Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7360 |
| ensemblid | ENSG00000169764.16 |
| hgncid | 12527 |
| symbol | UGP2 |
| name | UDP-glucose pyrophosphorylase 2 |
| refseq_nuc | NM_006759.4 |
| refseq_prot | NP_006750.3 |
| ensembl_nuc | ENST00000337130.10 |
| ensembl_prot | ENSP00000338703.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 63841896 |
| end | 63891560 |
| strand | + |
| ver | v1.2 |
| region | chr2:63841896-63891560 |
| region5000 | chr2:63836896-63896560 |
| regionname0 | UGP2_chr2_63841896_63891560 |
| regionname5000 | UGP2_chr2_63836896_63896560 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 508 | 332 | 94 | 74 | 104 | 16 | 42 | 78 | UGP2_chr2_63836896_63896560 | UGP2 | MSRFV others(503): Show |
chr2 | 63836896 | 63896560 |
| a0002 | 0/0 | 508 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | MSRFV others(503): Show |
chr2 | 63836896 | 63896560 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1524 | 327 | 94 | 74 | 102 | 14 | 41 | UGP2_chr2_63836896_63896560 | UGP2 | ATGTC others(1519): Show |
chr2 | 63836896 | 63896560 | ||
| a0001c0002 | 0/0 | 1524 | 3 | 0 | 0 | 0 | 2 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | ATGTC others(1519): Show |
chr2 | 63836896 | 63896560 | ||
| a0001c0004 | 0/0 | 1524 | 2 | 0 | 0 | 2 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | ATGTC others(1519): Show |
chr2 | 63836896 | 63896560 | ||
| a0002c0003 | 0/0 | 1524 | 2 | 0 | 0 | 0 | 2 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | ATGTC others(1519): Show |
chr2 | 63836896 | 63896560 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2150 | 269 | 85 | 58 | 84 | 12 | 28 | UGP2_chr2_63836896_63896560 | UGP2 | GGGAG others(2145): Show |
chr2 | 63836896 | 63896560 |
| a0001c0001t0002 | 0/0 | 2150 | 38 | 2 | 14 | 14 | 1 | 7 | UGP2_chr2_63836896_63896560 | UGP2 | GGGAG others(2145): Show |
chr2 | 63836896 | 63896560 |
| a0001c0001t0003 | 0/0 | 2149 | 18 | 7 | 2 | 2 | 1 | 6 | UGP2_chr2_63836896_63896560 | UGP2 | GGGAG others(2144): Show |
chr2 | 63836896 | 63896560 |
| a0001c0001t0004 | 0/0 | 2150 | 2 | 0 | 0 | 2 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | GGGAG others(2145): Show |
chr2 | 63836896 | 63896560 |
| a0001c0002t0001 | 0/0 | 2150 | 2 | 0 | 0 | 0 | 2 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | GGGAG others(2145): Show |
chr2 | 63836896 | 63896560 |
| a0001c0002t0002 | 0/0 | 2150 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | GGGAG others(2145): Show |
chr2 | 63836896 | 63896560 |
| a0001c0004t0001 | 0/0 | 2150 | 2 | 0 | 0 | 2 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | GGGAG others(2145): Show |
chr2 | 63836896 | 63896560 |
| a0002c0003t0001 | 0/0 | 2150 | 2 | 0 | 0 | 0 | 2 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | GGGAG others(2145): Show |
chr2 | 63836896 | 63896560 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0045 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0275 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0007 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| a0002c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | GBR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0068 | EUR | GBR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0097 | EUR | FIN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0241 | EUR | FIN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0067 | EUR | FIN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01516 | hp1 | a0002 | c0003 | t0001 | g0012 | EUR | IBS | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01517 | hp2 | a0002 | c0003 | t0001 | g0012 | EUR | IBS | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0258 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | MSL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | MSL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0083 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | GWD | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | STU | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0087 | SAS | STU | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0143 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | BEB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | STU | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | STU | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CHB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | YRI | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18974 | hp2 | a0001 | c0004 | t0001 | g0223 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0231 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | TSI | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0086 | SAS | GIH | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | USA | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | USA | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | USA | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | USA | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0045 | REF | REF | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0275 | REF | REF | UGP2_chr2_63836896_63896560 | UGP2 | chr2 | 63836896 | 63896560 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:63882520 | G | A | 1 | a0002 | 2 | HG01516.hp1 HG01517.hp2 |
missense_variant | MODERATE | c.310G>A | p.Val104Met | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 4/10 | 600/2150 | 310/1527 | 104/508 | chr2 | 63882520 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:63887419 | G | A | 1 | a0001c0002 | 3 | HG00140.hp2 HG00323.hp2 HG02683.hp1 |
synonymous_variant | LOW | c.1089G>A | p.Leu363Leu | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/10 | 1379/2150 | 1089/1527 | 363/508 | chr2 | 63887419 | |||
| chr2:63887629 | C | T | 1 | a0001c0004 | 2 | NA18974.hp2 NA18999.hp2 |
synonymous_variant | LOW | c.1299C>T | p.Gly433Gly | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/10 | 1589/2150 | 1299/1527 | 433/508 | chr2 | 63887629 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:63841969 | C | T | 1 | a0001c0001t0004 | 2 | NA18989.hp2 NA19076.hp2 |
5_prime_UTR_variant | MODIFIER | c.-217C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/10 | 217 | chr2 | 63841969 | ||||||
| chr2:63842143 | GA | G | 1 | a0001c0001t0003 | 18 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-28delA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/10 | 28 | INFO_REALIGN_3_PRIME | chr2 | 63842143 | |||||
| chr2:63842177 | G | C | 2 | a0001c0001t0002 a0001c0002t0002 |
39 | HG00280.hp2 HG00738.hp2 HG01099.hp2 others(36): Show |
5_prime_UTR_variant | MODIFIER | c.-9G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/10 | 9 | chr2 | 63842177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:63842363 | T | A | 1 | a0001c0001t0001g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.19+159T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63842363 | |||||||
| chr2:63842373 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.19+169T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63842373 | |||||||
| chr2:63842536 | A | G | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | NA18612.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.19+332A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63842536 | |||||||
| chr2:63842598 | G | A | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(248): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.19+394G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63842598 | |||||||
| chr2:63842804 | G | T | 1 | a0001c0001t0001g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.19+600G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63842804 | |||||||
| chr2:63843279 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19+1075T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63843279 | |||||||
| chr2:63843316 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.19+1112T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63843316 | |||||||
| chr2:63843421 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.19+1217G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63843421 | |||||||
| chr2:63843463 | G | T | 1 | a0001c0001t0001g0287 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.19+1259G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63843463 | |||||||
| chr2:63843473 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.19+1269A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63843473 | |||||||
| chr2:63843856 | T | G | 1 | a0001c0001t0002g0039 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.19+1652T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63843856 | |||||||
| chr2:63843886 | TTTTC | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+1689_19+1692del others(4): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63843886 | ||||||
| chr2:63843945 | G | T | 1 | a0001c0002t0002g0258 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.19+1741G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63843945 | |||||||
| chr2:63844057 | G | A | 1 | a0001c0001t0001g0288 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.19+1853G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63844057 | |||||||
| chr2:63844098 | A | C | 28 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(25): Show |
37 | HG00280.hp2 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.19+1894A>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63844098 | |||||||
| chr2:63844321 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0260 a0001c0001t0001g0261 others(1): Show |
5 | HG02257.hp1 HG02572.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+2117G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63844321 | |||||||
| chr2:63844435 | CT | C | 31 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(28): Show |
41 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.19+2241delT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63844435 | ||||||
| chr2:63844444 | TTCATGGG others(5): Show |
T | 12 | a0001c0001t0001g0036 a0001c0001t0001g0046 a0001c0001t0001g0047 others(9): Show |
12 | HG00639.hp2 HG01099.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.19+2244_19+2255del others(12): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63844444 | ||||||
| chr2:63844466 | A | G | 31 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(28): Show |
41 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.19+2262A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63844466 | |||||||
| chr2:63844517 | G | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(249): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.19+2313G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63844517 | |||||||
| chr2:63844681 | C | G | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(218): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.19+2477C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63844681 | |||||||
| chr2:63844777 | G | A | 1 | a0001c0001t0001g0011 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19+2573G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63844777 | |||||||
| chr2:63844800 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.19+2596G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63844800 | |||||||
| chr2:63845278 | G | A | 2 | a0001c0001t0002g0237 a0001c0001t0002g0238 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.19+3074G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63845278 | |||||||
| chr2:63845318 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0236 |
2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.19+3114A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63845318 | |||||||
| chr2:63845519 | T | TA | 62 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(59): Show |
68 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.19+3332dupA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63845519 | ||||||
| chr2:63845519 | TA | T | 41 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(38): Show |
51 | HG00280.hp2 HG00738.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.19+3332delA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63845519 | ||||||
| chr2:63845541 | C | T | 3 | a0001c0001t0002g0255 a0001c0001t0002g0256 a0001c0001t0002g0257 |
3 | HG00738.hp2 HG01361.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.19+3337C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63845541 | |||||||
| chr2:63845613 | A | C | 100 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(97): Show |
106 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.19+3409A>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63845613 | |||||||
