Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80146 |
| ensemblid | ENSG00000115652.15 |
| hgncid | 17729 |
| symbol | UXS1 |
| name | UDP-glucuronate decarboxylase 1 |
| refseq_nuc | NM_001253875.2 |
| refseq_prot | NP_001240804.1 |
| ensembl_nuc | ENST00000283148.12 |
| ensembl_prot | ENSP00000283148.7 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 106093311 |
| end | 106194301 |
| strand | - |
| ver | v1.2 |
| region | chr2:106093311-106194301 |
| region5000 | chr2:106088311-106199301 |
| regionname0 | UXS1_chr2_106093311_106194301 |
| regionname5000 | UXS1_chr2_106088311_106199301 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1275 | 301 | 67 | 56 | 128 | 12 | 36 | UXS1_chr2_106088311_106199301 | UXS1 | ATGGT others(1270): Show |
chr2 | 106088311 | 106199301 | ||
| a0001c0002 | 0/0 | 1275 | 3 | 3 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | ATGGT others(1270): Show |
chr2 | 106088311 | 106199301 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2053 | 254 | 49 | 56 | 105 | 12 | 32 | UXS1_chr2_106088311_106199301 | UXS1 | GCATT others(2048): Show |
chr2 | 106088311 | 106199301 |
| a0001c0001t0002 | 0/0 | 2053 | 25 | 0 | 0 | 21 | 0 | 4 | UXS1_chr2_106088311_106199301 | UXS1 | GCATT others(2048): Show |
chr2 | 106088311 | 106199301 |
| a0001c0001t0003 | 1/0 | 2053 | 12 | 11 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | GCATT others(2048): Show |
chr2 | 106088311 | 106199301 |
| a0001c0001t0005 | 0/0 | 2051 | 3 | 3 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | GCATT others(2046): Show |
chr2 | 106088311 | 106199301 |
| a0001c0001t0006 | 0/0 | 2053 | 2 | 2 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | GCATT others(2048): Show |
chr2 | 106088311 | 106199301 |
| a0001c0001t0007 | 0/0 | 2053 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | GCATT others(2048): Show |
chr2 | 106088311 | 106199301 |
| a0001c0001t0008 | 0/0 | 2053 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | GCATT others(2048): Show |
chr2 | 106088311 | 106199301 |
| a0001c0001t0009 | 0/1 | 2053 | 1 | 0 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | GCATT others(2048): Show |
chr2 | 106088311 | 106199301 |
| a0001c0001t0010 | 0/0 | 2053 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | GCATT others(2048): Show |
chr2 | 106088311 | 106199301 |
| a0001c0001t0011 | 0/0 | 2053 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | GCATT others(2048): Show |
chr2 | 106088311 | 106199301 |
| a0001c0002t0004 | 0/0 | 2053 | 3 | 3 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | GCATT others(2048): Show |
chr2 | 106088311 | 106199301 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0003g0278 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0007g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0008g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0009g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0001t0011g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0002t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0002t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| a0001c0002t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | GBR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | GBR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | FIN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | FIN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | FIN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | FIN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0182 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | CDX | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CDX | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0276 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0273 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0279 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0280 | AFR | ESN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0272 | AFR | ESN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0269 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03130 | hp2 | a0001 | c0002 | t0004 | g0030 | AFR | ESN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0089 | AFR | MSL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0248 | AFR | MSL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | ESN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | BEB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | STU | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | STU | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | STU | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | STU | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | YRI | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19011 | hp1 | a0001 | c0001 | t0007 | g0096 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0032 | AFR | LWK | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19054 | hp2 | a0001 | c0001 | t0008 | g0116 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ASW | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ASW | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | TSI | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0029 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0274 | AFR | MSL | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | USA | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0281 | AFR | USA | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0009 | g0214 | REF | REF | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0278 | REF | REF | UXS1_chr2_106088311_106199301 | UXS1 | chr2 | 106088311 | 106199301 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:106094104 | G | A | 1 | a0001c0002 | 3 | HG02559.hp1 HG03130.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.1200C>T | p.Leu400Leu | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 15/15 | 1260/2053 | 1200/1278 | 400/425 | chr2 | 106094104 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:106093323 | A | G | 1 | a0001c0001t0006 | 2 | HG01884.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*703T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 15/15 | 703 | chr2 | 106093323 | ||||||
| chr2:106093432 | C | T | 1 | a0001c0001t0007 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*594G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 15/15 | 594 | chr2 | 106093432 | ||||||
| chr2:106093501 | A | G | 1 | a0001c0002t0004 | 3 | HG02559.hp1 HG03130.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*525T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 15/15 | 525 | chr2 | 106093501 | ||||||
| chr2:106093505 | ACT | A | 1 | a0001c0001t0005 | 3 | HG02055.hp2 HG02886.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*519_*520delAG | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 15/15 | 519 | chr2 | 106093505 | ||||||
| chr2:106093520 | A | G | 1 | a0001c0001t0008 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*506T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 15/15 | 506 | chr2 | 106093520 | ||||||
| chr2:106093652 | C | T | 8 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(5): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*374G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 15/15 | 374 | chr2 | 106093652 | ||||||
| chr2:106093743 | A | G | 2 | a0001c0001t0002 a0001c0001t0007 |
26 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*283T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 15/15 | 283 | chr2 | 106093743 | ||||||
| chr2:106194247 | G | A | 1 | a0001c0001t0011 | 1 | HG03041.hp1 | 5_prime_UTR_variant | MODIFIER | c.-6C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/15 | 6 | chr2 | 106194247 | ||||||
| chr2:106194271 | A | G | 9 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(6): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
5_prime_UTR_variant | MODIFIER | c.-30T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/15 | 30 | chr2 | 106194271 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:106094212 | C | CGCAGGAA others(14): Show |
183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1147-76_1147-56dup others(21): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106094212 | |||||||
| chr2:106094212 | C | CGCAGGAA others(35): Show |
3 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0158 |
3 | HG02145.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1147-97_1147-56dup others(42): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106094212 | |||||||
| chr2:106094212 | CGCAGGAA others(14): Show |
C | 1 | a0001c0001t0001g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1147-76_1147-56del others(21): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106094212 | |||||||
| chr2:106094327 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1147-170C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106094327 | |||||||
| chr2:106094334 | C | A | 1 | a0001c0001t0006g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1147-177G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106094334 | |||||||
| chr2:106094361 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1147-204G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106094361 | |||||||
| chr2:106094372 | T | G | 3 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0089 |
3 | HG02055.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1147-215A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106094372 | |||||||
| chr2:106094512 | T | C | 2 | a0001c0001t0002g0093 a0001c0001t0002g0094 |
2 | HG03834.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1147-355A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106094512 | |||||||
| chr2:106094607 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0091 |
2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1147-450G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106094607 | |||||||
| chr2:106094944 | A | G | 13 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0039 others(10): Show |
13 | HG00140.hp1 HG00621.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1147-787T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106094944 | |||||||
| chr2:106094985 | A | G | 3 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0089 |
3 | HG02055.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1147-828T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106094985 | |||||||
| chr2:106095150 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1147-993G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106095150 | |||||||
| chr2:106095404 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1147-1247A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106095404 | |||||||
| chr2:106095633 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1146+1085C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106095633 | |||||||
| chr2:106095675 | C | T | 2 | a0001c0001t0005g0037 a0001c0001t0005g0038 |
2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1146+1043G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106095675 | |||||||
| chr2:106095703 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1146+1015G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106095703 | |||||||
| chr2:106095854 | G | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0166 |
3 | HG02015.hp2 NA18972.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1146+864C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106095854 | |||||||
| chr2:106096060 | C | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0022 others(53): Show |
63 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1146+658G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106096060 | |||||||
| chr2:106096183 | GGT | G | 80 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1146+533_1146+534d others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106096183 | |||||||
| chr2:106096185 | T | G | 4 | a0001c0001t0001g0081 a0001c0002t0004g0029 a0001c0002t0004g0030 others(1): Show |
4 | HG02559.hp1 HG03130.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146+533A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106096185 | |||||||
| chr2:106096202 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1146+516C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106096202 | |||||||
| chr2:106096211 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1146+507A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106096211 | |||||||
| chr2:106096260 | G | A | 21 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(18): Show |
26 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.1146+458C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106096260 | |||||||
| chr2:106096307 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01891.hp2 HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1146+411A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106096307 | |||||||
| chr2:106096323 | AGT | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0087 others(5): Show |
9 | HG01069.hp1 HG01071.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1146+393_1146+394d others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106096323 | |||||||
| chr2:106096387 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1146+331C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106096387 | |||||||
| chr2:106096587 | C | T | 6 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0105 others(3): Show |
6 | NA18947.hp1 NA18968.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146+131G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106096587 | |||||||
| chr2:106096602 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0084 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1146+116G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106096602 | |||||||
| chr2:106096668 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1146+50C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 14/14 | chr2 | 106096668 | |||||||
| chr2:106096934 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1043-113G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106096934 | |||||||
| chr2:106097024 | C | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0086 others(6): Show |
10 | HG01069.hp1 HG01071.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1043-203G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106097024 | |||||||
| chr2:106097044 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1043-223G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106097044 | |||||||
| chr2:106097149 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1043-328T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106097149 | |||||||
| chr2:106097378 | C | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1043-557G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106097378 | |||||||
| chr2:106097427 | G | C | 1 | a0001c0001t0001g0013 | 2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1043-606C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106097427 | |||||||
| chr2:106097568 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1043-747A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106097568 | |||||||
| chr2:106097582 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1043-761A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106097582 | |||||||
| chr2:106097686 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1043-865G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106097686 | |||||||
| chr2:106097687 | A | G | 275 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1043-866T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106097687 | |||||||
| chr2:106097861 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0086 others(6): Show |
10 | HG01069.hp1 HG01071.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1042+855T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106097861 | |||||||
| chr2:106098040 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1042+676T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106098040 | |||||||
| chr2:106098229 | T | G | 1 | a0001c0001t0001g0020 | 2 | NA18941.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1042+487A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106098229 | |||||||
| chr2:106098259 | G | C | 77 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(74): Show |
83 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1042+457C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106098259 | |||||||
| chr2:106098300 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1042+416T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106098300 | |||||||
| chr2:106098453 | G | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1042+263C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106098453 | |||||||
| chr2:106098497 | A | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1042+219T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 13/14 | chr2 | 106098497 | |||||||
| chr2:106098886 | G | A | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.985-113C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106098886 | |||||||
| chr2:106098886 | G | T | 30 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0124 others(27): Show |
32 | HG00408.hp1 HG00597.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.985-113C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106098886 | |||||||
| chr2:106099150 | G | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(264): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.985-377C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106099150 | |||||||
| chr2:106099229 | G | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.985-456C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106099229 | |||||||
| chr2:106099252 | C | T | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.985-479G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106099252 | |||||||
| chr2:106099483 | G | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.985-710C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106099483 | |||||||
| chr2:106099542 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.985-769A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106099542 | |||||||
| chr2:106099549 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.985-776T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106099549 | |||||||
| chr2:106099597 | C | T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0080 |
3 | HG01167.hp2 HG01169.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.985-824G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106099597 | |||||||
| chr2:106099618 | T | C | 3 | a0001c0002t0004g0029 a0001c0002t0004g0030 a0001c0002t0004g0032 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.985-845A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106099618 | |||||||
| chr2:106099632 | C | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.985-859G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106099632 | |||||||
| chr2:106099677 | C | T | 62 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
68 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.985-904G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106099677 | |||||||
| chr2:106099940 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.984+1118T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106099940 | |||||||
| chr2:106100072 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.984+986C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106100072 | |||||||
| chr2:106100073 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.984+985A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106100073 | |||||||
| chr2:106100073 | T | G | 1 | a0001c0001t0001g0137 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.984+985A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106100073 | |||||||
| chr2:106100074 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.984+984C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106100074 | |||||||
| chr2:106100103 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.984+955T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106100103 | |||||||
| chr2:106100104 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.984+954C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106100104 | |||||||
| chr2:106100336 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.984+722T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106100336 | |||||||
| chr2:106100622 | C | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0158 |
3 | HG02145.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.984+436G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106100622 | |||||||
| chr2:106100715 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.984+343A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106100715 | |||||||
| chr2:106100742 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0158 |
2 | HG00642.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.984+316C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106100742 | |||||||
| chr2:106100818 | A | G | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.984+240T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 12/14 | chr2 | 106100818 | |||||||
| chr2:106101200 | G | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.924-82C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106101200 | |||||||
| chr2:106101287 | C | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.924-169G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106101287 | |||||||
| chr2:106101527 | T | C | 3 | a0001c0002t0004g0029 a0001c0002t0004g0030 a0001c0002t0004g0032 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.924-409A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106101527 | |||||||
| chr2:106101537 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.924-419G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106101537 | |||||||
| chr2:106101907 | C | T | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(1): Show |
4 | HG00323.hp2 HG01346.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-789G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106101907 | |||||||
| chr2:106102292 | G | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.924-1174C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106102292 | |||||||
| chr2:106102429 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.924-1311C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106102429 | |||||||
| chr2:106102451 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.924-1333G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106102451 | |||||||
| chr2:106102626 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.924-1508G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106102626 | |||||||
| chr2:106102702 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.924-1584C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106102702 | |||||||
| chr2:106102746 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.924-1628G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106102746 | |||||||
| chr2:106102808 | T | G | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.924-1690A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106102808 | |||||||
| chr2:106102840 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.924-1722T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106102840 | |||||||
| chr2:106102949 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.924-1831C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106102949 | |||||||
| chr2:106102952 | G | A | 21 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(18): Show |
26 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.924-1834C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106102952 | |||||||
| chr2:106103029 | T | A | 1 | a0001c0001t0001g0203 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.923+1765A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103029 | |||||||
| chr2:106103049 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.923+1745G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103049 | |||||||
| chr2:106103150 | A | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.923+1644T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103150 | |||||||
| chr2:106103306 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.923+1488A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103306 | |||||||
| chr2:106103311 | C | T | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.923+1483G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103311 | |||||||
