Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7374 |
| ensemblid | ENSG00000076248.12 |
| hgncid | 12572 |
| symbol | UNG |
| name | uracil DNA glycosylase |
| refseq_nuc | NM_080911.3 |
| refseq_prot | NP_550433.1 |
| ensembl_nuc | ENST00000242576.7 |
| ensembl_prot | ENSP00000242576.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 109097597 |
| end | 109110992 |
| strand | + |
| ver | v1.2 |
| region | chr12:109097597-109110992 |
| region5000 | chr12:109092597-109115992 |
| regionname0 | UNG_chr12_109097597_109110992 |
| regionname5000 | UNG_chr12_109092597_109115992 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 313 | 451 | 93 | 70 | 226 | 14 | 46 | 182 | UNG_chr12_109092597_109115992 | UNG | MIGQK others(308): Show |
chr12 | 109092597 | 109115992 |
| a0002 | 0/0 | 313 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | MIGQK others(308): Show |
chr12 | 109092597 | 109115992 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 939 | 440 | 84 | 68 | 226 | 14 | 46 | UNG_chr12_109092597_109115992 | UNG | ATGAT others(934): Show |
chr12 | 109092597 | 109115992 | ||
| a0001c0002 | 0/0 | 939 | 6 | 5 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | ATGAT others(934): Show |
chr12 | 109092597 | 109115992 | ||
| a0001c0003 | 0/0 | 939 | 3 | 3 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | ATGAT others(934): Show |
chr12 | 109092597 | 109115992 | ||
| a0001c0005 | 0/0 | 939 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | ATGAT others(934): Show |
chr12 | 109092597 | 109115992 | ||
| a0001c0006 | 0/0 | 939 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | ATGAT others(934): Show |
chr12 | 109092597 | 109115992 | ||
| a0002c0004 | 0/0 | 939 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | ATGAT others(934): Show |
chr12 | 109092597 | 109115992 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2048 | 379 | 69 | 59 | 199 | 12 | 38 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2043): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0002 | 0/0 | 2050 | 37 | 3 | 3 | 22 | 2 | 7 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2045): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0003 | 0/0 | 2049 | 7 | 4 | 3 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2044): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0004 | 0/0 | 2020 | 4 | 4 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2015): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0005 | 0/0 | 2048 | 2 | 2 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2043): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0006 | 0/0 | 2048 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2043): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0007 | 0/0 | 2048 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2043): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0008 | 0/0 | 2048 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2043): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0009 | 0/0 | 2050 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2045): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0010 | 0/0 | 2048 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2043): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0011 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2044): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0012 | 0/0 | 2050 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2045): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0013 | 0/0 | 2048 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2043): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0014 | 0/0 | 2048 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2043): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0015 | 0/0 | 2050 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2045): Show |
chr12 | 109092597 | 109115992 |
| a0001c0001t0016 | 0/0 | 2050 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2045): Show |
chr12 | 109092597 | 109115992 |
| a0001c0002t0001 | 0/0 | 2048 | 6 | 5 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2043): Show |
chr12 | 109092597 | 109115992 |
| a0001c0003t0001 | 0/0 | 2048 | 3 | 3 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2043): Show |
chr12 | 109092597 | 109115992 |
| a0001c0005t0001 | 0/0 | 2048 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2043): Show |
chr12 | 109092597 | 109115992 |
| a0001c0006t0001 | 0/0 | 2048 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2043): Show |
chr12 | 109092597 | 109115992 |
| a0002c0004t0001 | 0/0 | 2048 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | AATTG others(2043): Show |
chr12 | 109092597 | 109115992 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 0 | 1 | 20 | 1 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0002 | 0/0 | 11 | 2 | 3 | 4 | 0 | 2 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 2 | 7 | 1 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 8 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 5 | 0 | 0 | 2 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0015 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0020 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0025 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0055 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0132 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0005 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0003g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0004g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0006g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0007g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0008g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0009g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0010g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0011g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0012g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0013g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0014g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0015g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0001t0016g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0002t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0005t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0001c0006t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| a0002c0004t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0027 | EUR | GBR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0027 | EUR | FIN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0295 | EUR | FIN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | FIN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00738 | hp2 | a0001 | c0001 | t0014 | g0152 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01074 | hp2 | a0001 | c0001 | t0008 | g0131 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01175 | hp1 | a0001 | c0005 | t0001 | g0161 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0283 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01433 | hp1 | a0001 | c0001 | t0013 | g0289 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | IBS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | IBS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0073 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0071 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0285 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0286 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02622 | hp2 | a0002 | c0004 | t0001 | g0265 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0284 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0074 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | MSL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0233 | AFR | MSL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | STU | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | BEB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG04184 | hp1 | a0001 | c0001 | t0010 | g0021 | SAS | BEB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | STU | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18522 | hp1 | a0001 | c0006 | t0001 | g0076 | AFR | YRI | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | YRI | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | YRI | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19010 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0278 | AFR | LWK | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | LWK | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19070 | hp1 | a0001 | c0001 | t0015 | g0183 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19079 | hp1 | a0001 | c0001 | t0011 | g0023 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19079 | hp2 | a0001 | c0001 | t0009 | g0186 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19086 | hp1 | a0001 | c0001 | t0012 | g0113 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | YRI | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ASW | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ASW | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | TSI | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | GIH | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | GIH | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | USA | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | USA | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA20300 | hp1 | a0001 | c0001 | t0016 | g0290 | AFR | USA | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | USA | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | LWK | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0132 | REF | REF | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0104 | REF | REF | UNG_chr12_109092597_109115992 | UNG | chr12 | 109092597 | 109115992 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109097803 | G | C | 1 | a0002 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.124G>C | p.Asp42His | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 1/7 | 207/2048 | 124/942 | 42/313 | chr12 | 109097803 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109098545 | G | C | 1 | a0001c0005 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.246G>C | p.Leu82Leu | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 2/7 | 329/2048 | 246/942 | 82/313 | chr12 | 109098545 | |||
| chr12:109098590 | C | T | 1 | a0001c0003 | 3 | HG01884.hp2 HG01891.hp1 HG03041.hp1 |
synonymous_variant | LOW | c.291C>T | p.Ser97Ser | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 2/7 | 374/2048 | 291/942 | 97/313 | chr12 | 109098590 | |||