| chr2:63845756 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.19+3552G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63845756 | |||||||
| chr2:63845810 | C | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0146 |
3 | HG01515.hp2 HG01517.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.19+3606C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63845810 | |||||||
| chr2:63846041 | C | A | 1 | a0001c0001t0001g0265 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.19+3837C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63846041 | |||||||
| chr2:63846135 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.19+3931C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63846135 | |||||||
| chr2:63846185 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.19+3981T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63846185 | |||||||
| chr2:63846233 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.19+4029G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63846233 | |||||||
| chr2:63846274 | A | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0144 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+4070A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63846274 | |||||||
| chr2:63846445 | T | TA | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(248): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.19+4249dupA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63846445 | ||||||
| chr2:63846734 | G | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0227 |
2 | HG02135.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.19+4530G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63846734 | |||||||
| chr2:63846753 | A | G | 32 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(29): Show |
42 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.19+4549A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63846753 | |||||||
| chr2:63846903 | A | G | 29 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0079 others(26): Show |
32 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.19+4699A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63846903 | |||||||
| chr2:63847066 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.19+4862G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63847066 | |||||||
| chr2:63847496 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19+5292A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63847496 | |||||||
| chr2:63847506 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.19+5302G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63847506 | |||||||
| chr2:63847649 | C | T | 28 | a0001c0001t0001g0013 a0001c0001t0001g0079 a0001c0001t0001g0088 others(25): Show |
30 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.19+5445C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63847649 | |||||||
| chr2:63847738 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.19+5534C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63847738 | |||||||
| chr2:63847777 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19+5573G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63847777 | |||||||
| chr2:63847942 | A | C | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.19+5738A>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63847942 | |||||||
| chr2:63848424 | T | C | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(249): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.19+6220T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63848424 | |||||||
| chr2:63848435 | C | T | 32 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(29): Show |
42 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.19+6231C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63848435 | |||||||
| chr2:63848791 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG01168.hp1 HG01169.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.19+6587T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63848791 | |||||||
| chr2:63849166 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.19+6962A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63849166 | |||||||
| chr2:63849349 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-6957A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63849349 | |||||||
| chr2:63849453 | G | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0097 a0001c0001t0003g0098 others(1): Show |
5 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-6853G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63849453 | |||||||
| chr2:63849638 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.20-6668G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63849638 | |||||||
| chr2:63849727 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20-6579C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63849727 | |||||||
| chr2:63849755 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.20-6551G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63849755 | |||||||
| chr2:63849828 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0226 |
2 | NA19011.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.20-6478C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63849828 | |||||||
| chr2:63849859 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG02970.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.20-6447T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63849859 | |||||||
| chr2:63849931 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.20-6375G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63849931 | |||||||
| chr2:63850171 | C | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(227): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.20-6135C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63850171 | |||||||
| chr2:63850181 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.20-6125G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63850181 | |||||||
| chr2:63850186 | T | C | 1 | a0001c0001t0003g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.20-6120T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63850186 | |||||||
| chr2:63850216 | A | T | 1 | a0001c0002t0002g0258 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.20-6090A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63850216 | |||||||
| chr2:63850312 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.20-5994G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63850312 | |||||||
| chr2:63850314 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.20-5992T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63850314 | |||||||
| chr2:63850610 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.20-5696A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63850610 | |||||||
| chr2:63850731 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG00642.hp2 HG01192.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-5575C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63850731 | |||||||
| chr2:63850993 | C | G | 10 | a0001c0001t0001g0095 a0001c0001t0003g0014 a0001c0001t0003g0083 others(7): Show |
11 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-5313C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63850993 | |||||||
| chr2:63851079 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.20-5227A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63851079 | |||||||
| chr2:63851268 | A | G | 1 | a0001c0001t0003g0082 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.20-5038A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63851268 | |||||||
| chr2:63851776 | A | G | 1 | a0001c0004t0001g0223 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.20-4530A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63851776 | |||||||
| chr2:63851844 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02055.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.20-4462C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63851844 | |||||||
| chr2:63852038 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.20-4268T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63852038 | |||||||
| chr2:63852054 | A | G | 1 | a0001c0002t0002g0258 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.20-4252A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63852054 | |||||||
| chr2:63852129 | GAA | G | 101 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(98): Show |
107 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.20-4175_20-4174del others(2): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63852129 | ||||||
| chr2:63852453 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.20-3853G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63852453 | |||||||
| chr2:63852727 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.20-3579A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63852727 | |||||||
| chr2:63852921 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.20-3385A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63852921 | |||||||
| chr2:63853006 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG01168.hp1 HG01169.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.20-3300A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63853006 | |||||||
| chr2:63853011 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.20-3295G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63853011 | |||||||
| chr2:63853475 | G | A | 1 | a0001c0002t0002g0258 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.20-2831G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63853475 | |||||||
| chr2:63853554 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.20-2752T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63853554 | |||||||
| chr2:63853683 | A | G | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02055.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.20-2623A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63853683 | |||||||
| chr2:63853685 | T | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02055.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.20-2621T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63853685 | |||||||
| chr2:63853687 | T | G | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02055.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.20-2619T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63853687 | |||||||
| chr2:63853689 | T | G | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02055.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.20-2617T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63853689 | |||||||
| chr2:63853691 | T | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02055.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.20-2615T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63853691 | |||||||
| chr2:63853692 | C | G | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02055.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.20-2614C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63853692 | |||||||
| chr2:63853693 | C | G | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02055.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.20-2613C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63853693 | |||||||
| chr2:63853694 | C | G | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02055.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.20-2612C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63853694 | |||||||
| chr2:63853859 | G | T | 1 | a0001c0001t0001g0094 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.20-2447G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63853859 | |||||||
| chr2:63853959 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.20-2347G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63853959 | |||||||
| chr2:63854199 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0236 |
2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.20-2107C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63854199 | |||||||
| chr2:63854332 | C | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(249): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.20-1974C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63854332 | |||||||
| chr2:63854404 | G | A | 32 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(29): Show |
42 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.20-1902G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63854404 | |||||||
| chr2:63854554 | CCCTGCTC others(7): Show |
C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(216): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.20-1747_20-1734del others(14): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63854554 | ||||||
