Item | Value |
---|---|
geneid | 7358 |
ensemblid | ENSG00000109814.12 |
hgncid | 12525 |
symbol | UGDH |
name | UDP-glucose 6-dehydrogenase |
refseq_nuc | NM_003359.4 |
refseq_prot | NP_003350.1 |
ensembl_nuc | ENST00000316423.11 |
ensembl_prot | ENSP00000319501.6 |
mane_status | MANE Select |
chr | chr4 |
start | 39498755 |
end | 39527439 |
strand | - |
ver | v1.2 |
region | chr4:39498755-39527439 |
region5000 | chr4:39493755-39532439 |
regionname0 | UGDH_chr4_39498755_39527439 |
regionname5000 | UGDH_chr4_39493755_39532439 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 494 | 413 | 93 | 74 | 185 | 15 | 44 | 143 | UGDH_chr4_39493755_39532439 | UGDH | MFEIK others(489): Show |
chr4 | 39493755 | 39532439 |
a0002 | 0/0 | 494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | MFEIK others(489): Show |
chr4 | 39493755 | 39532439 |
a0003 | 0/0 | 494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | MFEIK others(489): Show |
chr4 | 39493755 | 39532439 |
a0004 | 0/0 | 494 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | MFEIK others(489): Show |
chr4 | 39493755 | 39532439 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1482 | 261 | 48 | 57 | 113 | 8 | 33 | UGDH_chr4_39493755_39532439 | UGDH | ATGTT others(1477): Show |
chr4 | 39493755 | 39532439 | ||
a0001c0002 | 0/0 | 1482 | 130 | 42 | 14 | 64 | 3 | 7 | UGDH_chr4_39493755_39532439 | UGDH | ATGTT others(1477): Show |
chr4 | 39493755 | 39532439 | ||
a0001c0003 | 0/0 | 1482 | 17 | 1 | 3 | 6 | 4 | 3 | UGDH_chr4_39493755_39532439 | UGDH | ATGTT others(1477): Show |
chr4 | 39493755 | 39532439 | ||
a0001c0004 | 0/0 | 1482 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | ATGTT others(1477): Show |
chr4 | 39493755 | 39532439 | ||
a0001c0005 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | ATGTT others(1477): Show |
chr4 | 39493755 | 39532439 | ||
a0001c0008 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | ATGTT others(1477): Show |
chr4 | 39493755 | 39532439 | ||
a0001c0010 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | ATGTT others(1477): Show |
chr4 | 39493755 | 39532439 | ||
a0002c0009 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | ATGTT others(1477): Show |
chr4 | 39493755 | 39532439 | ||
a0003c0006 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | ATGTT others(1477): Show |
chr4 | 39493755 | 39532439 | ||
a0004c0007 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | ATGTT others(1477): Show |
chr4 | 39493755 | 39532439 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3034 | 63 | 0 | 19 | 29 | 1 | 13 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0002 | 0/0 | 3037 | 36 | 8 | 12 | 11 | 3 | 2 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0003 | 0/0 | 3035 | 9 | 0 | 0 | 8 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0004 | 0/0 | 3036 | 34 | 3 | 8 | 16 | 1 | 6 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3031): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0005 | 0/0 | 3034 | 29 | 0 | 3 | 24 | 1 | 1 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0006 | 1/0 | 3037 | 30 | 23 | 3 | 0 | 1 | 2 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0007 | 0/0 | 3038 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3033): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0008 | 0/0 | 3036 | 2 | 1 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3031): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0010 | 0/0 | 3034 | 9 | 0 | 5 | 1 | 1 | 2 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0011 | 0/0 | 3036 | 6 | 0 | 1 | 3 | 0 | 2 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3031): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0012 | 0/0 | 3038 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3033): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0013 | 0/0 | 3035 | 3 | 3 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0014 | 0/0 | 3034 | 4 | 0 | 0 | 4 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0015 | 0/0 | 3034 | 3 | 0 | 0 | 3 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0017 | 0/0 | 3036 | 2 | 0 | 1 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3031): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0018 | 0/0 | 3035 | 3 | 1 | 1 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0020 | 0/0 | 3037 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0021 | 0/0 | 3037 | 2 | 0 | 1 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0022 | 0/0 | 3035 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0023 | 0/0 | 3035 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0024 | 0/0 | 3036 | 2 | 0 | 2 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3031): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0027 | 0/0 | 3033 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3028): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0028 | 0/0 | 3034 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0029 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3028): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0030 | 0/0 | 3035 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0031 | 0/0 | 3035 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0032 | 0/0 | 3037 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0033 | 0/0 | 3037 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0035 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0036 | 0/0 | 3035 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0037 | 0/0 | 3037 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0038 | 0/0 | 3037 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0039 | 0/0 | 3037 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0043 | 0/0 | 3035 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0045 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3031): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0047 | 0/0 | 3037 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0048 | 0/0 | 3037 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0001t0049 | 0/0 | 3037 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0001 | 0/0 | 3034 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0002 | 0/0 | 3037 | 15 | 12 | 0 | 3 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0003 | 0/0 | 3035 | 40 | 15 | 3 | 22 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0005 | 0/0 | 3034 | 2 | 0 | 0 | 1 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0007 | 0/0 | 3038 | 24 | 3 | 1 | 18 | 0 | 2 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3033): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0008 | 0/0 | 3036 | 9 | 1 | 1 | 7 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3031): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0009 | 0/0 | 3034 | 11 | 0 | 2 | 6 | 0 | 3 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0010 | 0/0 | 3034 | 2 | 0 | 1 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0012 | 0/0 | 3038 | 4 | 0 | 0 | 4 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3033): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0013 | 0/0 | 3035 | 2 | 1 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0016 | 0/0 | 3035 | 4 | 1 | 3 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0017 | 0/0 | 3036 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3031): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0019 | 0/0 | 3034 | 3 | 3 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0020 | 0/0 | 3037 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0022 | 0/0 | 3035 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0023 | 0/0 | 3035 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0025 | 0/0 | 3036 | 2 | 1 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3031): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0026 | 0/0 | 3038 | 2 | 1 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3033): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0034 | 0/0 | 3038 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3033): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0041 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0044 | 0/0 | 3035 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0046 | 0/0 | 3037 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0001c0002t0050 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0003t0001 | 0/0 | 3034 | 16 | 1 | 3 | 6 | 3 | 3 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0003t0040 | 0/0 | 3034 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0004t0003 | 0/0 | 3035 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0004t0015 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0005t0018 | 0/0 | 3035 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0001c0008t0005 | 0/0 | 3034 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0001c0010t0042 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3029): Show |
chr4 | 39493755 | 39532439 |
a0002c0009t0002 | 0/0 | 3037 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3032): Show |
chr4 | 39493755 | 39532439 |
a0003c0006t0013 | 0/0 | 3035 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3030): Show |
chr4 | 39493755 | 39532439 |
a0004c0007t0017 | 0/0 | 3036 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | GTGTA others(3031): Show |
chr4 | 39493755 | 39532439 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 13 | 0 | 3 | 8 | 1 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0007 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0016 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0005g0001 | 0/0 | 17 | 0 | 2 | 14 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0005g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0008 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0017 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0006g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0007g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0008g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0010g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0010g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0010g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0010g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0010g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0010g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0010g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0011g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0011g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0011g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0011g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0011g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0011g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0012g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0012g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0013g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0013g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0013g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0014g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0014g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0014g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0015g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0015g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0015g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0017g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0017g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0018g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0018g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0018g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0020g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0020g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0021g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0022g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0023g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0024g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0024g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0027g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0028g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0029g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0030g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0031g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0032g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0033g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0035g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0036g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0037g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0038g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0039g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0043g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0045g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0047g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0048g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0001t0049g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0002 | 0/0 | 15 | 0 | 1 | 14 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0004 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0005g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0012 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0007g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0008g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0008g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0008g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0008g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0009g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0009g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0009g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0009g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0009g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0009g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0009g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0009g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0009g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0009g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0009g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0010g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0010g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0012g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0012g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0013g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0013g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0016g0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0016g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0017g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0019g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0019g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0019g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0020g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0022g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0023g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0025g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0025g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0026g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0026g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0034g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0041g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0044g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0046g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0002t0050g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0003t0001g0005 | 0/0 | 7 | 0 | 1 | 4 | 0 | 2 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0003t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0003t0040g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0004t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0004t0015g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0005t0018g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0008t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0001c0010t0042g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0002c0009t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0003c0006t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
