t0001 | g0177 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02559 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | USA | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0092 | AFR | USA | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | LWK | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0090 | AFR | LWK | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0053 | REF | REF | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0223 | REF | REF | HMGXB4_chr22_35252493_35300807 | HMGXB4 | chr22 | 35252493 | 35300807 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:35264882 | G | T | 1 | a0002 | 131 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(128): Show |
missense_variant | MODERATE | c.494G>T | p.Gly165Val | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/11 | 627/4095 | 494/1806 | 165/601 | chr22 | 35264882 | |||
chr22:35265425 | T | C | 1 | a0003 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.1037T>C | p.Leu346Ser | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/11 | 1170/4095 | 1037/1806 | 346/601 | chr22 | 35265425 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:35257497 | C | T | 1 | a0001c0001t0018 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-129C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/11 | 4894 | chr22 | 35257497 | ||||||
chr22:35257528 | T | A | 1 | a0001c0001t0009 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-98T>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/11 | 4863 | chr22 | 35257528 | ||||||
chr22:35257539 | C | G | 1 | a0002c0002t0017 | 1 | NA18984.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-87C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/11 | chr22 | 35257539 | |||||||
chr22:35262386 | C | T | 1 | a0001c0001t0007 | 4 | HG00642.hp1 HG02735.hp2 HG03710.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-5C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 2/11 | 5 | chr22 | 35262386 | ||||||
chr22:35293899 | T | C | 1 | a0001c0001t0008 | 2 | NA18950.hp2 NA18954.hp2 |
3_prime_UTR_variant | MODIFIER | c.*248T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 248 | chr22 | 35293899 | ||||||
chr22:35293961 | C | T | 1 | a0002c0002t0016 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*310C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 310 | chr22 | 35293961 | ||||||
chr22:35294186 | T | C | 11 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0014 others(8): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*535T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 535 | chr22 | 35294186 | ||||||
chr22:35294190 | A | G | 11 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0014 others(8): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*539A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 539 | chr22 | 35294190 | ||||||
chr22:35294340 | G | C | 1 | a0001c0001t0010 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*689G>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 689 | chr22 | 35294340 | ||||||
chr22:35294355 | A | G | 1 | a0002c0002t0015 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*704A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 704 | chr22 | 35294355 | ||||||
chr22:35294425 | TGTCTTTC others(26): Show |
T | 1 | a0002c0002t0011 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*778_*810delTTTCAC others(27): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 778 | INFO_REALIGN_3_PRIME | chr22 | 35294425 | |||||
chr22:35294491 | T | A | 1 | a0002c0002t0012 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*840T>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 840 | chr22 | 35294491 | ||||||
chr22:35294539 | A | G | 11 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0014 others(8): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*888A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 888 | chr22 | 35294539 | ||||||
chr22:35294796 | C | G | 1 | a0002c0002t0005 | 7 | NA18943.hp1 NA18945.hp1 NA18988.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1145C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 1145 | chr22 | 35294796 | ||||||
chr22:35294806 | C | T | 1 | a0001c0001t0014 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1155C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 1155 | chr22 | 35294806 | ||||||
chr22:35295113 | C | T | 1 | a0001c0001t0004 | 10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1462C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 1462 | chr22 | 35295113 | ||||||
chr22:35295124 | CT | C | 11 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0014 others(8): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1474delT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 1474 | chr22 | 35295124 | ||||||
chr22:35295215 | C | A | 1 | a0002c0002t0013 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1564C>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 1564 | chr22 | 35295215 | ||||||
chr22:35295603 | C | T | 1 | a0001c0001t0006 | 4 | HG01168.hp1 HG01169.hp2 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1952C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 1952 | chr22 | 35295603 | ||||||
chr22:35295689 | ATTGTT | A | 1 | a0001c0001t0003 | 42 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2041_*2045delGTTT others(1): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 2041 | INFO_REALIGN_3_PRIME | chr22 | 35295689 | |||||
chr22:35295752 | T | TAAAGAAA others(26): Show |
1 | a0002c0002t0011 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2104_*2136dupAGAA others(29): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 11/11 | 2137 | INFO_REALIGN_3_PRIME | chr22 | 35295752 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:35257594 | G | C | 1 | a0001c0001t0003g0039 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-69+37G>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35257594 | |||||||
chr22:35257598 | C | A | 1 | a0001c0001t0003g0039 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-69+41C>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35257598 | |||||||
chr22:35257602 | C | T | 1 | a0001c0001t0014g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-69+45C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35257602 | |||||||
chr22:35257946 | T | C | 7 | a0001c0001t0004g0019 a0001c0001t0004g0040 a0001c0001t0004g0041 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-69+389T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35257946 | |||||||
chr22:35257951 | G | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0048 |
3 | HG00621.hp2 HG02165.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.-69+394G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35257951 | |||||||
chr22:35258065 | T | G | 1 | a0001c0001t0003g0039 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-69+508T>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35258065 | |||||||
chr22:35258140 | T | G | 102 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0050 others(99): Show |
140 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.-69+583T>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35258140 | |||||||
chr22:35258270 | C | T | 1 | a0001c0001t0009g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-69+713C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35258270 | |||||||
chr22:35258642 | C | T | 97 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(94): Show |
134 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-69+1085C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35258642 | |||||||
chr22:35258830 | A | T | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-69+1273A>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35258830 | |||||||
chr22:35258890 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-69+1333G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35258890 | |||||||
chr22:35258950 | G | C | 20 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0133 others(17): Show |
23 | HG02027.hp1 HG02132.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.-69+1393G>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35258950 | |||||||
chr22:35258963 | C | G | 2 | a0001c0001t0002g0130 a0001c0001t0010g0131 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-69+1406C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35258963 | |||||||
chr22:35259148 | TA | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
6 | HG02451.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-69+1592delA | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35259148 | |||||||
chr22:35259557 | TA | T | 95 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(92): Show |
132 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-69+2003delA | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 35259557 | ||||||
chr22:35259619 | C | G | 1 | a0001c0001t0001g0146 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-69+2062C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35259619 | |||||||
chr22:35259793 | CCTT | C | 4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69+2240_-69+2242d others(5): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 35259793 | ||||||
chr22:35259961 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-68-2362A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35259961 | |||||||