| chr2:106103317 | A | T | 3 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0089 |
3 | HG02055.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.923+1477T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103317 | |||||||
| chr2:106103319 | A | T | 3 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0089 |
3 | HG02055.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.923+1475T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103319 | |||||||
| chr2:106103320 | T | C | 3 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0089 |
3 | HG02055.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.923+1474A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103320 | |||||||
| chr2:106103326 | T | G | 9 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0069 others(6): Show |
9 | HG02451.hp1 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+1468A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103326 | |||||||
| chr2:106103336 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0082 |
3 | HG01167.hp1 HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.923+1458A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103336 | |||||||
| chr2:106103377 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(48): Show |
55 | HG00323.hp2 HG00423.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.923+1417C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103377 | |||||||
| chr2:106103526 | C | G | 1 | a0001c0001t0001g0218 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.923+1268G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103526 | |||||||
| chr2:106103619 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.923+1175A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103619 | |||||||
| chr2:106103654 | T | C | 14 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0039 others(11): Show |
14 | HG00140.hp1 HG00621.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.923+1140A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103654 | |||||||
| chr2:106103663 | C | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.923+1131G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106103663 | |||||||
| chr2:106104112 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.923+682A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106104112 | |||||||
| chr2:106104330 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.923+464T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106104330 | |||||||
| chr2:106104369 | A | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.923+425T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106104369 | |||||||
| chr2:106104422 | C | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.923+372G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106104422 | |||||||
| chr2:106104438 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.923+356A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106104438 | |||||||
| chr2:106104502 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.923+292C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106104502 | |||||||
| chr2:106104540 | T | G | 2 | a0001c0001t0005g0037 a0001c0001t0005g0038 |
2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.923+254A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106104540 | |||||||
| chr2:106104552 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
7 | HG00642.hp1 HG01928.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.923+242G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 11/14 | chr2 | 106104552 | |||||||
| chr2:106104923 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.880-86C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106104923 | |||||||
| chr2:106104984 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.880-147C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106104984 | |||||||
| chr2:106105099 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.880-262C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106105099 | |||||||
| chr2:106105289 | G | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.880-452C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106105289 | |||||||
| chr2:106105399 | A | AG | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.880-563dupC | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106105399 | |||||||
| chr2:106105430 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.880-593G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106105430 | |||||||
| chr2:106105489 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.880-652C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106105489 | |||||||
| chr2:106105676 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.880-839A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106105676 | |||||||
| chr2:106105739 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.880-902C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106105739 | |||||||
| chr2:106105794 | C | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.880-957G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106105794 | |||||||
| chr2:106106087 | T | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.880-1250A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106106087 | |||||||
| chr2:106106091 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0118 |
2 | NA18978.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.880-1254C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106106091 | |||||||
| chr2:106106357 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.880-1520A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106106357 | |||||||
| chr2:106106364 | C | CA | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.880-1528dupT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106106364 | |||||||
| chr2:106106364 | CA | C | 83 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(80): Show |
90 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.880-1528delT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106106364 | |||||||
| chr2:106106389 | C | T | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.880-1552G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106106389 | |||||||
| chr2:106106497 | T | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(64): Show |
72 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.880-1660A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106106497 | |||||||
| chr2:106106501 | T | C | 5 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0092 others(2): Show |
7 | HG02155.hp1 NA18993.hp1 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-1664A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106106501 | |||||||
| chr2:106106589 | T | A | 1 | a0001c0001t0001g0221 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.880-1752A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106106589 | |||||||
| chr2:106106971 | A | G | 9 | a0001c0001t0001g0014 a0001c0001t0001g0110 a0001c0001t0001g0129 others(6): Show |
10 | HG02015.hp2 HG02523.hp2 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-2134T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106106971 | |||||||
| chr2:106107062 | G | C | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.880-2225C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106107062 | |||||||
| chr2:106107102 | G | C | 21 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(18): Show |
26 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.880-2265C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106107102 | |||||||
| chr2:106107144 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0217 |
2 | HG00099.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.880-2307G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106107144 | |||||||
| chr2:106107167 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.880-2330G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106107167 | |||||||
| chr2:106107398 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.880-2561C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106107398 | |||||||
| chr2:106107450 | G | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.880-2613C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106107450 | |||||||
| chr2:106107497 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.880-2660G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106107497 | |||||||
| chr2:106107645 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.880-2808C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106107645 | |||||||
| chr2:106107653 | G | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.880-2816C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106107653 | |||||||
| chr2:106108567 | A | G | 3 | a0001c0002t0004g0029 a0001c0002t0004g0030 a0001c0002t0004g0032 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.880-3730T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106108567 | |||||||
| chr2:106108582 | C | T | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.880-3745G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106108582 | |||||||
| chr2:106108616 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.880-3779C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106108616 | |||||||
| chr2:106108631 | G | A | 9 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0002g0103 others(6): Show |
9 | HG03834.hp1 HG04115.hp2 HG04204.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-3794C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106108631 | |||||||
| chr2:106108653 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.880-3816A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106108653 | |||||||
| chr2:106108741 | G | A | 1 | a0001c0001t0006g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.880-3904C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106108741 | |||||||
| chr2:106108786 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0054 |
2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.879+3860G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106108786 | |||||||
| chr2:106108788 | G | A | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.879+3858C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106108788 | |||||||
| chr2:106108904 | A | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0188 |
2 | HG00438.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.879+3742T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106108904 | |||||||
| chr2:106108941 | TACCCTCG others(10): Show |
T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG03834.hp2 NA18942.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.879+3688_879+3704d others(19): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106108941 | |||||||
| chr2:106108948 | G | C | 6 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0069 others(3): Show |
6 | HG02630.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.879+3698C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106108948 | |||||||
| chr2:106108950 | TATCTGAT others(10): Show |
T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0132 others(23): Show |
31 | HG00673.hp1 HG00673.hp2 HG02080.hp2 others(28): Show |
intron_variant | MODIFIER | c.879+3679_879+3695d others(19): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106108950 | |||||||
| chr2:106108959 | ACCCTCGA others(5): Show |
A | 1 | a0001c0001t0001g0127 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.879+3675_879+3686d others(14): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106108959 | |||||||
| chr2:106109162 | T | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0023 |
3 | HG01928.hp1 HG01943.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.879+3484A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106109162 | |||||||
| chr2:106109172 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.879+3474A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106109172 | |||||||
| chr2:106109174 | T | G | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.879+3472A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106109174 | |||||||
| chr2:106109304 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.879+3342G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106109304 | |||||||
| chr2:106109472 | C | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.879+3174G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106109472 | |||||||
| chr2:106109664 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.879+2982A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106109664 | |||||||
| chr2:106109717 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.879+2929G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106109717 | |||||||
| chr2:106109728 | C | T | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.879+2918G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106109728 | |||||||
| chr2:106109907 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.879+2739G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106109907 | |||||||
| chr2:106109910 | G | A | 1 | a0001c0001t0003g0273 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.879+2736C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106109910 | |||||||
| chr2:106110224 | A | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.879+2422T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106110224 | |||||||
| chr2:106110235 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.879+2411C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106110235 | |||||||
| chr2:106110505 | C | A | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.879+2141G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106110505 | |||||||
| chr2:106110554 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(27): Show |
32 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.879+2092C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106110554 | |||||||
| chr2:106110574 | G | A | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.879+2072C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106110574 | |||||||
| chr2:106110672 | T | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.879+1974A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106110672 | |||||||
| chr2:106110690 | C | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0135 |
2 | NA18998.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.879+1956G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106110690 | |||||||
| chr2:106111000 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(27): Show |
32 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.879+1646C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106111000 | |||||||
| chr2:106111755 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.879+891T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106111755 | |||||||
| chr2:106111758 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.879+888T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106111758 | |||||||
| chr2:106111917 | C | G | 1 | a0001c0001t0006g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.879+729G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106111917 | |||||||
| chr2:106111947 | G | T | 3 | a0001c0002t0004g0029 a0001c0002t0004g0030 a0001c0002t0004g0032 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.879+699C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106111947 | |||||||
| chr2:106112040 | A | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(261): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.879+606T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106112040 | |||||||
| chr2:106112097 | G | A | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.879+549C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106112097 | |||||||
| chr2:106112145 | C | T | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.879+501G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106112145 | |||||||
| chr2:106112166 | G | C | 1 | a0001c0001t0001g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.879+480C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106112166 | |||||||
| chr2:106112339 | T | G | 36 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0039 others(33): Show |
41 | HG00140.hp1 HG00621.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.879+307A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106112339 | |||||||
| chr2:106112417 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.879+229C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106112417 | |||||||
| chr2:106112583 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.879+63A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 10/14 | chr2 | 106112583 | |||||||
| chr2:106112814 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.760-49G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106112814 | |||||||
| chr2:106112937 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.760-172C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106112937 | |||||||
| chr2:106113055 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.760-290G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106113055 | |||||||
| chr2:106113231 | T | C | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.760-466A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106113231 | |||||||
| chr2:106113536 | A | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(95): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.760-771T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106113536 | |||||||
| chr2:106113691 | C | T | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.760-926G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106113691 | |||||||
| chr2:106113778 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.760-1013C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106113778 | |||||||
| chr2:106114020 | A | T | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(1): Show |
4 | HG00323.hp2 HG01346.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-1255T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106114020 | |||||||
| chr2:106114120 | A | T | 13 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0039 others(10): Show |
13 | HG00140.hp1 HG00621.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.760-1355T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106114120 | |||||||
| chr2:106114403 | G | T | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.760-1638C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106114403 | |||||||
| chr2:106114477 | G | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(56): Show |
64 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.760-1712C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106114477 | |||||||
| chr2:106114816 | C | G | 1 | a0001c0001t0001g0173 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.760-2051G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106114816 | |||||||
| chr2:106114877 | C | A | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.760-2112G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106114877 | |||||||
| chr2:106114942 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.760-2177A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106114942 | |||||||
| chr2:106114960 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
7 | HG00642.hp1 HG01928.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.760-2195G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106114960 | |||||||
| chr2:106115008 | C | T | 1 | a0001c0001t0001g0012 | 2 | NA18944.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.760-2243G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106115008 | |||||||
| chr2:106115167 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.760-2402A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106115167 | |||||||
| chr2:106115336 | T | C | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.760-2571A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106115336 | |||||||
| chr2:106115556 | C | T | 67 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(64): Show |
73 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.760-2791G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106115556 | |||||||
| chr2:106115878 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.760-3113A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106115878 | |||||||
| chr2:106115987 | A | C | 1 | a0001c0001t0002g0105 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.760-3222T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106115987 | |||||||
| chr2:106115988 | C | A | 1 | a0001c0001t0002g0105 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.760-3223G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106115988 | |||||||
| chr2:106116075 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.760-3310A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106116075 | |||||||
| chr2:106116089 | C | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(138): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.760-3324G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106116089 | |||||||
| chr2:106116110 | G | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0054 |
2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.760-3345C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106116110 | |||||||
| chr2:106116123 | G | A | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.760-3358C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106116123 | |||||||
| chr2:106116251 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.760-3486A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106116251 | |||||||
| chr2:106116415 | C | T | 21 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(18): Show |
26 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.760-3650G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106116415 | |||||||
| chr2:106116423 | C | T | 23 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(20): Show |
24 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.760-3658G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106116423 | |||||||
| chr2:106116605 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0142 |
3 | NA18953.hp2 NA18962.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.760-3840G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106116605 | |||||||
| chr2:106116975 | A | G | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.760-4210T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106116975 | |||||||
| chr2:106117040 | G | C | 1 | a0001c0001t0001g0034 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.760-4275C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106117040 | |||||||
| chr2:106117062 | C | T | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.760-4297G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106117062 | |||||||
| chr2:106117098 | C | T | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.760-4333G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106117098 | |||||||
| chr2:106117172 | C | G | 1 | a0001c0002t0004g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.760-4407G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106117172 | |||||||
| chr2:106117533 | G | GT | 68 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(65): Show |
73 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.760-4769dupA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106117533 | |||||||
| chr2:106117609 | G | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(20): Show |
24 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.760-4844C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106117609 | |||||||
| chr2:106117685 | C | G | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.760-4920G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106117685 | |||||||
| chr2:106117808 | G | A | 21 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(18): Show |
26 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.760-5043C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106117808 | |||||||
| chr2:106118195 | G | C | 1 | a0001c0001t0006g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.759+4775C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106118195 | |||||||
| chr2:106118222 | CT | C | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.759+4747delA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106118222 | |||||||
| chr2:106118421 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.759+4549C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106118421 | |||||||