a0004c0007t0017g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0005 | g0121 | EUR | GBR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | GBR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00140 | hp1 | a0001 | c0003 | t0001 | g0022 | EUR | GBR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0044 | EUR | GBR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00280 | hp1 | a0001 | c0003 | t0040 | g0196 | EUR | FIN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00280 | hp2 | a0001 | c0001 | t0006 | g0207 | EUR | FIN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00323 | hp1 | a0001 | c0001 | t0010 | g0233 | EUR | FIN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00408 | hp1 | a0001 | c0002 | t0007 | g0012 | EAS | CHS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00408 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | CHS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00423 | hp2 | a0001 | c0002 | t0009 | g0268 | EAS | CHS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | CHS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00558 | hp1 | a0001 | c0002 | t0003 | g0116 | EAS | CHS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | CHS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00609 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | CHS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00609 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00639 | hp1 | a0001 | c0001 | t0010 | g0239 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00642 | hp1 | a0001 | c0001 | t0021 | g0020 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00733 | hp1 | a0001 | c0001 | t0005 | g0188 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01069 | hp1 | a0001 | c0001 | t0024 | g0247 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01069 | hp2 | a0001 | c0001 | t0018 | g0241 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01070 | hp2 | a0001 | c0001 | t0010 | g0039 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01071 | hp1 | a0001 | c0001 | t0024 | g0248 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0022 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01074 | hp2 | a0001 | c0001 | t0006 | g0229 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01081 | hp1 | a0001 | c0001 | t0008 | g0171 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0240 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01099 | hp2 | a0001 | c0002 | t0034 | g0046 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01109 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0242 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01167 | hp1 | a0001 | c0002 | t0016 | g0119 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01167 | hp2 | a0001 | c0002 | t0025 | g0272 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01168 | hp1 | a0001 | c0001 | t0010 | g0205 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01168 | hp2 | a0001 | c0002 | t0010 | g0291 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01169 | hp1 | a0001 | c0001 | t0010 | g0039 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01169 | hp2 | a0001 | c0002 | t0016 | g0015 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0243 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01175 | hp2 | a0001 | c0002 | t0020 | g0126 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01243 | hp1 | a0001 | c0002 | t0003 | g0133 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01243 | hp2 | a0001 | c0002 | t0009 | g0261 | AMR | PUR | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01255 | hp2 | a0001 | c0002 | t0016 | g0015 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0246 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0245 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0238 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01361 | hp2 | a0001 | c0002 | t0003 | g0123 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0059 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0055 | EUR | IBS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0172 | EUR | IBS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01516 | hp1 | a0001 | c0003 | t0001 | g0099 | EUR | IBS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0047 | EUR | IBS | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0137 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01952 | hp1 | a0001 | c0002 | t0007 | g0275 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01978 | hp2 | a0001 | c0002 | t0008 | g0014 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01993 | hp1 | a0001 | c0001 | t0006 | g0199 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01993 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02004 | hp2 | a0001 | c0002 | t0009 | g0263 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02015 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02015 | hp2 | a0001 | c0003 | t0001 | g0060 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02027 | hp1 | a0001 | c0002 | t0003 | g0118 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02040 | hp2 | a0001 | c0001 | t0011 | g0054 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0056 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02056 | hp1 | a0001 | c0002 | t0008 | g0014 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02056 | hp2 | a0001 | c0001 | t0011 | g0075 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02071 | hp1 | a0001 | c0002 | t0009 | g0264 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02071 | hp2 | a0001 | c0002 | t0007 | g0012 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02074 | hp1 | a0001 | c0002 | t0007 | g0276 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02074 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02080 | hp1 | a0001 | c0001 | t0014 | g0069 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02129 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02129 | hp2 | a0001 | c0002 | t0009 | g0258 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02135 | hp1 | a0001 | c0002 | t0007 | g0280 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02135 | hp2 | a0001 | c0001 | t0018 | g0209 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0228 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02145 | hp2 | a0001 | c0001 | t0035 | g0194 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02155 | hp1 | a0001 | c0002 | t0009 | g0269 | EAS | CDX | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02155 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | CDX | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02165 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | CDX | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | CDX | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02257 | hp1 | a0001 | c0001 | t0049 | g0250 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02257 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02258 | hp1 | a0001 | c0001 | t0047 | g0251 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0230 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02273 | hp2 | a0001 | c0001 | t0011 | g0096 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02280 | hp2 | a0001 | c0001 | t0023 | g0217 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02293 | hp2 | a0001 | c0001 | t0017 | g0156 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02300 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0294 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02523 | hp1 | a0001 | c0002 | t0003 | g0109 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | KHV | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0293 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0192 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0231 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02622 | hp2 | a0001 | c0002 | t0044 | g0286 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02630 | hp1 | a0001 | c0002 | t0022 | g0257 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02630 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0226 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02647 | hp2 | a0001 | c0002 | t0003 | g0131 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02698 | hp2 | a0001 | c0001 | t0010 | g0289 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02717 | hp1 | a0001 | c0002 | t0019 | g0130 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02723 | hp2 | a0001 | c0002 | t0016 | g0015 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02735 | hp1 | a0001 | c0002 | t0007 | g0012 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02738 | hp1 | a0001 | c0002 | t0017 | g0122 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0125 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02809 | hp2 | a0001 | c0002 | t0007 | g0018 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02818 | hp1 | a0001 | c0002 | t0023 | g0281 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02818 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02886 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02886 | hp2 | a0001 | c0002 | t0025 | g0285 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0223 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02895 | hp2 | a0001 | c0002 | t0013 | g0256 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02897 | hp1 | a0001 | c0002 | t0019 | g0140 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02897 | hp2 | a0001 | c0002 | t0041 | g0255 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02922 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0224 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02965 | hp1 | a0001 | c0002 | t0019 | g0132 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02970 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02976 | hp1 | a0001 | c0001 | t0045 | g0236 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0041 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03098 | hp2 | a0001 | c0002 | t0003 | g0135 | AFR | MSL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03130 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03139 | hp2 | a0001 | c0001 | t0013 | g0249 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0127 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03195 | hp2 | a0001 | c0002 | t0007 | g0018 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03209 | hp1 | a0001 | c0002 | t0026 | g0277 | AFR | MSL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0222 | AFR | MSL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03239 | hp1 | a0001 | c0001 | t0028 | g0097 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03239 | hp2 | a0001 | c0002 | t0009 | g0259 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03453 | hp1 | a0001 | c0001 | t0013 | g0237 | AFR | MSL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0134 | AFR | MSL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | MSL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | MSL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03490 | hp1 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0211 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03491 | hp2 | a0001 | c0003 | t0001 | g0058 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03516 | hp1 | a0001 | c0002 | t0008 | g0120 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0129 | AFR | ESN | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03540 | hp2 | a0001 | c0001 | t0048 | g0244 | AFR | GWD | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | MSL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03579 | hp2 | a0001 | c0001 | t0037 | g0195 | AFR | MSL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03654 | hp2 | a0001 | c0001 | t0006 | g0040 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03669 | hp1 | a0001 | c0002 | t0007 | g0271 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03669 | hp2 | a0001 | c0002 | t0009 | g0262 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03688 | hp1 | a0001 | c0001 | t0006 | g0040 | SAS | STU | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03704 | hp2 | a0001 | c0001 | t0039 | g0174 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03710 | hp1 | a0001 | c0002 | t0010 | g0265 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03710 | hp2 | a0001 | c0001 | t0011 | g0061 | SAS | PJL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0220 | SAS | BEB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03831 | hp2 | a0001 | c0001 | t0027 | g0095 | SAS | BEB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03834 | hp2 | a0001 | c0001 | t0030 | g0064 | SAS | BEB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03927 | hp1 | a0001 | c0008 | t0005 | g0110 | SAS | BEB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | BEB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0005 | SAS | STU | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG04204 | hp2 | a0001 | c0002 | t0009 | g0270 | SAS | STU | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG04228 | hp1 | a0001 | c0001 | t0010 | g0216 | SAS | STU | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG04228 | hp2 | a0001 | c0001 | t0011 | g0079 | SAS | STU | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18522 | hp1 | a0001 | c0002 | t0003 | g0031 | AFR | YRI | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0186 | AFR | YRI | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18612 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | CHB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18747 | hp1 | a0001 | c0001 | t0005 | g0154 | EAS | CHB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | CHB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | YRI | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0139 | AFR | YRI | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18939 | hp1 | a0001 | c0002 | t0046 | g0279 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18940 | hp1 | a0001 | c0001 | t0010 | g0214 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18940 | hp2 | a0001 | c0002 | t0007 | g0282 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18943 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18945 | hp1 | a0001 | c0002 | t0012 | g0013 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18946 | hp2 | a0001 | c0002 | t0003 | g0115 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18948 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18949 | hp2 | a0001 | c0001 | t0036 | g0162 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18951 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18951 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18952 