chr22:35260102 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-68-2221C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35260102 | |||||||
chr22:35260247 | A | G | 20 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0133 others(17): Show |
23 | HG02027.hp1 HG02132.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.-68-2076A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35260247 | |||||||
chr22:35261203 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-68-1120C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35261203 | |||||||
chr22:35261293 | A | G | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.-68-1030A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35261293 | |||||||
chr22:35261299 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-68-1024G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35261299 | |||||||
chr22:35261360 | C | T | 1 | a0002c0002t0002g0129 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-68-963C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35261360 | |||||||
chr22:35261388 | A | C | 95 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(92): Show |
132 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-68-935A>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35261388 | |||||||
chr22:35261391 | G | A | 1 | a0002c0002t0002g0052 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-68-932G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35261391 | |||||||
chr22:35261435 | C | CA | 99 | a0001c0001t0001g0051 a0001c0001t0001g0133 a0001c0001t0001g0151 others(96): Show |
136 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-68-871dupA | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 35261435 | ||||||
chr22:35261548 | TA | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0133 others(16): Show |
22 | HG02027.hp1 HG02132.hp1 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.-68-769delA | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 35261548 | ||||||
chr22:35261615 | A | G | 1 | a0002c0002t0002g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-68-708A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35261615 | |||||||
chr22:35261665 | T | A | 2 | a0001c0001t0003g0154 a0001c0001t0003g0155 |
2 | NA18940.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-68-658T>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35261665 | |||||||
chr22:35261770 | G | A | 1 | a0001c0001t0009g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-68-553G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35261770 | |||||||
chr22:35261846 | A | G | 2 | a0002c0002t0002g0123 a0002c0002t0002g0128 |
2 | NA18974.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-68-477A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35261846 | |||||||
chr22:35261909 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-68-414A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35261909 | |||||||
chr22:35262029 | G | A | 95 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(92): Show |
132 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-68-294G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35262029 | |||||||
chr22:35262044 | A | T | 1 | a0001c0001t0001g0238 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-68-279A>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35262044 | |||||||
chr22:35262232 | A | G | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.-68-91A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35262232 | |||||||
chr22:35262249 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-68-74G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 1/10 | chr22 | 35262249 | |||||||
chr22:35262696 | G | A | 1 | a0002c0002t0002g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.31+275G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 2/10 | chr22 | 35262696 | |||||||
chr22:35262781 | C | T | 1 | a0002c0002t0002g0122 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.32-297C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 2/10 | chr22 | 35262781 | |||||||
chr22:35262860 | A | G | 1 | a0002c0002t0002g0121 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.32-218A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 2/10 | chr22 | 35262860 | |||||||
chr22:35263300 | G | GT | 6 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0007g0237 others(3): Show |
6 | HG00544.hp1 HG00642.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.180+88dupT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr22 | 35263300 | ||||||
chr22:35263300 | G | T | 1 | a0001c0001t0014g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.180+74G>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 3/10 | chr22 | 35263300 | |||||||
chr22:35263300 | GT | G | 9 | a0001c0001t0004g0019 a0001c0001t0004g0040 a0001c0001t0004g0041 others(6): Show |
10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.180+88delT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr22 | 35263300 | ||||||
chr22:35263306 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.180+80T>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 3/10 | chr22 | 35263306 | |||||||
chr22:35263307 | T | G | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.180+81T>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 3/10 | chr22 | 35263307 | |||||||
chr22:35263335 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.180+109A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 3/10 | chr22 | 35263335 | |||||||
chr22:35263387 | G | A | 4 | a0002c0002t0005g0021 a0002c0002t0005g0055 a0002c0002t0005g0056 others(1): Show |
5 | NA18945.hp1 NA18988.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+161G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 3/10 | chr22 | 35263387 | |||||||
chr22:35263627 | G | A | 8 | a0002c0002t0002g0058 a0002c0002t0002g0059 a0002c0002t0002g0060 others(5): Show |
8 | HG00642.hp2 HG00738.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.181-169G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 3/10 | chr22 | 35263627 | |||||||
chr22:35263746 | C | G | 1 | a0001c0001t0003g0234 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.181-50C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 3/10 | chr22 | 35263746 | |||||||
chr22:35263776 | C | G | 1 | a0001c0001t0003g0233 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.181-20C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 3/10 | chr22 | 35263776 | |||||||
chr22:35263777 | A | G | 1 | a0001c0001t0001g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.181-19A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 3/10 | chr22 | 35263777 | |||||||
chr22:35264124 | T | C | 2 | a0002c0002t0002g0065 a0002c0002t0002g0124 |
2 | HG03491.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.259+250T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 4/10 | chr22 | 35264124 | |||||||
chr22:35264214 | T | C | 1 | a0001c0001t0006g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.259+340T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 4/10 | chr22 | 35264214 | |||||||
chr22:35264265 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.260-383T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 4/10 | chr22 | 35264265 | |||||||
chr22:35264612 | C | A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0031 others(12): Show |
22 | HG00423.hp2 HG00609.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.260-36C>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 4/10 | chr22 | 35264612 | |||||||
chr22:35265789 | C | CT | 17 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0135 others(14): Show |
18 | HG01069.hp2 HG01071.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1215+201dupT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35265789 | ||||||
chr22:35265846 | G | A | 1 | a0001c0001t0004g0167 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1215+243G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35265846 | |||||||
chr22:35265942 | A | AT | 13 | a0001c0001t0001g0145 a0001c0001t0001g0156 a0001c0001t0001g0224 others(10): Show |
13 | HG01106.hp1 HG01192.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.1215+357dupT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35265942 | ||||||
chr22:35265942 | AT | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0049 others(11): Show |
17 | HG02155.hp2 HG02280.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1215+357delT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35265942 | ||||||
chr22:35266029 | T | G | 2 | a0002c0002t0002g0008 a0002c0002t0002g0066 |
4 | HG03704.hp2 HG03834.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+426T>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35266029 | |||||||
chr22:35266043 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1215+440C>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35266043 | |||||||
chr22:35266084 | C | T | 6 | a0001c0001t0004g0019 a0001c0001t0004g0041 a0001c0001t0004g0042 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1215+481C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35266084 | |||||||
chr22:35266085 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1215+482G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35266085 | |||||||
chr22:35266245 | A | G | 2 | a0002c0002t0002g0115 a0002c0002t0002g0116 |