| chr2:63854594 | ATAGCTAC others(8): Show |
A | 1 | a0001c0001t0001g0011 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.20-1710_20-1696del others(15): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63854594 | ||||||
| chr2:63854655 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.20-1651G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63854655 | |||||||
| chr2:63854675 | C | T | 3 | a0001c0001t0003g0014 a0001c0001t0003g0097 a0001c0001t0003g0098 |
4 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-1631C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63854675 | |||||||
| chr2:63854690 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.20-1616A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63854690 | |||||||
| chr2:63854891 | C | T | 1 | a0001c0001t0003g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.20-1415C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63854891 | |||||||
| chr2:63854964 | C | G | 9 | a0001c0001t0003g0014 a0001c0001t0003g0083 a0001c0001t0003g0084 others(6): Show |
10 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-1342C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63854964 | |||||||
| chr2:63855239 | G | A | 11 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0001g0106 others(8): Show |
11 | HG01243.hp1 HG01261.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-1067G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63855239 | |||||||
| chr2:63855262 | A | T | 32 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(29): Show |
42 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.20-1044A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63855262 | |||||||
| chr2:63855485 | G | C | 35 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(32): Show |
45 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.20-821G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63855485 | |||||||
| chr2:63855520 | G | GT | 33 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0034 others(30): Show |
37 | HG00099.hp2 HG00544.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.20-765dupT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63855520 | ||||||
| chr2:63855520 | G | GTT | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0055 others(8): Show |
13 | HG00639.hp2 HG01346.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.20-766_20-765dupTT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63855520 | ||||||
| chr2:63855520 | GT | G | 41 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0016 others(38): Show |
44 | HG00140.hp2 HG00323.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.20-765delT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63855520 | ||||||
| chr2:63855520 | GTT | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(43): Show |
59 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.20-766_20-765delTT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63855520 | ||||||
| chr2:63855520 | GTTT | G | 30 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0059 others(27): Show |
33 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.20-767_20-765delTT others(1): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63855520 | ||||||
| chr2:63855520 | GTTTT | G | 87 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(84): Show |
92 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.20-768_20-765delTT others(2): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 63855520 | ||||||
| chr2:63855521 | T | G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG02280.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.20-785T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63855521 | |||||||
| chr2:63855547 | T | C | 1 | a0001c0001t0003g0080 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.20-759T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63855547 | |||||||
| chr2:63855587 | G | A | 32 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(29): Show |
42 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.20-719G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63855587 | |||||||
| chr2:63855611 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.20-695G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63855611 | |||||||
| chr2:63855635 | C | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0036 others(31): Show |
38 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.20-671C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63855635 | |||||||
| chr2:63855895 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.20-411G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63855895 | |||||||
| chr2:63855905 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.20-401G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63855905 | |||||||
| chr2:63856065 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0038 others(9): Show |
15 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.20-241G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 1/9 | chr2 | 63856065 | |||||||
| chr2:63856871 | G | A | 35 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(32): Show |
45 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.147+438G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63856871 | |||||||
| chr2:63856873 | A | C | 10 | a0001c0001t0001g0095 a0001c0001t0003g0014 a0001c0001t0003g0083 others(7): Show |
11 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+440A>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63856873 | |||||||
| chr2:63856894 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.147+461C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63856894 | |||||||
| chr2:63856909 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG02970.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.147+476A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63856909 | |||||||
| chr2:63856940 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.147+507T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63856940 | |||||||
| chr2:63856964 | T | C | 32 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(29): Show |
42 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.147+531T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63856964 | |||||||
| chr2:63857000 | T | C | 1 | a0001c0001t0001g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.147+567T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63857000 | |||||||
| chr2:63857048 | C | T | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
6 | HG01175.hp2 NA18946.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+615C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63857048 | |||||||
| chr2:63857149 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.148-680A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63857149 | |||||||
| chr2:63857178 | G | A | 51 | a0001c0001t0001g0017 a0001c0001t0001g0099 a0001c0001t0001g0147 others(48): Show |
52 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.148-651G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63857178 | |||||||
| chr2:63857230 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.148-599G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63857230 | |||||||
| chr2:63857282 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.148-547C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63857282 | |||||||
| chr2:63857300 | C | CA | 8 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
9 | HG00280.hp1 HG01167.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-513dupA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 63857300 | ||||||
| chr2:63857328 | G | C | 1 | a0001c0001t0001g0219 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.148-501G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63857328 | |||||||
| chr2:63857469 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.148-360T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63857469 | |||||||
| chr2:63857735 | A | G | 10 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0001g0106 others(7): Show |
10 | HG01261.hp1 HG01496.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.148-94A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63857735 | |||||||
| chr2:63857737 | G | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0142 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.148-92G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 2/9 | chr2 | 63857737 | |||||||
| chr2:63857980 | G | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(249): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.255+44G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63857980 | |||||||
| chr2:63858197 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.255+261G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858197 | |||||||
| chr2:63858210 | C | T | 250 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(247): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.255+274C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858210 | |||||||
| chr2:63858287 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.255+351G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858287 | |||||||
| chr2:63858356 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0038 others(11): Show |
17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.255+420C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858356 | |||||||
| chr2:63858376 | A | G | 9 | a0001c0001t0001g0079 a0001c0001t0001g0263 a0001c0001t0003g0075 others(6): Show |
9 | HG01891.hp2 HG02886.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+440A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858376 | |||||||
| chr2:63858504 | C | T | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(249): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.255+568C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858504 | |||||||
| chr2:63858577 | C | G | 1 | a0001c0001t0001g0056 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.255+641C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858577 | |||||||
| chr2:63858580 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.255+644C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858580 | |||||||
| chr2:63858589 | G | T | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
6 | HG01175.hp2 NA18946.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+653G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858589 | |||||||
| chr2:63858675 | T | G | 1 | a0001c0001t0001g0059 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.255+739T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858675 | |||||||
| chr2:63858822 | T | A | 2 | a0001c0002t0001g0067 a0001c0002t0001g0068 |
2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.255+886T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858822 | |||||||
| chr2:63858880 | A | AC | 18 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0102 others(15): Show |
18 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.255+951dupC | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63858880 | ||||||
| chr2:63858880 | AC | A | 27 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0016 others(24): Show |
32 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.255+951delC | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63858880 | ||||||
| chr2:63858888 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.255+952G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858888 | |||||||
| chr2:63858906 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 |
4 | HG01167.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.255+970T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858906 | |||||||
| chr2:63858950 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+1014T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858950 | |||||||
| chr2:63858951 | A | G | 21 | a0001c0001t0001g0026 a0001c0001t0001g0061 a0001c0001t0001g0079 others(18): Show |
23 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.255+1015A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858951 | |||||||
| chr2:63858973 | G | A | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.255+1037G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63858973 | |||||||
| chr2:63859003 | C | CT | 11 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0001g0106 others(8): Show |
11 | HG01243.hp1 HG01261.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+1079dupT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63859003 | ||||||
| chr2:63859131 | C | A | 1 | a0001c0001t0001g0205 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.255+1195C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63859131 | |||||||