| chr12:109103548 | G | A | 1 | a0001c0006 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.738G>A | p.Ser246Ser | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/7 | 821/2048 | 738/942 | 246/313 | chr12 | 109103548 | |||
| chr12:109103569 | C | G | 1 | a0001c0002 | 6 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(3): Show |
synonymous_variant | LOW | c.759C>G | p.Leu253Leu | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/7 | 842/2048 | 759/942 | 253/313 | chr12 | 109103569 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109110010 | G | A | 1 | a0001c0001t0006 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*41G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 41 | chr12 | 109110010 | ||||||
| chr12:109110078 | A | G | 1 | a0001c0001t0016 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*109A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 109 | chr12 | 109110078 | ||||||
| chr12:109110309 | C | T | 1 | a0001c0001t0015 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*340C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 340 | chr12 | 109110309 | ||||||
| chr12:109110332 | C | G | 1 | a0001c0001t0014 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*363C>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 363 | chr12 | 109110332 | ||||||
| chr12:109110432 | C | T | 1 | a0001c0001t0013 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*463C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 463 | chr12 | 109110432 | ||||||
| chr12:109110443 | A | C | 1 | a0001c0001t0012 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*474A>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 474 | chr12 | 109110443 | ||||||
| chr12:109110445 | C | A | 1 | a0001c0001t0007 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*476C>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 476 | chr12 | 109110445 | ||||||
| chr12:109110470 | G | A | 1 | a0001c0001t0008 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*501G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 501 | chr12 | 109110470 | ||||||
| chr12:109110561 | G | A | 1 | a0001c0001t0009 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*592G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 592 | chr12 | 109110561 | ||||||
| chr12:109110633 | TGGAATTT others(21): Show |
T | 1 | a0001c0001t0004 | 4 | HG03139.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*672_*699delGAACAA others(22): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 672 | INFO_REALIGN_3_PRIME | chr12 | 109110633 | |||||
| chr12:109110749 | G | GT | 2 | a0001c0001t0003 a0001c0001t0011 |
8 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*788dupT | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 789 | INFO_REALIGN_3_PRIME | chr12 | 109110749 | |||||
| chr12:109110761 | C | T | 1 | a0001c0001t0005 | 2 | HG03195.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*792C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 792 | chr12 | 109110761 | ||||||
| chr12:109110834 | G | GAT | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0012 others(2): Show |
41 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*880_*881dupAT | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 882 | INFO_REALIGN_3_PRIME | chr12 | 109110834 | |||||
| chr12:109110855 | C | T | 1 | a0001c0001t0011 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*886C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 886 | chr12 | 109110855 | ||||||
| chr12:109110982 | T | A | 1 | a0001c0001t0003 | 7 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1013T>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 1013 | chr12 | 109110982 | ||||||
| chr12:109110985 | T | G | 1 | a0001c0001t0012 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1016T>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 1016 | chr12 | 109110985 | ||||||
| chr12:109110986 | A | T | 1 | a0001c0001t0012 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1017A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 1017 | chr12 | 109110986 | ||||||
| chr12:109110987 | A | G | 1 | a0001c0001t0010 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1018A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 7/7 | 1018 | chr12 | 109110987 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109097903 | A | T | 1 | a0001c0001t0001g0301 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.132+92A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 1/6 | chr12 | 109097903 | |||||||
| chr12:109097967 | C | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0293 a0001c0001t0001g0294 others(6): Show |
13 | HG00323.hp1 HG02258.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.132+156C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 1/6 | chr12 | 109097967 | |||||||
| chr12:109097991 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0002g0027 |
3 | HG00099.hp2 HG00280.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.132+180G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 1/6 | chr12 | 109097991 | |||||||
| chr12:109098004 | A | G | 50 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(47): Show |
71 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(68): Show |
intron_variant | MODIFIER | c.132+193A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 1/6 | chr12 | 109098004 | |||||||
| chr12:109098052 | T | A | 46 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
67 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(64): Show |
intron_variant | MODIFIER | c.132+241T>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 1/6 | chr12 | 109098052 | |||||||
| chr12:109098157 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG01515.hp1 HG02738.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.133-275G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 1/6 | chr12 | 109098157 | |||||||
| chr12:109098178 | G | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0062 |
3 | HG00741.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.133-254G>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 1/6 | chr12 | 109098178 | |||||||
| chr12:109098185 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.133-247A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 1/6 | chr12 | 109098185 | |||||||
| chr12:109098211 | C | T | 8 | a0001c0001t0001g0057 a0001c0001t0001g0287 a0001c0001t0001g0288 others(5): Show |
10 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.133-221C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 1/6 | chr12 | 109098211 | |||||||
| chr12:109098229 | C | G | 1 | a0001c0001t0001g0300 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.133-203C>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 1/6 | chr12 | 109098229 | |||||||
| chr12:109098391 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.133-41C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 1/6 | chr12 | 109098391 | |||||||
| chr12:109098746 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.339+108C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 2/6 | chr12 | 109098746 | |||||||
| chr12:109098754 | A | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(68): Show |
100 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.339+116A>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 2/6 | chr12 | 109098754 | |||||||
| chr12:109098776 | G | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0250 |
3 | HG02257.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.339+138G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 2/6 | chr12 | 109098776 | |||||||
| chr12:109098802 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.339+164T>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 2/6 | chr12 | 109098802 | |||||||
| chr12:109098854 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.339+216G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 2/6 | chr12 | 109098854 | |||||||
| chr12:109098918 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | NA18941.hp1 NA18949.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-271C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 2/6 | chr12 | 109098918 | |||||||
| chr12:109099020 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.340-169A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 2/6 | chr12 | 109099020 | |||||||
| chr12:109099312 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.435+28T>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109099312 | |||||||
| chr12:109099618 | T | TTA | 72 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(69): Show |
106 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.435+337_435+338dup others(2): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 109099618 | ||||||
| chr12:109099757 | T | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0253 others(1): Show |
11 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.435+473T>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109099757 | |||||||
| chr12:109099759 | G | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0020 others(62): Show |
86 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.435+475G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109099759 | |||||||
| chr12:109099784 | G | A | 4 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0013g0289 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.435+500G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109099784 | |||||||
| chr12:109099791 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.435+507G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109099791 | |||||||
| chr12:109099882 | A | G | 3 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0016g0290 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.435+598A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109099882 | |||||||
| chr12:109099960 | G | C | 1 | a0001c0001t0001g0029 | 2 | HG02135.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.435+676G>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109099960 | |||||||
| chr12:109100066 | C | CA | 9 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0126 others(6): Show |
9 | HG01167.hp2 HG01515.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.435+792dupA | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 109100066 | ||||||
| chr12:109100076 | AC | A | 4 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0013g0289 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.435+794delC | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 109100076 | ||||||
| chr12:109100084 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.435+800T>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109100084 | |||||||
