Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23190 |
| ensemblid | ENSG00000144224.17 |
| hgncid | 14860 |
| symbol | UBXN4 |
| name | UBX domain protein 4 |
| refseq_nuc | NM_014607.4 |
| refseq_prot | NP_055422.1 |
| ensembl_nuc | ENST00000272638.14 |
| ensembl_prot | ENSP00000272638.9 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 135741855 |
| end | 135785056 |
| strand | + |
| ver | v1.2 |
| region | chr2:135741855-135785056 |
| region5000 | chr2:135736855-135790056 |
| regionname0 | UBXN4_chr2_135741855_135785056 |
| regionname5000 | UBXN4_chr2_135736855_135790056 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 508 | 367 | 86 | 64 | 173 | 6 | 36 | 138 | UBXN4_chr2_135736855_135790056 | UBXN4 | MLWFQ others(503): Show |
chr2 | 135736855 | 135790056 |
| a0002 | 0/0 | 508 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | MLWFQ others(503): Show |
chr2 | 135736855 | 135790056 |
| a0003 | 0/0 | 508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | MLWFQ others(503): Show |
chr2 | 135736855 | 135790056 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1524 | 270 | 76 | 41 | 120 | 4 | 27 | UBXN4_chr2_135736855_135790056 | UBXN4 | ATGCT others(1519): Show |
chr2 | 135736855 | 135790056 | ||
| a0001c0002 | 0/0 | 1524 | 62 | 10 | 17 | 28 | 2 | 5 | UBXN4_chr2_135736855_135790056 | UBXN4 | ATGCT others(1519): Show |
chr2 | 135736855 | 135790056 | ||
| a0001c0003 | 0/0 | 1524 | 25 | 0 | 2 | 22 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | ATGCT others(1519): Show |
chr2 | 135736855 | 135790056 | ||
| a0001c0004 | 0/0 | 1524 | 8 | 0 | 3 | 3 | 0 | 2 | UBXN4_chr2_135736855_135790056 | UBXN4 | ATGCT others(1519): Show |
chr2 | 135736855 | 135790056 | ||
| a0001c0007 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | ATGCT others(1519): Show |
chr2 | 135736855 | 135790056 | ||
| a0001c0008 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | ATGCT others(1519): Show |
chr2 | 135736855 | 135790056 | ||
| a0002c0005 | 0/0 | 1524 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | ATGCT others(1519): Show |
chr2 | 135736855 | 135790056 | ||
| a0003c0006 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | ATGCT others(1519): Show |
chr2 | 135736855 | 135790056 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3770 | 133 | 26 | 23 | 68 | 3 | 13 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3765): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0002 | 0/0 | 3771 | 16 | 2 | 7 | 3 | 1 | 3 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3766): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0003 | 0/0 | 3768 | 65 | 22 | 6 | 32 | 0 | 5 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3763): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0004 | 0/0 | 3770 | 25 | 15 | 4 | 4 | 0 | 2 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3765): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0005 | 1/0 | 3771 | 12 | 2 | 0 | 6 | 0 | 3 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3766): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0006 | 0/0 | 3771 | 4 | 4 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3766): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0007 | 0/0 | 3768 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3763): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0008 | 0/0 | 3770 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3765): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0009 | 0/0 | 3770 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3765): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0010 | 0/0 | 3770 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3765): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0011 | 0/0 | 3770 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3765): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0012 | 0/0 | 3770 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3765): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0013 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3763): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0014 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3763): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0015 | 0/0 | 3770 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3765): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0016 | 0/1 | 3771 | 1 | 0 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3766): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0017 | 0/0 | 3770 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3765): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0018 | 0/0 | 3769 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3764): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0021 | 0/0 | 3770 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3765): Show |
chr2 | 135736855 | 135790056 |
| a0001c0001t0022 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3763): Show |
chr2 | 135736855 | 135790056 |
| a0001c0002t0002 | 0/0 | 3771 | 61 | 10 | 16 | 28 | 2 | 5 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3766): Show |
chr2 | 135736855 | 135790056 |
| a0001c0002t0019 | 0/0 | 3771 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3766): Show |
chr2 | 135736855 | 135790056 |
| a0001c0003t0001 | 0/0 | 3770 | 25 | 0 | 2 | 22 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3765): Show |
chr2 | 135736855 | 135790056 |
| a0001c0004t0003 | 0/0 | 3768 | 8 | 0 | 3 | 3 | 0 | 2 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3763): Show |
chr2 | 135736855 | 135790056 |
| a0001c0007t0020 | 0/0 | 3771 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3766): Show |
chr2 | 135736855 | 135790056 |
| a0001c0008t0002 | 0/0 | 3771 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3766): Show |
chr2 | 135736855 | 135790056 |
| a0002c0005t0002 | 0/0 | 3771 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3766): Show |
chr2 | 135736855 | 135790056 |
| a0003c0006t0001 | 0/0 | 3770 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | GAAGA others(3765): Show |
chr2 | 135736855 | 135790056 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 17 | 1 | 10 | 1 | 1 | 4 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0002 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0002g0006 | 0/0 | 5 | 0 | 3 | 1 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0003 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0005g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0005g0282 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0008g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0009g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0010g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0011g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0012g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0013g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0014g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0015g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0016g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0017g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0018g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0021g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0001t0022g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0004 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0005 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0007 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0002t0019g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0004t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0004t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0004t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0004t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0004t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0004t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0004t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0004t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0007t0020g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0001c0008t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0002c0005t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0002c0005t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| a0003c0006t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | FIN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0052 