2 | HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1215+642A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35266245 | |||||||
chr22:35266256 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1215+653T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35266256 | |||||||
chr22:35266731 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1215+1128C>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35266731 | |||||||
chr22:35266841 | T | C | 3 | a0001c0001t0002g0130 a0001c0001t0010g0131 a0001c0001t0014g0247 |
3 | HG02055.hp1 HG03927.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1215+1238T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35266841 | |||||||
chr22:35266857 | A | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG02280.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+1254A>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35266857 | |||||||
chr22:35266933 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1215+1330A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35266933 | |||||||
chr22:35266942 | C | G | 1 | a0001c0001t0009g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1215+1339C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35266942 | |||||||
chr22:35267083 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1215+1480T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267083 | |||||||
chr22:35267085 | CTTATATC others(7): Show |
C | 93 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(90): Show |
128 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1215+1497_1215+151 others(18): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35267085 | ||||||
chr22:35267146 | G | A | 1 | a0001c0001t0004g0167 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1215+1543G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267146 | |||||||
chr22:35267148 | A | ATATATAT others(2): Show |
122 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0030 others(119): Show |
163 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1215+1551_1215+155 others(13): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35267148 | ||||||
chr22:35267149 | T | TATATA | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(121): Show |
176 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.1215+1552_1215+155 others(9): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35267149 | ||||||
chr22:35267155 | A | T | 1 | a0001c0001t0014g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1215+1552A>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267155 | |||||||
chr22:35267156 | T | A | 1 | a0001c0001t0014g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1215+1553T>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267156 | |||||||
chr22:35267157 | A | T | 1 | a0001c0001t0014g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1215+1554A>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267157 | |||||||
chr22:35267165 | A | T | 1 | a0001c0001t0014g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1215+1562A>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267165 | |||||||
chr22:35267170 | T | A | 1 | a0001c0001t0014g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1215+1567T>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267170 | |||||||
chr22:35267174 | T | A | 1 | a0001c0001t0014g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1215+1571T>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267174 | |||||||
chr22:35267275 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1215+1672A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267275 | |||||||
chr22:35267479 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1215+1876C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267479 | |||||||
chr22:35267496 | A | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0222 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1215+1893A>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267496 | |||||||
chr22:35267530 | C | T | 93 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(90): Show |
128 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1215+1927C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267530 | |||||||
chr22:35267661 | C | G | 1 | a0001c0001t0003g0221 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1215+2058C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267661 | |||||||
chr22:35267743 | T | C | 1 | a0001c0001t0003g0221 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1215+2140T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267743 | |||||||
chr22:35267916 | T | C | 1 | a0002c0002t0002g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1215+2313T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35267916 | |||||||
chr22:35268128 | T | C | 1 | a0002c0002t0002g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1215+2525T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35268128 | |||||||
chr22:35268306 | C | G | 1 | a0002c0002t0013g0113 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1215+2703C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35268306 | |||||||
chr22:35268311 | C | G | 1 | a0002c0002t0002g0002 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1215+2708C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35268311 | |||||||
chr22:35268334 | T | C | 123 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0030 others(120): Show |
164 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1215+2731T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35268334 | |||||||
chr22:35268354 | T | C | 1 | a0002c0002t0002g0068 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1215+2751T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35268354 | |||||||
chr22:35268369 | A | G | 1 | a0002c0002t0002g0120 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1215+2766A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35268369 | |||||||
chr22:35268434 | A | G | 1 | a0002c0002t0002g0054 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1215+2831A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35268434 | |||||||
chr22:35268548 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1215+2945T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35268548 | |||||||
chr22:35268945 | C | T | 1 | a0002c0002t0002g0112 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1215+3342C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35268945 | |||||||
chr22:35268948 | T | C | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1215+3345T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35268948 | |||||||
chr22:35269014 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1215+3411T>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35269014 | |||||||
chr22:35269943 | A | C | 3 | a0001c0001t0003g0218 a0001c0001t0003g0219 a0001c0001t0003g0220 |
3 | NA18998.hp1 NA19070.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1215+4340A>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35269943 | |||||||
chr22:35270030 | G | A | 2 | a0001c0001t0004g0041 a0001c0001t0004g0042 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1215+4427G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35270030 | |||||||
chr22:35270092 | G | A | 22 | a0002c0002t0002g0009 a0002c0002t0002g0054 a0002c0002t0002g0067 others(19): Show |
26 | HG00558.hp2 HG00673.hp1 HG02523.hp1 others(23): Show |
intron_variant | MODIFIER | c.1215+4489G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35270092 | |||||||
chr22:35270522 | A | G | 165 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0030 others(162): Show |
222 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.1215+4919A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35270522 | |||||||
chr22:35270714 | G | T | 3 | a0002c0002t0002g0012 a0002c0002t0002g0110 a0002c0002t0002g0111 |
5 | NA18942.hp1 NA18944.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215+5111G>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35270714 | |||||||
chr22:35270771 | G | T | 1 | a0001c0001t0003g0217 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1215+5168G>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35270771 | |||||||
chr22:35270862 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0010g0131 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1215+5259G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35270862 | |||||||
chr22:35271150 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1215+5547A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35271150 | |||||||
chr22:35271348 | C | T | 1 | a0002c0002t0002g0109 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1215+5745C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35271348 | |||||||
chr22:35271389 | C | T | 3 | a0001c0001t0002g0130 a0001c0001t0010g0131 a0001c0001t0014g0247 |
3 | HG02055.hp1 HG03927.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1215+5786C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35271389 | |||||||
chr22:35271409 | GAGA | G | 3 | a0002c0002t0002g0029 a0002c0002t0002g0107 a0002c0002t0002g0108 |
4 | HG00438.hp2 NA18949.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+5809_1215+581 others(7): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35271409 | ||||||
chr22:35271468 | A | G | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1215+5865A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35271468 | |||||||