| chr12:109100161 | C | G | 10 | a0001c0001t0001g0037 a0001c0001t0001g0167 a0001c0001t0001g0168 others(7): Show |
11 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(8): Show |
intron_variant | MODIFIER | c.435+877C>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109100161 | |||||||
| chr12:109100228 | C | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0287 a0001c0001t0001g0288 |
4 | HG02809.hp1 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.435+944C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109100228 | |||||||
| chr12:109100235 | A | G | 1 | a0001c0001t0001g0053 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.435+951A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109100235 | |||||||
| chr12:109100428 | G | A | 1 | a0001c0001t0001g0041 | 2 | NA18747.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.435+1144G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109100428 | |||||||
| chr12:109100430 | A | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(22): Show |
61 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.435+1146A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109100430 | |||||||
| chr12:109100679 | T | C | 1 | a0001c0001t0002g0177 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.436-1223T>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109100679 | |||||||
| chr12:109100843 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.436-1059G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109100843 | |||||||
| chr12:109100902 | CTAGG | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0281 a0001c0001t0001g0282 |
6 | HG02109.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.436-998_436-995del others(4): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 109100902 | ||||||
| chr12:109100919 | G | A | 1 | a0001c0001t0013g0289 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.436-983G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109100919 | |||||||
| chr12:109100940 | C | G | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.436-962C>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109100940 | |||||||
| chr12:109100958 | C | T | 4 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0013g0289 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.436-944C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109100958 | |||||||
| chr12:109100969 | CTTCAT | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0293 a0001c0001t0001g0294 others(6): Show |
13 | HG00323.hp1 HG02258.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.436-921_436-917del others(5): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 109100969 | ||||||
| chr12:109100977 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.436-925C>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109100977 | |||||||
| chr12:109101025 | C | G | 3 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0016g0290 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.436-877C>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109101025 | |||||||
| chr12:109101106 | C | CT | 6 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
7 | HG00558.hp1 HG01496.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-767dupT | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 109101106 | ||||||
| chr12:109101106 | CT | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0021 others(68): Show |
100 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.436-767delT | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 109101106 | ||||||
| chr12:109101106 | CTT | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(64): Show |
101 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.436-768_436-767del others(2): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 109101106 | ||||||
| chr12:109101106 | CTTT | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(36): Show |
82 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.436-769_436-767del others(3): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 109101106 | ||||||
| chr12:109101106 | CTTTT | C | 41 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0023 others(38): Show |
50 | HG00323.hp1 HG00544.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.436-770_436-767del others(4): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 109101106 | ||||||
| chr12:109101106 | CTTTTT | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0041 others(46): Show |
72 | HG00408.hp1 HG00639.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.436-771_436-767del others(5): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 109101106 | ||||||
| chr12:109101106 | CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0003g0009 others(3): Show |
10 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-777_436-767del others(11): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 109101106 | ||||||
| chr12:109101106 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0016g0290 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.436-778_436-767del others(12): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 109101106 | ||||||
| chr12:109101110 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.436-792T>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109101110 | |||||||
| chr12:109101147 | C | T | 1 | a0001c0001t0013g0289 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.436-755C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109101147 | |||||||
| chr12:109101148 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.436-754A>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109101148 | |||||||
| chr12:109101184 | C | T | 1 | a0001c0001t0007g0233 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.436-718C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109101184 | |||||||
| chr12:109101185 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.436-717T>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109101185 | |||||||
| chr12:109101312 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.436-590G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109101312 | |||||||
| chr12:109101472 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0293 a0001c0001t0001g0294 others(6): Show |
13 | HG00323.hp1 HG02258.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.436-430G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109101472 | |||||||
| chr12:109101530 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.436-372G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109101530 | |||||||
| chr12:109101594 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-308C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 3/6 | chr12 | 109101594 | |||||||
| chr12:109102005 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG01074.hp1 | splice_region_variant&intron_variant | LOW | c.533+6G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 4/6 | chr12 | 109102005 | |||||||
| chr12:109102106 | G | A | 1 | a0001c0001t0002g0182 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.533+107G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 4/6 | chr12 | 109102106 | |||||||
| chr12:109102232 | C | G | 3 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0016g0290 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.533+233C>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 4/6 | chr12 | 109102232 | |||||||
| chr12:109102265 | T | C | 1 | a0001c0001t0015g0183 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.533+266T>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 4/6 | chr12 | 109102265 | |||||||
| chr12:109102296 | C | G | 4 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0013g0289 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.533+297C>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 4/6 | chr12 | 109102296 | |||||||
| chr12:109102356 | T | A | 1 | a0001c0001t0001g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.533+357T>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 4/6 | chr12 | 109102356 | |||||||
| chr12:109102578 | G | A | 4 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0013g0289 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-261G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 4/6 | chr12 | 109102578 | |||||||
| chr12:109102588 | G | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0084 a0001c0001t0001g0085 others(2): Show |
13 | HG01070.hp1 HG01123.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.534-251G>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 4/6 | chr12 | 109102588 | |||||||
| chr12:109102750 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG01081.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.534-89A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 4/6 | chr12 | 109102750 | |||||||
| chr12:109102763 | A | G | 3 | a0001c0003t0001g0071 a0001c0003t0001g0073 a0001c0003t0001g0074 |
3 | HG01884.hp2 HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.534-76A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 4/6 | chr12 | 109102763 | |||||||
| chr12:109102808 | G | GT | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(68): Show |
100 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.534-25dupT | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 109102808 | ||||||
| chr12:109102937 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.622+10C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 5/6 | chr12 | 109102937 | |||||||
| chr12:109102947 | A | AT | 35 | a0001c0001t0001g0061 a0001c0001t0001g0066 a0001c0001t0001g0081 others(32): Show |
36 | HG00438.hp2 HG00597.hp2 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.622+42dupT | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr12 | 109102947 | ||||||
| chr12:109102947 | A | ATT | 62 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(59): Show |
89 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.622+41_622+42dupTT | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr12 | 109102947 | ||||||
| chr12:109102947 | A | ATTT | 16 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(13): Show |
18 | HG00673.hp2 HG01891.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.622+40_622+42dupTT others(1): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr12 | 109102947 | ||||||
| chr12:109102947 | AT | A | 6 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0150 others(3): Show |
6 | HG00323.hp1 HG01515.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.622+42delT | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr12 | 109102947 | ||||||