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18952 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18953 | hp1 | a0001 | c0002 | t0003 | g0108 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18959 | hp1 | a0001 | c0001 | t0005 | g0164 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18960 | hp1 | a0001 | c0001 | t0014 | g0086 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18962 | hp1 | a0001 | c0002 | t0012 | g0013 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18962 | hp2 | a0001 | c0001 | t0014 | g0024 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18963 | hp1 | a0001 | c0002 | t0007 | g0283 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18964 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18967 | hp1 | a0001 | c0002 | t0009 | g0267 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18967 | hp2 | a0001 | c0001 | t0005 | g0160 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18968 | hp1 | a0001 | c0001 | t0012 | g0159 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18970 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18970 | hp2 | a0001 | c0002 | t0007 | g0012 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18971 | hp2 | a0001 | c0002 | t0007 | g0274 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18972 | hp1 | a0001 | c0001 | t0005 | g0149 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18972 | hp2 | a0001 | c0002 | t0012 | g0102 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18974 | hp2 | a0001 | c0001 | t0005 | g0142 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18975 | hp1 | a0001 | c0002 | t0008 | g0107 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18978 | hp2 | a0001 | c0002 | t0008 | g0014 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18979 | hp1 | a0001 | c0002 | t0005 | g0141 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18979 | hp2 | a0001 | c0002 | t0007 | g0284 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18980 | hp1 | a0001 | c0001 | t0020 | g0157 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18980 | hp2 | a0001 | c0002 | t0007 | g0278 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18984 | hp1 | a0001 | c0002 | t0008 | g0027 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18985 | hp1 | a0001 | c0002 | t0007 | g0288 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18985 | hp2 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18987 | hp1 | a0001 | c0001 | t0014 | g0024 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18987 | hp2 | a0001 | c0001 | t0015 | g0191 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18989 | hp2 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18990 | hp1 | a0001 | c0001 | t0007 | g0213 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18991 | hp2 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18992 | hp1 | a0001 | c0002 | t0008 | g0112 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18993 | hp1 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18993 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18995 | hp1 | a0001 | c0002 | t0003 | g0111 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18998 | hp1 | a0001 | c0001 | t0038 | g0158 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19002 | hp2 | a0001 | c0001 | t0031 | g0070 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19003 | hp1 | a0001 | c0002 | t0007 | g0253 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19003 | hp2 | a0001 | c0001 | t0033 | g0098 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19005 | hp2 | a0002 | c0009 | t0002 | g0155 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19007 | hp1 | a0001 | c0002 | t0012 | g0013 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19030 | hp1 | a0003 | c0006 | t0013 | g0198 | AFR | LWK | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0234 | AFR | LWK | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | LWK | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19043 | hp2 | a0001 | c0005 | t0018 | g0197 | AFR | LWK | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19054 | hp1 | a0001 | c0001 | t0012 | g0187 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19055 | hp2 | a0001 | c0002 | t0007 | g0254 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19056 | hp1 | a0001 | c0001 | t0032 | g0088 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19058 | hp2 | a0001 | c0002 | t0013 | g0260 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19060 | hp2 | a0001 | c0001 | t0017 | g0176 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19062 | hp2 | a0001 | c0002 | t0008 | g0027 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19063 | hp1 | a0001 | c0002 | t0003 | g0104 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19063 | hp2 | a0001 | c0002 | t0007 | g0019 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19064 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19065 | hp1 | a0001 | c0002 | t0050 | g0295 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19066 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19066 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19068 | hp2 | a0001 | c0001 | t0015 | g0182 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19072 | hp1 | a0001 | c0002 | t0007 | g0287 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19072 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19074 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19074 | hp2 | a0001 | c0001 | t0011 | g0074 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19075 | hp1 | a0001 | c0001 | t0015 | g0181 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19075 | hp2 | a0001 | c0001 | t0029 | g0062 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19077 | hp2 | a0001 | c0002 | t0007 | g0290 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19080 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19082 | hp1 | a0001 | c0002 | t0009 | g0266 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19082 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19083 | hp1 | a0001 | c0004 | t0015 | g0105 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19083 | hp2 | a0001 | c0004 | t0003 | g0106 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19084 | hp1 | a0001 | c0001 | t0021 | g0020 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19087 | hp1 | a0001 | c0002 | t0007 | g0019 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19087 | hp2 | a0001 | c0002 | t0003 | g0103 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19088 | hp1 | a0001 | c0002 | t0007 | g0019 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19089 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19089 | hp2 | a0001 | c0002 | t0008 | g0113 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19091 | hp1 | a0001 | c0001 | t0020 | g0177 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19091 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0227 | AFR | YRI | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA19240 | hp2 | a0001 | c0002 | t0003 | g0031 | AFR | YRI | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA20752 | hp1 | a0001 | c0002 | t0026 | g0273 | EUR | TSI | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0035 | EUR | TSI | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0173 | EUR | TSI | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA20805 | hp2 | a0004 | c0007 | t0017 | g0114 | EUR | TSI | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA20905 | hp1 | a0001 | c0003 | t0001 | g0005 | SAS | GIH | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0221 | SAS | GIH | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG01123 | hp2 | a0001 | c0001 | t0010 | g0206 | AMR | CLM | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0124 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02486 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02559 | hp1 | a0001 | c0002 | t0007 | g0018 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG02559 | hp2 | a0001 | c0002 | t0003 | g0136 | AFR | ACB | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03471 | hp1 | a0001 | c0001 | t0043 | g0203 | AFR | MSL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG03471 | hp2 | a0001 | c0010 | t0042 | g0252 | AFR | MSL | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG06807 | hp1 | a0001 | c0001 | t0013 | g0232 | AFR | USA | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
HG06807 | hp2 | a0001 | c0001 | t0022 | g0292 | AFR | USA | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | USA | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | USA | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0138 | AFR | LWK | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
NA21309 | hp2 | a0001 | c0001 | t0018 | g0235 | AFR | LWK | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0078 | REF | REF | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0017 | REF | REF | UGDH_chr4_39493755_39532439 | UGDH | chr4 | 39493755 | 39532439 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:39504432 | C | G | 1 | a0004 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1248G>C | p.Glu416Asp | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 10/12 | 1412/3037 | 1248/1485 | 416/494 | chr4 | 39504432 | |||
chr4:39505258 | C | T | 1 | a0002 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.1150G>A | p.Gly384Ser | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 9/12 | 1314/3037 | 1150/1485 | 384/494 | chr4 | 39505258 | |||
chr4:39510705 | G | A | 1 | a0003 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.421C>T | p.Arg141Cys | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 4/12 | 585/3037 | 421/1485 | 141/494 | chr4 | 39510705 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:39500188 | C | T | 1 | a0001c0008 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.1440G>A | p.Pro480Pro | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 1604/3037 | 1440/1485 | 480/494 | chr4 | 39500188 | |||
chr4:39503941 | G | C | 1 | a0001c0010 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.1308C>G | p.Ala436Ala | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/12 | 1472/3037 | 1308/1485 | 436/494 | chr4 | 39503941 | |||
chr4:39508644 | A | G | 6 | a0001c0002 a0001c0004 a0001c0005 others(3): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
synonymous_variant | LOW | c.828T>C | p.Cys276Cys | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/12 | 992/3037 | 828/1485 | 276/494 | chr4 | 39508644 | |||
chr4:39509809 | C | T | 1 | a0001c0004 | 2 | NA19083.hp1 NA19083.hp2 |
synonymous_variant | LOW | c.762G>A | p.Ala254Ala | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 6/12 | 926/3037 | 762/1485 | 254/494 | chr4 | 39509809 | |||
chr4:39510727 | T | C | 1 | a0001c0003 | 17 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(14): Show |
synonymous_variant | LOW | c.399A>G | p.Pro133Pro | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 4/12 | 563/3037 | 399/1485 | 133/494 | chr4 | 39510727 | |||
chr4:39514116 | A | G | 4 | a0001c0002 a0001c0004 a0001c0008 others(1): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
synonymous_variant | LOW | c.231T>C | p.Asp77Asp | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/12 | 395/3037 | 231/1485 | 77/494 | chr4 | 39514116 | |||
chr4:39521375 | A | G | 2 | a0001c0005 a0003c0006 |
2 | NA19030.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.138T>C | p.Asn46Asn | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/12 | 302/3037 | 138/1485 | 46/494 | chr4 | 39521375 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:39498844 | T | C | 1 | a0001c0001t0035 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1299A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 1299 | chr4 | 39498844 | ||||||
chr4:39498869 | G | A | 2 | a0001c0001t0014 a0001c0001t0031 |
5 | HG02080.hp1 NA18960.hp1 NA18962.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1274C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 1274 | chr4 | 39498869 | ||||||
chr4:39498894 | T | C | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0010 others(13): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*1249A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 1249 | chr4 | 39498894 | ||||||
chr4:39498994 | C | G | 6 | a0001c0001t0015 a0001c0001t0022 a0001c0001t0028 others(3): Show |
18 | HG00423.hp2 HG01243.hp2 HG02004.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1149G>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 1149 | chr4 | 39498994 | ||||||
chr4:39499186 | TA | T | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0010 others(13): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*956delT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 956 | chr4 | 39499186 | ||||||
chr4:39499217 | T | G | 27 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0010 others(24): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*926A>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 926 | chr4 | 39499217 | ||||||
chr4:39499221 | T | A | 1 | a0001c0001t0035 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*922A>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 922 | chr4 | 39499221 | ||||||
chr4:39499400 | G | A | 6 | a0001c0001t0015 a0001c0001t0022 a0001c0001t0028 others(3): Show |
18 | HG00423.hp2 HG01243.hp2 HG02004.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*743C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 743 | chr4 | 39499400 | ||||||
chr4:39499466 | G | A | 43 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(40): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*677C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 677 | chr4 | 39499466 | ||||||
chr4:39499494 | G | A | 1 | a0001c0001t0035 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*649C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 649 | chr4 | 39499494 | ||||||
chr4:39499576 | T | C | 2 | a0001c0001t0045 a0001c0001t0048 |
2 | HG02976.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*567A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 567 | chr4 | 39499576 | ||||||
chr4:39499622 | C | A | 1 | a0001c0002t0044 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*521G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 521 | chr4 | 39499622 | ||||||
chr4:39499665 | C | T | 1 | a0001c0001t0047 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*478G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 478 | chr4 | 39499665 | ||||||
chr4:39499813 | A | G | 6 | a0001c0001t0015 a0001c0001t0022 a0001c0001t0028 others(3): Show |
18 | HG00423.hp2 HG01243.hp2 HG02004.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*330T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 330 | chr4 | 39499813 | ||||||
chr4:39499892 | C | T | 7 | a0001c0001t0007 a0001c0001t0012 a0001c0002t0007 others(4): Show |
35 | HG00408.hp1 HG01099.hp2 HG01952.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*251G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 251 | chr4 | 39499892 | ||||||
chr4:39499898 | C | T | 3 | a0001c0001t0043 a0001c0002t0026 a0001c0002t0034 |
4 | HG01099.hp2 HG03209.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*245G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 245 | chr4 | 39499898 | ||||||
chr4:39499929 | C | T | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0010 others(13): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*214G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 214 | chr4 | 39499929 | ||||||