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0058 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0061 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00558 | hp2 | a0001 | c0001 | t0009 | g0117 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00639 | hp1 | a0001 | c0007 | t0020 | g0041 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0129 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0246 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0130 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0259 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0237 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0116 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0047 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0234 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0239 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0072 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01358 | hp1 | a0001 | c0004 | t0003 | g0066 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01358 | hp2 | a0001 | c0002 | t0019 | g0004 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0232 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0257 | EUR | IBS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0084 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0121 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01993 | hp1 | a0001 | c0004 | t0003 | g0064 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0049 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0238 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0294 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02074 | hp2 | a0002 | c0005 | t0002 | g0254 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02132 | hp2 | a0001 | c0001 | t0013 | g0088 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0261 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0290 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | CDX | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0279 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02280 | hp1 | a0001 | c0001 | t0014 | g0035 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02293 | hp1 | a0001 | c0004 | t0003 | g0065 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0122 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0255 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0048 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0114 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0245 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0280 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03017 | hp1 | a0001 | c0004 | t0003 | g0291 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0281 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0241 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0287 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0242 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0133 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0262 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0278 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03579 | hp1 | a0001 | c0001 | t0015 | g0295 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0283 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0126 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03704 | hp1 | a0001 | c0001 | t0021 | g0002 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0288 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | BEB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0012 | SAS | BEB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | BEB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0106 | SAS | BEB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG04115 | hp1 | a0001 | c0008 | t0002 | g0256 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0267 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG04184 | hp2 | a0001 | c0004 | t0003 | g0296 | SAS | BEB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0233 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0240 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0067 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | YRI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | YRI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | CHB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | CHB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0243 | AFR | YRI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | YRI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18944 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18950 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18952 | hp2 | a0001 | c0001 | t0005 | g0289 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18959 | hp2 | a0001 | c0001 | t0018 | g0009 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18967 | hp1 | a0001 | c0001 | t0012 | g0150 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0059 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0284 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18971 | hp2 | a0001 | c0001 | t0017 | g0204 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18981 | hp2 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18986 | hp2 | a0002 | c0005 | t0002 | g0004 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18988 | hp2 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0286 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18993 | hp1 | a0001 | c0001 | t0022 | g0090 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19001 | hp2 | a0001 | c0003 | t0001 | g0055 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19002 | hp1 | a0001 | c0004 | t0003 | g0027 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19004 | hp2 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19006 | hp1 | a0001 | c0004 | t0003 | g0026 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19006 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19009 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19030 | hp1 | a0001 | c0001 | t0011 | g0147 | AFR | LWK | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | LWK | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | LWK | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0277 | AFR | LWK | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19058 | hp1 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19062 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19063 | hp1 | a0003 | c0006 | t0001 | g0202 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19075 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19077 | hp2 | a0001 | c0004 | t0003 | g0028 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19083 | hp1 | a0001 | c0001 | t0005 | g0285 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19089 | hp2 | a0001 | c0001 | t0008 | g0120 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | YRI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | YRI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0292 | AFR | ASW | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | ASW | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | TSI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0007 | EUR | TSI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0086 | SAS | GIH | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA18955 | hp2 | a0001 | c0003 | t0001 | g0063 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0244 | AFR | USA | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0100 | AFR | USA | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | LWK | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | LWK | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0016 | g0200 | REF | REF | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0282 | REF | REF | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:135769798 | A | C | 1 | a0003 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.632A>C | p.Glu211Ala | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/13 | 707/3771 | 632/1527 | 211/508 | chr2 | 135769798 | |||
| chr2:135780371 | C | G | 1 | a0002 | 2 | HG02074.hp2 NA18986.hp2 |