| chr12:109103047 | G | T | 1 | a0001c0001t0005g0030 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.622+120G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 5/6 | chr12 | 109103047 | |||||||
| chr12:109103110 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.622+183G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 5/6 | chr12 | 109103110 | |||||||
| chr12:109103176 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622+249G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 5/6 | chr12 | 109103176 | |||||||
| chr12:109103208 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0293 a0001c0001t0001g0294 others(6): Show |
13 | HG00323.hp1 HG02258.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.623-225G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 5/6 | chr12 | 109103208 | |||||||
| chr12:109103366 | T | C | 9 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0060 others(6): Show |
12 | HG00738.hp2 HG01074.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.623-67T>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 5/6 | chr12 | 109103366 | |||||||
| chr12:109103630 | CTTTT | C | 7 | a0001c0001t0001g0255 a0001c0001t0001g0258 a0001c0001t0001g0259 others(4): Show |
7 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.801+24_801+27delTT others(2): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109103630 | ||||||
| chr12:109103880 | G | T | 2 | a0001c0001t0004g0026 a0001c0001t0004g0278 |
4 | HG03139.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.801+269G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109103880 | |||||||
| chr12:109103979 | C | A | 1 | a0001c0001t0001g0031 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.801+368C>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109103979 | |||||||
| chr12:109104055 | G | GTTTTTTG others(6): Show |
1 | a0001c0001t0013g0289 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.801+451_801+452ins others(13): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109104055 | ||||||
| chr12:109104055 | G | GTTTTTTG others(7): Show |
3 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0016g0290 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.801+451_801+452ins others(14): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109104055 | ||||||
| chr12:109104055 | G | GTTTTTTG others(6): Show |
63 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0023 others(60): Show |
92 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.801+445_801+457dup others(13): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109104055 | ||||||
| chr12:109104055 | G | GTTTTTTG others(8): Show |
85 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0016 others(82): Show |
123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.801+458_801+459ins others(15): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109104055 | ||||||
| chr12:109104055 | G | GTTTTTTG others(7): Show |
28 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(25): Show |
65 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.801+457_801+458ins others(14): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109104055 | ||||||
| chr12:109104055 | G | GTTTTTTG others(8): Show |
2 | a0001c0001t0001g0121 a0001c0001t0001g0123 |
2 | NA18973.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.801+457_801+458ins others(15): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109104055 | ||||||
| chr12:109104062 | G | GTTTTTTT others(6): Show |
6 | a0001c0001t0001g0022 a0001c0001t0001g0205 a0001c0001t0001g0224 others(3): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.801+457_801+458ins others(13): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109104062 | ||||||
| chr12:109104062 | G | GTTTTTTT others(7): Show |
2 | a0001c0001t0001g0227 a0001c0001t0001g0246 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.801+457_801+458ins others(14): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109104062 | ||||||
| chr12:109104100 | G | A | 1 | a0001c0001t0013g0289 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.801+489G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109104100 | |||||||
| chr12:109104184 | T | C | 3 | a0001c0003t0001g0071 a0001c0003t0001g0073 a0001c0003t0001g0074 |
3 | HG01884.hp2 HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.801+573T>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109104184 | |||||||
| chr12:109104207 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.801+596G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109104207 | |||||||
| chr12:109104238 | A | G | 4 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0013g0289 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.801+627A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109104238 | |||||||
| chr12:109104258 | A | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0095 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.801+647A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109104258 | |||||||
| chr12:109104444 | C | T | 3 | a0001c0001t0003g0009 a0001c0001t0003g0069 a0001c0001t0003g0070 |
7 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.801+833C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109104444 | |||||||
| chr12:109104587 | T | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(68): Show |
98 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.801+976T>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109104587 | |||||||
| chr12:109104589 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0176 a0001c0001t0002g0189 others(1): Show |
5 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(2): Show |
intron_variant | MODIFIER | c.801+978C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109104589 | |||||||
| chr12:109104677 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.801+1066G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109104677 | |||||||
| chr12:109104726 | G | T | 6 | a0001c0001t0001g0255 a0001c0001t0001g0258 a0001c0001t0001g0260 others(3): Show |
6 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.801+1115G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109104726 | |||||||
| chr12:109104860 | G | A | 7 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0003g0009 others(4): Show |
11 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.801+1249G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109104860 | |||||||
| chr12:109104905 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG02257.hp1 HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.801+1294G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109104905 | |||||||
| chr12:109104907 | G | T | 1 | a0001c0001t0001g0222 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.801+1296G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109104907 | |||||||
| chr12:109105000 | C | T | 4 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0013g0289 others(1): Show |
4 | HG01433.hp1 HG01891.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.801+1389C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109105000 | |||||||
| chr12:109105351 | C | T | 3 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0016g0290 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.801+1740C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109105351 | |||||||
| chr12:109105352 | G | C | 1 | a0001c0001t0001g0300 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.801+1741G>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109105352 | |||||||
| chr12:109105411 | G | A | 3 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0016g0290 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.801+1800G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109105411 | |||||||
| chr12:109105568 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0068 |
2 | HG00323.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.801+1957A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109105568 | |||||||
| chr12:109105584 | GTTTCTCC others(20): Show |
G | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.801+1975_801+2001d others(29): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109105584 | ||||||
| chr12:109105679 | C | A | 3 | a0001c0001t0003g0009 a0001c0001t0003g0069 a0001c0001t0003g0070 |
7 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.801+2068C>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109105679 | |||||||
| chr12:109105730 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.801+2119T>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109105730 | |||||||
| chr12:109105768 | CT | C | 5 | a0001c0001t0001g0082 a0001c0001t0001g0122 a0001c0001t0001g0198 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.801+2160delT | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109105768 | ||||||
| chr12:109105791 | C | G | 3 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0016g0290 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.801+2180C>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109105791 | |||||||
| chr12:109105842 | G | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.801+2231G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109105842 | |||||||
| chr12:109105909 | A | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(300): Show |
448 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(445): Show |
intron_variant | MODIFIER | c.801+2298A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109105909 | |||||||
| chr12:109105963 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.801+2352G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109105963 | |||||||
| chr12:109106122 | G | A | 9 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0051 others(6): Show |
12 | HG00735.hp1 HG01109.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.801+2511G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106122 | |||||||
| chr12:109106208 | G | A | 3 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0016g0290 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.801+2597G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106208 | |||||||
| chr12:109106494 | A | G | 8 | a0001c0001t0001g0022 a0001c0001t0001g0205 a0001c0001t0001g0224 others(5): Show |
10 | HG02280.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.801+2883A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106494 | |||||||
| chr12:109106581 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.801+2970A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106581 | |||||||