chr4:39500024 | T | C | 1 | a0001c0001t0037 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 119 | chr4 | 39500024 | ||||||
chr4:39500027 | C | CA | 23 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(20): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*115dupT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 115 | chr4 | 39500027 | ||||||
chr4:39500038 | C | A | 2 | a0001c0001t0029 a0001c0001t0038 |
2 | NA18998.hp1 NA19075.hp2 |
3_prime_UTR_variant | MODIFIER | c.*105G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 105 | chr4 | 39500038 | ||||||
chr4:39500053 | G | A | 1 | a0001c0001t0049 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*90C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 90 | chr4 | 39500053 | ||||||
chr4:39500085 | T | C | 1 | a0001c0001t0039 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*58A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 58 | chr4 | 39500085 | ||||||
chr4:39500102 | CA | C | 13 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(10): Show |
63 | HG00140.hp2 HG00558.hp2 HG00738.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*40delT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 40 | chr4 | 39500102 | ||||||
chr4:39500102 | CAA | C | 18 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0018 others(15): Show |
73 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*39_*40delTT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 39 | chr4 | 39500102 | ||||||
chr4:39500102 | CAAA | C | 21 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0010 others(18): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*38_*40delTTT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 12/12 | 38 | chr4 | 39500102 | ||||||
chr4:39527318 | T | A | 14 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(11): Show |
98 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(95): Show |
5_prime_UTR_variant | MODIFIER | c.-43A>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/12 | 5806 | chr4 | 39527318 | ||||||
chr4:39527319 | C | T | 14 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(11): Show |
98 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(95): Show |
5_prime_UTR_variant | MODIFIER | c.-44G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/12 | 5807 | chr4 | 39527319 | ||||||
chr4:39527354 | G | C | 1 | a0001c0003t0040 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-79C>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/12 | 5842 | chr4 | 39527354 | ||||||
chr4:39527356 | C | T | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(40): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
5_prime_UTR_variant | MODIFIER | c.-81G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/12 | 5844 | chr4 | 39527356 | ||||||
chr4:39527357 | G | A | 1 | a0001c0002t0050 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-82C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/12 | 5845 | chr4 | 39527357 | ||||||
chr4:39527433 | G | T | 1 | a0001c0001t0021 | 2 | HG00642.hp1 NA19084.hp1 |
5_prime_UTR_variant | MODIFIER | c.-158C>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/12 | 5921 | chr4 | 39527433 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:39500350 | T | A | 1 | a0001c0002t0008g0113 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1375-97A>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39500350 | |||||||
chr4:39500436 | G | A | 276 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(273): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.1375-183C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39500436 | |||||||
chr4:39500512 | A | T | 1 | a0001c0002t0008g0113 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1375-259T>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39500512 | |||||||
chr4:39500649 | T | TTC | 17 | a0001c0001t0015g0181 a0001c0001t0015g0182 a0001c0001t0015g0191 others(14): Show |
17 | HG00423.hp2 HG02004.hp2 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1375-398_1375-397d others(4): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39500649 | |||||||
chr4:39500653 | C | CT | 49 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0038 others(46): Show |
58 | HG00140.hp2 HG00558.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1375-401dupA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39500653 | |||||||
chr4:39500653 | CT | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(96): Show |
153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1375-401delA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39500653 | |||||||
chr4:39500653 | CTTT | C | 37 | a0001c0001t0003g0033 a0001c0001t0003g0036 a0001c0001t0003g0169 others(34): Show |
65 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1375-403_1375-401d others(5): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39500653 | |||||||
chr4:39500655 | T | C | 17 | a0001c0001t0015g0181 a0001c0001t0015g0182 a0001c0001t0015g0191 others(14): Show |
17 | HG00423.hp2 HG02004.hp2 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1375-402A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39500655 | |||||||
chr4:39500766 | C | T | 1 | a0001c0002t0017g0122 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1375-513G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39500766 | |||||||
chr4:39500814 | C | A | 1 | a0001c0002t0008g0113 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1375-561G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39500814 | |||||||
chr4:39500968 | G | T | 276 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(273): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.1375-715C>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39500968 | |||||||
chr4:39500969 | C | CT | 18 | a0001c0001t0015g0181 a0001c0001t0015g0182 a0001c0001t0015g0191 others(15): Show |
18 | HG00423.hp2 HG01243.hp2 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.1375-717dupA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39500969 | |||||||
chr4:39501051 | G | A | 1 | a0001c0002t0003g0115 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1375-798C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501051 | |||||||
chr4:39501077 | C | T | 1 | a0001c0001t0043g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1375-824G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501077 | |||||||
chr4:39501114 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1375-861G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501114 | |||||||
chr4:39501198 | C | T | 8 | a0001c0001t0006g0009 a0001c0001t0006g0199 a0001c0001t0006g0207 others(5): Show |
12 | HG00280.hp2 HG01074.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1375-945G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501198 | |||||||
chr4:39501212 | C | T | 1 | a0001c0002t0034g0046 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1375-959G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501212 | |||||||
chr4:39501213 | G | A | 34 | a0001c0001t0002g0007 a0001c0001t0002g0032 a0001c0001t0002g0034 others(31): Show |
44 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.1375-960C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501213 | |||||||
chr4:39501257 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1375-1004A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501257 | |||||||
chr4:39501275 | A | C | 45 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0038 others(42): Show |
53 | HG00140.hp2 HG00558.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.1375-1022T>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501275 | |||||||
chr4:39501276 | A | T | 1 | a0001c0002t0020g0126 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1375-1023T>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501276 | |||||||
chr4:39501276 | AT | A | 194 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(191): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1375-1024delA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501276 | |||||||
chr4:39501276 | ATT | A | 6 | a0001c0001t0023g0217 a0001c0002t0016g0015 a0001c0002t0016g0119 others(3): Show |
8 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-1025_1375-102 others(6): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501276 | |||||||
chr4:39501337 | T | C | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG00733.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1375-1084A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501337 | |||||||
chr4:39501422 | T | C | 2 | a0001c0002t0002g0128 a0001c0002t0002g0138 |
2 | HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1375-1169A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501422 | |||||||
chr4:39501467 | T | G | 276 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(273): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.1375-1214A>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501467 | |||||||
chr4:39501475 | G | A | 3 | a0001c0001t0010g0039 a0001c0001t0010g0205 a0001c0001t0010g0206 |
4 | HG01070.hp2 HG01123.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1375-1222C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501475 | |||||||
chr4:39501490 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1375-1237C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501490 | |||||||
chr4:39501552 | C | T | 1 | a0001c0002t0007g0283 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1375-1299G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501552 | |||||||
chr4:39501576 | A | G | 12 | a0001c0001t0006g0009 a0001c0001t0006g0199 a0001c0001t0006g0207 others(9): Show |
17 | HG00280.hp2 HG01074.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1375-1323T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501576 | |||||||
chr4:39501939 | C | T | 18 | a0001c0001t0015g0181 a0001c0001t0015g0182 a0001c0001t0015g0191 others(15): Show |
18 | HG00423.hp2 HG01243.hp2 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.1375-1686G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39501939 | |||||||
chr4:39502074 | A | G | 1 | a0003c0006t0013g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1374+1801T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39502074 | |||||||
chr4:39502296 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0089 a0001c0001t0021g0020 |
4 | HG00642.hp1 NA18988.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1374+1579A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39502296 | |||||||
chr4:39502303 | C | G | 21 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0089 others(18): Show |
28 | HG00423.hp2 HG00642.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.1374+1572G>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39502303 | |||||||
chr4:39502311 | C | T | 1 | a0001c0002t0002g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1374+1564G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39502311 | |||||||
chr4:39502649 | C | T | 235 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(232): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1374+1226G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39502649 | |||||||
chr4:39502653 | G | T | 3 | a0001c0001t0006g0230 a0001c0001t0035g0194 a0001c0001t0037g0195 |
3 | HG02145.hp2 HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1374+1222C>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39502653 | |||||||
chr4:39502685 | C | A | 209 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(206): Show |
308 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1374+1190G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39502685 | |||||||
chr4:39502721 | G | C | 2 | a0001c0002t0007g0019 a0001c0002t0007g0290 |
4 | NA19063.hp2 NA19077.hp2 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.1374+1154C>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39502721 | |||||||
chr4:39502779 | C | G | 1 | a0001c0001t0002g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1374+1096G>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39502779 | |||||||
chr4:39502857 | C | T | 1 | a0001c0001t0047g0251 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1374+1018G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39502857 | |||||||
chr4:39502861 | G | C | 1 | a0001c0001t0043g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1374+1014C>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39502861 | |||||||
chr4:39502869 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0077 |
3 | HG01255.hp1 HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1374+1006G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39502869 | |||||||
chr4:39502922 | A | T | 23 | a0001c0001t0010g0239 a0001c0002t0007g0012 a0001c0002t0007g0019 others(20): Show |
28 | HG00408.hp1 HG00639.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1374+953T>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39502922 | |||||||
chr4:39502949 | C | T | 45 | a0001c0001t0002g0007 a0001c0001t0002g0032 a0001c0001t0002g0034 others(42): Show |
69 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1374+926G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39502949 | |||||||
chr4:39503002 | C | T | 1 | a0001c0001t0043g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1374+873G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39503002 | |||||||
chr4:39503012 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0092 a0001c0001t0001g0094 |
4 | NA18612.hp1 NA18984.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.1374+863C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39503012 | |||||||
chr4:39503019 | C | T | 3 | a0001c0001t0006g0008 a0001c0001t0006g0222 a0001c0001t0006g0226 |
7 | HG01109.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1374+856G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39503019 | |||||||
chr4:39503158 | G | A | 60 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0032 others(57): Show |
88 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1374+717C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39503158 | |||||||
chr4:39503162 | G | A | 2 | a0001c0001t0006g0293 a0001c0001t0006g0294 |
2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1374+713C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39503162 | |||||||
chr4:39503190 | T | C | 62 | a0001c0001t0001g0073 a0001c0001t0003g0033 a0001c0001t0003g0169 others(59): Show |
96 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1374+685A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39503190 | |||||||
chr4:39503197 | G | A | 20 | a0001c0001t0043g0203 a0001c0002t0001g0047 a0001c0002t0007g0012 others(17): Show |
25 | HG00408.hp1 HG01099.hp2 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.1374+678C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39503197 | |||||||
chr4:39503207 | G | A | 1 | a0001c0002t0023g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1374+668C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39503207 | |||||||
chr4:39503209 | C | T | 1 | a0001c0001t0047g0251 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1374+666G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39503209 | |||||||
chr4:39503534 | G | A | 1 | a0001c0001t0006g0207 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1374+341C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 11/11 | chr4 | 39503534 | |||||||