| chr2:106118436 | C | CA | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(48): Show |
58 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.759+4533dupT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106118436 | |||||||
| chr2:106118932 | T | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0158 |
3 | HG02145.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.759+4038A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106118932 | |||||||
| chr2:106118937 | T | G | 70 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(67): Show |
77 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.759+4033A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106118937 | |||||||
| chr2:106118997 | T | G | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.759+3973A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106118997 | |||||||
| chr2:106119034 | C | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(20): Show |
24 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.759+3936G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106119034 | |||||||
| chr2:106119062 | T | G | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.759+3908A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106119062 | |||||||
| chr2:106119074 | T | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0210 a0001c0001t0001g0213 others(2): Show |
6 | HG02523.hp1 NA18940.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.759+3896A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106119074 | |||||||
| chr2:106119626 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.759+3344C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106119626 | |||||||
| chr2:106119645 | C | G | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.759+3325G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106119645 | |||||||
| chr2:106119857 | T | C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(48): Show |
58 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.759+3113A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106119857 | |||||||
| chr2:106119889 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.759+3081A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106119889 | |||||||
| chr2:106120312 | A | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.759+2658T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106120312 | |||||||
| chr2:106120376 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.759+2594C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106120376 | |||||||
| chr2:106120438 | G | A | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.759+2532C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106120438 | |||||||
| chr2:106120521 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.759+2449G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106120521 | |||||||
| chr2:106120574 | T | C | 3 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0250 |
3 | HG00423.hp2 NA18998.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.759+2396A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106120574 | |||||||
| chr2:106120753 | C | G | 62 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
68 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.759+2217G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106120753 | |||||||
| chr2:106120814 | A | G | 72 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
79 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.759+2156T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106120814 | |||||||
| chr2:106120844 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.759+2126G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106120844 | |||||||
| chr2:106120845 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.759+2125C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106120845 | |||||||
| chr2:106120879 | C | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.759+2091G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106120879 | |||||||
| chr2:106120934 | C | T | 1 | a0001c0001t0003g0271 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.759+2036G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106120934 | |||||||
| chr2:106121462 | G | A | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.759+1508C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106121462 | |||||||
| chr2:106121469 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.759+1501T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106121469 | |||||||
| chr2:106121525 | T | C | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.759+1445A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106121525 | |||||||
| chr2:106121528 | T | A | 1 | a0001c0001t0001g0066 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.759+1442A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106121528 | |||||||
| chr2:106121604 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.759+1366A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106121604 | |||||||
| chr2:106121661 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.759+1309A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106121661 | |||||||
| chr2:106122136 | G | A | 1 | a0001c0001t0003g0281 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.759+834C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106122136 | |||||||
| chr2:106122169 | C | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(141): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.759+801G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106122169 | |||||||
| chr2:106122379 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.759+591T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106122379 | |||||||
| chr2:106122460 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.759+510C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106122460 | |||||||
| chr2:106122615 | T | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.759+355A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106122615 | |||||||
| chr2:106122686 | T | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0137 |
2 | HG00621.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.759+284A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106122686 | |||||||
| chr2:106122866 | C | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG00642.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.759+104G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106122866 | |||||||
| chr2:106122911 | C | T | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG02015.hp2 NA18972.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.759+59G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 9/14 | chr2 | 106122911 | |||||||
| chr2:106123142 | A | C | 21 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(18): Show |
26 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.638-51T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106123142 | |||||||
| chr2:106123296 | AG | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.638-206delC | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106123296 | |||||||
| chr2:106123299 | GGA | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
10 | HG00642.hp1 HG01928.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-210_638-209del others(2): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106123299 | |||||||
| chr2:106123300 | G | A | 80 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(77): Show |
87 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.638-209C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106123300 | |||||||
| chr2:106123401 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.638-310A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106123401 | |||||||
| chr2:106123496 | C | T | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.638-405G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106123496 | |||||||
| chr2:106123679 | T | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0158 |
3 | HG02145.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.638-588A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106123679 | |||||||
| chr2:106123959 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0080 others(1): Show |
4 | HG00099.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-868C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106123959 | |||||||
| chr2:106124132 | T | C | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.638-1041A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106124132 | |||||||
| chr2:106124176 | C | G | 14 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0039 others(11): Show |
14 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.638-1085G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106124176 | |||||||
| chr2:106124393 | T | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.637+1227A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106124393 | |||||||
| chr2:106124867 | A | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0086 others(2): Show |
6 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+753T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106124867 | |||||||
| chr2:106124875 | G | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0054 |
2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.637+745C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106124875 | |||||||
| chr2:106125080 | T | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.637+540A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106125080 | |||||||
| chr2:106125316 | G | A | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.637+304C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106125316 | |||||||
| chr2:106125358 | C | A | 2 | a0001c0001t0005g0089 a0001c0001t0010g0248 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.637+262G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106125358 | |||||||
| chr2:106125363 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.637+257C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106125363 | |||||||
| chr2:106125397 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0170 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.637+223C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106125397 | |||||||
| chr2:106125469 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.637+151G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106125469 | |||||||
| chr2:106125475 | G | A | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.637+145C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106125475 | |||||||
| chr2:106125501 | C | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(21): Show |
28 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.637+119G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 8/14 | chr2 | 106125501 | |||||||
| chr2:106125683 | C | T | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(264): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
splice_region_variant&intron_variant | LOW | c.578-4G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106125683 | |||||||
| chr2:106125721 | T | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.578-42A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106125721 | |||||||
| chr2:106125731 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.578-52G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106125731 | |||||||
| chr2:106125752 | A | G | 1 | a0001c0001t0003g0270 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.578-73T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106125752 | |||||||
| chr2:106125900 | C | T | 69 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(66): Show |
76 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.578-221G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106125900 | |||||||
| chr2:106126204 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(162): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.578-525T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106126204 | |||||||
| chr2:106126261 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.578-582G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106126261 | |||||||
| chr2:106126322 | T | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0042 others(16): Show |
20 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.578-643A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106126322 | |||||||
| chr2:106126363 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.578-684C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106126363 | |||||||
| chr2:106126390 | G | A | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.578-711C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106126390 | |||||||
| chr2:106126395 | AC | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.578-717delG | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106126395 | |||||||
| chr2:106126527 | T | C | 70 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(67): Show |
77 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.578-848A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106126527 | |||||||
| chr2:106127063 | T | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0185 a0001c0001t0001g0188 |
4 | HG00438.hp1 HG02165.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.578-1384A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106127063 | |||||||
| chr2:106127238 | T | C | 24 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0158 others(21): Show |
29 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.578-1559A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106127238 | |||||||
| chr2:106127303 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.578-1624A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106127303 | |||||||
| chr2:106127594 | A | T | 1 | a0001c0001t0001g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.578-1915T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106127594 | |||||||
| chr2:106127851 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0184 |
2 | HG00639.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.577+1823A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106127851 | |||||||
| chr2:106127861 | C | A | 3 | a0001c0002t0004g0029 a0001c0002t0004g0030 a0001c0002t0004g0032 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.577+1813G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106127861 | |||||||
| chr2:106127875 | T | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(264): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.577+1799A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106127875 | |||||||
| chr2:106128147 | T | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.577+1527A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106128147 | |||||||
| chr2:106128148 | G | A | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.577+1526C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106128148 | |||||||
| chr2:106128218 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.577+1456C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106128218 | |||||||
| chr2:106128277 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.577+1397C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106128277 | |||||||
| chr2:106128401 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0159 a0001c0001t0001g0165 |
4 | HG02451.hp1 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.577+1273A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106128401 | |||||||
| chr2:106128440 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.577+1234C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106128440 | |||||||
| chr2:106128470 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.577+1204C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106128470 | |||||||
| chr2:106128588 | C | T | 27 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0035 others(24): Show |
29 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.577+1086G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106128588 | |||||||
| chr2:106129121 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0267 |
2 | HG00642.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.577+553A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106129121 | |||||||
| chr2:106129360 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0088 |
2 | HG00738.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.577+314C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106129360 | |||||||
| chr2:106129459 | G | A | 1 | a0001c0001t0006g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.577+215C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106129459 | |||||||
| chr2:106129487 | T | C | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.577+187A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 7/14 | chr2 | 106129487 | |||||||
| chr2:106130193 | A | C | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.473-415T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106130193 | |||||||
| chr2:106130553 | G | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(163): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.473-775C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106130553 | |||||||
| chr2:106130624 | T | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(264): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.473-846A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106130624 | |||||||
| chr2:106130701 | G | A | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.473-923C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106130701 | |||||||
| chr2:106130811 | C | T | 3 | a0001c0002t0004g0029 a0001c0002t0004g0030 a0001c0002t0004g0032 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.473-1033G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106130811 | |||||||
| chr2:106130955 | C | T | 67 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(64): Show |
73 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.473-1177G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106130955 | |||||||
| chr2:106131060 | G | A | 2 | a0001c0001t0005g0037 a0001c0001t0005g0038 |
2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.473-1282C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131060 | |||||||
| chr2:106131125 | G | C | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.473-1347C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131125 | |||||||
| chr2:106131139 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0057 |
2 | HG01192.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.473-1361C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131139 | |||||||
| chr2:106131211 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.473-1433C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131211 | |||||||
| chr2:106131214 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.473-1436C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131214 | |||||||
| chr2:106131221 | G | A | 27 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0035 others(24): Show |
29 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.473-1443C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131221 | |||||||
| chr2:106131232 | C | T | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(48): Show |
58 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.473-1454G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131232 | |||||||
| chr2:106131336 | G | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.473-1558C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131336 | |||||||
| chr2:106131376 | G | T | 24 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0158 others(21): Show |
29 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.473-1598C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131376 | |||||||
| chr2:106131385 | G | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG03927.hp2 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.473-1607C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131385 | |||||||
| chr2:106131390 | G | C | 1 | a0001c0001t0001g0026 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.473-1612C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131390 | |||||||
| chr2:106131473 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.473-1695T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131473 | |||||||
| chr2:106131597 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.473-1819G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131597 | |||||||
| chr2:106131633 | C | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0053 |
2 | HG01928.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.473-1855G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131633 | |||||||
| chr2:106131640 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0053 |
2 | HG01928.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.473-1862C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131640 | |||||||
| chr2:106131662 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.473-1884C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131662 | |||||||
| chr2:106131664 | A | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0068 a0001c0001t0001g0113 others(1): Show |
4 | HG00280.hp1 HG01106.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-1886T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131664 | |||||||
| chr2:106131670 | T | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0068 a0001c0001t0001g0113 others(1): Show |
4 | HG00280.hp1 HG01106.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-1892A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131670 | |||||||
| chr2:106131691 | G | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0068 a0001c0001t0001g0113 others(1): Show |
4 | HG00280.hp1 HG01106.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-1913C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131691 | |||||||
| chr2:106131932 | A | G | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(48): Show |
58 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.473-2154T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131932 | |||||||
| chr2:106131933 | A | C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(48): Show |
58 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.473-2155T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106131933 | |||||||
| chr2:106132403 | G | C | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.473-2625C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106132403 | |||||||
| chr2:106132432 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.473-2654C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106132432 | |||||||
| chr2:106132569 | C | A | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.473-2791G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106132569 | |||||||
| chr2:106132819 | C | T | 22 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
23 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.473-3041G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106132819 | |||||||
| chr2:106132823 | C | T | 30 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0129 others(27): Show |
32 | HG00597.hp1 HG00735.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.473-3045G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106132823 | |||||||
| chr2:106133011 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.473-3233G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106133011 | |||||||
| chr2:106133129 | T | G | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.473-3351A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106133129 | |||||||
| chr2:106133402 | C | T | 32 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0153 others(29): Show |
34 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.473-3624G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106133402 | |||||||
| chr2:106133614 | C | T | 24 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0158 others(21): Show |
29 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.473-3836G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106133614 | |||||||
| chr2:106133662 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.473-3884C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106133662 | |||||||
| chr2:106133671 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.473-3893C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106133671 | |||||||
| chr2:106133746 | G | A | 24 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0158 others(21): Show |