missense_variant | MODERATE | c.1374C>G | p.Ser458Arg | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/13 | 1449/3771 | 1374/1527 | 458/508 | chr2 | 135780371 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:135754247 | A | G | 3 | a0001c0002 a0001c0008 a0002c0005 |
65 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(62): Show |
synonymous_variant | LOW | c.303A>G | p.Glu101Glu | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/13 | 378/3771 | 303/1527 | 101/508 | chr2 | 135754247 | |||
| chr2:135754272 | C | A | 1 | a0001c0003 | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
synonymous_variant | LOW | c.328C>A | p.Arg110Arg | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/13 | 403/3771 | 328/1527 | 110/508 | chr2 | 135754272 | |||
| chr2:135755609 | C | T | 1 | a0001c0007 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.426C>T | p.Asn142Asn | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/13 | 501/3771 | 426/1527 | 142/508 | chr2 | 135755609 | |||
| chr2:135761846 | C | G | 1 | a0001c0008 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.537C>G | p.Ser179Ser | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/13 | 612/3771 | 537/1527 | 179/508 | chr2 | 135761846 | |||
| chr2:135780341 | G | A | 1 | a0001c0004 | 8 | HG01358.hp1 HG01993.hp1 HG02293.hp1 others(5): Show |
synonymous_variant | LOW | c.1344G>A | p.Ser448Ser | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/13 | 1419/3771 | 1344/1527 | 448/508 | chr2 | 135780341 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:135741872 | C | T | 1 | a0001c0001t0022 | 1 | NA18993.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/13 | 58 | chr2 | 135741872 | ||||||
| chr2:135741879 | C | T | 1 | a0001c0001t0021 | 1 | HG03704.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-51C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/13 | chr2 | 135741879 | |||||||
| chr2:135741888 | G | A | 4 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0009 others(1): Show |
28 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-42G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/13 | 42 | chr2 | 135741888 | ||||||
| chr2:135783082 | C | G | 1 | a0001c0001t0010 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*195C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 195 | chr2 | 135783082 | ||||||
| chr2:135783342 | T | C | 1 | a0001c0001t0011 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*455T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 455 | chr2 | 135783342 | ||||||
| chr2:135783439 | T | C | 1 | a0001c0001t0006 | 4 | HG02258.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*552T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 552 | chr2 | 135783439 | ||||||
| chr2:135783491 | AT | A | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
270 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*615delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 615 | INFO_REALIGN_3_PRIME | chr2 | 135783491 | |||||
| chr2:135783543 | C | T | 1 | a0001c0001t0009 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*656C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 656 | chr2 | 135783543 | ||||||
| chr2:135783546 | G | C | 1 | a0001c0001t0012 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*659G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 659 | chr2 | 135783546 | ||||||
| chr2:135783644 | G | A | 1 | a0001c0001t0013 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*757G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 757 | chr2 | 135783644 | ||||||
| chr2:135783885 | A | G | 1 | a0001c0001t0017 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*998A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 998 | chr2 | 135783885 | ||||||
| chr2:135784017 | TTC | T | 7 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0013 others(4): Show |
79 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1132_*1133delCT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 1132 | INFO_REALIGN_3_PRIME | chr2 | 135784017 | |||||
| chr2:135784284 | T | C | 1 | a0001c0001t0015 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1397T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 1397 | chr2 | 135784284 | ||||||
| chr2:135784374 | A | G | 1 | a0001c0001t0007 | 2 | HG03225.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1487A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 1487 | chr2 | 135784374 | ||||||
| chr2:135784464 | T | C | 1 | a0001c0001t0014 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1577T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 1577 | chr2 | 135784464 | ||||||
| chr2:135784824 | G | T | 1 | a0001c0001t0008 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1937G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 1937 | chr2 | 135784824 | ||||||
| chr2:135784989 | G | A | 6 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0019 others(3): Show |
82 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2102G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 2102 | chr2 | 135784989 | ||||||
| chr2:135784990 | A | G | 6 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0019 others(3): Show |
82 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2103A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 2103 | chr2 | 135784990 | ||||||
| chr2:135785003 | G | A | 1 | a0001c0002t0019 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2116G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 2116 | chr2 | 135785003 | ||||||
| chr2:135785019 | G | A | 1 | a0001c0007t0020 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2132G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 2132 | chr2 | 135785019 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:135742031 | G | C | 3 | a0001c0004t0003g0026 a0001c0004t0003g0027 a0001c0004t0003g0028 |
3 | NA19002.hp1 NA19006.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.82+20G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742031 | |||||||
| chr2:135742090 | G | T | 1 | a0001c0004t0003g0296 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.82+79G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742090 | |||||||
| chr2:135742184 | C | G | 1 | a0001c0001t0015g0295 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.82+173C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742184 | |||||||
| chr2:135742228 | G | T | 1 | a0001c0001t0003g0294 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.82+217G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742228 | |||||||
| chr2:135742237 | G | T | 1 | a0001c0001t0001g0293 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.82+226G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742237 | |||||||
| chr2:135742300 | C | T | 1 | a0001c0001t0005g0292 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.82+289C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742300 | |||||||
| chr2:135742326 | C | T | 1 | a0001c0004t0003g0291 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.82+315C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742326 | |||||||
| chr2:135742653 | G | C | 1 | a0001c0001t0001g0029 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.82+642G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742653 | |||||||
| chr2:135742728 | A | G | 1 | a0001c0003t0001g0290 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.82+717A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742728 | |||||||
| chr2:135742768 | T | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.82+757T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742768 | |||||||
| chr2:135742905 | A | G | 63 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0275 others(60): Show |
85 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.82+894A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742905 | |||||||
| chr2:135742938 | T | A | 1 | a0001c0001t0004g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.82+927T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742938 | |||||||
| chr2:135742939 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.82+928C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742939 | |||||||