chr22:35271473 | A | C | 2 | a0001c0001t0002g0130 a0001c0001t0010g0131 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1215+5870A>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35271473 | |||||||
chr22:35271493 | G | A | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1215+5890G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35271493 | |||||||
chr22:35271534 | A | G | 1 | a0001c0001t0004g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1215+5931A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35271534 | |||||||
chr22:35271717 | G | A | 1 | a0001c0001t0009g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1215+6114G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35271717 | |||||||
chr22:35271727 | T | C | 1 | a0001c0001t0004g0167 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1215+6124T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35271727 | |||||||
chr22:35271767 | T | C | 9 | a0001c0001t0004g0019 a0001c0001t0004g0040 a0001c0001t0004g0041 others(6): Show |
10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1215+6164T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35271767 | |||||||
chr22:35271777 | T | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG02280.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+6174T>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35271777 | |||||||
chr22:35271917 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1215+6314C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35271917 | |||||||
chr22:35271982 | A | G | 95 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(92): Show |
132 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1215+6379A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35271982 | |||||||
chr22:35272059 | T | C | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1215+6456T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35272059 | |||||||
chr22:35272060 | G | A | 1 | a0001c0001t0014g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1215+6457G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35272060 | |||||||
chr22:35272309 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1215+6706C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35272309 | |||||||
chr22:35272365 | CAAAG | C | 95 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(92): Show |
132 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1215+6765_1215+676 others(8): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35272365 | ||||||
chr22:35272438 | G | T | 14 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(11): Show |
20 | HG00423.hp2 HG00609.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1215+6835G>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35272438 | |||||||
chr22:35272563 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG02280.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+6960A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35272563 | |||||||
chr22:35272750 | T | G | 4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+7147T>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35272750 | |||||||
chr22:35272786 | T | G | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1215+7183T>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35272786 | |||||||
chr22:35272859 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG02280.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+7256G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35272859 | |||||||
chr22:35272891 | G | A | 1 | a0002c0002t0011g0080 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1215+7288G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35272891 | |||||||
chr22:35272904 | A | G | 1 | a0002c0002t0002g0011 | 3 | HG03492.hp1 NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1215+7301A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35272904 | |||||||
chr22:35272955 | C | T | 1 | a0001c0001t0003g0216 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1215+7352C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35272955 | |||||||
chr22:35273448 | A | G | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1215+7845A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35273448 | |||||||
chr22:35273501 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18951.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1215+7898C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35273501 | |||||||
chr22:35273520 | T | C | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1215+7917T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35273520 | |||||||
chr22:35273532 | C | G | 1 | a0001c0001t0003g0048 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1215+7929C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35273532 | |||||||
chr22:35273549 | G | A | 1 | a0002c0002t0002g0081 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1215+7946G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35273549 | |||||||
chr22:35273564 | A | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0201 others(5): Show |
12 | HG02717.hp2 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1215+7961A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35273564 | |||||||
chr22:35273802 | T | C | 95 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(92): Show |
132 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1215+8199T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35273802 | |||||||
chr22:35273816 | C | T | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1215+8213C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35273816 | |||||||
chr22:35273859 | C | T | 3 | a0001c0001t0002g0130 a0001c0001t0010g0131 a0001c0001t0014g0247 |
3 | HG02055.hp1 HG03927.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1215+8256C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35273859 | |||||||
chr22:35273994 | G | T | 3 | a0001c0001t0002g0130 a0001c0001t0010g0131 a0001c0001t0014g0247 |
3 | HG02055.hp1 HG03927.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1215+8391G>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35273994 | |||||||
chr22:35274008 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1215+8405C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35274008 | |||||||
chr22:35274702 | A | G | 4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+9099A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35274702 | |||||||
chr22:35274729 | G | GT | 2 | a0001c0001t0001g0020 a0001c0001t0001g0049 |
3 | HG02280.hp2 HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1215+9127dupT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35274729 | ||||||
chr22:35274744 | G | C | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1215+9141G>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35274744 | |||||||
chr22:35274852 | T | A | 9 | a0001c0001t0004g0019 a0001c0001t0004g0040 a0001c0001t0004g0041 others(6): Show |
10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1216-9110T>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35274852 | |||||||
chr22:35274856 | G | A | 9 | a0001c0001t0004g0019 a0001c0001t0004g0040 a0001c0001t0004g0041 others(6): Show |
10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1216-9106G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35274856 | |||||||
chr22:35274955 | C | T | 1 | a0002c0002t0002g0079 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1216-9007C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35274955 | |||||||
chr22:35275087 | G | A | 1 | a0001c0001t0003g0207 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1216-8875G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35275087 | |||||||
chr22:35275110 | C | CT | 32 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0051 others(29): Show |
35 | HG00423.hp2 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1216-8826dupT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35275110 | ||||||
chr22:35275110 | CT | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0049 others(5): Show |
10 | HG02280.hp2 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1216-8826delT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35275110 | ||||||
chr22:35275110 | CTTTTTT | C | 7 | a0001c0001t0001g0204 a0001c0001t0002g0130 a0002c0002t0002g0012 others(4): Show |
10 | HG02071.hp1 HG03209.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.1216-8831_1216-882 others(10): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35275110 | ||||||
chr22:35275110 | CTTTTTTT | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0203 a0001c0001t0014g0247 others(19): Show |
36 | HG00423.hp1 HG00609.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.1216-8832_1216-882 others(11): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35275110 | ||||||
chr22:35275110 | CTTTTTTT others(1): Show |
C | 75 | a0001c0001t0001g0036 a0001c0001t0001g0201 a0001c0001t0001g0202 others(72): Show |
99 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1216-8833_1216-882 others(12): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35275110 | ||||||
chr22:35275142 | G | A | 20 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0133 others(17): Show |
23 | HG02027.hp1 HG02132.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.1216-8820G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35275142 | |||||||