29 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.473-3968C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106133746 | |||||||
| chr2:106133791 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.473-4013A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106133791 | |||||||
| chr2:106133819 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(123): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.473-4041A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106133819 | |||||||
| chr2:106133825 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0091 |
2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.473-4047G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106133825 | |||||||
| chr2:106133877 | A | G | 3 | a0001c0002t0004g0029 a0001c0002t0004g0030 a0001c0002t0004g0032 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.473-4099T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106133877 | |||||||
| chr2:106134007 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.473-4229C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134007 | |||||||
| chr2:106134081 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0158 |
3 | HG02145.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.473-4303G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134081 | |||||||
| chr2:106134085 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.473-4307G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134085 | |||||||
| chr2:106134137 | G | A | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.473-4359C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134137 | |||||||
| chr2:106134179 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(141): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.473-4401C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134179 | |||||||
| chr2:106134337 | G | A | 3 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 |
3 | HG02109.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.473-4559C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134337 | |||||||
| chr2:106134527 | C | A | 1 | a0001c0001t0001g0199 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.473-4749G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134527 | |||||||
| chr2:106134528 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.473-4750C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134528 | |||||||
| chr2:106134531 | T | C | 3 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 |
3 | HG02109.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.473-4753A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134531 | |||||||
| chr2:106134585 | C | G | 30 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(27): Show |
32 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.473-4807G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134585 | |||||||
| chr2:106134711 | C | G | 3 | a0001c0002t0004g0029 a0001c0002t0004g0030 a0001c0002t0004g0032 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.473-4933G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134711 | |||||||
| chr2:106134874 | G | A | 4 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0250 others(1): Show |
4 | HG00423.hp2 HG00597.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.473-5096C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134874 | |||||||
| chr2:106134888 | T | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(65): Show |
73 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.473-5110A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134888 | |||||||
| chr2:106134900 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.473-5122A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134900 | |||||||
| chr2:106134925 | G | A | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.473-5147C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134925 | |||||||
| chr2:106134972 | C | G | 1 | a0001c0001t0001g0202 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.473-5194G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134972 | |||||||
| chr2:106134985 | C | T | 21 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(18): Show |
26 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.473-5207G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106134985 | |||||||
| chr2:106135016 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.473-5238C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106135016 | |||||||
| chr2:106135040 | C | T | 22 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
23 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.473-5262G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106135040 | |||||||
| chr2:106135102 | C | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0069 others(1): Show |
4 | HG02630.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.473-5324G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106135102 | |||||||
| chr2:106135106 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.473-5328A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106135106 | |||||||
| chr2:106135445 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.473-5667T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106135445 | |||||||
| chr2:106135520 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(141): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.473-5742C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106135520 | |||||||
| chr2:106135606 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0158 |
3 | HG02145.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.473-5828C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106135606 | |||||||
| chr2:106135687 | C | T | 3 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0002g0160 |
3 | HG03834.hp1 HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.473-5909G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106135687 | |||||||
| chr2:106135847 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0006g0182 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.473-6069C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106135847 | |||||||
| chr2:106135977 | T | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.473-6199A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106135977 | |||||||
| chr2:106136097 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.473-6319G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136097 | |||||||
| chr2:106136098 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.473-6320C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136098 | |||||||
| chr2:106136108 | A | C | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.473-6330T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136108 | |||||||
| chr2:106136145 | A | G | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.473-6367T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136145 | |||||||
| chr2:106136236 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.473-6458C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136236 | |||||||
| chr2:106136243 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.473-6465T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136243 | |||||||
| chr2:106136382 | C | T | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.473-6604G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136382 | |||||||
| chr2:106136412 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.473-6634C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136412 | |||||||
| chr2:106136512 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.473-6734G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136512 | |||||||
| chr2:106136612 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.473-6834C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136612 | |||||||
| chr2:106136655 | C | T | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.473-6877G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136655 | |||||||
| chr2:106136704 | T | C | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | NA18969.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.473-6926A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136704 | |||||||
| chr2:106136777 | G | C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(48): Show |
58 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.473-6999C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136777 | |||||||
| chr2:106136965 | C | CA | 38 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0033 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.473-7188dupT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136965 | |||||||
| chr2:106136965 | CA | C | 8 | a0001c0001t0001g0146 a0001c0001t0001g0177 a0001c0001t0001g0183 others(5): Show |
8 | HG00438.hp1 HG00639.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.473-7188delT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136965 | |||||||
| chr2:106136967 | A | C | 2 | a0001c0001t0005g0037 a0001c0001t0005g0038 |
2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.473-7189T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136967 | |||||||
| chr2:106136983 | A | G | 21 | a0001c0001t0001g0196 a0001c0001t0002g0001 a0001c0001t0002g0007 others(18): Show |
26 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.473-7205T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106136983 | |||||||
| chr2:106137008 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.473-7230C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106137008 | |||||||
| chr2:106137143 | TAAAA | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.473-7369_473-7366d others(6): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106137143 | |||||||
| chr2:106137274 | G | T | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.473-7496C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106137274 | |||||||
| chr2:106137645 | A | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.472+7545T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106137645 | |||||||
| chr2:106137887 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.472+7303G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106137887 | |||||||
| chr2:106138236 | G | A | 67 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(64): Show |
73 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.472+6954C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106138236 | |||||||
| chr2:106138263 | C | T | 62 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
68 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.472+6927G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106138263 | |||||||
| chr2:106138278 | A | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.472+6912T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106138278 | |||||||
| chr2:106138390 | T | C | 67 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(64): Show |
73 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.472+6800A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106138390 | |||||||
| chr2:106138451 | C | T | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.472+6739G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106138451 | |||||||
| chr2:106138735 | G | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.472+6455C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106138735 | |||||||
| chr2:106139037 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.472+6153T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106139037 | |||||||
| chr2:106139060 | C | G | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.472+6130G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106139060 | |||||||
| chr2:106139066 | AGCCCAGG others(6): Show |
A | 21 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(18): Show |
26 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.472+6111_472+6123d others(15): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106139066 | |||||||
| chr2:106139098 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.472+6092G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106139098 | |||||||
| chr2:106139108 | C | G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0063 others(12): Show |
16 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.472+6082G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106139108 | |||||||
| chr2:106139204 | C | A | 1 | a0001c0001t0001g0231 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.472+5986G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106139204 | |||||||
| chr2:106139225 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0267 |
3 | HG00642.hp1 HG02300.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.472+5965C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106139225 | |||||||
| chr2:106139241 | C | G | 24 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0158 others(21): Show |
29 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.472+5949G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106139241 | |||||||
| chr2:106139529 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.472+5661G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106139529 | |||||||
| chr2:106139539 | A | G | 4 | a0001c0001t0001g0084 a0001c0001t0005g0037 a0001c0001t0005g0038 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.472+5651T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106139539 | |||||||
| chr2:106139569 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.472+5621C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106139569 | |||||||
| chr2:106139788 | T | C | 3 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0002g0160 |
3 | HG03834.hp1 HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.472+5402A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106139788 | |||||||
| chr2:106139971 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.472+5219G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106139971 | |||||||
| chr2:106139977 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.472+5213A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106139977 | |||||||
| chr2:106140044 | T | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0023 |
3 | HG01928.hp1 HG01943.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.472+5146A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106140044 | |||||||
| chr2:106140154 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.472+5036G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106140154 | |||||||
| chr2:106140214 | C | A | 1 | a0001c0001t0001g0117 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.472+4976G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106140214 | |||||||
| chr2:106140235 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.472+4955C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106140235 | |||||||
| chr2:106140273 | AT | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.472+4916delA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106140273 | |||||||
| chr2:106140469 | T | C | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.472+4721A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106140469 | |||||||
| chr2:106140528 | G | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0001g0203 others(2): Show |
6 | HG01099.hp2 HG01496.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.472+4662C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106140528 | |||||||
| chr2:106140687 | G | A | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(48): Show |
58 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.472+4503C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106140687 | |||||||
| chr2:106140838 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01891.hp2 HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.472+4352G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106140838 | |||||||
| chr2:106140909 | G | C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(48): Show |
58 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.472+4281C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106140909 | |||||||
| chr2:106141033 | A | C | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.472+4157T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106141033 | |||||||
| chr2:106141116 | G | C | 24 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0158 others(21): Show |
29 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.472+4074C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106141116 | |||||||
| chr2:106141167 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.472+4023T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106141167 | |||||||
| chr2:106141396 | G | C | 21 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(18): Show |
26 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.472+3794C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106141396 | |||||||
| chr2:106141608 | C | T | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(48): Show |
58 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.472+3582G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106141608 | |||||||
| chr2:106141865 | G | GT | 171 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.472+3324dupA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106141865 | |||||||
| chr2:106141865 | G | GTT | 8 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
9 | HG00642.hp1 HG01928.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.472+3323_472+3324d others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106141865 | |||||||
| chr2:106141877 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.472+3313C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106141877 | |||||||
| chr2:106142005 | C | T | 2 | a0001c0001t0002g0103 a0001c0001t0002g0107 |
2 | NA18947.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.472+3185G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106142005 | |||||||
| chr2:106142006 | G | A | 1 | a0001c0001t0006g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.472+3184C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106142006 | |||||||
| chr2:106142021 | C | T | 3 | a0001c0002t0004g0029 a0001c0002t0004g0030 a0001c0002t0004g0032 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.472+3169G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106142021 | |||||||
| chr2:106142161 | C | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.472+3029G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106142161 | |||||||
| chr2:106142162 | A | G | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.472+3028T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106142162 | |||||||
| chr2:106142173 | A | G | 27 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0035 others(24): Show |
29 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.472+3017T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106142173 | |||||||
| chr2:106142397 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472+2793A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106142397 | |||||||
| chr2:106142599 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.472+2591A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106142599 | |||||||
| chr2:106142707 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.472+2483G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106142707 | |||||||
| chr2:106142923 | A | ATG | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.472+2265_472+2266d others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106142923 | |||||||
| chr2:106143089 | A | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
10 | HG00642.hp1 HG01928.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.472+2101T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143089 | |||||||
| chr2:106143148 | A | G | 6 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0249 others(3): Show |
6 | HG01891.hp1 HG02258.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.472+2042T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143148 | |||||||
| chr2:106143232 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.472+1958G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143232 | |||||||
| chr2:106143272 | G | C | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.472+1918C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143272 | |||||||
| chr2:106143336 | G | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0057 |
2 | HG01192.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.472+1854C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143336 | |||||||
| chr2:106143341 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.472+1849T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143341 | |||||||
| chr2:106143349 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.472+1841G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143349 | |||||||
| chr2:106143380 | GCC | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0001g0203 others(2): Show |
6 | HG01099.hp2 HG01496.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.472+1808_472+1809d others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143380 | |||||||
| chr2:106143385 | G | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0001g0203 others(2): Show |
6 | HG01099.hp2 HG01496.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.472+1805C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143385 | |||||||
| chr2:106143386 | G | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0001g0203 others(2): Show |
6 | HG01099.hp2 HG01496.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.472+1804C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143386 | |||||||
| chr2:106143387 | CAACAGAG others(43): Show |
C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0001g0203 others(2): Show |
6 | HG01099.hp2 HG01496.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.472+1753_472+1802d others(52): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143387 | |||||||
| chr2:106143408 | C | CA | 16 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0050 others(13): Show |
16 | HG01106.hp2 HG01891.hp2 HG02300.hp1 others(13): Show |
intron_variant | MODIFIER | c.472+1781dupT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143408 | |||||||
| chr2:106143408 | C | CAAAAAAA others(1): Show |
23 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0023 others(20): Show |
24 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.472+1774_472+1781d others(10): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143408 | |||||||
| chr2:106143408 | C | CAAAAAAA others(2): Show |
42 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
43 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.472+1773_472+1781d others(11): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143408 | |||||||
| chr2:106143408 | C | CAAAAAAA others(3): Show |
20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0040 others(17): Show |
20 | HG00323.hp2 HG00639.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.472+1772_472+1781d others(12): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143408 | |||||||
| chr2:106143408 | C | CAAAAAAA others(4): Show |
7 | a0001c0001t0001g0172 a0001c0001t0001g0209 a0001c0001t0001g0225 others(4): Show |
7 | HG00408.hp2 HG02040.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.472+1771_472+1781d others(13): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143408 | |||||||
| chr2:106143408 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0213 a0001c0001t0001g0229 |
2 | NA19005.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.472+1770_472+1781d others(14): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143408 | |||||||
| chr2:106143408 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.472+1763_472+1781d others(21): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143408 | |||||||
| chr2:106143408 | CAA | C | 18 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(15): Show |
18 | HG00597.hp2 HG01123.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.472+1780_472+1781d others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143408 | |||||||
| chr2:106143408 | CAAA | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
53 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.472+1779_472+1781d others(5): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143408 | |||||||
| chr2:106143408 | CAAAA | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0017 others(15): Show |
20 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.472+1778_472+1781d others(6): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143408 | |||||||