| chr2:135743027 | A | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.82+1016A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135743027 | |||||||
| chr2:135743107 | G | A | 3 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 |
3 | HG02559.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.82+1096G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135743107 | |||||||
| chr2:135743339 | C | T | 4 | a0001c0001t0003g0219 a0001c0001t0003g0220 a0001c0001t0003g0221 others(1): Show |
4 | NA18967.hp2 NA18972.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+1328C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135743339 | |||||||
| chr2:135743725 | G | A | 1 | a0001c0002t0002g0224 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.82+1714G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135743725 | |||||||
| chr2:135743863 | G | GTA | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(85): Show |
124 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.82+1863_82+1864dup others(2): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135743863 | ||||||
| chr2:135743939 | T | G | 58 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(55): Show |
80 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.82+1928T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135743939 | |||||||
| chr2:135744091 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+2080C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744091 | |||||||
| chr2:135744117 | C | G | 2 | a0001c0004t0003g0291 a0001c0004t0003g0296 |
2 | HG03017.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.82+2106C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744117 | |||||||
| chr2:135744270 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(114): Show |
159 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.82+2259A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744270 | |||||||
| chr2:135744362 | A | G | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | NA18945.hp2 NA18957.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+2351A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744362 | |||||||
| chr2:135744368 | C | T | 1 | a0001c0001t0005g0289 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.82+2357C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744368 | |||||||
| chr2:135744374 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.82+2363A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744374 | |||||||
| chr2:135744394 | C | CAAATTAA others(1470): Show |
1 | a0001c0001t0001g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.82+2400_82+2401ins others(1477): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135744394 | ||||||
| chr2:135744394 | C | CAAATTAA others(1471): Show |
1 | a0001c0001t0001g0212 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.82+2400_82+2401ins others(1478): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135744394 | ||||||
| chr2:135744394 | CAAATT | C | 66 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0067 others(63): Show |
68 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(65): Show |
intron_variant | MODIFIER | c.82+2386_82+2390del others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135744394 | ||||||
| chr2:135744460 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0210 a0001c0001t0001g0211 |
5 | HG00621.hp2 NA18983.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+2449A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744460 | |||||||
| chr2:135744610 | T | C | 8 | a0001c0004t0003g0026 a0001c0004t0003g0027 a0001c0004t0003g0028 others(5): Show |
8 | HG01358.hp1 HG01993.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.82+2599T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744610 | |||||||
| chr2:135744625 | A | ATT | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.82+2616_82+2617dup others(2): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135744625 | ||||||
| chr2:135744629 | A | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.82+2618A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744629 | |||||||
| chr2:135744725 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.82+2714G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744725 | |||||||
| chr2:135745050 | G | C | 1 | a0001c0001t0004g0116 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.82+3039G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745050 | |||||||
| chr2:135745058 | C | G | 2 | a0001c0001t0003g0144 a0001c0001t0003g0145 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.82+3047C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745058 | |||||||
| chr2:135745103 | G | A | 4 | a0001c0001t0006g0277 a0001c0001t0006g0278 a0001c0001t0006g0279 others(1): Show |
4 | HG02258.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+3092G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745103 | |||||||
| chr2:135745204 | G | A | 1 | a0001c0001t0004g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.83-3063G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745204 | |||||||
| chr2:135745222 | C | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(81): Show |
120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.83-3045C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745222 | |||||||
| chr2:135745549 | A | G | 1 | a0001c0002t0002g0271 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.83-2718A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745549 | |||||||
| chr2:135745587 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(81): Show |
120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.83-2680A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745587 | |||||||
| chr2:135745748 | G | T | 1 | a0001c0001t0004g0140 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.83-2519G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745748 | |||||||
| chr2:135745818 | CTAATGGA others(7): Show |
C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0208 a0001c0001t0001g0209 |
4 | HG00673.hp1 HG01993.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-2436_83-2423del others(14): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745818 | ||||||
| chr2:135745875 | C | CTT | 43 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0275 others(40): Show |
59 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.83-2372_83-2371dup others(2): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | ||||||
| chr2:135745875 | C | CTTT | 7 | a0001c0002t0002g0012 a0001c0002t0002g0224 a0001c0002t0002g0259 others(4): Show |
9 | HG01175.hp2 HG02080.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.83-2373_83-2371dup others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | ||||||
| chr2:135745875 | C | CTTTTTTT others(1): Show |
64 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0148 others(61): Show |
70 | HG00280.hp1 HG01256.hp1 HG01433.hp1 others(67): Show |
intron_variant | MODIFIER | c.83-2378_83-2371dup others(8): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | ||||||
| chr2:135745875 | C | CTTTTTTT others(2): Show |
89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(86): Show |
130 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.83-2379_83-2371dup others(9): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | ||||||
| chr2:135745875 | C | CTTTTTTT others(3): Show |
26 | a0001c0001t0001g0021 a0001c0001t0001g0132 a0001c0001t0001g0134 others(23): Show |
27 | HG00621.hp1 HG00639.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.83-2380_83-2371dup others(10): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | ||||||
| chr2:135745875 | C | CTTTTTTT others(4): Show |
23 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0206 others(20): Show |
24 | HG00408.hp2 HG00544.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.83-2381_83-2371dup others(11): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | ||||||
| chr2:135745875 | C | CTTTTTTT others(5): Show |
4 | a0001c0001t0004g0116 a0001c0003t0001g0061 a0001c0003t0001g0062 others(1): Show |
4 | HG00558.hp1 HG01243.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2382_83-2371dup others(12): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | ||||||