chr22:35275159 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1216-8803G>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35275159 | |||||||
chr22:35275212 | C | T | 1 | a0001c0001t0003g0214 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1216-8750C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35275212 | |||||||
chr22:35275213 | G | A | 1 | a0002c0002t0002g0115 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1216-8749G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35275213 | |||||||
chr22:35275232 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1216-8730G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35275232 | |||||||
chr22:35275510 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1216-8452T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35275510 | |||||||
chr22:35275562 | A | T | 1 | a0002c0002t0002g0100 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1216-8400A>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35275562 | |||||||
chr22:35275608 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
6 | HG02451.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1216-8354G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35275608 | |||||||
chr22:35275967 | A | T | 1 | a0001c0001t0001g0200 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1216-7995A>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35275967 | |||||||
chr22:35276190 | G | A | 95 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(92): Show |
132 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1216-7772G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35276190 | |||||||
chr22:35276462 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1216-7500A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35276462 | |||||||
chr22:35276519 | G | A | 95 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(92): Show |
132 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1216-7443G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35276519 | |||||||
chr22:35276777 | C | T | 1 | a0002c0002t0002g0105 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1216-7185C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35276777 | |||||||
chr22:35276850 | T | G | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1216-7112T>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35276850 | |||||||
chr22:35276958 | C | T | 1 | a0001c0001t0009g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1216-7004C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35276958 | |||||||
chr22:35277006 | C | G | 27 | a0001c0001t0003g0001 a0001c0001t0003g0037 a0001c0001t0003g0038 others(24): Show |
42 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1216-6956C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35277006 | |||||||
chr22:35277108 | C | G | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1216-6854C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35277108 | |||||||
chr22:35277405 | A | G | 1 | a0001c0001t0003g0221 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1216-6557A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35277405 | |||||||
chr22:35277850 | T | C | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1216-6112T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35277850 | |||||||
chr22:35278175 | C | T | 1 | a0002c0002t0002g0078 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1216-5787C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35278175 | |||||||
chr22:35278176 | G | A | 1 | a0001c0001t0009g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1216-5786G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35278176 | |||||||
chr22:35278657 | A | AT | 97 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(94): Show |
132 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1216-5296dupT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35278657 | ||||||
chr22:35278784 | G | A | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1216-5178G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35278784 | |||||||
chr22:35278877 | C | CA | 7 | a0001c0001t0001g0137 a0001c0001t0001g0164 a0001c0001t0001g0168 others(4): Show |
7 | HG02486.hp2 NA19001.hp1 NA19006.hp2 others(4): Show |
intron_variant | MODIFIER | c.1216-5065dupA | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35278877 | ||||||
chr22:35278877 | CA | C | 6 | a0001c0001t0001g0143 a0001c0001t0001g0171 a0001c0001t0001g0190 others(3): Show |
8 | HG00642.hp1 HG01255.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1216-5065delA | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35278877 | ||||||
chr22:35278877 | CAAA | C | 6 | a0001c0001t0014g0247 a0002c0002t0002g0069 a0002c0002t0005g0021 others(3): Show |
8 | HG03927.hp1 NA18943.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.1216-5067_1216-506 others(7): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35278877 | ||||||
chr22:35278877 | CAAAA | C | 93 | a0001c0001t0001g0192 a0001c0001t0002g0088 a0001c0001t0002g0130 others(90): Show |
128 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1216-5068_1216-506 others(8): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35278877 | ||||||
chr22:35278918 | G | A | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1216-5044G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35278918 | |||||||
chr22:35278987 | T | A | 1 | a0001c0001t0001g0168 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1216-4975T>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35278987 | |||||||
chr22:35279118 | A | T | 4 | a0002c0002t0002g0024 a0002c0002t0002g0098 a0002c0002t0002g0099 others(1): Show |
5 | NA18939.hp2 NA18955.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.1216-4844A>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279118 | |||||||
chr22:35279132 | C | CT | 8 | a0001c0001t0001g0017 a0001c0001t0001g0151 a0001c0001t0001g0191 others(5): Show |
10 | HG01081.hp2 HG01175.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1216-4799dupT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279132 | ||||||
chr22:35279132 | CT | C | 59 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(56): Show |
90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1216-4799delT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279132 | ||||||
chr22:35279132 | CTT | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0051 others(10): Show |
17 | HG01069.hp2 HG02717.hp2 HG02723.hp2 others(14): Show |
intron_variant | MODIFIER | c.1216-4800_1216-479 others(6): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279132 | ||||||
chr22:35279132 | CTTT | C | 25 | a0001c0001t0001g0135 a0001c0001t0001g0138 a0001c0001t0001g0140 others(22): Show |
27 | HG00438.hp2 HG01928.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.1216-4801_1216-479 others(7): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279132 | ||||||
chr22:35279132 | CTTTT | C | 80 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0133 others(77): Show |
118 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1216-4802_1216-479 others(8): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279132 | ||||||
chr22:35279132 | CTTTTT | C | 9 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0002c0002t0002g0067 others(6): Show |
9 | HG00558.hp2 HG01169.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1216-4803_1216-479 others(9): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279132 | ||||||
chr22:35279132 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1216-4810_1216-479 others(16): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279132 | ||||||
chr22:35279132 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0050 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1216-4812_1216-479 others(18): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279132 | ||||||
chr22:35279132 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0049 |
3 | HG02280.hp2 HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1216-4813_1216-479 others(19): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279132 | ||||||
chr22:35279223 | C | T | 4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-4739C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279223 | |||||||
chr22:35279274 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1216-4688G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279274 | |||||||
chr22:35279331 | A | G | 1 | a0002c0002t0016g0095 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1216-4631A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279331 | |||||||
chr22:35279348 | A | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0133 a0001c0001t0001g0134 others(11): Show |
16 | HG02027.hp1 HG02132.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.1216-4614A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279348 | |||||||
chr22:35279359 | G | A | 1 | a0002c0002t0002g0024 | 2 | NA18939.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1216-4603G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279359 | |||||||
chr22:35279382 | G | A | 2 | a0001c0001t0003g0211 a0001c0001t0003g0234 |
2 | HG02015.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1216-4580G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279382 | |||||||