| chr2:63859238 | A | G | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(249): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.255+1302A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63859238 | |||||||
| chr2:63859367 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.255+1431G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63859367 | |||||||
| chr2:63859382 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.255+1446T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63859382 | |||||||
| chr2:63859396 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+1460G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63859396 | |||||||
| chr2:63859415 | T | C | 34 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(31): Show |
44 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.255+1479T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63859415 | |||||||
| chr2:63859780 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.255+1844A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63859780 | |||||||
| chr2:63859824 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.255+1888G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63859824 | |||||||
| chr2:63859893 | T | A | 34 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(31): Show |
44 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.255+1957T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63859893 | |||||||
| chr2:63859928 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+1992G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63859928 | |||||||
| chr2:63860016 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0133 |
3 | HG02895.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.255+2080A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63860016 | |||||||
| chr2:63860136 | T | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(249): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.255+2200T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63860136 | |||||||
| chr2:63860297 | T | A | 12 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0062 others(9): Show |
12 | HG02145.hp2 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.255+2361T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63860297 | |||||||
| chr2:63860309 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.255+2373C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63860309 | |||||||
| chr2:63860370 | T | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18974.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.255+2434T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63860370 | |||||||
| chr2:63860476 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.255+2540C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63860476 | |||||||
| chr2:63860555 | C | G | 3 | a0001c0001t0001g0178 a0001c0001t0001g0224 a0001c0001t0001g0226 |
3 | NA18984.hp1 NA19011.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.255+2619C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63860555 | |||||||
| chr2:63860558 | T | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0185 |
3 | NA18948.hp1 NA18963.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.255+2622T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63860558 | |||||||
| chr2:63860762 | A | AT | 93 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(90): Show |
99 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.255+2848dupT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63860762 | ||||||
| chr2:63860762 | A | ATT | 12 | a0001c0001t0001g0152 a0001c0001t0001g0155 a0001c0001t0001g0176 others(9): Show |
12 | HG01175.hp2 HG01261.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.255+2847_255+2848d others(4): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63860762 | ||||||
| chr2:63860762 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255+2838_255+2848d others(13): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63860762 | ||||||
| chr2:63861180 | AGGTTAAT others(1669): Show |
A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0283 |
3 | HG01109.hp1 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.255+3247_255+4922d others(2): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63861180 | ||||||
| chr2:63861248 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.255+3312G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63861248 | |||||||
| chr2:63861254 | C | T | 1 | a0001c0001t0003g0078 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.255+3318C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63861254 | |||||||
| chr2:63861305 | T | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0122 a0001c0001t0001g0123 others(3): Show |
6 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+3369T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63861305 | |||||||
| chr2:63861359 | G | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0146 a0001c0001t0001g0228 |
4 | HG01070.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+3423G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63861359 | |||||||
| chr2:63861524 | A | AT | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0036 others(21): Show |
28 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.255+3600dupT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63861524 | ||||||
| chr2:63861630 | G | C | 1 | a0001c0001t0002g0005 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.255+3694G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63861630 | |||||||
| chr2:63861687 | C | CA | 77 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(74): Show |
87 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.255+3767dupA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63861687 | ||||||
| chr2:63861687 | C | CAA | 10 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0128 others(7): Show |
11 | HG01192.hp2 HG02004.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+3766_255+3767d others(4): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63861687 | ||||||
| chr2:63861704 | C | A | 13 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0122 others(10): Show |
13 | HG02055.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.255+3768C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63861704 | |||||||
| chr2:63861710 | A | T | 1 | a0001c0001t0001g0210 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.255+3774A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63861710 | |||||||
| chr2:63862011 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.255+4075G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63862011 | |||||||
| chr2:63862077 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.255+4141A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63862077 | |||||||
| chr2:63862239 | G | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(31): Show |
44 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.255+4303G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63862239 | |||||||
| chr2:63862336 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.255+4400G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63862336 | |||||||
| chr2:63862465 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.255+4529T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63862465 | |||||||
| chr2:63862602 | T | G | 2 | a0001c0001t0001g0116 a0001c0001t0002g0057 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.255+4666T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63862602 | |||||||
| chr2:63862614 | C | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(249): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.255+4678C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63862614 | |||||||
| chr2:63862739 | T | A | 1 | a0001c0001t0003g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.255+4803T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63862739 | |||||||
| chr2:63862773 | C | T | 5 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | NA18747.hp1 NA18948.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+4837C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63862773 | |||||||
| chr2:63863018 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255+5082G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63863018 | |||||||
| chr2:63863065 | T | A | 1 | a0001c0001t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255+5129T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63863065 | |||||||
| chr2:63863116 | G | C | 1 | a0001c0001t0001g0028 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.255+5180G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63863116 | |||||||
| chr2:63863585 | A | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0268 others(3): Show |
12 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.255+5649A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63863585 | |||||||
| chr2:63863593 | A | G | 1 | a0001c0001t0002g0251 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.255+5657A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63863593 | |||||||
| chr2:63863651 | A | G | 3 | a0001c0002t0001g0067 a0001c0002t0001g0068 a0001c0002t0002g0258 |
3 | HG00140.hp2 HG00323.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.255+5715A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63863651 | |||||||
| chr2:63863751 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.255+5815A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63863751 | |||||||
| chr2:63863807 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.255+5871T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63863807 | |||||||
| chr2:63863915 | A | C | 1 | a0001c0001t0003g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.255+5979A>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63863915 | |||||||
| chr2:63863916 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0212 |
3 | HG01884.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255+5980G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63863916 | |||||||
| chr2:63864275 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.255+6339A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63864275 | |||||||
| chr2:63864295 | C | T | 22 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0037 others(19): Show |
24 | HG01070.hp1 HG01074.hp2 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.255+6359C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63864295 | |||||||
| chr2:63864322 | C | A | 1 | a0001c0001t0001g0262 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.255+6386C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63864322 | |||||||
| chr2:63864399 | T | C | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(249): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.255+6463T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63864399 | |||||||
| chr2:63864607 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.255+6671A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63864607 | |||||||
| chr2:63864663 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.255+6727G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63864663 | |||||||
| chr2:63864961 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.255+7025C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63864961 | |||||||
| chr2:63865197 | C | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(241): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.255+7261C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63865197 | |||||||
| chr2:63865481 | CCTAGAGA others(8): Show |
C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0227 |
2 | HG02135.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.255+7546_255+7560d others(17): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63865481 | |||||||
| chr2:63865532 | A | AT | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(203): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.255+7617dupT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63865532 | ||||||
| chr2:63865532 | A | ATT | 13 | a0001c0001t0001g0044 a0001c0001t0001g0112 a0001c0001t0001g0113 others(10): Show |
13 | HG01109.hp2 HG02109.hp1 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.255+7616_255+7617d others(4): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63865532 | ||||||
| chr2:63865719 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.255+7783T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63865719 | |||||||
| chr2:63865735 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255+7799C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63865735 | |||||||