| chr2:106143408 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0268 |
3 | HG00738.hp1 HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.472+1772_472+1781d others(12): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143408 | |||||||
| chr2:106143408 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.472+1769_472+1781d others(15): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143408 | |||||||
| chr2:106143408 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.472+1768_472+1781d others(16): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143408 | |||||||
| chr2:106143408 | CAAAAAAA others(14): Show |
C | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.472+1761_472+1781d others(23): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143408 | |||||||
| chr2:106143431 | AAAAAAAA others(1): Show |
A | 18 | a0001c0001t0001g0031 a0001c0001t0001g0097 a0001c0001t0002g0001 others(15): Show |
22 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.472+1751_472+1758d others(10): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143431 | |||||||
| chr2:106143432 | AAAAAAAG | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0086 others(9): Show |
13 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.472+1751_472+1757d others(9): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143432 | |||||||
| chr2:106143439 | G | A | 29 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(26): Show |
30 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.472+1751C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143439 | |||||||
| chr2:106143545 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.472+1645G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143545 | |||||||
| chr2:106143562 | T | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.472+1628A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143562 | |||||||
| chr2:106143579 | C | T | 1 | a0001c0002t0004g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.472+1611G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143579 | |||||||
| chr2:106143580 | G | A | 1 | a0001c0001t0003g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.472+1610C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143580 | |||||||
| chr2:106143651 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.472+1539C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143651 | |||||||
| chr2:106143870 | C | G | 1 | a0001c0001t0001g0005 | 2 | HG00099.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.472+1320G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143870 | |||||||
| chr2:106143872 | C | A | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.472+1318G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106143872 | |||||||
| chr2:106144111 | G | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.472+1079C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106144111 | |||||||
| chr2:106144377 | A | T | 1 | a0001c0001t0001g0218 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.472+813T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106144377 | |||||||
| chr2:106144715 | G | A | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(138): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.472+475C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106144715 | |||||||
| chr2:106144894 | T | C | 265 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(262): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.472+296A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106144894 | |||||||
| chr2:106144980 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.472+210C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 6/14 | chr2 | 106144980 | |||||||
| chr2:106145535 | AC | A | 6 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0105 others(3): Show |
6 | NA18947.hp1 NA18968.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-166delG | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106145535 | |||||||
| chr2:106145693 | C | A | 1 | a0001c0001t0001g0040 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.292-323G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106145693 | |||||||
| chr2:106145910 | T | C | 143 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(140): Show |
156 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.292-540A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106145910 | |||||||
| chr2:106146007 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.292-637A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146007 | |||||||
| chr2:106146032 | G | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.292-662C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146032 | |||||||
| chr2:106146049 | A | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
5 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-679T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146049 | |||||||
| chr2:106146085 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.292-715G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146085 | |||||||
| chr2:106146188 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0224 |
2 | HG01069.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.292-818C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146188 | |||||||
| chr2:106146280 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.292-910A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146280 | |||||||
| chr2:106146303 | T | G | 1 | a0001c0001t0001g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.292-933A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146303 | |||||||
| chr2:106146329 | T | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.292-959A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146329 | |||||||
| chr2:106146331 | T | C | 11 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0040 others(8): Show |
11 | HG00140.hp1 HG00408.hp2 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-961A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146331 | |||||||
| chr2:106146388 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.292-1018A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146388 | |||||||
| chr2:106146470 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.292-1100G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146470 | |||||||
| chr2:106146587 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.292-1217C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146587 | |||||||
| chr2:106146588 | G | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.292-1218C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146588 | |||||||
| chr2:106146606 | C | G | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(1): Show |
4 | HG00735.hp2 HG01071.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-1236G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146606 | |||||||
| chr2:106146630 | A | AT | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.292-1261dupA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146630 | |||||||
| chr2:106146648 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.292-1278G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146648 | |||||||
| chr2:106146772 | C | CA | 44 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(41): Show |
47 | HG00597.hp1 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.292-1403dupT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146772 | |||||||
| chr2:106146772 | C | CAA | 39 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(36): Show |
41 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.292-1404_292-1403d others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146772 | |||||||
| chr2:106146772 | C | CAAA | 10 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0045 others(7): Show |
10 | HG00280.hp1 HG00621.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.292-1405_292-1403d others(5): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146772 | |||||||
| chr2:106146772 | CA | C | 31 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0031 others(28): Show |
36 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(33): Show |
intron_variant | MODIFIER | c.292-1403delT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146772 | |||||||
| chr2:106146772 | CAAAAAAA others(3): Show |
C | 60 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
66 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.292-1412_292-1403d others(12): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146772 | |||||||
| chr2:106146772 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0229 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.292-1413_292-1403d others(13): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146772 | |||||||
| chr2:106146870 | T | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.292-1500A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146870 | |||||||
| chr2:106146901 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.292-1531G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146901 | |||||||
| chr2:106146958 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-1588C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106146958 | |||||||
| chr2:106147013 | C | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0043 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.292-1643G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106147013 | |||||||
| chr2:106147197 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.292-1827C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106147197 | |||||||
| chr2:106147295 | A | G | 26 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(23): Show |
31 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(28): Show |
intron_variant | MODIFIER | c.292-1925T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106147295 | |||||||
| chr2:106147634 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.292-2264G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106147634 | |||||||
| chr2:106148159 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.292-2789T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106148159 | |||||||
| chr2:106148330 | T | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.292-2960A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106148330 | |||||||
| chr2:106148677 | G | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.292-3307C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106148677 | |||||||
| chr2:106148742 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.292-3372A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106148742 | |||||||
| chr2:106149190 | A | G | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.292-3820T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106149190 | |||||||
| chr2:106149352 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.292-3982G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106149352 | |||||||
| chr2:106149364 | T | C | 22 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0007 others(19): Show |
27 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.292-3994A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106149364 | |||||||
| chr2:106149526 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.292-4156A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106149526 | |||||||
| chr2:106149666 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.292-4296G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106149666 | |||||||
| chr2:106149816 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
7 | HG00642.hp1 HG01928.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.292-4446T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106149816 | |||||||
| chr2:106149950 | T | C | 2 | a0001c0001t0002g0008 a0001c0001t0002g0152 |
3 | HG02080.hp2 HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.292-4580A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106149950 | |||||||
| chr2:106150024 | G | A | 56 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(53): Show |
58 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.292-4654C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106150024 | |||||||
| chr2:106150257 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.292-4887G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106150257 | |||||||
| chr2:106150451 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.292-5081C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106150451 | |||||||
| chr2:106150558 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0042 |
3 | HG03540.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.292-5188C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106150558 | |||||||
| chr2:106150666 | T | G | 1 | a0001c0001t0001g0134 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.292-5296A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106150666 | |||||||
| chr2:106150700 | G | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0098 |
3 | NA18993.hp1 NA18999.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.292-5330C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106150700 | |||||||
| chr2:106150760 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.292-5390C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106150760 | |||||||
| chr2:106150819 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0063 others(10): Show |
14 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.292-5449G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106150819 | |||||||
| chr2:106151123 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.292-5753T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106151123 | |||||||
| chr2:106151327 | T | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.292-5957A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106151327 | |||||||
| chr2:106151381 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.292-6011A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106151381 | |||||||
| chr2:106151522 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.292-6152C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106151522 | |||||||
| chr2:106151754 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.291+6304T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106151754 | |||||||
| chr2:106151866 | A | G | 13 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0063 others(10): Show |
14 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.291+6192T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106151866 | |||||||
| chr2:106152494 | AGAGG | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.291+5560_291+5563d others(6): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106152494 | |||||||
| chr2:106152557 | AGAAAGGA others(2): Show |
A | 46 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0034 others(43): Show |
47 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.291+5492_291+5500d others(11): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106152557 | |||||||
| chr2:106152575 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.291+5483C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106152575 | |||||||
| chr2:106152576 | GAAAGGAA others(7): Show |
G | 1 | a0001c0001t0001g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.291+5468_291+5481d others(16): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106152576 | |||||||
| chr2:106152756 | A | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.291+5302T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106152756 | |||||||
| chr2:106152775 | A | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.291+5283T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106152775 | |||||||
| chr2:106152873 | GA | G | 52 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0033 others(49): Show |
54 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.291+5184delT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106152873 | |||||||
| chr2:106153131 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.291+4927C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106153131 | |||||||
| chr2:106153158 | CA | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+4899delT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106153158 | |||||||
| chr2:106153268 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0042 |
3 | HG03540.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.291+4790G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106153268 | |||||||
| chr2:106153376 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.291+4682T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106153376 | |||||||
| chr2:106153603 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.291+4455C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106153603 | |||||||
| chr2:106154065 | CA | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01891.hp2 HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.291+3992delT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106154065 | |||||||
| chr2:106154188 | T | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG03927.hp2 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.291+3870A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106154188 | |||||||
| chr2:106154282 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.291+3776C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106154282 | |||||||
| chr2:106154338 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.291+3720G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106154338 | |||||||
| chr2:106154442 | G | A | 46 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0034 others(43): Show |
47 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.291+3616C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106154442 | |||||||
| chr2:106154826 | C | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.291+3232G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106154826 | |||||||
| chr2:106154844 | G | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG02723.hp2 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.291+3214C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106154844 | |||||||
| chr2:106154978 | A | G | 22 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0007 others(19): Show |
27 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.291+3080T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106154978 | |||||||
| chr2:106155063 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0063 others(10): Show |
14 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.291+2995G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106155063 | |||||||
| chr2:106155132 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+2926G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106155132 | |||||||
| chr2:106155135 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.291+2923T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106155135 | |||||||
| chr2:106155334 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0054 |
2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.291+2724G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106155334 | |||||||
| chr2:106155357 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+2701C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106155357 | |||||||
| chr2:106155369 | G | C | 60 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
66 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.291+2689C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106155369 | |||||||
| chr2:106155618 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.291+2440T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106155618 | |||||||
| chr2:106155656 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.291+2402C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106155656 | |||||||
| chr2:106155659 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.291+2399C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106155659 | |||||||
| chr2:106155734 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.291+2324G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106155734 | |||||||
| chr2:106155869 | A | T | 1 | a0001c0001t0001g0221 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.291+2189T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106155869 | |||||||
| chr2:106155915 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.291+2143G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106155915 | |||||||
| chr2:106155933 | C | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0085 others(9): Show |
14 | HG02129.hp2 HG02148.hp1 HG03490.hp1 others(11): Show |
intron_variant | MODIFIER | c.291+2125G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106155933 | |||||||
| chr2:106155933 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.291+2125G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106155933 | |||||||
| chr2:106156020 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.291+2038T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106156020 | |||||||
| chr2:106156140 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.291+1918A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106156140 | |||||||
| chr2:106156221 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.291+1837C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106156221 | |||||||
| chr2:106156589 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.291+1469G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106156589 | |||||||
| chr2:106156622 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.291+1436A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106156622 | |||||||
| chr2:106156671 | A | T | 3 | a0001c0002t0004g0029 a0001c0002t0004g0030 a0001c0002t0004g0032 |
3 | HG02559.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.291+1387T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106156671 | |||||||
| chr2:106157055 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.291+1003T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106157055 | |||||||
| chr2:106157276 | T | TA | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.291+781dupT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106157276 | |||||||
| chr2:106157593 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.291+465C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106157593 | |||||||
| chr2:106157652 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0244 |
2 | NA18979.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.291+406T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106157652 | |||||||
| chr2:106157842 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.291+216T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106157842 | |||||||
| chr2:106157963 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.291+95A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106157963 | |||||||
| chr2:106157969 | A | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0244 |
2 | NA18979.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.291+89T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 5/14 | chr2 | 106157969 | |||||||
| chr2:106158122 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG02630.hp2 | splice_region_variant&intron_variant | LOW | c.231-4A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106158122 | |||||||
| chr2:106158174 | T | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.231-56A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106158174 | |||||||
| chr2:106158686 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
7 | HG00642.hp1 HG01928.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.231-568C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106158686 | |||||||
| chr2:106158767 | C | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.231-649G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106158767 | |||||||
| chr2:106158919 | C | T | 47 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0034 others(44): Show |
48 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.231-801G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106158919 | |||||||
| chr2:106159174 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.231-1056C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106159174 | |||||||
| chr2:106159687 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | NA18972.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.231-1569G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106159687 | |||||||