| chr12:109106705 | C | T | 1 | a0001c0001t0013g0289 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.801+3094C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106705 | |||||||
| chr12:109106730 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3099C>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106730 | |||||||
| chr12:109106732 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3097C>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106732 | |||||||
| chr12:109106736 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3093T>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106736 | |||||||
| chr12:109106737 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3092A>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106737 | |||||||
| chr12:109106739 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3090A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106739 | |||||||
| chr12:109106743 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3086C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106743 | |||||||
| chr12:109106746 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3083A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106746 | |||||||
| chr12:109106748 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3081A>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106748 | |||||||
| chr12:109106753 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3076G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106753 | |||||||
| chr12:109106754 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3075C>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106754 | |||||||
| chr12:109106755 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3074C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106755 | |||||||
| chr12:109106757 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3072G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106757 | |||||||
| chr12:109106758 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3071G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106758 | |||||||
| chr12:109106765 | G | A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0122 a0001c0001t0001g0198 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.802-3064G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106765 | |||||||
| chr12:109106768 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3061G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106768 | |||||||
| chr12:109106770 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3059G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106770 | |||||||
| chr12:109106772 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3057G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106772 | |||||||
| chr12:109106772 | G | T | 1 | a0001c0001t0001g0280 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.802-3057G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106772 | |||||||
| chr12:109106773 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3056C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106773 | |||||||
| chr12:109106774 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3055C>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106774 | |||||||
| chr12:109106776 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3053G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106776 | |||||||
| chr12:109106779 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3050G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106779 | |||||||
| chr12:109106780 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3049T>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106780 | |||||||
| chr12:109106782 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3047C>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106782 | |||||||
| chr12:109106785 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3044G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106785 | |||||||
| chr12:109106786 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3043C>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106786 | |||||||
| chr12:109106788 | ACTTGGGA others(64): Show |
A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-3040_802-2970d others(73): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106788 | |||||||
| chr12:109106791 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.802-3038T>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106791 | |||||||
| chr12:109106825 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0201 |
3 | HG00639.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.802-3004C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106825 | |||||||
| chr12:109106863 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-2966C>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106863 | |||||||
| chr12:109106865 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-2964C>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106865 | |||||||
| chr12:109106865 | C | CA | 73 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(70): Show |
101 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.802-2954dupA | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106865 | ||||||
| chr12:109106866 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-2963A>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106866 | |||||||
| chr12:109106868 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-2961A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106868 | |||||||
| chr12:109106870 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG01081.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.802-2959A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106870 | |||||||
| chr12:109106870 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-2959A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106870 | |||||||
| chr12:109106872 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-2957A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106872 | |||||||
| chr12:109106874 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-2955A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106874 | |||||||
| chr12:109106876 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-2953C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106876 | |||||||
| chr12:109106888 | T | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0256 others(8): Show |
17 | HG01361.hp1 HG02109.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.802-2941T>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106888 | |||||||
| chr12:109106890 | C | T | 6 | a0001c0001t0001g0193 a0001c0001t0001g0216 a0001c0001t0001g0217 others(3): Show |
6 | HG01891.hp2 HG03130.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.802-2939C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106890 | |||||||
| chr12:109106891 | A | ATATATAT others(339): Show |
1 | a0001c0001t0016g0290 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.802-2938_802-2937i others(348): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106891 | |||||||
| chr12:109106892 | C | CACATATA others(129): Show |
1 | a0001c0001t0001g0216 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.802-2936_802-2935i others(138): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CACATATA others(127): Show |
1 | a0001c0001t0001g0217 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.802-2936_802-2935i others(136): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(261): Show |
1 | a0001c0001t0001g0099 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(270): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(233): Show |
1 | a0001c0001t0001g0068 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(242): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(235): Show |
1 | a0001c0001t0001g0085 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(244): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(232): Show |
1 | a0001c0001t0001g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(241): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(234): Show |
2 | a0001c0001t0001g0080 a0001c0006t0001g0076 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(243): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(237): Show |
2 | a0001c0001t0001g0096 a0001c0001t0001g0154 |
2 | HG02074.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(246): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(239): Show |
1 | a0001c0001t0001g0077 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(248): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(233): Show |
6 | a0001c0001t0001g0013 a0001c0001t0001g0078 a0001c0001t0001g0086 others(3): Show |
9 | NA18612.hp2 NA18942.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.802-2913_802-2912i others(242): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(235): Show |
18 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0032 others(15): Show |
30 | HG00323.hp2 HG00597.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.802-2913_802-2912i others(244): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(263): Show |
1 | a0001c0001t0001g0018 | 3 | HG02615.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(272): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(235): Show |
2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(244): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(233): Show |
1 | a0001c0001t0001g0103 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(242): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(236): Show |
1 | a0001c0001t0001g0091 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(245): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(235): Show |
1 | a0001c0001t0001g0037 | 2 | HG00558.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(244): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(233): Show |
1 | a0001c0001t0001g0172 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(242): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(233): Show |
1 | a0001c0001t0001g0133 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(242): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(289): Show |
1 | a0001c0001t0001g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(298): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(262): Show |
1 | a0001c0001t0001g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(271): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(261): Show |
1 | a0001c0001t0001g0155 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(270): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(261): Show |