chr4:39504031 | G | A | 1 | a0001c0001t0048g0244 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1264-46C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 10/11 | chr4 | 39504031 | |||||||
chr4:39504233 | A | G | 98 | a0001c0001t0047g0251 a0001c0002t0001g0047 a0001c0002t0002g0028 others(95): Show |
138 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1263+184T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 10/11 | chr4 | 39504233 | |||||||
chr4:39504285 | G | A | 1 | a0001c0002t0007g0280 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1263+132C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 10/11 | chr4 | 39504285 | |||||||
chr4:39504317 | A | C | 3 | a0001c0001t0010g0206 a0001c0002t0016g0015 a0001c0002t0016g0119 |
5 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263+100T>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 10/11 | chr4 | 39504317 | |||||||
chr4:39504318 | A | C | 1 | a0001c0010t0042g0252 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1263+99T>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 10/11 | chr4 | 39504318 | |||||||
chr4:39504319 | C | A | 1 | a0001c0010t0042g0252 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1263+98G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 10/11 | chr4 | 39504319 | |||||||
chr4:39504523 | A | G | 1 | a0001c0002t0002g0029 | 2 | HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1172-15T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 9/11 | chr4 | 39504523 | |||||||
chr4:39504524 | C | T | 53 | a0001c0002t0002g0028 a0001c0002t0002g0029 a0001c0002t0002g0030 others(50): Show |
86 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.1172-16G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 9/11 | chr4 | 39504524 | |||||||
chr4:39504860 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0094 |
3 | NA18984.hp2 NA19001.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1172-352C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 9/11 | chr4 | 39504860 | |||||||
chr4:39505015 | G | A | 1 | a0001c0010t0042g0252 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1171+222C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 9/11 | chr4 | 39505015 | |||||||
chr4:39505377 | GA | G | 97 | a0001c0001t0004g0044 a0001c0002t0001g0047 a0001c0002t0002g0028 others(94): Show |
138 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(135): Show |
splice_region_variant&intron_variant | LOW | c.1038-8delT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 8/11 | chr4 | 39505377 | |||||||
chr4:39505434 | GT | G | 3 | a0001c0002t0023g0281 a0001c0002t0025g0272 a0001c0002t0025g0285 |
3 | HG01167.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1038-65delA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 8/11 | chr4 | 39505434 | |||||||
chr4:39505463 | G | T | 163 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0032 others(160): Show |
232 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1038-93C>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 8/11 | chr4 | 39505463 | |||||||
chr4:39505837 | T | C | 96 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(93): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.907-89A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39505837 | |||||||
chr4:39505904 | T | TA | 58 | a0001c0001t0001g0077 a0001c0001t0004g0220 a0001c0001t0004g0221 others(55): Show |
92 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.907-157dupT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39505904 | |||||||
chr4:39505904 | T | TAA | 42 | a0001c0002t0001g0047 a0001c0002t0007g0012 a0001c0002t0007g0018 others(39): Show |
49 | HG00408.hp1 HG00423.hp2 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.907-158_907-157dup others(2): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39505904 | |||||||
chr4:39505904 | TA | T | 47 | a0001c0001t0002g0007 a0001c0001t0002g0032 a0001c0001t0002g0034 others(44): Show |
72 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.907-157delT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39505904 | |||||||
chr4:39505979 | C | T | 43 | a0001c0002t0001g0047 a0001c0002t0007g0012 a0001c0002t0007g0018 others(40): Show |
50 | HG00408.hp1 HG00423.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.907-231G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39505979 | |||||||
chr4:39506010 | T | C | 1 | a0001c0001t0004g0043 | 2 | NA18961.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.907-262A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506010 | |||||||
chr4:39506056 | C | T | 1 | a0001c0002t0002g0134 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.907-308G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506056 | |||||||
chr4:39506196 | C | T | 1 | a0001c0001t0043g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.907-448G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506196 | |||||||
chr4:39506233 | T | TAAAAAA | 54 | a0001c0001t0001g0073 a0001c0001t0001g0087 a0001c0001t0002g0146 others(51): Show |
61 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.907-491_907-486dup others(6): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506233 | |||||||
chr4:39506233 | T | TAAAAAAA | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(143): Show |
232 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.907-492_907-486dup others(7): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506233 | |||||||
chr4:39506233 | T | TAAAAAAA others(1): Show |
17 | a0001c0001t0001g0025 a0001c0001t0001g0067 a0001c0001t0001g0072 others(14): Show |
18 | HG00423.hp1 HG01081.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.907-493_907-486dup others(8): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506233 | |||||||
chr4:39506406 | A | C | 96 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(93): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.907-658T>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506406 | |||||||
chr4:39506414 | T | C | 96 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(93): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.907-666A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506414 | |||||||
chr4:39506417 | G | A | 2 | a0001c0001t0035g0194 a0001c0001t0037g0195 |
2 | HG02145.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.907-669C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506417 | |||||||
chr4:39506566 | T | C | 1 | a0001c0004t0003g0106 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.907-818A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506566 | |||||||
chr4:39506586 | A | G | 2 | a0001c0005t0018g0197 a0003c0006t0013g0198 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.907-838T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506586 | |||||||
chr4:39506664 | G | A | 222 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(219): Show |
316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.907-916C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506664 | |||||||
chr4:39506672 | G | A | 222 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(219): Show |
316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.907-924C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506672 | |||||||
chr4:39506751 | C | A | 1 | a0001c0001t0022g0292 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.907-1003G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506751 | |||||||
chr4:39506796 | G | C | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.907-1048C>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506796 | |||||||
chr4:39506891 | G | A | 2 | a0001c0005t0018g0197 a0003c0006t0013g0198 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.907-1143C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506891 | |||||||
chr4:39506960 | C | G | 96 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(93): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.907-1212G>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506960 | |||||||
chr4:39506970 | C | A | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.907-1222G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39506970 | |||||||
chr4:39507147 | T | C | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.907-1399A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39507147 | |||||||
chr4:39507157 | C | T | 5 | a0001c0002t0003g0108 a0001c0002t0008g0027 a0001c0002t0008g0107 others(2): Show |
6 | NA18953.hp1 NA18975.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.906+1409G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39507157 | |||||||
chr4:39507364 | A | C | 51 | a0001c0002t0002g0028 a0001c0002t0002g0029 a0001c0002t0002g0030 others(48): Show |
84 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.906+1202T>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39507364 | |||||||
chr4:39507569 | A | G | 232 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(229): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.906+997T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39507569 | |||||||
chr4:39507616 | T | G | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.906+950A>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39507616 | |||||||
chr4:39507648 | T | C | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.906+918A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39507648 | |||||||
chr4:39507716 | AGATGGGA others(1): Show |
A | 3 | a0001c0002t0002g0127 a0001c0002t0002g0129 a0001c0002t0003g0031 |
4 | HG03195.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+842_906+849del others(8): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39507716 | |||||||
chr4:39507788 | C | A | 218 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(215): Show |
312 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(309): Show |
intron_variant | MODIFIER | c.906+778G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39507788 | |||||||
chr4:39507814 | C | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(51): Show |
79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.906+752G>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39507814 | |||||||
chr4:39507827 | G | A | 2 | a0001c0001t0003g0033 a0001c0001t0003g0169 |
3 | HG02132.hp1 NA19001.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.906+739C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39507827 | |||||||
chr4:39507942 | CA | C | 12 | a0001c0001t0001g0049 a0001c0001t0001g0066 a0001c0001t0001g0067 others(9): Show |
12 | HG00323.hp1 HG01069.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.906+623delT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39507942 | |||||||
chr4:39507942 | CAA | C | 94 | a0001c0001t0047g0251 a0001c0002t0001g0047 a0001c0002t0002g0028 others(91): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.906+622_906+623del others(2): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39507942 | |||||||
chr4:39507984 | G | A | 96 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(93): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.906+582C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39507984 | |||||||
chr4:39508230 | G | A | 96 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(93): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.906+336C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39508230 | |||||||
chr4:39508502 | G | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(51): Show |
79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.906+64C>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39508502 | |||||||
chr4:39508555 | G | A | 96 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(93): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.906+11C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 7/11 | chr4 | 39508555 | |||||||
chr4:39508663 | G | A | 2 | a0001c0005t0018g0197 a0003c0006t0013g0198 |
2 | NA19030.hp1 NA19043.hp2 |
splice_region_variant&intron_variant | LOW | c.812-3C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 6/11 | chr4 | 39508663 | |||||||
chr4:39508709 | C | T | 47 | a0001c0001t0002g0007 a0001c0001t0002g0032 a0001c0001t0002g0034 others(44): Show |
72 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.812-49G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 6/11 | chr4 | 39508709 | |||||||
chr4:39508883 | C | T | 5 | a0001c0001t0002g0145 a0001c0001t0002g0147 a0001c0001t0002g0150 others(2): Show |
5 | HG01257.hp2 HG01928.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.812-223G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 6/11 | chr4 | 39508883 | |||||||
chr4:39508898 | T | C | 1 | a0001c0002t0007g0282 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.812-238A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 6/11 | chr4 | 39508898 | |||||||
chr4:39509128 | T | A | 1 | a0001c0002t0007g0283 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.812-468A>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 6/11 | chr4 | 39509128 | |||||||
chr4:39509138 | C | T | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.812-478G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 6/11 | chr4 | 39509138 | |||||||
chr4:39509150 | C | CT | 11 | a0001c0001t0001g0021 a0001c0001t0002g0035 a0001c0001t0004g0041 others(8): Show |
14 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.812-491dupA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 6/11 | chr4 | 39509150 | |||||||
chr4:39509157 | T | C | 2 | a0001c0002t0003g0133 a0001c0002t0019g0140 |
2 | HG01243.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.812-497A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 6/11 | chr4 | 39509157 | |||||||
chr4:39509208 | A | G | 221 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(218): Show |
315 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(312): Show |
intron_variant | MODIFIER | c.812-548T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 6/11 | chr4 | 39509208 | |||||||
chr4:39509680 | T | C | 6 | a0001c0001t0006g0009 a0001c0001t0006g0199 a0001c0001t0006g0223 others(3): Show |
10 | HG01074.hp2 HG01884.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.811+80A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 6/11 | chr4 | 39509680 | |||||||
chr4:39509739 | T | C | 96 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(93): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.811+21A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 6/11 | chr4 | 39509739 | |||||||
chr4:39509910 | T | TA | 104 | a0001c0001t0001g0026 a0001c0001t0001g0045 a0001c0001t0001g0065 others(101): Show |
137 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(134): Show |
splice_region_variant&intron_variant | LOW | c.664-4dupT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 5/11 | chr4 | 39509910 | |||||||
chr4:39509990 | C | T | 1 | a0001c0001t0047g0251 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.664-83G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 5/11 | chr4 | 39509990 | |||||||
chr4:39510200 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.663+153C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 5/11 | chr4 | 39510200 | |||||||
chr4:39510951 | A | G | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.265-90T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39510951 | |||||||
chr4:39510966 | C | T | 1 | a0001c0002t0003g0115 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.265-105G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39510966 | |||||||