| chr2:106160050 | C | A | 1 | a0001c0001t0001g0202 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.231-1932G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106160050 | |||||||
| chr2:106160161 | T | C | 2 | a0001c0001t0003g0280 a0001c0001t0003g0281 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.231-2043A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106160161 | |||||||
| chr2:106160199 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0135 |
2 | NA18998.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.231-2081C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106160199 | |||||||
| chr2:106160402 | G | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0043 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.231-2284C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106160402 | |||||||
| chr2:106160407 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.231-2289C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106160407 | |||||||
| chr2:106160420 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.231-2302C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106160420 | |||||||
| chr2:106160460 | G | A | 1 | a0001c0001t0002g0098 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.231-2342C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106160460 | |||||||
| chr2:106160479 | A | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(129): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.231-2361T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106160479 | |||||||
| chr2:106160673 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.231-2555G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106160673 | |||||||
| chr2:106160830 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.231-2712G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106160830 | |||||||
| chr2:106160904 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.230+2763G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106160904 | |||||||
| chr2:106160939 | T | C | 59 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(56): Show |
65 | HG00621.hp2 HG00639.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.230+2728A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106160939 | |||||||
| chr2:106160998 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.230+2669C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106160998 | |||||||
| chr2:106161133 | TG | T | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.230+2533delC | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106161133 | |||||||
| chr2:106161188 | C | CT | 7 | a0001c0001t0001g0177 a0001c0001t0001g0193 a0001c0001t0001g0264 others(4): Show |
7 | HG00738.hp1 HG01981.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.230+2478dupA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106161188 | |||||||
| chr2:106161288 | T | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
9 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.230+2379A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106161288 | |||||||
| chr2:106161478 | A | C | 21 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0007 others(18): Show |
26 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.230+2189T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106161478 | |||||||
| chr2:106161556 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.230+2111C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106161556 | |||||||
| chr2:106161820 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.230+1847G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106161820 | |||||||
| chr2:106161882 | C | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.230+1785G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106161882 | |||||||
| chr2:106162002 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.230+1665T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106162002 | |||||||
| chr2:106162103 | A | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0212 a0001c0001t0001g0239 others(4): Show |
8 | NA18941.hp2 NA18942.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.230+1564T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106162103 | |||||||
| chr2:106162166 | C | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.230+1501G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106162166 | |||||||
| chr2:106162212 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.230+1455A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106162212 | |||||||
| chr2:106162297 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
9 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.230+1370A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106162297 | |||||||
| chr2:106162688 | T | C | 1 | a0001c0001t0003g0270 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.230+979A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106162688 | |||||||
| chr2:106162724 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
13 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.230+943G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106162724 | |||||||
| chr2:106162837 | T | G | 4 | a0001c0001t0001g0031 a0001c0002t0004g0029 a0001c0002t0004g0030 others(1): Show |
4 | HG02559.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.230+830A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106162837 | |||||||
| chr2:106162839 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0054 |
2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.230+828C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106162839 | |||||||
| chr2:106163044 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.230+623A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106163044 | |||||||
| chr2:106163087 | G | A | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0158 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.230+580C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106163087 | |||||||
| chr2:106163093 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.230+574C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106163093 | |||||||
| chr2:106163306 | T | G | 1 | a0001c0001t0005g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.230+361A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106163306 | |||||||
| chr2:106163329 | G | GTAC | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.230+335_230+337dup others(3): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106163329 | |||||||
| chr2:106163559 | C | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.230+108G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106163559 | |||||||
| chr2:106163599 | C | CTG | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.230+67_230+68insCA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 4/14 | chr2 | 106163599 | |||||||
| chr2:106163794 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0224 |
2 | HG01069.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.187-84C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 3/14 | chr2 | 106163794 | |||||||
| chr2:106163799 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.187-89T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 3/14 | chr2 | 106163799 | |||||||
| chr2:106163931 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.187-221C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 3/14 | chr2 | 106163931 | |||||||
| chr2:106164270 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.186+466G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 3/14 | chr2 | 106164270 | |||||||
| chr2:106164369 | C | CGTGGATG others(12): Show |
268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.186+366_186+367ins others(19): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 3/14 | chr2 | 106164369 | |||||||
| chr2:106164617 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0158 |
3 | HG02145.hp1 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.186+119G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 3/14 | chr2 | 106164617 | |||||||
| chr2:106165124 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0024 |
2 | HG00642.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.123-325G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 2/14 | chr2 | 106165124 | |||||||
| chr2:106165214 | C | A | 61 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
67 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.123-415G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 2/14 | chr2 | 106165214 | |||||||
| chr2:106165345 | T | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(26): Show |
33 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.123-546A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 2/14 | chr2 | 106165345 | |||||||
| chr2:106165421 | A | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.123-622T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 2/14 | chr2 | 106165421 | |||||||
| chr2:106165515 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.122+541A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 2/14 | chr2 | 106165515 | |||||||
| chr2:106165520 | G | T | 2 | a0001c0001t0005g0037 a0001c0001t0005g0038 |
2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.122+536C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 2/14 | chr2 | 106165520 | |||||||
| chr2:106165532 | T | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.122+524A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 2/14 | chr2 | 106165532 | |||||||
| chr2:106165816 | A | AG | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.122+239dupC | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 2/14 | chr2 | 106165816 | |||||||
| chr2:106165818 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.122+238G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 2/14 | chr2 | 106165818 | |||||||
| chr2:106165818 | C | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.122+238G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 2/14 | chr2 | 106165818 | |||||||
| chr2:106165887 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0240 |
3 | NA18941.hp2 NA18953.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.122+169C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 2/14 | chr2 | 106165887 | |||||||
| chr2:106165890 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.122+166T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 2/14 | chr2 | 106165890 | |||||||
| chr2:106165942 | C | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.122+114G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 2/14 | chr2 | 106165942 | |||||||
| chr2:106166263 | A | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-180T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166263 | |||||||
| chr2:106166273 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.95-190A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166273 | |||||||
| chr2:106166294 | T | G | 1 | a0001c0001t0001g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.95-211A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166294 | |||||||
| chr2:106166367 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.95-284C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166367 | |||||||
| chr2:106166485 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.95-402C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166485 | |||||||
| chr2:106166677 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.95-594C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166677 | |||||||
| chr2:106166690 | C | A | 10 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(7): Show |
10 | HG00323.hp2 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-607G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166690 | |||||||
| chr2:106166693 | G | C | 10 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(7): Show |
10 | HG00323.hp2 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-610C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166693 | |||||||
| chr2:106166694 | TGAAGC | T | 10 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(7): Show |
10 | HG00323.hp2 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-616_95-612delGC others(3): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166694 | |||||||
| chr2:106166699 | C | CT | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
160 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.95-617dupA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166699 | |||||||
| chr2:106166699 | C | CTT | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.95-618_95-617dupAA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166699 | |||||||
| chr2:106166717 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.95-634A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166717 | |||||||
| chr2:106166717 | T | TC | 2 | a0001c0001t0001g0016 a0001c0001t0001g0061 |
3 | HG02809.hp2 HG03225.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.95-635dupG | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166717 | |||||||
| chr2:106166722 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
9 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-639C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166722 | |||||||
| chr2:106166775 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.95-692G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166775 | |||||||
| chr2:106166806 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.95-723G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166806 | |||||||
| chr2:106166885 | C | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
9 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-802G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106166885 | |||||||
| chr2:106167180 | A | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
9 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-1097T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106167180 | |||||||
| chr2:106167259 | T | TA | 8 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(5): Show |
8 | HG00323.hp2 HG01099.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-1177dupT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106167259 | |||||||
| chr2:106167332 | G | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-1249C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106167332 | |||||||
| chr2:106167338 | G | A | 4 | a0001c0001t0001g0031 a0001c0002t0004g0029 a0001c0002t0004g0030 others(1): Show |
4 | HG02559.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-1255C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106167338 | |||||||
| chr2:106167568 | T | C | 1 | a0001c0001t0002g0107 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.95-1485A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106167568 | |||||||
| chr2:106167585 | TCAAA | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0109 a0001c0001t0001g0114 others(1): Show |
5 | HG02129.hp2 HG03490.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-1506_95-1503del others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106167585 | |||||||
| chr2:106167598 | A | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-1515T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106167598 | |||||||
| chr2:106167610 | A | T | 1 | a0001c0001t0001g0264 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.95-1527T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106167610 | |||||||
| chr2:106167836 | A | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.95-1753T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106167836 | |||||||
| chr2:106167884 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.95-1801C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106167884 | |||||||
| chr2:106167977 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.95-1894G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106167977 | |||||||
| chr2:106168035 | C | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0170 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.95-1952G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106168035 | |||||||
| chr2:106168122 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.95-2039A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106168122 | |||||||
| chr2:106168308 | GT | G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
13 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.95-2226delA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106168308 | |||||||
| chr2:106168365 | T | C | 61 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
67 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.95-2282A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106168365 | |||||||
| chr2:106168582 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.95-2499C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106168582 | |||||||
| chr2:106168789 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.95-2706T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106168789 | |||||||
| chr2:106168995 | G | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-2912C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106168995 | |||||||
| chr2:106169084 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-3001C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106169084 | |||||||
| chr2:106169121 | C | A | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.95-3038G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106169121 | |||||||
| chr2:106169274 | T | C | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0158 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-3191A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106169274 | |||||||
| chr2:106169418 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-3335A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106169418 | |||||||
| chr2:106169424 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.95-3341G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106169424 | |||||||
| chr2:106169437 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.95-3354G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106169437 | |||||||
| chr2:106169545 | G | C | 2 | a0001c0002t0004g0029 a0001c0002t0004g0030 |
2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.95-3462C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106169545 | |||||||
| chr2:106169579 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0137 |
2 | HG00621.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.95-3496A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106169579 | |||||||
| chr2:106169779 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0043 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.95-3696C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106169779 | |||||||
| chr2:106169951 | A | C | 25 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0097 others(22): Show |
30 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-3868T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106169951 | |||||||
| chr2:106170297 | C | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-4214G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106170297 | |||||||
| chr2:106170439 | C | A | 5 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0106 others(2): Show |
5 | NA18947.hp1 NA18968.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-4356G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106170439 | |||||||
| chr2:106170734 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.95-4651T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106170734 | |||||||
| chr2:106170793 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.95-4710C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106170793 | |||||||
| chr2:106170801 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.95-4718G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106170801 | |||||||
| chr2:106170905 | C | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0073 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-4822G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106170905 | |||||||
| chr2:106171008 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.95-4925A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106171008 | |||||||
| chr2:106171109 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.95-5026G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106171109 | |||||||
| chr2:106171128 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.95-5045A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106171128 | |||||||
| chr2:106171171 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0006g0182 |
2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.95-5088T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106171171 | |||||||
| chr2:106171306 | A | ATC | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-5225_95-5224dup others(2): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106171306 | |||||||
| chr2:106171439 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.95-5356C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106171439 | |||||||
| chr2:106171689 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.95-5606A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106171689 | |||||||
| chr2:106171788 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-5705C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106171788 | |||||||
| chr2:106171837 | G | C | 1 | a0001c0001t0001g0260 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.95-5754C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106171837 | |||||||
| chr2:106171873 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0069 others(1): Show |
4 | HG02630.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-5790G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106171873 | |||||||
| chr2:106172045 | TC | T | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0158 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-5963delG | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106172045 | |||||||
| chr2:106172098 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.95-6015C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106172098 | |||||||
| chr2:106172125 | G | A | 25 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0097 others(22): Show |
30 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-6042C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106172125 | |||||||
| chr2:106172230 | G | A | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0158 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-6147C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106172230 | |||||||
| chr2:106172240 | C | T | 3 | a0001c0001t0001g0181 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG00099.hp1 HG01258.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.95-6157G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106172240 | |||||||
| chr2:106172334 | T | G | 1 | a0001c0001t0001g0191 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.95-6251A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106172334 | |||||||
| chr2:106172354 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.95-6271C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106172354 | |||||||
| chr2:106172497 | T | C | 29 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0206 others(26): Show |
31 | HG00597.hp1 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.95-6414A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106172497 | |||||||
| chr2:106172500 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.95-6417C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106172500 | |||||||
| chr2:106172635 | C | G | 25 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0097 others(22): Show |
30 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-6552G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106172635 | |||||||
| chr2:106172681 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.95-6598G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106172681 | |||||||
| chr2:106172912 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.95-6829A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106172912 | |||||||
| chr2:106173204 | T | C | 62 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
68 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.95-7121A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106173204 | |||||||
| chr2:106173294 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.95-7211C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106173294 | |||||||