| chr2:135745875 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0136 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.83-2384_83-2371dup others(14): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | ||||||
| chr2:135745875 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0137 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.83-2387_83-2371dup others(17): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | ||||||
| chr2:135745875 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.83-2388_83-2371dup others(18): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | ||||||
| chr2:135745875 | CTTT | C | 13 | a0001c0001t0001g0151 a0001c0001t0003g0008 a0001c0001t0003g0034 others(10): Show |
14 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.83-2373_83-2371del others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | ||||||
| chr2:135745998 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.83-2269C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745998 | |||||||
| chr2:135746034 | C | T | 1 | a0001c0001t0004g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.83-2233C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135746034 | |||||||
| chr2:135746161 | G | A | 1 | a0001c0003t0001g0061 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.83-2106G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135746161 | |||||||
| chr2:135746531 | A | C | 57 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(54): Show |
79 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.83-1736A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135746531 | |||||||
| chr2:135746579 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.83-1688C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135746579 | |||||||
| chr2:135746668 | G | A | 1 | a0001c0003t0001g0046 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.83-1599G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135746668 | |||||||
| chr2:135746882 | C | CT | 63 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0275 others(60): Show |
85 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.83-1374dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135746882 | ||||||
| chr2:135746882 | CT | C | 8 | a0001c0004t0003g0026 a0001c0004t0003g0027 a0001c0004t0003g0028 others(5): Show |
8 | HG01358.hp1 HG01993.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.83-1374delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135746882 | ||||||
| chr2:135746993 | TTAG | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0207 |
3 | HG00733.hp2 HG01192.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.83-1269_83-1267del others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135746993 | ||||||
| chr2:135747158 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-1109C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747158 | |||||||
| chr2:135747191 | CA | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(217): Show |
266 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(263): Show |
intron_variant | MODIFIER | c.83-1069delA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135747191 | ||||||
| chr2:135747284 | A | G | 1 | a0001c0001t0004g0116 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.83-983A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747284 | |||||||
| chr2:135747290 | A | G | 1 | a0001c0003t0001g0290 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.83-977A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747290 | |||||||
| chr2:135747348 | CA | C | 84 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 others(81): Show |
107 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.83-895delA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135747348 | ||||||
| chr2:135747348 | CAA | C | 19 | a0001c0001t0001g0015 a0001c0001t0001g0156 a0001c0001t0001g0157 others(16): Show |
21 | HG00423.hp1 HG00558.hp2 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.83-896_83-895delAA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135747348 | ||||||
| chr2:135747348 | CAAA | C | 30 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0124 others(27): Show |
38 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.83-897_83-895delAA others(1): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135747348 | ||||||
| chr2:135747348 | CAAAA | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(80): Show |
116 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.83-898_83-895delAA others(2): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135747348 | ||||||
| chr2:135747348 | CAAAAA | C | 65 | a0001c0001t0001g0190 a0001c0001t0003g0009 a0001c0001t0003g0014 others(62): Show |
67 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(64): Show |
intron_variant | MODIFIER | c.83-899_83-895delAA others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135747348 | ||||||
| chr2:135747348 | CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0002g0258 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.83-906_83-895delAA others(10): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135747348 | ||||||
| chr2:135747398 | G | A | 2 | a0001c0003t0001g0047 a0001c0003t0001g0290 |
2 | HG01255.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.83-869G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747398 | |||||||
| chr2:135747693 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.83-574G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747693 | |||||||
| chr2:135747701 | C | G | 1 | a0001c0001t0001g0272 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.83-566C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747701 | |||||||
| chr2:135747754 | C | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.83-513C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747754 | |||||||
| chr2:135747833 | C | T | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.83-434C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747833 | |||||||
| chr2:135747868 | G | A | 10 | a0001c0001t0003g0008 a0001c0001t0003g0034 a0001c0001t0003g0036 others(7): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.83-399G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747868 | |||||||
| chr2:135747894 | T | A | 1 | a0001c0002t0002g0259 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.83-373T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747894 | |||||||
| chr2:135747972 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.83-295G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747972 | |||||||
| chr2:135747976 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(137): Show |
183 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.83-291C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747976 | |||||||
| chr2:135748233 | A | G | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | NA18939.hp2 NA18941.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.83-34A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135748233 | |||||||
| chr2:135748510 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.185+141G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135748510 | |||||||
| chr2:135748566 | T | G | 1 | a0001c0001t0003g0075 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.185+197T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135748566 | |||||||
| chr2:135748724 | CA | C | 135 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(132): Show |
145 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.185+371delA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135748724 | ||||||
| chr2:135748724 | CAA | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(82): Show |
121 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.185+370_185+371del others(2): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135748724 | ||||||
| chr2:135748805 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(217): Show |
266 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(263): Show |
intron_variant | MODIFIER | c.185+436G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135748805 | |||||||
| chr2:135749044 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.185+675A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749044 | |||||||