chr4:39510993 | T | C | 1 | a0001c0002t0010g0265 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.265-132A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39510993 | |||||||
chr4:39511017 | T | C | 1 | a0001c0010t0042g0252 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.265-156A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39511017 | |||||||
chr4:39511097 | G | A | 94 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(91): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.265-236C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39511097 | |||||||
chr4:39511110 | A | T | 1 | a0001c0001t0006g0229 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.265-249T>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39511110 | |||||||
chr4:39511265 | C | CT | 92 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(89): Show |
132 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.265-405dupA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39511265 | |||||||
chr4:39511265 | CT | C | 11 | a0001c0001t0002g0179 a0001c0001t0002g0190 a0001c0001t0004g0037 others(8): Show |
13 | HG00558.hp2 HG01257.hp2 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.265-405delA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39511265 | |||||||
chr4:39511312 | G | A | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.265-451C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39511312 | |||||||
chr4:39511409 | C | T | 51 | a0001c0002t0002g0028 a0001c0002t0002g0029 a0001c0002t0002g0030 others(48): Show |
84 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.265-548G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39511409 | |||||||
chr4:39511410 | G | A | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.265-549C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39511410 | |||||||
chr4:39511447 | G | C | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG00733.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.265-586C>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39511447 | |||||||
chr4:39511498 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0082 |
2 | NA18949.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.265-637C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39511498 | |||||||
chr4:39511552 | C | T | 1 | a0001c0001t0008g0171 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.265-691G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39511552 | |||||||
chr4:39511710 | CT | C | 6 | a0001c0001t0003g0169 a0001c0001t0006g0225 a0001c0001t0033g0098 others(3): Show |
6 | HG02015.hp2 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.265-850delA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39511710 | |||||||
chr4:39511856 | C | T | 15 | a0001c0001t0002g0011 a0001c0001t0002g0184 a0001c0001t0002g0185 others(12): Show |
19 | HG00438.hp2 HG00733.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.265-995G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39511856 | |||||||
chr4:39512007 | G | A | 1 | a0001c0010t0042g0252 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.265-1146C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512007 | |||||||
chr4:39512025 | G | GA | 178 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(175): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.265-1165dupT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512025 | |||||||
chr4:39512025 | G | GAA | 9 | a0001c0001t0001g0083 a0001c0001t0003g0192 a0001c0001t0005g0149 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.265-1166_265-1165d others(4): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512025 | |||||||
chr4:39512161 | C | T | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.265-1300G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512161 | |||||||
chr4:39512211 | T | G | 1 | a0001c0002t0007g0284 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.265-1350A>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512211 | |||||||
chr4:39512218 | T | C | 2 | a0001c0005t0018g0197 a0003c0006t0013g0198 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.265-1357A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512218 | |||||||
chr4:39512414 | A | G | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.265-1553T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512414 | |||||||
chr4:39512415 | T | C | 1 | a0001c0001t0043g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.265-1554A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512415 | |||||||
chr4:39512428 | G | A | 1 | a0001c0001t0010g0239 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.265-1567C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512428 | |||||||
chr4:39512643 | T | C | 15 | a0001c0001t0002g0011 a0001c0001t0002g0184 a0001c0001t0002g0185 others(12): Show |
19 | HG00438.hp2 HG00733.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.264+1440A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512643 | |||||||
chr4:39512662 | A | AT | 25 | a0001c0002t0002g0028 a0001c0002t0002g0117 a0001c0002t0003g0002 others(22): Show |
47 | HG00558.hp1 HG00609.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.264+1420dupA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512662 | |||||||
chr4:39512751 | G | A | 10 | a0001c0003t0001g0005 a0001c0003t0001g0022 a0001c0003t0001g0055 others(7): Show |
17 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(14): Show |
intron_variant | MODIFIER | c.264+1332C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512751 | |||||||
chr4:39512819 | A | AT | 23 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0065 others(20): Show |
29 | HG01257.hp2 HG01346.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.264+1263dupA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512819 | |||||||
chr4:39512819 | A | ATT | 44 | a0001c0001t0002g0007 a0001c0001t0002g0032 a0001c0001t0002g0034 others(41): Show |
69 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.264+1262_264+1263d others(4): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512819 | |||||||
chr4:39512819 | AT | A | 9 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0092 others(6): Show |
9 | HG01070.hp1 HG01256.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.264+1263delA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512819 | |||||||
chr4:39512819 | ATTTT | A | 94 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(91): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.264+1260_264+1263d others(6): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512819 | |||||||
chr4:39512989 | G | T | 1 | a0001c0002t0009g0259 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.264+1094C>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39512989 | |||||||
chr4:39513324 | G | A | 1 | a0001c0001t0002g0101 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.264+759C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513324 | |||||||
chr4:39513325 | T | A | 94 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(91): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.264+758A>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513325 | |||||||
chr4:39513502 | T | G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(64): Show |
99 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.264+581A>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513502 | |||||||
chr4:39513531 | C | CT | 10 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0170 others(7): Show |
10 | HG01928.hp2 HG02145.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.264+551dupA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513531 | |||||||
chr4:39513531 | CT | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(75): Show |
113 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.264+551delA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513531 | |||||||
chr4:39513531 | CTT | C | 7 | a0001c0001t0001g0051 a0001c0001t0001g0087 a0001c0001t0001g0089 others(4): Show |
7 | NA18960.hp1 NA18975.hp2 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+550_264+551del others(2): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513531 | |||||||
chr4:39513531 | CTTT | C | 49 | a0001c0002t0002g0028 a0001c0002t0002g0029 a0001c0002t0002g0030 others(46): Show |
82 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.264+549_264+551del others(3): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513531 | |||||||
chr4:39513531 | CTTTT | C | 41 | a0001c0002t0001g0047 a0001c0002t0007g0012 a0001c0002t0007g0018 others(38): Show |
48 | HG00408.hp1 HG00423.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.264+548_264+551del others(4): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513531 | |||||||
chr4:39513678 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.264+405C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513678 | |||||||
chr4:39513725 | C | T | 1 | a0001c0002t0044g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.264+358G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513725 | |||||||
chr4:39513768 | CT | C | 37 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0038 others(34): Show |
47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.264+314delA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513768 | |||||||
chr4:39513796 | C | A | 165 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0032 others(162): Show |
234 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.264+287G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513796 | |||||||
chr4:39513856 | A | G | 165 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0032 others(162): Show |
234 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.264+227T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513856 | |||||||
chr4:39513917 | C | T | 4 | a0001c0001t0047g0251 a0001c0005t0018g0197 a0001c0010t0042g0252 others(1): Show |
4 | HG02258.hp1 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+166G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513917 | |||||||
chr4:39513955 | A | T | 94 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(91): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.264+128T>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39513955 | |||||||
chr4:39514010 | CT | C | 94 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(91): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.264+72delA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39514010 | |||||||
chr4:39514026 | A | G | 51 | a0001c0002t0002g0028 a0001c0002t0002g0029 a0001c0002t0002g0030 others(48): Show |
84 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.264+57T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39514026 | |||||||
chr4:39514035 | T | C | 94 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(91): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.264+48A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 3/11 | chr4 | 39514035 | |||||||
chr4:39514186 | TAAAAAGA | T | 51 | a0001c0002t0002g0028 a0001c0002t0002g0029 a0001c0002t0002g0030 others(48): Show |
84 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(81): Show |
splice_region_variant&intron_variant | LOW | c.163-9_163-3delTCTT others(3): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39514186 | |||||||
chr4:39514233 | T | C | 15 | a0001c0001t0002g0011 a0001c0001t0002g0184 a0001c0001t0002g0185 others(12): Show |
19 | HG00438.hp2 HG00733.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-49A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39514233 | |||||||
chr4:39514542 | T | C | 232 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(229): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.163-358A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39514542 | |||||||
chr4:39514686 | A | AT | 13 | a0001c0001t0002g0011 a0001c0001t0002g0184 a0001c0001t0002g0185 others(10): Show |
17 | HG00438.hp2 HG00733.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.163-503dupA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39514686 | |||||||
chr4:39514691 | A | T | 15 | a0001c0001t0002g0011 a0001c0001t0002g0184 a0001c0001t0002g0185 others(12): Show |
19 | HG00438.hp2 HG00733.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-507T>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39514691 | |||||||
chr4:39514752 | G | A | 47 | a0001c0001t0002g0007 a0001c0001t0002g0032 a0001c0001t0002g0034 others(44): Show |
72 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.163-568C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39514752 | |||||||
chr4:39514761 | C | A | 3 | a0001c0001t0047g0251 a0001c0001t0049g0250 a0001c0010t0042g0252 |
3 | HG02257.hp1 HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.163-577G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39514761 | |||||||
chr4:39514762 | G | A | 161 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0032 others(158): Show |
230 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.163-578C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39514762 | |||||||
chr4:39514922 | T | C | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.163-738A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39514922 | |||||||
chr4:39515038 | G | A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(61): Show |
96 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.163-854C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39515038 | |||||||
chr4:39515103 | T | G | 1 | a0001c0001t0010g0239 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.163-919A>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39515103 | |||||||
chr4:39515436 | T | TTTTTCTA others(29): Show |
1 | a0001c0002t0003g0104 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.163-1288_163-1253d others(38): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39515436 | |||||||
chr4:39515499 | T | TA | 62 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(59): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.163-1316dupT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39515499 | |||||||
chr4:39515499 | TA | T | 95 | a0001c0001t0015g0181 a0001c0002t0001g0047 a0001c0002t0002g0028 others(92): Show |
135 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.163-1316delT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39515499 | |||||||
chr4:39515582 | T | TA | 51 | a0001c0001t0002g0007 a0001c0001t0002g0032 a0001c0001t0002g0034 others(48): Show |
76 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.163-1399dupT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39515582 | |||||||
chr4:39515707 | A | T | 1 | a0001c0001t0004g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.163-1523T>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39515707 | |||||||
chr4:39515712 | T | C | 1 | a0001c0002t0002g0134 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.163-1528A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39515712 | |||||||
chr4:39515723 | A | G | 1 | a0001c0002t0002g0127 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.163-1539T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39515723 | |||||||
chr4:39516049 | T | C | 2 | a0001c0005t0018g0197 a0003c0006t0013g0198 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.163-1865A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516049 | |||||||
chr4:39516079 | G | T | 1 | a0001c0001t0043g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.163-1895C>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516079 | |||||||