| chr2:106173309 | C | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.95-7226G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106173309 | |||||||
| chr2:106173606 | A | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG01884.hp1 HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.95-7523T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106173606 | |||||||
| chr2:106173660 | G | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0033 others(52): Show |
57 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.95-7577C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106173660 | |||||||
| chr2:106173797 | T | C | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0033 others(52): Show |
57 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.95-7714A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106173797 | |||||||
| chr2:106173931 | G | A | 25 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0097 others(22): Show |
30 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-7848C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106173931 | |||||||
| chr2:106174027 | C | T | 10 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(7): Show |
10 | HG00323.hp2 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-7944G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106174027 | |||||||
| chr2:106174037 | G | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-7954C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106174037 | |||||||
| chr2:106174089 | T | TG | 30 | a0001c0001t0001g0024 a0001c0001t0001g0057 a0001c0001t0001g0058 others(27): Show |
30 | HG00597.hp2 HG01123.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-8007dupC | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106174089 | |||||||
| chr2:106174101 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.95-8018C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106174101 | |||||||
| chr2:106174417 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0011g0269 |
2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.95-8334G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106174417 | |||||||
| chr2:106174424 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-8341C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106174424 | |||||||
| chr2:106174594 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-8511A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106174594 | |||||||
| chr2:106174796 | C | CAGCGGAA others(1): Show |
19 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(16): Show |
19 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(16): Show |
intron_variant | MODIFIER | c.95-8721_95-8714dup others(8): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106174796 | |||||||
| chr2:106174888 | A | T | 12 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0007 others(9): Show |
17 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-8805T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106174888 | |||||||
| chr2:106174901 | A | C | 3 | a0001c0001t0001g0176 a0001c0001t0001g0258 a0001c0001t0006g0182 |
3 | HG01884.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.95-8818T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106174901 | |||||||
| chr2:106175001 | T | C | 5 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(2): Show |
5 | HG00738.hp1 HG01981.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8918A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106175001 | |||||||
| chr2:106175014 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-8931C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106175014 | |||||||
| chr2:106175072 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.95-8989C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106175072 | |||||||
| chr2:106175538 | T | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-9455A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106175538 | |||||||
| chr2:106175672 | G | C | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG03834.hp2 HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.95-9589C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106175672 | |||||||
| chr2:106175793 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.95-9710C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106175793 | |||||||
| chr2:106175831 | C | A | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0158 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-9748G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106175831 | |||||||
| chr2:106175838 | G | A | 4 | a0001c0001t0001g0031 a0001c0002t0004g0029 a0001c0002t0004g0030 others(1): Show |
4 | HG02559.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-9755C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106175838 | |||||||
| chr2:106175844 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
9 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-9761C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106175844 | |||||||
| chr2:106176352 | G | C | 1 | a0001c0001t0002g0092 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.95-10269C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106176352 | |||||||
| chr2:106176435 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.95-10352G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106176435 | |||||||
| chr2:106176626 | T | C | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG00642.hp2 HG00738.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-10543A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106176626 | |||||||
| chr2:106176662 | C | T | 62 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
68 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.95-10579G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106176662 | |||||||
| chr2:106176663 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.95-10580C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106176663 | |||||||
| chr2:106176826 | C | T | 61 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
67 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.95-10743G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106176826 | |||||||
| chr2:106176859 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
13 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.95-10776G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106176859 | |||||||
| chr2:106176927 | C | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-10844G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106176927 | |||||||
| chr2:106176929 | A | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-10846T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106176929 | |||||||
| chr2:106177026 | C | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-10943G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106177026 | |||||||
| chr2:106177066 | A | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-10983T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106177066 | |||||||
| chr2:106177106 | A | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-11023T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106177106 | |||||||
| chr2:106177200 | C | CT | 6 | a0001c0001t0001g0062 a0001c0001t0001g0136 a0001c0001t0001g0158 others(3): Show |
6 | HG00323.hp1 HG02145.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-11118dupA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106177200 | |||||||
| chr2:106177200 | C | CTT | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(256): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.95-11119_95-11118d others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106177200 | |||||||
| chr2:106177200 | CT | C | 7 | a0001c0001t0003g0270 a0001c0001t0003g0271 a0001c0001t0003g0272 others(4): Show |
7 | HG02109.hp1 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-11118delA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106177200 | |||||||
| chr2:106177536 | T | G | 1 | a0001c0001t0001g0207 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.95-11453A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106177536 | |||||||
| chr2:106177635 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.95-11552A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106177635 | |||||||
| chr2:106177673 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0023 |
3 | HG01928.hp1 HG01943.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.95-11590T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106177673 | |||||||
| chr2:106177731 | C | A | 25 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0097 others(22): Show |
30 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-11648G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106177731 | |||||||
| chr2:106178024 | A | T | 62 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
68 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.95-11941T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106178024 | |||||||
| chr2:106178033 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-11950A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106178033 | |||||||
| chr2:106178163 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.95-12080G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106178163 | |||||||
| chr2:106178202 | T | C | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | NA18942.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.95-12119A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106178202 | |||||||
| chr2:106178288 | T | C | 275 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.95-12205A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106178288 | |||||||
| chr2:106178404 | G | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-12321C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106178404 | |||||||
| chr2:106178480 | G | GTA | 29 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(26): Show |
33 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.95-12399_95-12398d others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106178480 | |||||||
| chr2:106178520 | CTATG | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-12441_95-12438d others(6): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106178520 | |||||||
| chr2:106178568 | GTA | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
15 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.95-12487_95-12486d others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106178568 | |||||||
| chr2:106178578 | A | G | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0158 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-12495T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106178578 | |||||||
| chr2:106178598 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.95-12515C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106178598 | |||||||
| chr2:106178924 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.95-12841A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106178924 | |||||||
| chr2:106179030 | T | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.95-12947A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106179030 | |||||||
| chr2:106179105 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.95-13022A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106179105 | |||||||
| chr2:106179164 | G | C | 27 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0097 others(24): Show |
32 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(29): Show |
intron_variant | MODIFIER | c.95-13081C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106179164 | |||||||
| chr2:106179224 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.95-13141A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106179224 | |||||||
| chr2:106179263 | C | T | 25 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0097 others(22): Show |
30 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-13180G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106179263 | |||||||
| chr2:106179385 | A | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.95-13302T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106179385 | |||||||
| chr2:106179484 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-13401A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106179484 | |||||||
| chr2:106179535 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.95-13452T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106179535 | |||||||
| chr2:106179638 | T | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0063 others(2): Show |
6 | HG00099.hp2 HG01169.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-13555A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106179638 | |||||||
| chr2:106179770 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.95-13687A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106179770 | |||||||
| chr2:106179780 | C | A | 1 | a0001c0001t0001g0254 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.95-13697G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106179780 | |||||||
| chr2:106179871 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-13788C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106179871 | |||||||
| chr2:106179923 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.95-13840A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106179923 | |||||||
| chr2:106179966 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0186 a0001c0001t0001g0203 others(3): Show |
7 | HG01099.hp2 HG01123.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-13883C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106179966 | |||||||
| chr2:106180046 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | NA18962.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.95-13963A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106180046 | |||||||
| chr2:106180295 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.94+13853G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106180295 | |||||||
| chr2:106180311 | CTG | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.94+13835_94+13836d others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106180311 | |||||||
| chr2:106180351 | T | G | 11 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(8): Show |
11 | HG00323.hp2 HG01099.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+13797A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106180351 | |||||||
| chr2:106180376 | G | A | 60 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
66 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.94+13772C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106180376 | |||||||
| chr2:106180441 | T | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(104): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.94+13707A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106180441 | |||||||
| chr2:106180624 | C | A | 1 | a0001c0001t0001g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.94+13524G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106180624 | |||||||
| chr2:106180637 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.94+13511G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106180637 | |||||||
| chr2:106180790 | A | T | 2 | a0001c0001t0002g0093 a0001c0001t0002g0094 |
2 | HG03834.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.94+13358T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106180790 | |||||||
| chr2:106180934 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+13214C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106180934 | |||||||
| chr2:106180959 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.94+13189G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106180959 | |||||||
| chr2:106181009 | A | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.94+13139T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106181009 | |||||||
| chr2:106181207 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+12941A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106181207 | |||||||
| chr2:106181328 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.94+12820C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106181328 | |||||||
| chr2:106181368 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.94+12780G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106181368 | |||||||
| chr2:106181411 | T | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0212 a0001c0001t0001g0239 others(4): Show |
8 | NA18941.hp2 NA18942.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+12737A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106181411 | |||||||
| chr2:106181444 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0023 |
3 | HG01928.hp1 HG01943.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.94+12704G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106181444 | |||||||
| chr2:106181588 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
10 | HG00642.hp1 HG01928.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+12560C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106181588 | |||||||
| chr2:106181627 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.94+12521C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106181627 | |||||||
| chr2:106181739 | A | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG03927.hp2 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.94+12409T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106181739 | |||||||
| chr2:106181887 | G | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+12261C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106181887 | |||||||
| chr2:106181973 | A | G | 6 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0105 others(3): Show |
6 | NA18947.hp1 NA18968.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+12175T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106181973 | |||||||
| chr2:106182000 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.94+12148A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106182000 | |||||||
| chr2:106182018 | A | C | 1 | a0001c0001t0001g0203 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.94+12130T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106182018 | |||||||
| chr2:106182071 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.94+12077C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106182071 | |||||||
| chr2:106182150 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.94+11998A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106182150 | |||||||
| chr2:106182157 | T | C | 4 | a0001c0001t0001g0031 a0001c0002t0004g0029 a0001c0002t0004g0030 others(1): Show |
4 | HG02559.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+11991A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106182157 | |||||||
| chr2:106182159 | T | C | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0158 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+11989A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106182159 | |||||||
| chr2:106182330 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.94+11818C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106182330 | |||||||
| chr2:106182500 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.94+11648C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106182500 | |||||||
| chr2:106182501 | G | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(94): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.94+11647C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106182501 | |||||||
| chr2:106182569 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.94+11579C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106182569 | |||||||
| chr2:106182629 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+11519A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106182629 | |||||||
| chr2:106182684 | C | T | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0158 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+11464G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106182684 | |||||||
| chr2:106182894 | T | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+11254A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106182894 | |||||||
| chr2:106183074 | C | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+11074G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183074 | |||||||
| chr2:106183234 | CT | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.94+10913delA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183234 | |||||||
| chr2:106183240 | TA | T | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.94+10907delT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183240 | |||||||
| chr2:106183240 | TAA | T | 21 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0031 others(18): Show |
21 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.94+10906_94+10907d others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183240 | |||||||
| chr2:106183241 | A | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0244 |
2 | NA18979.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.94+10907T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183241 | |||||||
| chr2:106183242 | A | T | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.94+10906T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183242 | |||||||
| chr2:106183243 | A | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0014 others(70): Show |
81 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.94+10905T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183243 | |||||||
| chr2:106183244 | A | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0026 others(6): Show |
10 | HG00323.hp2 HG01167.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+10904T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183244 | |||||||
| chr2:106183245 | A | T | 1 | a0001c0001t0001g0023 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.94+10903T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183245 | |||||||
| chr2:106183275 | A | G | 25 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0097 others(22): Show |
30 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.94+10873T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183275 | |||||||
| chr2:106183609 | G | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.94+10539C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183609 | |||||||
| chr2:106183628 | G | A | 61 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
67 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.94+10520C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183628 | |||||||
| chr2:106183696 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.94+10452T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183696 | |||||||
| chr2:106183725 | T | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.94+10423A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183725 | |||||||
| chr2:106183804 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+10344C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183804 | |||||||
| chr2:106183860 | T | G | 1 | a0001c0001t0001g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.94+10288A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183860 | |||||||
| chr2:106183990 | G | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.94+10158C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106183990 | |||||||
| chr2:106184052 | C | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+10096G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106184052 | |||||||
| chr2:106184121 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.94+10027C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106184121 | |||||||
| chr2:106184131 | A | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+10017T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106184131 | |||||||
| chr2:106184605 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.94+9543G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106184605 | |||||||
| chr2:106184678 | T | C | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG02683.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.94+9470A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106184678 | |||||||
| chr2:106184740 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.94+9408A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106184740 | |||||||
| chr2:106184797 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.94+9351C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106184797 | |||||||
| chr2:106184800 | C | T | 166 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.94+9348G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106184800 | |||||||