| chr2:63865829 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.255+7893C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63865829 | |||||||
| chr2:63865925 | A | G | 1 | a0001c0002t0002g0258 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.255+7989A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63865925 | |||||||
| chr2:63866007 | A | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+8071A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63866007 | |||||||
| chr2:63866194 | C | G | 3 | a0001c0002t0001g0067 a0001c0002t0001g0068 a0001c0002t0002g0258 |
3 | HG00140.hp2 HG00323.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.255+8258C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63866194 | |||||||
| chr2:63866261 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.255+8325C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63866261 | |||||||
| chr2:63866334 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0280 a0001c0001t0001g0281 others(2): Show |
6 | HG01358.hp2 HG01928.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+8398G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63866334 | |||||||
| chr2:63866424 | G | GTT | 3 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG00642.hp2 HG01192.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.255+8490_255+8491d others(4): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63866424 | ||||||
| chr2:63866762 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0038 others(7): Show |
13 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.255+8826G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63866762 | |||||||
| chr2:63866803 | A | G | 38 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(35): Show |
49 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.255+8867A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63866803 | |||||||
| chr2:63866831 | T | G | 1 | a0001c0001t0001g0264 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.255+8895T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63866831 | |||||||
| chr2:63866985 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.255+9049T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63866985 | |||||||
| chr2:63867357 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.255+9421T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63867357 | |||||||
| chr2:63867364 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.255+9428C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63867364 | |||||||
| chr2:63867372 | G | C | 262 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(259): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.255+9436G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63867372 | |||||||
| chr2:63867376 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.255+9440G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63867376 | |||||||
| chr2:63867497 | A | G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG02280.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.255+9561A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63867497 | |||||||
| chr2:63867577 | A | C | 1 | a0001c0001t0002g0249 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.255+9641A>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63867577 | |||||||
| chr2:63867684 | A | T | 3 | a0001c0002t0001g0067 a0001c0002t0001g0068 a0001c0002t0002g0258 |
3 | HG00140.hp2 HG00323.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.255+9748A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63867684 | |||||||
| chr2:63867695 | T | C | 20 | a0001c0001t0001g0026 a0001c0001t0001g0079 a0001c0001t0001g0095 others(17): Show |
22 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.255+9759T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63867695 | |||||||
| chr2:63867793 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.255+9857T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63867793 | |||||||
| chr2:63867861 | G | T | 37 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(34): Show |
47 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.255+9925G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63867861 | |||||||
| chr2:63867987 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.255+10051A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63867987 | |||||||
| chr2:63868369 | C | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(31): Show |
44 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.255+10433C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63868369 | |||||||
| chr2:63868461 | G | C | 1 | a0001c0001t0001g0232 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.255+10525G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63868461 | |||||||
| chr2:63868478 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.255+10542C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63868478 | |||||||
| chr2:63868584 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0283 a0001c0001t0001g0285 others(1): Show |
5 | HG01109.hp1 HG03098.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+10648A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63868584 | |||||||
| chr2:63868784 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.255+10848G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63868784 | |||||||
| chr2:63868785 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.255+10849C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63868785 | |||||||
| chr2:63868973 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.255+11037A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63868973 | |||||||
| chr2:63869457 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0003g0076 |
2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.255+11521T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63869457 | |||||||
| chr2:63869527 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.255+11591A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63869527 | |||||||
| chr2:63869543 | C | T | 1 | a0001c0001t0002g0250 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.255+11607C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63869543 | |||||||
| chr2:63869573 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.255+11637G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63869573 | |||||||
| chr2:63869672 | A | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0146 |
3 | HG01515.hp2 HG01517.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.255+11736A>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63869672 | |||||||
| chr2:63869718 | G | C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0236 a0001c0001t0002g0057 |
3 | HG02109.hp1 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.255+11782G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63869718 | |||||||
| chr2:63869790 | C | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0146 |
3 | HG01515.hp2 HG01517.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.255+11854C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63869790 | |||||||
| chr2:63869922 | A | AT | 40 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(37): Show |
50 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.255+12004dupT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63869922 | ||||||
| chr2:63869922 | A | T | 1 | a0001c0001t0003g0080 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.255+11986A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63869922 | |||||||
| chr2:63869922 | AT | A | 9 | a0001c0001t0001g0062 a0001c0001t0001g0116 a0001c0001t0001g0117 others(6): Show |
9 | HG02109.hp1 HG02280.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.255+12004delT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63869922 | ||||||
| chr2:63869923 | T | C | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0037 others(20): Show |
25 | HG01070.hp1 HG01074.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.255+11987T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63869923 | |||||||
| chr2:63869924 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.255+11988T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63869924 | |||||||
| chr2:63869983 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.255+12047C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63869983 | |||||||
| chr2:63870025 | C | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(196): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.255+12089C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63870025 | |||||||
| chr2:63870131 | C | A | 3 | a0001c0002t0001g0067 a0001c0002t0001g0068 a0001c0002t0002g0258 |
3 | HG00140.hp2 HG00323.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.255+12195C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63870131 | |||||||
| chr2:63870269 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG00642.hp2 HG01192.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.256-12197G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63870269 | |||||||
| chr2:63870319 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.256-12147A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63870319 | |||||||
| chr2:63870377 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.256-12089T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63870377 | |||||||
| chr2:63870734 | T | C | 38 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(35): Show |
49 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.256-11732T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63870734 | |||||||
| chr2:63870747 | A | G | 38 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(35): Show |
49 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.256-11719A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63870747 | |||||||
| chr2:63870870 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.256-11596C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63870870 | |||||||
| chr2:63871025 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.256-11441T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63871025 | |||||||
| chr2:63871223 | C | G | 34 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(31): Show |
44 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.256-11243C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63871223 | |||||||
| chr2:63871346 | T | C | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.256-11120T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63871346 | |||||||
| chr2:63871408 | C | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG00639.hp2 HG01515.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.256-11058C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63871408 | |||||||
| chr2:63871559 | T | A | 22 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0037 others(19): Show |
24 | HG01070.hp1 HG01074.hp2 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.256-10907T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63871559 | |||||||
| chr2:63871596 | T | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0133 |
3 | HG02572.hp2 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.256-10870T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63871596 | |||||||
| chr2:63871837 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.256-10629A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63871837 | |||||||
| chr2:63871972 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.256-10494A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63871972 | |||||||
| chr2:63871991 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.256-10475A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63871991 | |||||||
| chr2:63872036 | G | C | 3 | a0001c0002t0001g0067 a0001c0002t0001g0068 a0001c0002t0002g0258 |
3 | HG00140.hp2 HG00323.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.256-10430G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63872036 | |||||||
| chr2:63872050 | A | C | 3 | a0001c0002t0001g0067 a0001c0002t0001g0068 a0001c0002t0002g0258 |
3 | HG00140.hp2 HG00323.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.256-10416A>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63872050 | |||||||
| chr2:63872110 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0038 others(10): Show |
16 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.256-10356C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63872110 | |||||||
| chr2:63872137 | A | G | 3 | a0001c0001t0003g0014 a0001c0001t0003g0097 a0001c0001t0003g0098 |
4 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(1): Show |