chr4:39516110 | A | G | 1 | a0001c0003t0001g0022 | 2 | HG00140.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.163-1926T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516110 | |||||||
chr4:39516130 | A | T | 1 | a0001c0001t0006g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.163-1946T>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516130 | |||||||
chr4:39516148 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.163-1964C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516148 | |||||||
chr4:39516153 | G | A | 2 | a0001c0002t0025g0272 a0001c0002t0025g0285 |
2 | HG01167.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.163-1969C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516153 | |||||||
chr4:39516159 | C | T | 1 | a0001c0001t0030g0064 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.163-1975G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516159 | |||||||
chr4:39516216 | G | A | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.163-2032C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516216 | |||||||
chr4:39516239 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.163-2055C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516239 | |||||||
chr4:39516245 | C | G | 1 | a0001c0001t0002g0032 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.163-2061G>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516245 | |||||||
chr4:39516378 | T | G | 2 | a0001c0001t0002g0034 a0001c0001t0002g0170 |
3 | NA19011.hp2 NA19077.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.163-2194A>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516378 | |||||||
chr4:39516418 | C | T | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.163-2234G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516418 | |||||||
chr4:39516429 | T | C | 1 | a0001c0001t0006g0207 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.163-2245A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516429 | |||||||
chr4:39516467 | C | T | 161 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0032 others(158): Show |
230 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.163-2283G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516467 | |||||||
chr4:39516490 | T | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(227): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.163-2306A>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516490 | |||||||
chr4:39516508 | T | G | 1 | a0001c0001t0004g0218 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.163-2324A>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516508 | |||||||
chr4:39516606 | T | C | 1 | a0001c0002t0003g0115 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.163-2422A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516606 | |||||||
chr4:39516609 | G | A | 1 | a0001c0002t0009g0269 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.163-2425C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516609 | |||||||
chr4:39516638 | T | G | 1 | a0001c0002t0009g0268 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.163-2454A>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516638 | |||||||
chr4:39516644 | C | T | 232 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(229): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.163-2460G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516644 | |||||||
chr4:39516685 | G | A | 1 | a0001c0001t0043g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.163-2501C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39516685 | |||||||
chr4:39517008 | G | A | 6 | a0001c0001t0004g0042 a0001c0001t0004g0043 a0001c0001t0004g0204 others(3): Show |
8 | NA18947.hp1 NA18961.hp1 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-2824C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39517008 | |||||||
chr4:39517101 | C | G | 43 | a0001c0002t0001g0047 a0001c0002t0007g0012 a0001c0002t0007g0018 others(40): Show |
50 | HG00408.hp1 HG00423.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.163-2917G>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39517101 | |||||||
chr4:39517204 | AT | A | 57 | a0001c0001t0002g0145 a0001c0001t0002g0172 a0001c0001t0005g0142 others(54): Show |
90 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.163-3021delA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39517204 | |||||||
chr4:39517244 | C | T | 94 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(91): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.163-3060G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39517244 | |||||||
chr4:39517271 | C | G | 1 | a0001c0002t0007g0274 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.163-3087G>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39517271 | |||||||
chr4:39517348 | G | A | 1 | a0001c0001t0005g0173 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.163-3164C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39517348 | |||||||
chr4:39517480 | G | A | 1 | a0001c0001t0004g0240 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.163-3296C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39517480 | |||||||
chr4:39517503 | C | A | 2 | a0001c0001t0006g0293 a0001c0001t0006g0294 |
2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.163-3319G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39517503 | |||||||
chr4:39517527 | A | T | 94 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(91): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.163-3343T>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39517527 | |||||||
chr4:39517753 | A | AT | 5 | a0001c0001t0047g0251 a0001c0001t0049g0250 a0001c0005t0018g0197 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-3570dupA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39517753 | |||||||
chr4:39517767 | C | T | 14 | a0001c0001t0013g0249 a0001c0002t0002g0029 a0001c0002t0002g0124 others(11): Show |
23 | HG00099.hp1 HG01175.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-3583G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39517767 | |||||||
chr4:39517917 | C | T | 43 | a0001c0002t0001g0047 a0001c0002t0007g0012 a0001c0002t0007g0018 others(40): Show |
50 | HG00408.hp1 HG00423.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.162+3434G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39517917 | |||||||
chr4:39517924 | TTTTG | T | 43 | a0001c0001t0001g0063 a0001c0002t0001g0047 a0001c0002t0007g0012 others(40): Show |
50 | HG00408.hp1 HG00423.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.162+3423_162+3426d others(6): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39517924 | |||||||
chr4:39517994 | A | T | 94 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(91): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.162+3357T>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39517994 | |||||||
chr4:39518077 | T | C | 166 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0032 others(163): Show |
235 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.162+3274A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39518077 | |||||||
chr4:39518173 | C | T | 1 | a0001c0002t0026g0273 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.162+3178G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39518173 | |||||||
chr4:39518381 | C | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(51): Show |
79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.162+2970G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39518381 | |||||||
chr4:39518384 | T | C | 49 | a0001c0001t0002g0007 a0001c0001t0002g0032 a0001c0001t0002g0034 others(46): Show |
74 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.162+2967A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39518384 | |||||||
chr4:39518502 | C | T | 1 | a0001c0002t0003g0139 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+2849G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39518502 | |||||||
chr4:39518609 | G | A | 15 | a0001c0001t0002g0011 a0001c0001t0002g0184 a0001c0001t0002g0185 others(12): Show |
19 | HG00438.hp2 HG00733.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.162+2742C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39518609 | |||||||
chr4:39518619 | T | A | 1 | a0001c0002t0009g0269 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.162+2732A>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39518619 | |||||||
chr4:39518619 | TA | T | 67 | a0001c0001t0001g0048 a0001c0001t0002g0007 a0001c0001t0002g0011 others(64): Show |
95 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.162+2731delT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39518619 | |||||||
chr4:39518633 | A | G | 2 | a0001c0001t0006g0207 a0001c0002t0003g0135 |
2 | HG00280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.162+2718T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39518633 | |||||||
chr4:39518634 | A | G | 93 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(90): Show |
133 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.162+2717T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39518634 | |||||||
chr4:39518711 | G | A | 47 | a0001c0001t0002g0007 a0001c0001t0002g0032 a0001c0001t0002g0034 others(44): Show |
72 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.162+2640C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39518711 | |||||||
chr4:39518907 | T | C | 47 | a0001c0001t0004g0016 a0001c0001t0004g0037 a0001c0001t0004g0038 others(44): Show |
57 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.162+2444A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39518907 | |||||||
chr4:39518933 | T | C | 165 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0032 others(162): Show |
234 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.162+2418A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39518933 | |||||||
chr4:39519029 | G | A | 43 | a0001c0002t0001g0047 a0001c0002t0007g0012 a0001c0002t0007g0018 others(40): Show |
50 | HG00408.hp1 HG00423.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.162+2322C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39519029 | |||||||
chr4:39519169 | G | A | 1 | a0001c0002t0003g0116 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.162+2182C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39519169 | |||||||
chr4:39519219 | A | AT | 73 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0032 others(70): Show |
101 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.162+2131dupA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39519219 | |||||||
chr4:39519219 | A | ATT | 93 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(90): Show |
133 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.162+2130_162+2131d others(4): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39519219 | |||||||
chr4:39519507 | T | A | 1 | a0001c0002t0007g0287 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.162+1844A>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39519507 | |||||||
chr4:39519517 | C | T | 2 | a0001c0001t0006g0293 a0001c0001t0006g0294 |
2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.162+1834G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39519517 | |||||||
chr4:39519525 | A | C | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.162+1826T>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39519525 | |||||||
chr4:39519552 | A | T | 230 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(227): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.162+1799T>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39519552 | |||||||
chr4:39519561 | C | T | 94 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(91): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.162+1790G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39519561 | |||||||
chr4:39519608 | G | A | 2 | a0001c0005t0018g0197 a0003c0006t0013g0198 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.162+1743C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39519608 | |||||||
chr4:39519729 | G | A | 2 | a0001c0001t0006g0293 a0001c0001t0006g0294 |
2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.162+1622C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39519729 | |||||||
chr4:39519876 | A | C | 18 | a0001c0002t0007g0018 a0001c0002t0009g0258 a0001c0002t0009g0259 others(15): Show |
20 | HG00423.hp2 HG01168.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.162+1475T>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39519876 | |||||||
chr4:39520061 | G | A | 1 | a0001c0001t0017g0176 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.162+1290C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520061 | |||||||
chr4:39520086 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.162+1265G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520086 | |||||||
chr4:39520104 | C | T | 94 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(91): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.162+1247G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520104 | |||||||
chr4:39520114 | C | T | 94 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(91): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.162+1237G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520114 | |||||||
chr4:39520253 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.162+1098G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520253 | |||||||
chr4:39520273 | G | A | 1 | a0001c0001t0013g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.162+1078C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520273 | |||||||
chr4:39520282 | T | C | 2 | a0001c0001t0004g0242 a0001c0001t0018g0241 |
2 | HG01069.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.162+1069A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520282 | |||||||
chr4:39520313 | T | C | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.162+1038A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520313 | |||||||
chr4:39520334 | C | T | 1 | a0001c0001t0011g0061 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.162+1017G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520334 | |||||||
chr4:39520489 | T | TA | 64 | a0001c0002t0002g0028 a0001c0002t0002g0029 a0001c0002t0002g0030 others(61): Show |
97 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.162+861dupT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520489 | |||||||
chr4:39520588 | T | C | 2 | a0001c0005t0018g0197 a0003c0006t0013g0198 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.162+763A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520588 | |||||||
chr4:39520603 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(128): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.162+748G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520603 | |||||||
chr4:39520812 | G | A | 1 | a0001c0002t0002g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.162+539C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520812 | |||||||
chr4:39520845 | G | T | 3 | a0001c0001t0010g0039 a0001c0001t0010g0205 a0001c0001t0010g0206 |
4 | HG01070.hp2 HG01123.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+506C>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520845 | |||||||
chr4:39520857 | T | C | 2 | a0001c0005t0018g0197 a0003c0006t0013g0198 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.162+494A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520857 | |||||||