| chr2:106185071 | C | G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0158 |
3 | HG02145.hp1 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.94+9077G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106185071 | |||||||
| chr2:106185156 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+8992A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106185156 | |||||||
| chr2:106185409 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.94+8739G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106185409 | |||||||
| chr2:106185730 | G | C | 1 | a0001c0001t0001g0025 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.94+8418C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106185730 | |||||||
| chr2:106185820 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.94+8328A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106185820 | |||||||
| chr2:106185839 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
9 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+8309C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106185839 | |||||||
| chr2:106185871 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.94+8277G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106185871 | |||||||
| chr2:106185959 | CTT | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+8187_94+8188del others(2): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106185959 | |||||||
| chr2:106186029 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.94+8119C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186029 | |||||||
| chr2:106186058 | C | CACCACCA others(6): Show |
1 | a0001c0001t0001g0109 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.94+8077_94+8089dup others(13): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186058 | |||||||
| chr2:106186148 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+8000C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186148 | |||||||
| chr2:106186220 | G | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+7928C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186220 | |||||||
| chr2:106186291 | G | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+7857C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186291 | |||||||
| chr2:106186349 | T | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0031 others(56): Show |
61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.94+7799A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186349 | |||||||
| chr2:106186383 | A | C | 1 | a0001c0001t0010g0248 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.94+7765T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186383 | |||||||
| chr2:106186453 | T | TACACACA others(1): Show |
3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0247 |
3 | HG00408.hp1 HG00621.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.94+7694_94+7695ins others(8): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186453 | |||||||
| chr2:106186455 | T | C | 4 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0206 others(1): Show |
4 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+7693A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186455 | |||||||
| chr2:106186455 | T | TAC | 9 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
10 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+7692_94+7693ins others(2): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186455 | |||||||
| chr2:106186455 | T | TACAC | 63 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
69 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.94+7692_94+7693ins others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186455 | |||||||
| chr2:106186455 | T | TACACAC | 5 | a0001c0001t0001g0031 a0001c0001t0001g0164 a0001c0002t0004g0029 others(2): Show |
5 | HG02559.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+7692_94+7693ins others(6): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186455 | |||||||
| chr2:106186455 | T | TACACACA others(1): Show |
113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+7692_94+7693ins others(8): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186455 | |||||||
| chr2:106186455 | T | TACACACA others(3): Show |
15 | a0001c0001t0001g0018 a0001c0001t0001g0068 a0001c0001t0001g0179 others(12): Show |
16 | HG00280.hp2 HG00423.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.94+7692_94+7693ins others(10): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186455 | |||||||
| chr2:106186455 | T | TACACACA others(7): Show |
1 | a0001c0001t0001g0255 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.94+7692_94+7693ins others(14): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186455 | |||||||
| chr2:106186457 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.94+7691A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186457 | |||||||
| chr2:106186457 | T | TACAC | 3 | a0001c0001t0001g0016 a0001c0001t0001g0159 a0001c0001t0001g0165 |
4 | HG02451.hp1 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+7687_94+7690dup others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186457 | |||||||
| chr2:106186457 | T | TACACACA others(1): Show |
15 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0040 others(12): Show |
16 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.94+7683_94+7690dup others(8): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186457 | |||||||
| chr2:106186457 | T | TACACACA others(3): Show |
3 | a0001c0001t0001g0090 a0001c0001t0001g0158 a0001c0001t0001g0169 |
3 | HG02145.hp1 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.94+7681_94+7690dup others(10): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186457 | |||||||
| chr2:106186457 | T | TATACACA others(1): Show |
29 | a0001c0001t0001g0097 a0001c0001t0001g0167 a0001c0001t0001g0168 others(26): Show |
34 | HG00323.hp2 HG01099.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.94+7690_94+7691ins others(8): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186457 | |||||||
| chr2:106186457 | T | TATACACA others(3): Show |
5 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0087 others(2): Show |
6 | HG01069.hp1 HG01071.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+7690_94+7691ins others(10): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186457 | |||||||
| chr2:106186594 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.94+7554C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186594 | |||||||
| chr2:106186614 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.94+7534T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186614 | |||||||
| chr2:106186660 | A | T | 2 | a0001c0002t0004g0029 a0001c0002t0004g0030 |
2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.94+7488T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186660 | |||||||
| chr2:106186695 | G | C | 63 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
70 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.94+7453C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106186695 | |||||||
| chr2:106187007 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.94+7141C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106187007 | |||||||
| chr2:106187199 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.94+6949C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106187199 | |||||||
| chr2:106187347 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.94+6801A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106187347 | |||||||
| chr2:106187395 | A | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.94+6753T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106187395 | |||||||
| chr2:106187448 | A | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+6700T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106187448 | |||||||
| chr2:106187484 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.94+6664G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106187484 | |||||||
| chr2:106187688 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.94+6460G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106187688 | |||||||
| chr2:106187742 | C | CT | 27 | a0001c0001t0001g0036 a0001c0001t0001g0073 a0001c0001t0001g0074 others(24): Show |
32 | HG01123.hp1 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.94+6405dupA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106187742 | |||||||
| chr2:106187790 | G | T | 1 | a0001c0001t0001g0185 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.94+6358C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106187790 | |||||||
| chr2:106187791 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.94+6357C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106187791 | |||||||
| chr2:106187814 | C | CCACTGCA others(10): Show |
1 | a0001c0001t0001g0185 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.94+6333_94+6334ins others(17): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106187814 | |||||||
| chr2:106187841 | C | A | 1 | a0001c0001t0001g0260 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.94+6307G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106187841 | |||||||
| chr2:106187924 | T | A | 1 | a0001c0001t0001g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.94+6224A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106187924 | |||||||
| chr2:106187938 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(24): Show |
31 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.94+6210G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106187938 | |||||||
| chr2:106188025 | A | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0159 |
3 | HG02809.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.94+6123T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106188025 | |||||||
| chr2:106188031 | C | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+6117G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106188031 | |||||||
| chr2:106188136 | C | CT | 61 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
67 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.94+6011dupA | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106188136 | |||||||
| chr2:106188559 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.94+5589C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106188559 | |||||||
| chr2:106188630 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.94+5518G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106188630 | |||||||
| chr2:106188632 | C | G | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0158 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+5516G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106188632 | |||||||
| chr2:106188686 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.94+5462C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106188686 | |||||||
| chr2:106188756 | A | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.94+5392T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106188756 | |||||||
| chr2:106188763 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.94+5385G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106188763 | |||||||
| chr2:106189215 | C | CA | 60 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
66 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.94+4932dupT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106189215 | |||||||
| chr2:106189280 | C | T | 275 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.94+4868G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106189280 | |||||||
| chr2:106189304 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.94+4844A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106189304 | |||||||
| chr2:106189467 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+4681C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106189467 | |||||||
| chr2:106189470 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.94+4678C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106189470 | |||||||
| chr2:106189547 | T | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+4601A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106189547 | |||||||
| chr2:106189548 | C | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+4600G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106189548 | |||||||
| chr2:106189549 | C | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+4599G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106189549 | |||||||
| chr2:106189550 | T | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+4598A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106189550 | |||||||
| chr2:106189632 | G | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0073 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+4516C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106189632 | |||||||
| chr2:106189650 | CAT | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
9 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+4496_94+4497del others(2): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106189650 | |||||||
| chr2:106189711 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.94+4437T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106189711 | |||||||
| chr2:106189739 | A | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+4409T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106189739 | |||||||
| chr2:106189742 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0142 |
3 | NA18953.hp2 NA18962.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.94+4406C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106189742 | |||||||
| chr2:106190148 | C | T | 6 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0105 others(3): Show |
6 | NA18947.hp1 NA18968.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+4000G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190148 | |||||||
| chr2:106190186 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.94+3962G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190186 | |||||||
| chr2:106190242 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0006g0028 |
3 | HG01167.hp1 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.94+3906A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190242 | |||||||
| chr2:106190391 | C | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(104): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.94+3757G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190391 | |||||||
| chr2:106190465 | G | C | 10 | a0001c0001t0001g0015 a0001c0001t0001g0143 a0001c0001t0001g0144 others(7): Show |
11 | HG00639.hp2 HG00735.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+3683C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190465 | |||||||
| chr2:106190604 | G | A | 6 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0105 others(3): Show |
6 | NA18947.hp1 NA18968.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+3544C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190604 | |||||||
| chr2:106190669 | A | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+3479T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190669 | |||||||
| chr2:106190692 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | NA18962.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.94+3456C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190692 | |||||||
| chr2:106190700 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.94+3448C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190700 | |||||||
| chr2:106190720 | G | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02683.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.94+3428C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190720 | |||||||
| chr2:106190743 | C | CAA | 8 | a0001c0001t0001g0109 a0001c0001t0001g0149 a0001c0001t0001g0165 others(5): Show |
8 | HG01069.hp2 HG01261.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+3403_94+3404dup others(2): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190743 | |||||||
| chr2:106190743 | C | CAAA | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.94+3402_94+3404dup others(3): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190743 | |||||||
| chr2:106190743 | C | CAAAA | 8 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0087 others(5): Show |
9 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+3401_94+3404dup others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190743 | |||||||
| chr2:106190944 | A | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+3204T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190944 | |||||||
| chr2:106190945 | G | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+3203C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190945 | |||||||
| chr2:106190946 | A | C | 64 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(61): Show |
71 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.94+3202T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190946 | |||||||
| chr2:106190947 | A | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+3201T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190947 | |||||||
| chr2:106190972 | A | C | 1 | a0001c0001t0001g0180 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.94+3176T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106190972 | |||||||
| chr2:106191033 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.94+3115G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106191033 | |||||||
| chr2:106191063 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.94+3085A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106191063 | |||||||
| chr2:106191089 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.94+3059T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106191089 | |||||||
| chr2:106191092 | C | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0166 |
3 | HG02015.hp2 NA18972.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.94+3056G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106191092 | |||||||
| chr2:106191290 | T | C | 61 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
67 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.94+2858A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106191290 | |||||||
| chr2:106191322 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.94+2826G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106191322 | |||||||
| chr2:106191323 | A | T | 1 | a0001c0001t0001g0167 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.94+2825T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106191323 | |||||||
| chr2:106191359 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.94+2789A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106191359 | |||||||
| chr2:106191402 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.94+2746C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106191402 | |||||||
| chr2:106191413 | T | G | 1 | a0001c0001t0002g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.94+2735A>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106191413 | |||||||
| chr2:106191776 | G | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG01884.hp1 HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.94+2372C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106191776 | |||||||
| chr2:106191839 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.94+2309G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106191839 | |||||||
| chr2:106191989 | T | A | 1 | a0001c0001t0001g0085 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.94+2159A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106191989 | |||||||
| chr2:106192026 | C | G | 1 | a0001c0001t0001g0022 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.94+2122G>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192026 | |||||||
| chr2:106192071 | A | T | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 |
3 | NA18972.hp2 NA18993.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.94+2077T>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192071 | |||||||
| chr2:106192118 | C | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+2030G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192118 | |||||||
| chr2:106192166 | G | C | 1 | a0001c0001t0001g0260 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.94+1982C>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192166 | |||||||
| chr2:106192234 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.94+1914T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192234 | |||||||
| chr2:106192255 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
9 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+1893A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192255 | |||||||
| chr2:106192417 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.94+1731C>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192417 | |||||||
| chr2:106192449 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG00735.hp2 HG01071.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.94+1699C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192449 | |||||||
| chr2:106192485 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+1663A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192485 | |||||||
| chr2:106192497 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.94+1651A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192497 | |||||||
| chr2:106192548 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.94+1600A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192548 | |||||||
| chr2:106192549 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.94+1599G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192549 | |||||||
| chr2:106192555 | CA | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.94+1592delT | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192555 | |||||||
| chr2:106192621 | A | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
9 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+1527T>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192621 | |||||||
| chr2:106192728 | TCTTA | T | 4 | a0001c0001t0001g0031 a0001c0002t0004g0029 a0001c0002t0004g0030 others(1): Show |
4 | HG02559.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+1416_94+1419del others(4): Show |
UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192728 | |||||||
| chr2:106192831 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.94+1317G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192831 | |||||||
| chr2:106192991 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+1157A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106192991 | |||||||
| chr2:106193161 | A | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
9 | HG00642.hp1 HG01167.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+987T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106193161 | |||||||
| chr2:106193428 | A | G | 10 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(7): Show |
10 | HG00323.hp2 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+720T>C | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106193428 | |||||||
| chr2:106193504 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0031 others(56): Show |
61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.94+644G>A | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106193504 | |||||||
| chr2:106193592 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.94+556C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106193592 | |||||||
| chr2:106193599 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+549C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106193599 | |||||||
| chr2:106193739 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.94+409C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106193739 | |||||||
| chr2:106193777 | C | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(104): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.94+371G>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106193777 | |||||||
| chr2:106193794 | G | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.94+354C>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106193794 | |||||||
| chr2:106193959 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.94+189A>G | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106193959 | |||||||
| chr2:106194127 | T | A | 8 | a0001c0001t0001g0021 a0001c0001t0001g0262 a0001c0001t0001g0263 others(5): Show |
9 | HG00738.hp1 HG01123.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+21A>T | UXS1 | ENSG00000115652.15 | transcript | ENST00000283148.12 | protein_coding | 1/14 | chr2 | 106194127 |