intron_variant | MODIFIER | c.256-10329A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63872137 | |||||||
| chr2:63872244 | T | C | 1 | a0001c0001t0003g0084 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.256-10222T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63872244 | |||||||
| chr2:63872249 | T | A | 3 | a0001c0001t0002g0039 a0001c0001t0002g0240 a0001c0001t0002g0241 |
3 | HG00280.hp2 HG02135.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.256-10217T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63872249 | |||||||
| chr2:63872595 | T | C | 34 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(31): Show |
44 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.256-9871T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63872595 | |||||||
| chr2:63872691 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0036 others(23): Show |
30 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.256-9775G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63872691 | |||||||
| chr2:63872764 | A | C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0236 a0001c0001t0002g0057 |
3 | HG02109.hp1 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.256-9702A>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63872764 | |||||||
| chr2:63872787 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.256-9679C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63872787 | |||||||
| chr2:63872790 | C | CA | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0100 others(3): Show |
6 | HG02074.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.256-9660dupA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63872790 | ||||||
| chr2:63872809 | T | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0036 others(21): Show |
28 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.256-9657T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63872809 | |||||||
| chr2:63872880 | G | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0236 a0001c0001t0002g0057 |
3 | HG02109.hp1 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.256-9586G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63872880 | |||||||
| chr2:63872893 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.256-9573G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63872893 | |||||||
| chr2:63872965 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0003g0076 |
2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.256-9501C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63872965 | |||||||
| chr2:63873287 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.256-9179G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63873287 | |||||||
| chr2:63873400 | T | C | 1 | a0001c0001t0001g0018 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.256-9066T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63873400 | |||||||
| chr2:63873680 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.256-8786C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63873680 | |||||||
| chr2:63873707 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.256-8759G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63873707 | |||||||
| chr2:63873789 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.256-8677G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63873789 | |||||||
| chr2:63873893 | G | C | 1 | a0001c0001t0001g0191 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.256-8573G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63873893 | |||||||
| chr2:63873976 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.256-8490C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63873976 | |||||||
| chr2:63874328 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.256-8138G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63874328 | |||||||
| chr2:63874435 | A | T | 22 | a0001c0001t0001g0079 a0001c0001t0001g0095 a0001c0001t0001g0103 others(19): Show |
23 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.256-8031A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63874435 | |||||||
| chr2:63874441 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.256-8025A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63874441 | |||||||
| chr2:63874906 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.256-7560C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63874906 | |||||||
| chr2:63875047 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.256-7419T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63875047 | |||||||
| chr2:63875126 | T | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.256-7340T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63875126 | |||||||
| chr2:63875217 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.256-7249G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63875217 | |||||||
| chr2:63875540 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.256-6926A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63875540 | |||||||
| chr2:63875548 | C | A | 1 | a0001c0001t0001g0017 | 2 | HG01074.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.256-6918C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63875548 | |||||||
| chr2:63875584 | CTAGA | C | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
6 | HG01175.hp2 NA18946.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-6880_256-6877d others(6): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63875584 | ||||||
| chr2:63875922 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.256-6544C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63875922 | |||||||
| chr2:63875936 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.256-6530T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63875936 | |||||||
| chr2:63875946 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.256-6520A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63875946 | |||||||
| chr2:63875966 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.256-6500C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63875966 | |||||||
| chr2:63875992 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.256-6474A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63875992 | |||||||
| chr2:63876485 | G | A | 1 | a0001c0001t0002g0250 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.256-5981G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63876485 | |||||||
| chr2:63876607 | G | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(249): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.256-5859G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63876607 | |||||||
| chr2:63876998 | C | T | 210 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(207): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.256-5468C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63876998 | |||||||
| chr2:63877197 | G | GT | 13 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0038 others(10): Show |
16 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.256-5268dupT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63877197 | ||||||
| chr2:63877395 | A | G | 3 | a0001c0002t0001g0067 a0001c0002t0001g0068 a0001c0002t0002g0258 |
3 | HG00140.hp2 HG00323.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.256-5071A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63877395 | |||||||
| chr2:63877465 | C | A | 1 | a0001c0001t0002g0242 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.256-5001C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63877465 | |||||||
| chr2:63877563 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.256-4903T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63877563 | |||||||
| chr2:63877866 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.256-4600G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63877866 | |||||||
| chr2:63877917 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.256-4549C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63877917 | |||||||
| chr2:63877925 | G | A | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(210): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.256-4541G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63877925 | |||||||
| chr2:63877994 | C | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0036 others(20): Show |
27 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.256-4472C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63877994 | |||||||
| chr2:63877994 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.256-4472C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63877994 | |||||||
| chr2:63877999 | C | CA | 8 | a0001c0001t0001g0058 a0001c0001t0001g0269 a0001c0001t0001g0272 others(5): Show |
8 | HG02148.hp1 HG02300.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.256-4437dupA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63877999 | ||||||
| chr2:63877999 | CA | C | 36 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0029 others(33): Show |
48 | HG00642.hp2 HG00738.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.256-4437delA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63877999 | ||||||
| chr2:63877999 | CAA | C | 34 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0037 others(31): Show |
36 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.256-4438_256-4437d others(4): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63877999 | ||||||
| chr2:63877999 | CAAA | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(130): Show |
146 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.256-4439_256-4437d others(5): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63877999 | ||||||
| chr2:63877999 | CAAAA | C | 12 | a0001c0001t0001g0047 a0001c0001t0001g0052 a0001c0001t0001g0162 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.256-4440_256-4437d others(6): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63877999 | ||||||
| chr2:63877999 | CAAAAAAA others(2): Show |
C | 17 | a0001c0001t0001g0079 a0001c0001t0001g0263 a0001c0001t0003g0014 others(14): Show |
18 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.256-4445_256-4437d others(11): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63877999 | ||||||
| chr2:63877999 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.256-4450_256-4437d others(16): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63877999 | ||||||
| chr2:63878025 | AAAAAG | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0124 a0001c0001t0001g0125 others(4): Show |
8 | HG01070.hp1 HG01074.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.256-4438_256-4434d others(7): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63878025 | ||||||
| chr2:63878032 | A | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0100 |
3 | HG02622.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.256-4434A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63878032 | |||||||
| chr2:63878081 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.256-4385C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63878081 | |||||||
| chr2:63878082 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.256-4384G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63878082 | |||||||
| chr2:63878353 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.256-4113A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63878353 | |||||||
| chr2:63878419 | A | G | 39 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(36): Show |
50 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.256-4047A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63878419 | |||||||
| chr2:63878468 | G | C | 6 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0114 others(3): Show |
6 | HG01243.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.256-3998G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63878468 | |||||||
| chr2:63878711 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.256-3755G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63878711 | |||||||
| chr2:63879005 | T | TA | 82 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(79): Show |
93 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.256-3446dupA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63879005 | ||||||
| chr2:63879048 | C | G | 1 | a0001c0001t0003g0080 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.256-3418C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63879048 | |||||||
| chr2:63879052 | T | G | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0026 others(20): Show |
26 | HG01070.hp1 HG01074.hp2 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.256-3414T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63879052 | |||||||