| chr2:135749067 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0143 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.185+698T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749067 | |||||||
| chr2:135749357 | A | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(217): Show |
266 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(263): Show |
intron_variant | MODIFIER | c.185+988A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749357 | |||||||
| chr2:135749425 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.185+1056G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749425 | |||||||
| chr2:135749469 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(81): Show |
120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.185+1100A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749469 | |||||||
| chr2:135749578 | TCAC | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+1210_185+1212d others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749578 | |||||||
| chr2:135749633 | A | AGTATTGT others(348): Show |
1 | a0001c0001t0011g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.185+1280_185+1281i others(357): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135749633 | ||||||
| chr2:135749796 | G | A | 1 | a0001c0001t0005g0289 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.185+1427G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749796 | |||||||
| chr2:135749811 | G | A | 1 | a0001c0001t0003g0034 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.185+1442G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749811 | |||||||
| chr2:135749864 | A | T | 2 | a0001c0001t0003g0067 a0001c0001t0003g0106 |
2 | HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.185+1495A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749864 | |||||||
| chr2:135749946 | A | G | 1 | a0001c0001t0002g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+1577A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749946 | |||||||
| chr2:135749960 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.185+1591A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749960 | |||||||
| chr2:135750195 | A | C | 1 | a0001c0001t0001g0206 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.185+1826A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750195 | |||||||
| chr2:135750234 | A | G | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.185+1865A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750234 | |||||||
| chr2:135750249 | C | T | 1 | a0001c0004t0003g0027 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.185+1880C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750249 | |||||||
| chr2:135750308 | G | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+1939G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750308 | |||||||
| chr2:135750344 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.185+1975G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750344 | |||||||
| chr2:135750429 | C | T | 1 | a0001c0001t0011g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.185+2060C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750429 | |||||||
| chr2:135750437 | C | G | 1 | a0001c0001t0003g0067 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.185+2068C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750437 | |||||||
| chr2:135750553 | A | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0205 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.185+2184A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750553 | |||||||
| chr2:135750693 | CT | C | 19 | a0001c0001t0004g0003 a0001c0001t0004g0030 a0001c0001t0004g0116 others(16): Show |
25 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.185+2335delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750693 | ||||||
| chr2:135750802 | T | A | 10 | a0001c0001t0003g0008 a0001c0001t0003g0034 a0001c0001t0003g0036 others(7): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.185+2433T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750802 | |||||||
| chr2:135750835 | C | CTT | 7 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0040 others(4): Show |
7 | HG02055.hp2 HG02809.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+2503_185+2504d others(4): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | C | CTTTT | 7 | a0001c0001t0006g0279 a0001c0003t0001g0042 a0001c0003t0001g0044 others(4): Show |
7 | HG00408.hp2 HG02258.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+2501_185+2504d others(6): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | C | CTTTTT | 6 | a0001c0003t0001g0045 a0001c0003t0001g0047 a0001c0003t0001g0053 others(3): Show |
6 | HG01255.hp1 HG02148.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+2500_185+2504d others(7): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | C | CTTTTTT | 5 | a0001c0003t0001g0013 a0001c0003t0001g0046 a0001c0003t0001g0056 others(2): Show |
6 | HG02074.hp1 HG02129.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+2499_185+2504d others(8): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | C | CTTTTTTT others(3): Show |
2 | a0001c0003t0001g0043 a0001c0003t0001g0063 |
2 | HG00423.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.185+2495_185+2504d others(12): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | C | CTTTTTTT others(4): Show |
1 | a0001c0003t0001g0061 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.185+2494_185+2504d others(13): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | C | CTTTTTTT others(5): Show |
1 | a0001c0003t0001g0058 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.185+2493_185+2504d others(14): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | C | CTTTTTTT others(14): Show |
1 | a0001c0003t0001g0059 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.185+2484_185+2504d others(23): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | CT | C | 12 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0154 others(9): Show |
12 | HG01261.hp2 HG02300.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.185+2504delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | CTT | C | 10 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0097 others(7): Show |
10 | HG01346.hp1 HG02056.hp2 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+2503_185+2504d others(4): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | CTTT | C | 19 | a0001c0001t0001g0136 a0001c0001t0003g0009 a0001c0001t0003g0014 others(16): Show |
21 | HG01433.hp2 HG01978.hp1 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.185+2502_185+2504d others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | CTTTT | C | 18 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0001g0139 others(15): Show |
18 | HG01952.hp2 HG02132.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.185+2501_185+2504d others(6): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | CTTTTT | C | 16 | a0001c0001t0001g0124 a0001c0001t0001g0134 a0001c0001t0001g0135 others(13): Show |
16 | HG01358.hp1 HG02165.hp2 HG02293.hp1 others(13): Show |
intron_variant | MODIFIER | c.185+2500_185+2504d others(7): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | CTTTTTT | C | 7 | a0001c0001t0003g0076 a0001c0001t0003g0077 a0001c0001t0011g0147 others(4): Show |
7 | HG01993.hp1 HG02451.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+2499_185+2504d others(8): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | CTTTTTTT others(6): Show |
C | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0151 others(11): Show |
16 | HG00673.hp1 HG00738.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.185+2492_185+2504d others(15): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | CTTTTTTT others(7): Show |
C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(59): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.185+2491_185+2504d others(16): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0216 |
2 | NA18957.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.185+2490_185+2504d others(17): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0001g0152 a0001c0001t0004g0123 a0001c0001t0004g0131 |
3 | HG02109.hp1 HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.185+2489_185+2504d others(18): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | CTTTTTTT others(10): Show |