chr22:35279395 | T | C | 2 | a0002c0002t0002g0059 a0002c0002t0002g0060 |
2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1216-4567T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279395 | |||||||
chr22:35279402 | G | A | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1216-4560G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279402 | |||||||
chr22:35279489 | A | G | 95 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(92): Show |
132 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1216-4473A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279489 | |||||||
chr22:35279497 | T | G | 1 | a0001c0001t0001g0164 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1216-4465T>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279497 | |||||||
chr22:35279544 | G | A | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1216-4418G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279544 | |||||||
chr22:35279677 | C | CT | 35 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
47 | HG00609.hp1 HG00741.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.1216-4263dupT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279677 | ||||||
chr22:35279677 | C | CTT | 8 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0049 others(5): Show |
10 | HG00423.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1216-4264_1216-426 others(6): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279677 | ||||||
chr22:35279677 | CT | C | 10 | a0001c0001t0001g0034 a0001c0001t0001g0168 a0001c0001t0001g0176 others(7): Show |
11 | HG01074.hp2 HG01517.hp2 HG03239.hp2 others(8): Show |
intron_variant | MODIFIER | c.1216-4263delT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279677 | ||||||
chr22:35279677 | CTTTT | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(5): Show |
8 | HG02027.hp1 HG02132.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1216-4266_1216-426 others(8): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279677 | ||||||
chr22:35279677 | CTTTTT | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0133 a0001c0001t0001g0134 others(4): Show |
9 | HG02155.hp2 NA18941.hp1 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.1216-4267_1216-426 others(9): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279677 | ||||||
chr22:35279699 | T | TTTG | 82 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(79): Show |
118 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1216-4263_1216-426 others(7): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279699 | |||||||
chr22:35279699 | T | TTTTG | 13 | a0002c0002t0002g0026 a0002c0002t0002g0058 a0002c0002t0002g0060 others(10): Show |
14 | HG00438.hp2 HG01099.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.1216-4263_1216-426 others(8): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279699 | |||||||
chr22:35279921 | T | TCAGTCCT others(5): Show |
1 | a0001c0001t0001g0183 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1216-4040_1216-402 others(16): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35279921 | ||||||
chr22:35279981 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1216-3981T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35279981 | |||||||
chr22:35280116 | A | G | 5 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
5 | HG02027.hp1 NA18612.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1216-3846A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35280116 | |||||||
chr22:35280145 | C | CT | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1216-3815dupT | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35280145 | ||||||
chr22:35280158 | G | A | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1216-3804G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35280158 | |||||||
chr22:35280264 | C | T | 27 | a0001c0001t0003g0001 a0001c0001t0003g0037 a0001c0001t0003g0038 others(24): Show |
42 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1216-3698C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35280264 | |||||||
chr22:35280340 | C | T | 1 | a0002c0002t0002g0093 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1216-3622C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35280340 | |||||||
chr22:35280797 | C | G | 1 | a0002c0002t0002g0105 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1216-3165C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35280797 | |||||||
chr22:35281415 | G | A | 1 | a0002c0002t0002g0122 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1216-2547G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35281415 | |||||||
chr22:35281450 | C | G | 1 | a0001c0001t0009g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1216-2512C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35281450 | |||||||
chr22:35281578 | G | A | 95 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(92): Show |
132 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1216-2384G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35281578 | |||||||
chr22:35281585 | A | G | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1216-2377A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35281585 | |||||||
chr22:35281708 | T | C | 99 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0003g0215 others(96): Show |
136 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1216-2254T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35281708 | |||||||
chr22:35282176 | C | T | 1 | a0001c0001t0003g0046 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1216-1786C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282176 | |||||||
chr22:35282250 | T | C | 5 | a0001c0001t0003g0219 a0002c0002t0002g0012 a0002c0002t0002g0109 others(2): Show |
7 | NA18942.hp1 NA18944.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1216-1712T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282250 | |||||||
chr22:35282263 | A | G | 118 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0133 others(115): Show |
156 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.1216-1699A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282263 | |||||||
chr22:35282326 | A | G | 1 | a0002c0002t0017g0103 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1216-1636A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282326 | |||||||
chr22:35282333 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0185 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1216-1629T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282333 | |||||||
chr22:35282341 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0185 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1216-1621T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282341 | |||||||
chr22:35282368 | G | A | 6 | a0001c0001t0004g0019 a0001c0001t0004g0040 a0001c0001t0004g0043 others(3): Show |
7 | HG01884.hp2 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1216-1594G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282368 | |||||||
chr22:35282368 | G | C | 1 | a0001c0001t0001g0150 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1216-1594G>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282368 | |||||||
chr22:35282377 | C | A | 2 | a0001c0001t0003g0154 a0001c0001t0003g0155 |
2 | NA18940.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1216-1585C>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282377 | |||||||
chr22:35282378 | G | A | 4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-1584G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282378 | |||||||
chr22:35282387 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1216-1575A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282387 | |||||||
chr22:35282447 | T | C | 2 | a0001c0001t0007g0018 a0001c0001t0007g0237 |
4 | HG00642.hp1 HG02735.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-1515T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282447 | |||||||
chr22:35282451 | C | G | 2 | a0001c0001t0007g0018 a0001c0001t0007g0237 |
4 | HG00642.hp1 HG02735.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-1511C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282451 | |||||||
chr22:35282453 | A | T | 2 | a0001c0001t0007g0018 a0001c0001t0007g0237 |
4 | HG00642.hp1 HG02735.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-1509A>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282453 | |||||||
chr22:35282595 | A | G | 1 | a0001c0001t0014g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1216-1367A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282595 | |||||||
chr22:35282651 | G | A | 1 | a0002c0002t0002g0129 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1216-1311G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282651 | |||||||
chr22:35282890 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0161 |
2 | NA18986.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1216-1072G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282890 | |||||||
chr22:35282895 | A | T | 9 | a0001c0001t0004g0019 a0001c0001t0004g0040 a0001c0001t0004g0041 others(6): Show |
10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1216-1067A>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35282895 | |||||||
chr22:35283093 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1216-869A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35283093 | |||||||