1 | a0001c0001t0001g0160 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(270): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(234): Show |
7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0127 others(4): Show |
10 | HG00099.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.802-2913_802-2912i others(243): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(232): Show |
1 | a0001c0001t0001g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(241): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(232): Show |
1 | a0001c0001t0001g0028 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(241): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(233): Show |
1 | a0001c0001t0001g0167 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(242): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(235): Show |
1 | a0001c0001t0001g0137 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(244): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(236): Show |
1 | a0001c0001t0001g0146 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(245): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(235): Show |
20 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0034 others(17): Show |
35 | HG00423.hp1 HG00735.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.802-2913_802-2912i others(244): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(263): Show |
1 | a0001c0001t0001g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(272): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(231): Show |
1 | a0001c0001t0001g0138 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(240): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(233): Show |
2 | a0001c0001t0001g0139 a0001c0001t0014g0152 |
2 | HG00738.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(242): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(233): Show |
1 | a0001c0001t0001g0106 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(242): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(233): Show |
1 | a0001c0001t0001g0062 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(242): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(237): Show |
1 | a0001c0001t0001g0129 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(246): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(236): Show |
1 | a0001c0001t0001g0061 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(245): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(233): Show |
1 | a0001c0001t0001g0148 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(242): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(233): Show |
3 | a0001c0001t0001g0140 a0001c0001t0001g0162 a0001c0001t0001g0170 |
3 | HG00438.hp2 HG00597.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(242): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(231): Show |
1 | a0001c0001t0001g0149 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(240): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(235): Show |
1 | a0001c0001t0001g0251 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(244): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(234): Show |
2 | a0001c0001t0001g0126 a0001c0001t0001g0141 |
2 | NA19062.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(243): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(236): Show |
2 | a0001c0001t0001g0142 a0001c0001t0001g0157 |
2 | NA18999.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(245): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(265): Show |
1 | a0001c0001t0001g0143 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(274): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(235): Show |
1 | a0001c0001t0001g0094 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(244): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(237): Show |
5 | a0001c0001t0001g0036 a0001c0001t0001g0144 a0001c0001t0001g0150 others(2): Show |
6 | HG01074.hp2 HG02735.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.802-2913_802-2912i others(246): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(133): Show |
1 | a0001c0003t0001g0071 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(142): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(129): Show |
1 | a0001c0003t0001g0073 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(138): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(127): Show |
1 | a0001c0003t0001g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(136): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(93): Show |
1 | a0001c0001t0005g0030 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(102): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(127): Show |
17 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(14): Show |
21 | HG02132.hp1 HG02300.hp1 HG02738.hp1 others(18): Show |
intron_variant | MODIFIER | c.802-2923_802-2922i others(136): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(129): Show |
4 | a0001c0001t0001g0046 a0001c0001t0001g0229 a0001c0001t0001g0239 others(1): Show |
5 | HG00609.hp1 NA18942.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.802-2923_802-2922i others(138): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(125): Show |
1 | a0001c0001t0001g0230 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.802-2923_802-2922i others(134): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(125): Show |
1 | a0001c0001t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.802-2923_802-2922i others(134): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(127): Show |
30 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0023 others(27): Show |
49 | HG00544.hp1 HG00639.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.802-2923_802-2922i others(136): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(127): Show |
2 | a0001c0001t0001g0050 a0001c0001t0001g0214 |
3 | NA18949.hp1 NA19002.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.802-2923_802-2922i others(136): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(125): Show |
1 | a0001c0001t0001g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.802-2923_802-2922i others(134): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(123): Show |
1 | a0001c0001t0001g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.802-2923_802-2922i others(132): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CATATATA others(127): Show |
1 | a0001c0001t0001g0242 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.802-2923_802-2922i others(136): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106892 | ||||||
| chr12:109106892 | C | CGTATATA others(235): Show |
1 | a0001c0001t0001g0174 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.802-2937_802-2936i others(244): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106892 | |||||||
| chr12:109106892 | C | CGTGTATA others(117): Show |
1 | a0001c0001t0001g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.802-2937_802-2936i others(126): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106892 | |||||||
| chr12:109106892 | C | T | 3 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0016g0290 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.802-2937C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106892 | |||||||
| chr12:109106893 | A | ATATATAT others(135): Show |
2 | a0001c0001t0003g0069 a0001c0001t0003g0070 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.802-2923_802-2922i others(144): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106893 | ||||||
| chr12:109106893 | A | ATATATAT others(101): Show |
1 | a0001c0001t0003g0009 | 5 | HG01167.hp1 HG02280.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.802-2923_802-2922i others(110): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106893 | ||||||
| chr12:109106893 | A | ATATATGT others(311): Show |
2 | a0001c0001t0002g0291 a0001c0001t0002g0292 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.802-2931_802-2930i others(320): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106893 | ||||||
| chr12:109106903 | A | G | 1 | a0001c0001t0016g0290 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.802-2926A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106903 | |||||||
| chr12:109106904 | C | CGTATATA others(233): Show |
1 | a0001c0001t0001g0194 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(242): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106904 | ||||||
| chr12:109106904 | C | CGTGTATA others(73): Show |
1 | a0001c0001t0001g0272 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.802-2923_802-2922i others(82): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106904 | ||||||
| chr12:109106904 | C | T | 4 | a0001c0001t0001g0208 a0001c0001t0002g0291 a0001c0001t0002g0292 others(1): Show |
4 | HG00408.hp1 HG01891.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.802-2925C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106904 | |||||||
| chr12:109106906 | T | TGTATATA others(147): Show |
1 | a0001c0001t0001g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.802-2923_802-2922i others(156): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(147): Show |
1 | a0001c0001t0001g0110 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.802-2923_802-2922i others(156): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(173): Show |
2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.802-2923_802-2922i others(182): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(171): Show |
1 | a0001c0001t0001g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.802-2923_802-2922i others(180): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(123): Show |
1 | a0001c0001t0015g0183 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.802-2923_802-2922i others(132): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(145): Show |
1 | a0001c0001t0001g0117 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.802-2923_802-2922i others(154): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(109): Show |
1 | a0001c0001t0001g0294 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.802-2923_802-2922i others(118): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(111): Show |
1 | a0001c0001t0001g0297 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.802-2923_802-2922i others(120): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(113): Show |
5 | a0001c0001t0001g0011 a0001c0001t0001g0293 a0001c0001t0001g0295 others(2): Show |
9 | HG00323.hp1 HG03491.hp2 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.802-2923_802-2922i others(122): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(147): Show |