chr4:39520895 | G | A | 2 | a0001c0005t0018g0197 a0003c0006t0013g0198 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.162+456C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520895 | |||||||
chr4:39520925 | T | A | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.162+426A>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520925 | |||||||
chr4:39520975 | A | C | 2 | a0001c0001t0047g0251 a0001c0001t0049g0250 |
2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.162+376T>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39520975 | |||||||
chr4:39521068 | T | A | 3 | a0001c0001t0013g0249 a0001c0001t0043g0203 a0001c0010t0042g0252 |
3 | HG03139.hp2 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.162+283A>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39521068 | |||||||
chr4:39521069 | C | CA | 23 | a0001c0001t0002g0011 a0001c0001t0002g0184 a0001c0001t0002g0185 others(20): Show |
27 | HG00438.hp2 HG00733.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.162+281dupT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39521069 | |||||||
chr4:39521069 | CA | C | 14 | a0001c0001t0001g0052 a0001c0001t0002g0146 a0001c0001t0002g0179 others(11): Show |
14 | HG01069.hp1 HG01257.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.162+281delT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39521069 | |||||||
chr4:39521069 | CAA | C | 91 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0029 others(88): Show |
131 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.162+280_162+281del others(2): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39521069 | |||||||
chr4:39521079 | A | G | 2 | a0001c0001t0047g0251 a0001c0001t0049g0250 |
2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.162+272T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39521079 | |||||||
chr4:39521083 | A | C | 1 | a0001c0001t0004g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162+268T>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39521083 | |||||||
chr4:39521086 | A | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(59): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.162+265T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39521086 | |||||||
chr4:39521250 | C | T | 15 | a0001c0001t0002g0011 a0001c0001t0002g0184 a0001c0001t0002g0185 others(12): Show |
19 | HG00438.hp2 HG00733.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.162+101G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39521250 | |||||||
chr4:39521265 | A | G | 2 | a0001c0005t0018g0197 a0003c0006t0013g0198 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.162+86T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 2/11 | chr4 | 39521265 | |||||||
chr4:39521826 | A | T | 95 | a0001c0001t0010g0289 a0001c0002t0001g0047 a0001c0002t0002g0028 others(92): Show |
135 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.-7-307T>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39521826 | |||||||
chr4:39521959 | C | T | 1 | a0001c0001t0002g0032 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-7-440G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39521959 | |||||||
chr4:39521960 | G | A | 1 | a0001c0001t0002g0193 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-7-441C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39521960 | |||||||
chr4:39521989 | T | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(51): Show |
79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-7-470A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39521989 | |||||||
chr4:39522003 | CTGA | C | 95 | a0001c0001t0010g0289 a0001c0002t0001g0047 a0001c0002t0002g0028 others(92): Show |
135 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.-7-487_-7-485delTC others(1): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39522003 | |||||||
chr4:39522435 | T | C | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-7-916A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39522435 | |||||||
chr4:39522448 | C | A | 1 | a0001c0001t0043g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-7-929G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39522448 | |||||||
chr4:39522466 | G | A | 95 | a0001c0001t0010g0289 a0001c0002t0001g0047 a0001c0002t0002g0028 others(92): Show |
135 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.-7-947C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39522466 | |||||||
chr4:39522600 | C | T | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-7-1081G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39522600 | |||||||
chr4:39522683 | G | A | 1 | a0001c0002t0003g0139 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-7-1164C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39522683 | |||||||
chr4:39522684 | T | G | 98 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0010g0289 others(95): Show |
138 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.-7-1165A>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39522684 | |||||||
chr4:39522744 | T | C | 1 | a0001c0001t0011g0096 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-7-1225A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39522744 | |||||||
chr4:39522764 | C | CT | 18 | a0001c0002t0007g0018 a0001c0002t0009g0258 a0001c0002t0009g0259 others(15): Show |
20 | HG00423.hp2 HG01168.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.-7-1246dupA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39522764 | |||||||
chr4:39522764 | CT | C | 73 | a0001c0001t0002g0011 a0001c0001t0002g0145 a0001c0001t0002g0179 others(70): Show |
110 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.-7-1246delA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39522764 | |||||||
chr4:39522832 | G | A | 1 | a0001c0001t0048g0244 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-7-1313C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39522832 | |||||||
chr4:39523004 | A | G | 94 | a0001c0001t0010g0289 a0001c0002t0001g0047 a0001c0002t0002g0028 others(91): Show |
134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-7-1485T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39523004 | |||||||
chr4:39523198 | C | T | 2 | a0001c0001t0015g0181 a0001c0001t0015g0182 |
2 | NA19068.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-7-1679G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39523198 | |||||||
chr4:39523289 | C | T | 2 | a0001c0001t0011g0054 a0001c0001t0033g0098 |
2 | HG02040.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-7-1770G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39523289 | |||||||
chr4:39523484 | T | A | 1 | a0001c0001t0028g0097 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-7-1965A>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39523484 | |||||||
chr4:39523522 | T | C | 1 | a0001c0001t0010g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-7-2003A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39523522 | |||||||
chr4:39523578 | C | G | 233 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(230): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-7-2059G>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39523578 | |||||||
chr4:39523634 | A | G | 233 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(230): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-7-2115T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39523634 | |||||||
chr4:39523660 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-7-2141C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39523660 | |||||||
chr4:39523672 | C | G | 3 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 |
3 | HG02451.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-7-2153G>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39523672 | |||||||
chr4:39523729 | G | A | 15 | a0001c0001t0002g0011 a0001c0001t0002g0184 a0001c0001t0002g0185 others(12): Show |
19 | HG00438.hp2 HG00733.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-7-2210C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39523729 | |||||||
chr4:39523799 | T | C | 2 | a0001c0001t0035g0194 a0001c0001t0037g0195 |
2 | HG02145.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-7-2280A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39523799 | |||||||
chr4:39523806 | CA | C | 36 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0145 others(33): Show |
58 | HG00558.hp1 HG00609.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.-7-2288delT | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39523806 | |||||||
chr4:39523945 | A | G | 95 | a0001c0001t0010g0289 a0001c0002t0001g0047 a0001c0002t0002g0028 others(92): Show |
135 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.-7-2426T>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39523945 | |||||||
chr4:39524039 | A | C | 1 | a0001c0001t0002g0144 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-7-2520T>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39524039 | |||||||
chr4:39524285 | T | C | 1 | a0001c0003t0040g0196 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-7-2766A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39524285 | |||||||
chr4:39524503 | C | CT | 6 | a0001c0001t0001g0051 a0001c0001t0004g0218 a0001c0001t0005g0142 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+2779dupA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39524503 | |||||||
chr4:39524503 | CT | C | 9 | a0001c0001t0033g0098 a0001c0001t0047g0251 a0001c0001t0049g0250 others(6): Show |
10 | HG01516.hp1 HG02027.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+2779delA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39524503 | |||||||
chr4:39524579 | C | T | 21 | a0001c0001t0004g0016 a0001c0001t0004g0041 a0001c0001t0004g0042 others(18): Show |
28 | HG00280.hp2 HG01069.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.-8+2704G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39524579 | |||||||
chr4:39524847 | T | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(128): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-8+2436A>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39524847 | |||||||
chr4:39524863 | T | C | 1 | a0001c0001t0047g0251 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-8+2420A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39524863 | |||||||
chr4:39524995 | T | C | 2 | a0001c0001t0004g0245 a0001c0001t0004g0246 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-8+2288A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39524995 | |||||||
chr4:39525021 | G | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(59): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.-8+2262C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525021 | |||||||
chr4:39525199 | T | G | 1 | a0001c0001t0003g0036 | 2 | NA18959.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-8+2084A>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525199 | |||||||
chr4:39525235 | C | A | 51 | a0001c0002t0002g0028 a0001c0002t0002g0029 a0001c0002t0002g0030 others(48): Show |
84 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+2048G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525235 | |||||||
chr4:39525286 | T | C | 2 | a0001c0001t0024g0247 a0001c0001t0024g0248 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-8+1997A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525286 | |||||||
chr4:39525401 | T | C | 231 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(228): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-8+1882A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525401 | |||||||
chr4:39525405 | G | A | 95 | a0001c0001t0010g0289 a0001c0002t0001g0047 a0001c0002t0002g0028 others(92): Show |
135 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.-8+1878C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525405 | |||||||
chr4:39525501 | C | CTTT | 233 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(230): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-8+1779_-8+1781dup others(3): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525501 | |||||||
chr4:39525512 | C | CT | 91 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0023 others(88): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-8+1770dupA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525512 | |||||||
chr4:39525512 | C | CTT | 49 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0048 others(46): Show |
62 | HG00408.hp1 HG00423.hp2 HG01099.hp2 others(59): Show |
intron_variant | MODIFIER | c.-8+1769_-8+1770dup others(2): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525512 | |||||||
chr4:39525512 | C | CTTT | 24 | a0001c0002t0002g0028 a0001c0002t0002g0117 a0001c0002t0003g0002 others(21): Show |
44 | HG00558.hp1 HG00609.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+1768_-8+1770dup others(3): Show |
UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525512 | |||||||
chr4:39525673 | A | AT | 95 | a0001c0001t0010g0289 a0001c0002t0001g0047 a0001c0002t0002g0028 others(92): Show |
135 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.-8+1609dupA | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525673 | |||||||
chr4:39525804 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-8+1479G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525804 | |||||||
chr4:39525828 | T | C | 2 | a0001c0001t0013g0249 a0001c0010t0042g0252 |
2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-8+1455A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525828 | |||||||
chr4:39525841 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-8+1442A>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525841 | |||||||
chr4:39525853 | C | A | 1 | a0001c0002t0010g0291 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-8+1430G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525853 | |||||||
chr4:39525891 | G | T | 5 | a0001c0001t0004g0037 a0001c0001t0004g0038 a0001c0001t0004g0200 others(2): Show |
7 | HG00558.hp2 HG02165.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+1392C>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39525891 | |||||||
chr4:39526062 | C | T | 1 | a0001c0001t0006g0199 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-8+1221G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39526062 | |||||||
chr4:39526452 | C | A | 1 | a0001c0001t0021g0020 | 2 | HG00642.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-8+831G>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39526452 | |||||||
chr4:39526453 | C | G | 51 | a0001c0002t0002g0028 a0001c0002t0002g0029 a0001c0002t0002g0030 others(48): Show |
84 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+830G>C | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39526453 | |||||||
chr4:39526564 | G | C | 6 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0022g0292 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+719C>G | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39526564 | |||||||
chr4:39526770 | C | T | 1 | a0001c0001t0002g0101 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-8+513G>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39526770 | |||||||
chr4:39526778 | A | T | 2 | a0001c0005t0018g0197 a0003c0006t0013g0198 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-8+505T>A | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39526778 | |||||||
chr4:39527132 | G | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(223): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.-8+151C>T | UGDH | ENSG00000109814.12 | transcript | ENST00000316423.11 | protein_coding | 1/11 | chr4 | 39527132 |