| chr2:63879053 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-3413G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63879053 | |||||||
| chr2:63879259 | A | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-3207A>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63879259 | |||||||
| chr2:63879366 | T | G | 1 | a0001c0001t0001g0206 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.256-3100T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63879366 | |||||||
| chr2:63879448 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.256-3018G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63879448 | |||||||
| chr2:63879532 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.256-2934A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63879532 | |||||||
| chr2:63879708 | A | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.256-2758A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63879708 | |||||||
| chr2:63879750 | TTTTA | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0036 others(21): Show |
28 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.256-2714_256-2711d others(6): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63879750 | ||||||
| chr2:63879752 | T | G | 14 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0062 others(11): Show |
14 | HG02145.hp2 HG02559.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.256-2714T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63879752 | |||||||
| chr2:63879762 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.256-2704G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63879762 | |||||||
| chr2:63879827 | T | A | 1 | a0001c0001t0001g0236 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.256-2639T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63879827 | |||||||
| chr2:63880089 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.256-2377A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63880089 | |||||||
| chr2:63880152 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.256-2314C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63880152 | |||||||
| chr2:63880360 | G | C | 1 | a0001c0001t0002g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.256-2106G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63880360 | |||||||
| chr2:63880692 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.256-1774A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63880692 | |||||||
| chr2:63880725 | G | T | 8 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0171 others(5): Show |
8 | HG02132.hp2 NA18945.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.256-1741G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63880725 | |||||||
| chr2:63880787 | AGTGTGGT others(12): Show |
A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0204 |
2 | HG00597.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.256-1667_256-1649d others(21): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63880787 | ||||||
| chr2:63880806 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.256-1660G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63880806 | |||||||
| chr2:63880993 | A | T | 1 | a0001c0001t0002g0250 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.256-1473A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63880993 | |||||||
| chr2:63881348 | T | TAC | 94 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0016 others(91): Show |
111 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.256-1089_256-1088d others(4): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63881348 | ||||||
| chr2:63881348 | T | TACAC | 16 | a0001c0001t0001g0073 a0001c0001t0001g0103 a0001c0001t0001g0114 others(13): Show |
17 | HG00140.hp2 HG00323.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.256-1091_256-1088d others(6): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63881348 | ||||||
| chr2:63881348 | T | TACACAC | 4 | a0001c0001t0001g0070 a0001c0001t0003g0080 a0001c0001t0003g0081 others(1): Show |
4 | HG01891.hp2 HG02145.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.256-1093_256-1088d others(8): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63881348 | ||||||
| chr2:63881348 | T | TACACACA others(3): Show |
7 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0063 others(4): Show |
7 | HG02559.hp1 HG02630.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.256-1097_256-1088d others(12): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63881348 | ||||||
| chr2:63881348 | T | TACACACA others(5): Show |
1 | a0001c0001t0001g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.256-1099_256-1088d others(14): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63881348 | ||||||
| chr2:63881348 | TAC | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0003g0078 |
3 | HG02886.hp2 NA18952.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.256-1089_256-1088d others(4): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63881348 | ||||||
| chr2:63881348 | TACAC | T | 10 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0001g0106 others(7): Show |
10 | HG01261.hp1 HG01496.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.256-1091_256-1088d others(6): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63881348 | ||||||
| chr2:63881348 | TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0015 | 2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.256-1099_256-1088d others(14): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63881348 | ||||||
| chr2:63881348 | TACACACA others(7): Show |
T | 1 | a0001c0001t0002g0246 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.256-1101_256-1088d others(16): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 63881348 | ||||||
| chr2:63881434 | A | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0036 others(21): Show |
28 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.256-1032A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63881434 | |||||||
| chr2:63881697 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.256-769T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63881697 | |||||||
| chr2:63881766 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.256-700C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63881766 | |||||||
| chr2:63881869 | T | A | 2 | a0001c0001t0001g0079 a0001c0001t0003g0076 |
2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.256-597T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63881869 | |||||||
| chr2:63881884 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.256-582G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63881884 | |||||||
| chr2:63881935 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.256-531G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63881935 | |||||||
| chr2:63882162 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.256-304A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63882162 | |||||||
| chr2:63882233 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.256-233C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63882233 | |||||||
| chr2:63882408 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.256-58T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63882408 | |||||||
| chr2:63882416 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.256-50C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63882416 | |||||||
| chr2:63882453 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.256-13A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63882453 | |||||||
| chr2:63882455 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.256-11T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 3/9 | chr2 | 63882455 | |||||||
| chr2:63882672 | C | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG01891.hp1 HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.441+21C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 4/9 | chr2 | 63882672 | |||||||
| chr2:63882946 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.441+295C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 4/9 | chr2 | 63882946 | |||||||
| chr2:63883132 | A | T | 42 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(39): Show |
53 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.441+481A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 4/9 | chr2 | 63883132 | |||||||
| chr2:63883353 | ATAGT | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0036 others(22): Show |
29 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.442-602_442-599del others(4): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 63883353 | ||||||
| chr2:63883543 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.442-417C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 4/9 | chr2 | 63883543 | |||||||
| chr2:63883557 | T | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0260 a0001c0001t0001g0261 others(1): Show |
5 | HG02257.hp1 HG02572.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-403T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 4/9 | chr2 | 63883557 | |||||||
| chr2:63883848 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.442-112C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 4/9 | chr2 | 63883848 | |||||||
| chr2:63884175 | A | C | 1 | a0001c0001t0001g0051 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.575+82A>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | chr2 | 63884175 | |||||||
| chr2:63884196 | T | C | 8 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0171 others(5): Show |
8 | HG02132.hp2 NA18945.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.575+103T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | chr2 | 63884196 | |||||||
| chr2:63884798 | A | C | 3 | a0001c0001t0002g0255 a0001c0001t0002g0256 a0001c0001t0002g0257 |
3 | HG00738.hp2 HG01361.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.575+705A>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | chr2 | 63884798 | |||||||
| chr2:63884926 | GA | G | 5 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0130 others(2): Show |
5 | HG02258.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.576-661delA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 63884926 | ||||||
| chr2:63884993 | C | A | 1 | a0001c0001t0001g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.576-596C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | chr2 | 63884993 | |||||||
| chr2:63884993 | C | CT | 53 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0011 others(50): Show |
61 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.576-567dupT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 63884993 | ||||||
| chr2:63884993 | C | CTT | 71 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(68): Show |
74 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.576-568_576-567dup others(2): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 63884993 | ||||||
| chr2:63884993 | C | CTTT | 56 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0021 others(53): Show |
66 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.576-569_576-567dup others(3): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 63884993 | ||||||
| chr2:63884993 | C | CTTTT | 20 | a0001c0001t0001g0147 a0001c0001t0001g0159 a0001c0001t0001g0170 others(17): Show |
23 | HG00323.hp1 HG00741.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.576-570_576-567dup others(4): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 63884993 | ||||||
| chr2:63884993 | C | CTTTTT | 7 | a0001c0001t0001g0114 a0001c0001t0001g0157 a0001c0001t0001g0186 others(4): Show |
7 | HG00280.hp2 HG00438.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.576-571_576-567dup others(5): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 63884993 | ||||||
| chr2:63884993 | CTTT | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0036 others(21): Show |
28 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.576-569_576-567del others(3): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 63884993 | ||||||
| chr2:63884993 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.576-581_576-567del others(15): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 63884993 | ||||||
| chr2:63885068 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.576-521C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | chr2 | 63885068 | |||||||
| chr2:63885167 | T | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0270 a0001c0001t0001g0279 |
4 | HG01346.hp1 HG03239.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.576-422T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | chr2 | 63885167 | |||||||