chr22:35283131 | C | T | 6 | a0001c0001t0001g0156 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG01106.hp1 HG01192.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1216-831C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35283131 | |||||||
chr22:35283328 | C | T | 2 | a0001c0001t0002g0130 a0001c0001t0010g0131 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1216-634C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35283328 | |||||||
chr22:35283418 | G | A | 103 | a0001c0001t0001g0030 a0001c0001t0001g0147 a0001c0001t0001g0148 others(100): Show |
141 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.1216-544G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35283418 | |||||||
chr22:35283619 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1216-343A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35283619 | |||||||
chr22:35283665 | C | T | 103 | a0001c0001t0001g0030 a0001c0001t0001g0147 a0001c0001t0001g0148 others(100): Show |
141 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.1216-297C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35283665 | |||||||
chr22:35283722 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1216-240G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35283722 | |||||||
chr22:35283772 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1216-190A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35283772 | |||||||
chr22:35283794 | A | AAT | 92 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(89): Show |
129 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1216-153_1216-152d others(4): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr22 | 35283794 | ||||||
chr22:35283794 | A | T | 1 | a0002c0002t0002g0075 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1216-168A>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35283794 | |||||||
chr22:35283796 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1216-166T>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35283796 | |||||||
chr22:35283892 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1216-70A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35283892 | |||||||
chr22:35283958 | T | C | 122 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0030 others(119): Show |
163 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
splice_region_variant&intron_variant | LOW | c.1216-4T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 5/10 | chr22 | 35283958 | |||||||
chr22:35284102 | G | A | 165 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0030 others(162): Show |
222 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.1297+59G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35284102 | |||||||
chr22:35284232 | A | C | 1 | a0001c0001t0001g0132 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1297+189A>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35284232 | |||||||
chr22:35284282 | A | C | 1 | a0001c0001t0001g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1297+239A>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35284282 | |||||||
chr22:35284291 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1297+248C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35284291 | |||||||
chr22:35284334 | T | C | 1 | a0002c0002t0002g0127 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1297+291T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35284334 | |||||||
chr22:35284394 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1297+351T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35284394 | |||||||
chr22:35284473 | C | G | 1 | a0002c0002t0002g0097 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1297+430C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35284473 | |||||||
chr22:35284646 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1297+603A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35284646 | |||||||
chr22:35284822 | T | C | 1 | a0001c0001t0003g0048 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1297+779T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35284822 | |||||||
chr22:35284824 | T | G | 1 | a0002c0002t0013g0113 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1297+781T>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35284824 | |||||||
chr22:35284850 | G | C | 1 | a0002c0002t0002g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1297+807G>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35284850 | |||||||
chr22:35284885 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1297+842A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35284885 | |||||||
chr22:35284995 | G | C | 6 | a0001c0001t0002g0088 a0002c0002t0002g0082 a0002c0002t0002g0086 others(3): Show |
6 | HG01175.hp1 HG01257.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1297+952G>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35284995 | |||||||
chr22:35285184 | T | C | 1 | a0002c0002t0002g0011 | 3 | HG03492.hp1 NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1298-813T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35285184 | |||||||
chr22:35285255 | T | A | 1 | a0002c0002t0015g0083 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1298-742T>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35285255 | |||||||
chr22:35285284 | C | T | 1 | a0002c0002t0013g0113 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1298-713C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35285284 | |||||||
chr22:35285311 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1298-686G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35285311 | |||||||
chr22:35285373 | C | T | 95 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(92): Show |
132 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1298-624C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35285373 | |||||||
chr22:35285523 | C | T | 20 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0133 others(17): Show |
23 | HG02027.hp1 HG02132.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.1298-474C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35285523 | |||||||
chr22:35285826 | A | G | 4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1298-171A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35285826 | |||||||
chr22:35285844 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1298-153A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35285844 | |||||||
chr22:35285845 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1298-152G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35285845 | |||||||
chr22:35285900 | G | C | 99 | a0001c0001t0001g0051 a0001c0001t0002g0088 a0001c0001t0002g0130 others(96): Show |
136 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1298-97G>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 6/10 | chr22 | 35285900 | |||||||
chr22:35286451 | T | C | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1362+390T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 7/10 | chr22 | 35286451 | |||||||
chr22:35286491 | C | G | 1 | a0002c0002t0002g0091 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1362+430C>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 7/10 | chr22 | 35286491 | |||||||
chr22:35286745 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1363-602G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 7/10 | chr22 | 35286745 | |||||||
chr22:35286851 | C | CA | 18 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0146 others(15): Show |
19 | HG00733.hp1 HG00741.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.1363-475dupA | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 35286851 | ||||||
chr22:35286851 | C | CAA | 80 | a0001c0001t0001g0049 a0002c0002t0002g0002 a0002c0002t0002g0005 others(77): Show |
115 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1363-476_1363-475d others(4): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 35286851 | ||||||
chr22:35286851 | CA | C | 13 | a0001c0001t0001g0164 a0001c0001t0001g0183 a0001c0001t0001g0188 others(10): Show |
14 | HG01069.hp2 HG01071.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.1363-475delA | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 35286851 | ||||||
chr22:35286895 | TTATGA | T | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1363-446_1363-442d others(7): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 35286895 | ||||||
chr22:35287062 | G | T | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1363-285G>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 7/10 | chr22 | 35287062 | |||||||
chr22:35287245 | T | C | 95 | a0001c0001t0002g0088 a0002c0002t0002g0002 a0002c0002t0002g0005 others(92): Show |
132 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1363-102T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 7/10 | chr22 | 35287245 | |||||||
chr22:35287599 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1468+147G>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 8/10 | chr22 | 35287599 | |||||||
chr22:35287809 | G | A | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1468+357G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 8/10 | chr22 | 35287809 | |||||||
chr22:35287911 | G | A | 1 | a0002c0002t0002g0054 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1469-327G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 8/10 | chr22 | 35287911 | |||||||