18 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(15): Show |
49 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.802-2923_802-2922i others(156): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(145): Show |
4 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0123 others(1): Show |
9 | HG00438.hp1 HG00621.hp2 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.802-2923_802-2922i others(154): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(145): Show |
1 | a0001c0001t0001g0066 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.802-2923_802-2922i others(154): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(113): Show |
1 | a0001c0001t0001g0300 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.802-2923_802-2922i others(122): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(175): Show |
1 | a0001c0001t0001g0082 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.802-2923_802-2922i others(184): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(123): Show |
1 | a0001c0001t0001g0224 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.802-2923_802-2922i others(132): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(149): Show |
1 | a0001c0001t0001g0226 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.802-2923_802-2922i others(158): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(125): Show |
1 | a0001c0001t0001g0205 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.802-2923_802-2922i others(134): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(123): Show |
3 | a0001c0001t0001g0022 a0001c0001t0001g0227 a0001c0001t0001g0243 |
5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.802-2923_802-2922i others(132): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106906 | T | TGTATATA others(125): Show |
1 | a0001c0001t0001g0225 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.802-2923_802-2922i others(134): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106906 | |||||||
| chr12:109106907 | A | ATATATAT others(231): Show |
1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(240): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106907 | ||||||
| chr12:109106907 | A | ATATATAT others(230): Show |
1 | a0001c0001t0001g0095 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(239): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106907 | ||||||
| chr12:109106907 | A | ATATATAT others(229): Show |
1 | a0001c0001t0001g0031 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(238): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106907 | ||||||
| chr12:109106907 | A | ATATATAT others(251): Show |
1 | a0001c0001t0001g0019 | 3 | HG01884.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(260): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106907 | ||||||
| chr12:109106907 | A | ATATATAT others(232): Show |
1 | a0001c0001t0001g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(241): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106907 | ||||||
| chr12:109106907 | A | ATATATAT others(233): Show |
1 | a0001c0001t0001g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(242): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106907 | ||||||
| chr12:109106907 | A | ATATATAT others(149): Show |
1 | a0001c0001t0013g0289 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(158): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106907 | ||||||
| chr12:109106907 | A | ATATATAT others(169): Show |
1 | a0001c0001t0001g0122 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(178): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106907 | ||||||
| chr12:109106907 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.802-2922A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106907 | |||||||
| chr12:109106909 | A | ATATATAT others(121): Show |
1 | a0001c0001t0002g0181 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(130): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(119): Show |
1 | a0001c0001t0002g0184 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(128): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(125): Show |
1 | a0001c0001t0001g0179 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(134): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(99): Show |
1 | a0001c0001t0001g0180 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(108): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(123): Show |
2 | a0001c0001t0001g0262 a0001c0001t0001g0269 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(132): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(121): Show |
17 | a0001c0001t0002g0005 a0001c0001t0002g0024 a0001c0001t0002g0027 others(14): Show |
30 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.802-2913_802-2912i others(130): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(121): Show |
1 | a0001c0001t0001g0258 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(130): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(127): Show |
2 | a0001c0001t0001g0263 a0001c0001t0001g0271 |
2 | NA18961.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(136): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(123): Show |
4 | a0001c0001t0001g0260 a0001c0001t0001g0268 a0001c0001t0001g0276 others(1): Show |
4 | HG01099.hp1 HG01943.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.802-2913_802-2912i others(132): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(125): Show |
24 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(21): Show |
40 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.802-2913_802-2912i others(134): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(125): Show |
2 | a0001c0001t0001g0054 a0001c0001t0001g0266 |
3 | NA18974.hp2 NA18990.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(134): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(123): Show |
1 | a0001c0001t0001g0261 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(132): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(145): Show |
1 | a0001c0001t0001g0116 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(154): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(125): Show |
1 | a0001c0001t0001g0259 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(134): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(123): Show |
1 | a0001c0001t0002g0192 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(132): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(127): Show |
8 | a0001c0001t0001g0057 a0001c0001t0001g0287 a0001c0001t0001g0288 others(5): Show |
11 | HG02055.hp2 HG02145.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.802-2913_802-2912i others(136): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(127): Show |
1 | a0001c0002t0001g0056 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.802-2913_802-2912i others(136): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106909 | A | ATATATAT others(123): Show |
1 | a0001c0001t0001g0238 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.802-2913_802-2912i others(132): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106909 | ||||||
| chr12:109106915 | A | ATACACAT others(260): Show |
1 | a0001c0002t0001g0283 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(269): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106915 | ||||||
| chr12:109106916 | T | TACACATA others(9): Show |
1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.802-2913_802-2912i others(18): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106916 | |||||||
| chr12:109106917 | G | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(77): Show |
116 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.802-2912G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106917 | |||||||
| chr12:109106919 | G | A | 5 | a0001c0001t0001g0107 a0001c0002t0001g0283 a0001c0003t0001g0071 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.802-2910G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106919 | |||||||
| chr12:109106919 | GTA | G | 59 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0023 others(56): Show |
83 | HG00544.hp1 HG00609.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.802-2895_802-2894d others(4): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106919 | ||||||
| chr12:109106921 | A | ATATATAT others(191): Show |
1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.802-2898_802-2897i others(200): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109106921 | ||||||
| chr12:109106921 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0016 others(78): Show |
119 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.802-2908A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106921 | |||||||
| chr12:109106933 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.802-2896A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106933 | |||||||
| chr12:109106934 | T | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(66): Show |
96 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.802-2895T>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106934 | |||||||
| chr12:109106935 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.802-2894A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106935 | |||||||
| chr12:109106937 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.802-2892A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106937 | |||||||
| chr12:109106939 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.802-2890A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106939 | |||||||
| chr12:109106944 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.802-2885T>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106944 | |||||||
| chr12:109106946 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.802-2883T>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106946 | |||||||
| chr12:109106952 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.802-2877C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106952 | |||||||
| chr12:109106956 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.802-2873T>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106956 | |||||||
| chr12:109106958 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.802-2871T>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106958 | |||||||
| chr12:109106960 | C | A | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.802-2869C>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106960 | |||||||
| chr12:109106965 | T | TGTATATA others(244): Show |
1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.802-2864_802-2863i others(253): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109106965 | |||||||