| chr2:63885294 | C | T | 224 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(221): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.576-295C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | chr2 | 63885294 | |||||||
| chr2:63885451 | T | G | 1 | a0001c0001t0001g0018 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.576-138T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 5/9 | chr2 | 63885451 | |||||||
| chr2:63885933 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.873+47C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 6/9 | chr2 | 63885933 | |||||||
| chr2:63886068 | G | T | 32 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(29): Show |
42 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.873+182G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 6/9 | chr2 | 63886068 | |||||||
| chr2:63886552 | G | T | 17 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0023 others(14): Show |
23 | HG00280.hp2 HG01243.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1071+14G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 7/9 | chr2 | 63886552 | |||||||
| chr2:63886610 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1071+72G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 7/9 | chr2 | 63886610 | |||||||
| chr2:63886656 | C | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0210 |
2 | HG01175.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1071+118C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 7/9 | chr2 | 63886656 | |||||||
| chr2:63886743 | C | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0133 |
3 | HG02895.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1071+205C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 7/9 | chr2 | 63886743 | |||||||
| chr2:63886789 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1071+251C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 7/9 | chr2 | 63886789 | |||||||
| chr2:63886822 | A | G | 2 | a0001c0001t0002g0245 a0001c0001t0002g0251 |
2 | HG01361.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1071+284A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 7/9 | chr2 | 63886822 | |||||||
| chr2:63887149 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1072-253A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 7/9 | chr2 | 63887149 | |||||||
| chr2:63887157 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0236 a0001c0001t0002g0057 |
3 | HG02109.hp1 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1072-245G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 7/9 | chr2 | 63887157 | |||||||
| chr2:63887181 | T | G | 2 | a0001c0001t0001g0116 a0001c0001t0002g0057 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1072-221T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 7/9 | chr2 | 63887181 | |||||||
| chr2:63887264 | CA | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0038 others(12): Show |
18 | HG01168.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1072-123delA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 63887264 | ||||||
| chr2:63887279 | A | AT | 9 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0171 others(6): Show |
9 | HG01175.hp2 HG02132.hp2 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.1072-112dupT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 63887279 | ||||||
| chr2:63887279 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1072-123A>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 7/9 | chr2 | 63887279 | |||||||
| chr2:63887280 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1072-122T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 7/9 | chr2 | 63887280 | |||||||
| chr2:63887886 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1314+242G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63887886 | |||||||
| chr2:63887903 | T | C | 24 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0026 others(21): Show |
27 | HG01070.hp1 HG01074.hp2 HG01515.hp2 others(24): Show |
intron_variant | MODIFIER | c.1314+259T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63887903 | |||||||
| chr2:63888303 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1314+659A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63888303 | |||||||
| chr2:63888611 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1314+967C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63888611 | |||||||
| chr2:63888675 | A | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
8 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+1031A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63888675 | |||||||
| chr2:63888744 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1314+1100G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63888744 | |||||||
| chr2:63888790 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1314+1146T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63888790 | |||||||
| chr2:63889042 | A | C | 1 | a0001c0001t0001g0107 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1315-1039A>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63889042 | |||||||
| chr2:63889067 | G | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0166 others(1): Show |
4 | HG01934.hp1 HG02273.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315-1014G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63889067 | |||||||
| chr2:63889455 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1315-626G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63889455 | |||||||
| chr2:63889489 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1315-592T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63889489 | |||||||
| chr2:63889507 | T | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG02559.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1315-574T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63889507 | |||||||
| chr2:63889568 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1315-513A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63889568 | |||||||
| chr2:63889573 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1315-508G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63889573 | |||||||
| chr2:63889817 | T | TA | 8 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
9 | HG00140.hp2 HG00323.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.1315-253dupA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 63889817 | ||||||
| chr2:63889817 | T | TAA | 29 | a0001c0001t0001g0121 a0001c0001t0001g0184 a0001c0001t0002g0005 others(26): Show |
38 | HG00280.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.1315-254_1315-253d others(4): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 63889817 | ||||||
| chr2:63889913 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1315-168C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63889913 | |||||||
| chr2:63890018 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0133 |
3 | HG02895.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1315-63A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63890018 | |||||||
| chr2:63890044 | T | TA | 4 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1315-37_1315-36ins others(1): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63890044 | |||||||
| chr2:63890051 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1315-30C>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 8/9 | chr2 | 63890051 | |||||||
| chr2:63890289 | G | A | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(33): Show |
47 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1419+104G>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890289 | |||||||
| chr2:63890291 | G | T | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(33): Show |
47 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1419+106G>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890291 | |||||||
| chr2:63890292 | C | A | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(33): Show |
47 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1419+107C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890292 | |||||||
| chr2:63890295 | C | CT | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(33): Show |
47 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1419+110_1419+111i others(3): Show |
UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890295 | |||||||
| chr2:63890296 | C | A | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(33): Show |
47 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1419+111C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890296 | |||||||
| chr2:63890297 | T | G | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(33): Show |
47 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1419+112T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890297 | |||||||
| chr2:63890303 | AC | A | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(33): Show |
47 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1419+119delC | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890303 | |||||||
| chr2:63890305 | T | A | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(33): Show |
47 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1419+120T>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890305 | |||||||
| chr2:63890306 | A | G | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(33): Show |
47 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1419+121A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890306 | |||||||
| chr2:63890310 | T | G | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(33): Show |
47 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1419+125T>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890310 | |||||||
| chr2:63890311 | A | C | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(33): Show |
47 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1419+126A>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890311 | |||||||
| chr2:63890313 | T | C | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0040 others(33): Show |
47 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1419+128T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890313 | |||||||
| chr2:63890386 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1419+201A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890386 | |||||||
| chr2:63890506 | C | T | 34 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0041 others(31): Show |
45 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1419+321C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890506 | |||||||
| chr2:63890515 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1419+330T>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890515 | |||||||
| chr2:63890527 | G | C | 3 | a0001c0001t0001g0148 a0001c0001t0001g0221 a0001c0001t0001g0227 |
3 | HG02135.hp2 NA18992.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1419+342G>C | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890527 | |||||||
| chr2:63890724 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1420-396C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890724 | |||||||
| chr2:63890810 | A | G | 46 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0034 others(43): Show |
57 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1420-310A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890810 | |||||||
| chr2:63890855 | C | A | 1 | a0001c0001t0001g0261 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1420-265C>A | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890855 | |||||||
| chr2:63890860 | C | CT | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(31): Show |
51 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.1420-259dupT | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 63890860 | ||||||
| chr2:63890960 | A | G | 1 | a0001c0001t0002g0251 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1420-160A>G | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63890960 | |||||||
| chr2:63891024 | T | TA | 31 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0036 others(28): Show |
35 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1420-84dupA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 63891024 | ||||||
| chr2:63891024 | TA | T | 26 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0026 others(23): Show |
29 | HG01070.hp1 HG01074.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1420-84delA | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 63891024 | ||||||
| chr2:63891113 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA19240.hp1 | splice_region_variant&intron_variant | LOW | c.1420-7C>T | UGP2 | ENSG00000169764.16 | transcript | ENST00000337130.10 | protein_coding | 9/9 | chr2 | 63891113 |