chr22:35288066 | C | T | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1469-172C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 8/10 | chr22 | 35288066 | |||||||
chr22:35288441 | T | G | 1 | a0001c0001t0003g0037 | 2 | NA18963.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1638+34T>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35288441 | |||||||
chr22:35288540 | G | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(233): Show |
322 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(319): Show |
intron_variant | MODIFIER | c.1638+133G>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35288540 | |||||||
chr22:35288849 | A | T | 1 | a0002c0002t0002g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1638+442A>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35288849 | |||||||
chr22:35288860 | G | A | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1638+453G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35288860 | |||||||
chr22:35288965 | C | T | 1 | a0002c0002t0002g0127 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1638+558C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35288965 | |||||||
chr22:35289055 | A | G | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1638+648A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35289055 | |||||||
chr22:35289080 | C | T | 8 | a0001c0001t0004g0019 a0001c0001t0004g0040 a0001c0001t0004g0041 others(5): Show |
9 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1638+673C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35289080 | |||||||
chr22:35289081 | A | G | 97 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(94): Show |
134 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1638+674A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35289081 | |||||||
chr22:35289096 | C | T | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1638+689C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35289096 | |||||||
chr22:35289142 | AAAAG | A | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1638+755_1638+758d others(6): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr22 | 35289142 | ||||||
chr22:35289225 | A | G | 123 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0030 others(120): Show |
164 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1638+818A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35289225 | |||||||
chr22:35289238 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1638+831C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35289238 | |||||||
chr22:35289266 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1638+859C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35289266 | |||||||
chr22:35289362 | G | A | 1 | a0002c0002t0002g0072 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1638+955G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35289362 | |||||||
chr22:35289455 | A | G | 9 | a0001c0001t0004g0019 a0001c0001t0004g0040 a0001c0001t0004g0041 others(6): Show |
10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1638+1048A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35289455 | |||||||
chr22:35289471 | CAAAAA | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0160 |
4 | HG00741.hp1 HG01346.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638+1065_1638+106 others(9): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35289471 | |||||||
chr22:35289484 | G | C | 2 | a0001c0001t0002g0130 a0001c0001t0010g0131 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1638+1077G>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35289484 | |||||||
chr22:35289878 | A | T | 2 | a0002c0002t0002g0123 a0002c0002t0002g0128 |
2 | NA18974.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1638+1471A>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35289878 | |||||||
chr22:35290190 | A | G | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1638+1783A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35290190 | |||||||
chr22:35290400 | C | T | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1638+1993C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35290400 | |||||||
chr22:35290562 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1638+2155C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35290562 | |||||||
chr22:35290609 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1638+2202C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35290609 | |||||||
chr22:35290610 | G | A | 1 | a0001c0001t0014g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1638+2203G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35290610 | |||||||
chr22:35290612 | C | T | 5 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0200 others(2): Show |
7 | HG00642.hp1 HG01175.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1638+2205C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35290612 | |||||||
chr22:35290630 | C | CA | 61 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0050 others(58): Show |
77 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.1638+2246dupA | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr22 | 35290630 | ||||||
chr22:35290630 | C | CAA | 20 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0133 others(17): Show |
23 | HG01168.hp1 HG02027.hp1 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.1638+2245_1638+224 others(6): Show |
HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr22 | 35290630 | ||||||
chr22:35290630 | CA | C | 8 | a0001c0001t0001g0030 a0001c0001t0001g0148 a0001c0001t0001g0149 others(5): Show |
9 | HG02451.hp2 HG02486.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1638+2246delA | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr22 | 35290630 | ||||||
chr22:35290675 | G | A | 136 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0030 others(133): Show |
178 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.1638+2268G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35290675 | |||||||
chr22:35290680 | T | TC | 20 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0133 others(17): Show |
23 | HG02027.hp1 HG02132.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.1638+2277dupC | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr22 | 35290680 | ||||||
chr22:35290872 | G | A | 1 | a0002c0002t0002g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639-2120G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35290872 | |||||||
chr22:35291224 | T | C | 1 | a0001c0001t0003g0230 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1639-1768T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35291224 | |||||||
chr22:35291636 | C | A | 6 | a0002c0002t0002g0069 a0002c0002t0005g0021 a0002c0002t0005g0022 others(3): Show |
8 | NA18943.hp1 NA18945.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.1639-1356C>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35291636 | |||||||
chr22:35291797 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0185 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1639-1195T>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35291797 | |||||||
chr22:35291906 | G | C | 1 | a0001c0001t0008g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1639-1086G>C | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35291906 | |||||||
chr22:35292126 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0049 |
3 | HG02280.hp2 HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1639-866G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35292126 | |||||||
chr22:35292433 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG02280.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1639-559C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35292433 | |||||||
chr22:35292505 | T | A | 98 | a0001c0001t0002g0088 a0001c0001t0002g0130 a0001c0001t0010g0131 others(95): Show |
135 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1639-487T>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35292505 | |||||||
chr22:35292630 | C | T | 20 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0133 others(17): Show |
23 | HG02027.hp1 HG02132.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.1639-362C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35292630 | |||||||
chr22:35292668 | A | G | 9 | a0001c0001t0004g0019 a0001c0001t0004g0040 a0001c0001t0004g0041 others(6): Show |
10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1639-324A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 9/10 | chr22 | 35292668 | |||||||
chr22:35293194 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1761+80C>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 10/10 | chr22 | 35293194 | |||||||
chr22:35293214 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG01192.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1761+100A>G | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 10/10 | chr22 | 35293214 | |||||||
chr22:35293422 | G | T | 136 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0030 others(133): Show |
178 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.1762-185G>T | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 10/10 | chr22 | 35293422 | |||||||
chr22:35293425 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1762-182G>A | HMGXB4 | ENSG00000100281.14 | transcript | ENST00000216106.6 | protein_coding | 10/10 | chr22 | 35293425 |