C | 17 | a0001c0001t0004g0003 a0001c0001t0004g0030 a0001c0001t0004g0116 others(14): Show |
23 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.185+2488_185+2504d others(19): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | CTTTTTTT others(13): Show |
C | 6 | a0001c0001t0002g0230 a0001c0001t0002g0269 a0001c0002t0002g0234 others(3): Show |
6 | HG01255.hp2 HG01928.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+2485_185+2504d others(22): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750835 | CTTTTTTT others(14): Show |
C | 57 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0275 others(54): Show |
79 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.185+2484_185+2504d others(23): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | ||||||
| chr2:135750925 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG01433.hp2 HG03491.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+2556G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750925 | |||||||
| chr2:135750925 | G | T | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.185+2556G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750925 | |||||||
| chr2:135751022 | A | AT | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(105): Show |
144 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.186-2501dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135751022 | ||||||
| chr2:135751074 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.186-2465C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751074 | |||||||
| chr2:135751099 | C | T | 1 | a0001c0001t0011g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.186-2440C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751099 | |||||||
| chr2:135751249 | T | G | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.186-2290T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751249 | |||||||
| chr2:135751331 | C | T | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.186-2208C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751331 | |||||||
| chr2:135751436 | C | T | 1 | a0001c0001t0003g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.186-2103C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751436 | |||||||
| chr2:135751477 | C | T | 8 | a0001c0001t0005g0025 a0001c0001t0005g0281 a0001c0001t0005g0283 others(5): Show |
9 | HG03017.hp2 HG03654.hp2 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.186-2062C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751477 | |||||||
| chr2:135751561 | A | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG03491.hp2 HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.186-1978A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751561 | |||||||
| chr2:135751616 | C | T | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(294): Show |
366 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(363): Show |
intron_variant | MODIFIER | c.186-1923C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751616 | |||||||
| chr2:135751652 | T | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.186-1887T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751652 | |||||||
| chr2:135751685 | G | A | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.186-1854G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751685 | |||||||
| chr2:135751791 | A | C | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-1748A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751791 | |||||||
| chr2:135751890 | G | C | 26 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(23): Show |
32 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.186-1649G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751890 | |||||||
| chr2:135751900 | C | T | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG01433.hp2 HG03491.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-1639C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751900 | |||||||
| chr2:135751997 | A | G | 1 | a0001c0001t0003g0114 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.186-1542A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751997 | |||||||
| chr2:135752003 | T | C | 86 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(83): Show |
93 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(90): Show |
intron_variant | MODIFIER | c.186-1536T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752003 | |||||||
| chr2:135752009 | A | C | 1 | a0001c0001t0001g0179 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.186-1530A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752009 | |||||||
| chr2:135752057 | C | CT | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.186-1474dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135752057 | ||||||
| chr2:135752158 | C | G | 1 | a0001c0007t0020g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.186-1381C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752158 | |||||||
| chr2:135752268 | C | T | 3 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 |
3 | HG02559.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.186-1271C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752268 | |||||||
| chr2:135752298 | C | T | 59 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(56): Show |
81 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.186-1241C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752298 | |||||||
| chr2:135752385 | T | C | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-1154T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752385 | |||||||
| chr2:135752442 | T | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(221): Show |
270 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(267): Show |
intron_variant | MODIFIER | c.186-1097T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752442 | |||||||
| chr2:135752489 | G | A | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-1050G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752489 | |||||||
| chr2:135752521 | T | G | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.186-1018T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752521 | |||||||
| chr2:135752588 | G | C | 8 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(5): Show |
8 | HG01433.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-951G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752588 | |||||||
| chr2:135752643 | T | C | 1 | a0001c0007t0020g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.186-896T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752643 | |||||||
| chr2:135752732 | C | A | 40 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0067 others(37): Show |
42 | HG01346.hp1 HG01952.hp2 HG01978.hp1 others(39): Show |
intron_variant | MODIFIER | c.186-807C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752732 | |||||||
| chr2:135752966 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.186-573C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752966 | |||||||
| chr2:135753013 | C | T | 1 | a0001c0001t0005g0292 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.186-526C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135753013 | |||||||
| chr2:135753017 | CT | C | 86 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0001g0183 others(83): Show |
89 | HG00639.hp1 HG01261.hp2 HG01346.hp1 others(86): Show |
intron_variant | MODIFIER | c.186-499delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135753017 | ||||||
| chr2:135753017 | CTT | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(106): Show |
150 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.186-500_186-499del others(2): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135753017 | ||||||
| chr2:135753017 | CTTT | C | 23 | a0001c0001t0001g0018 a0001c0001t0001g0153 a0001c0001t0001g0188 others(20): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.186-501_186-499del others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135753017 | ||||||
| chr2:135753243 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.186-296C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135753243 | |||||||
| chr2:135753300 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.186-239A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135753300 | |||||||