| chr12:109107132 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.802-2697C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109107132 | |||||||
| chr12:109107383 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.802-2446T>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109107383 | |||||||
| chr12:109107457 | G | A | 1 | a0001c0001t0002g0184 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.802-2372G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109107457 | |||||||
| chr12:109107518 | C | CT | 29 | a0001c0001t0001g0049 a0001c0001t0001g0072 a0001c0001t0001g0088 others(26): Show |
30 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.802-2287dupT | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109107518 | ||||||
| chr12:109107518 | CT | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(77): Show |
140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.802-2287delT | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109107518 | ||||||
| chr12:109107548 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.802-2281A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109107548 | |||||||
| chr12:109107589 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG01081.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.802-2240G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109107589 | |||||||
| chr12:109107647 | T | A | 1 | a0001c0001t0001g0287 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.802-2182T>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109107647 | |||||||
| chr12:109107651 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.802-2178G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109107651 | |||||||
| chr12:109107821 | G | A | 3 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0016g0290 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.802-2008G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109107821 | |||||||
| chr12:109108000 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.802-1829A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109108000 | |||||||
| chr12:109108051 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0111 a0001c0001t0001g0116 others(1): Show |
7 | HG02040.hp1 HG02083.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.802-1778T>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109108051 | |||||||
| chr12:109108082 | C | T | 8 | a0001c0001t0001g0057 a0001c0001t0001g0287 a0001c0001t0001g0288 others(5): Show |
10 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.802-1747C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109108082 | |||||||
| chr12:109108146 | A | G | 25 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(22): Show |
38 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.802-1683A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109108146 | |||||||
| chr12:109108191 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0171 a0001c0001t0001g0173 |
3 | NA18951.hp1 NA19006.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.802-1638C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109108191 | |||||||
| chr12:109108273 | G | A | 1 | a0001c0001t0005g0030 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.802-1556G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109108273 | |||||||
| chr12:109108309 | C | T | 21 | a0001c0001t0002g0005 a0001c0001t0002g0024 a0001c0001t0002g0027 others(18): Show |
34 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.802-1520C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109108309 | |||||||
| chr12:109108451 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0077 |
4 | HG01109.hp2 HG02615.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.802-1378A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109108451 | |||||||
| chr12:109108505 | A | T | 1 | a0001c0001t0001g0253 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.802-1324A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109108505 | |||||||
| chr12:109108647 | A | T | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.802-1182A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109108647 | |||||||
| chr12:109108829 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.802-1000G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109108829 | |||||||
| chr12:109108854 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG01099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.802-975A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109108854 | |||||||
| chr12:109108896 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.802-933C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109108896 | |||||||
| chr12:109108966 | T | C | 3 | a0001c0001t0003g0009 a0001c0001t0003g0069 a0001c0001t0003g0070 |
7 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.802-863T>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109108966 | |||||||
| chr12:109109081 | T | G | 37 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(34): Show |
54 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.802-748T>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109081 | |||||||
| chr12:109109115 | T | C | 10 | a0001c0001t0001g0057 a0001c0001t0001g0287 a0001c0001t0001g0288 others(7): Show |
14 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.802-714T>C | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109115 | |||||||
| chr12:109109134 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.802-695G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109134 | |||||||
| chr12:109109178 | G | T | 3 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0016g0290 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.802-651G>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109178 | |||||||
| chr12:109109255 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
306 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.802-574A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109255 | |||||||
| chr12:109109281 | C | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0205 a0001c0001t0001g0224 others(3): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.802-548C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109281 | |||||||
| chr12:109109297 | C | T | 3 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0016g0290 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.802-532C>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109297 | |||||||
| chr12:109109479 | T | G | 1 | a0001c0001t0012g0113 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.802-350T>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109479 | |||||||
| chr12:109109482 | G | A | 1 | a0001c0001t0012g0113 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.802-347G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109482 | |||||||
| chr12:109109482 | G | GAA | 3 | a0001c0001t0001g0228 a0001c0001t0002g0292 a0001c0001t0016g0290 |
3 | HG03209.hp2 NA19059.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.802-347_802-346ins others(2): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109482 | |||||||
| chr12:109109482 | G | GAAA | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(68): Show |
98 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.802-347_802-346ins others(3): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109482 | |||||||
| chr12:109109483 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(187): Show |
296 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.802-346G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109483 | |||||||
| chr12:109109484 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.802-345A>G | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109484 | |||||||
| chr12:109109716 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.802-113G>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109716 | |||||||
| chr12:109109763 | C | CAAAA | 7 | a0001c0001t0001g0011 a0001c0001t0001g0293 a0001c0001t0001g0294 others(4): Show |
11 | HG00323.hp1 HG01884.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.802-51_802-48dupAA others(2): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109109763 | ||||||
| chr12:109109763 | C | CAAAAA | 8 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0213 others(5): Show |
9 | HG00673.hp2 HG01516.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.802-52_802-48dupAA others(3): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109109763 | ||||||
| chr12:109109763 | C | CAAAAAA | 60 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(57): Show |
89 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.802-53_802-48dupAA others(4): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109109763 | ||||||
| chr12:109109763 | C | CAAAAAAA | 9 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0214 others(6): Show |
11 | HG00639.hp1 HG01169.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.802-54_802-48dupAA others(5): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 109109763 | ||||||
| chr12:109109780 | A | T | 1 | a0001c0001t0001g0264 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.802-49A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109780 | |||||||
| chr12:109109781 | A | AAAAAT | 16 | a0001c0001t0001g0057 a0001c0001t0001g0082 a0001c0001t0001g0120 others(13): Show |
20 | HG00438.hp1 HG01243.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.802-48_802-47insAA others(3): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109781 | |||||||
| chr12:109109781 | A | AAAAT | 50 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(47): Show |
107 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.802-48_802-47insAA others(2): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109781 | |||||||
| chr12:109109781 | A | AAAT | 7 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0114 others(4): Show |
7 | HG01169.hp2 HG01496.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.802-48_802-47insAA others(1): Show |
UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109781 | |||||||
| chr12:109109781 | A | T | 37 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(34): Show |
54 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.802-48A>T | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109781 | |||||||
| chr12:109109782 | T | A | 3 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0016g0290 |
3 | HG01891.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.802-47T>A | UNG | ENSG00000076248.12 | transcript | ENST00000242576.7 | protein_coding | 6/6 | chr12 | 109109782 |