| chr2:135753721 | AT | A | 65 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(62): Show |
71 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(68): Show |
intron_variant | MODIFIER | c.214+155delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135753721 | |||||||
| chr2:135753852 | T | C | 1 | a0003c0006t0001g0202 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.214+285T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135753852 | |||||||
| chr2:135753852 | TA | T | 7 | a0001c0001t0003g0073 a0001c0001t0003g0087 a0001c0001t0003g0093 others(4): Show |
7 | NA18941.hp2 NA18945.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+286delA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135753852 | |||||||
| chr2:135753855 | A | T | 7 | a0001c0001t0003g0073 a0001c0001t0003g0087 a0001c0001t0003g0093 others(4): Show |
7 | NA18941.hp2 NA18945.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+288A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135753855 | |||||||
| chr2:135753925 | A | T | 1 | a0001c0007t0020g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.215-234A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135753925 | |||||||
| chr2:135753930 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215-229T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135753930 | |||||||
| chr2:135754005 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(81): Show |
120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.215-154A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135754005 | |||||||
| chr2:135754047 | G | T | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.215-112G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135754047 | |||||||
| chr2:135754304 | C | T | 76 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0014 others(73): Show |
79 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(76): Show |
intron_variant | MODIFIER | c.333+27C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754304 | |||||||
| chr2:135754316 | G | A | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.333+39G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754316 | |||||||
| chr2:135754328 | A | AT | 76 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(73): Show |
82 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(79): Show |
intron_variant | MODIFIER | c.333+62dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 135754328 | ||||||
| chr2:135754381 | G | C | 86 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(83): Show |
93 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(90): Show |
intron_variant | MODIFIER | c.333+104G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754381 | |||||||
| chr2:135754453 | G | A | 1 | a0001c0001t0006g0279 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.333+176G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754453 | |||||||
| chr2:135754565 | T | G | 2 | a0001c0001t0011g0147 a0001c0007t0020g0041 |
2 | HG00639.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.333+288T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754565 | |||||||
| chr2:135754569 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.333+292C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754569 | |||||||
| chr2:135754575 | G | A | 5 | a0001c0001t0003g0100 a0001c0001t0003g0109 a0001c0001t0003g0112 others(2): Show |
6 | HG02280.hp2 HG02486.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+298G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754575 | |||||||
| chr2:135754748 | G | A | 3 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 |
3 | HG02559.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.333+471G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754748 | |||||||
| chr2:135754765 | C | T | 3 | a0001c0001t0003g0076 a0001c0001t0003g0144 a0001c0001t0003g0145 |
3 | HG02451.hp1 HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.333+488C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754765 | |||||||
| chr2:135754929 | G | A | 1 | a0001c0007t0020g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.334-588G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754929 | |||||||
| chr2:135754972 | C | T | 1 | a0001c0001t0004g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.334-545C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754972 | |||||||
| chr2:135754975 | A | G | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.334-542A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754975 | |||||||
| chr2:135755013 | A | G | 4 | a0001c0001t0006g0277 a0001c0001t0006g0278 a0001c0001t0006g0279 others(1): Show |
4 | HG02258.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-504A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135755013 | |||||||
| chr2:135755031 | G | A | 3 | a0001c0001t0003g0014 a0001c0001t0003g0082 a0001c0001t0003g0110 |
4 | NA18955.hp1 NA18999.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-486G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135755031 | |||||||
| chr2:135755211 | T | TAATCATT others(17): Show |
1 | a0001c0001t0001g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.334-302_334-279dup others(24): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 135755211 | ||||||
| chr2:135755296 | G | T | 1 | a0001c0001t0003g0075 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.334-221G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135755296 | |||||||
| chr2:135755363 | A | T | 1 | a0001c0001t0002g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.334-154A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135755363 | |||||||
| chr2:135755703 | T | C | 1 | a0001c0001t0002g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.508+12T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135755703 | |||||||
| chr2:135755721 | A | G | 3 | a0001c0001t0006g0277 a0001c0001t0006g0278 a0001c0001t0006g0280 |
3 | HG02965.hp2 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.508+30A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135755721 | |||||||
| chr2:135755739 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.508+48C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135755739 | |||||||
| chr2:135755920 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0193 |
2 | HG02148.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.508+229T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135755920 | |||||||
| chr2:135755992 | A | G | 1 | a0001c0001t0011g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.508+301A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135755992 | |||||||
| chr2:135756100 | T | A | 47 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0007 others(44): Show |
65 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.508+409T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135756100 | |||||||
| chr2:135756131 | A | AAAT | 8 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(5): Show |
8 | HG01433.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.508+442_508+444dup others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135756131 | ||||||
| chr2:135756504 | A | T | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.508+813A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135756504 | |||||||
| chr2:135756594 | G | A | 10 | a0001c0001t0003g0008 a0001c0001t0003g0034 a0001c0001t0003g0036 others(7): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.508+903G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135756594 | |||||||
| chr2:135756881 | C | T | 1 | a0001c0001t0015g0295 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.508+1190C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135756881 | |||||||
| chr2:135757139 | G | T | 66 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0067 others(63): Show |
68 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(65): Show |
intron_variant | MODIFIER | c.508+1448G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757139 | |||||||
| chr2:135757276 | C | T | 10 | a0001c0001t0003g0008 a0001c0001t0003g0034 a0001c0001t0003g0036 others(7): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.508+1585C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757276 | |||||||
| chr2:135757431 | G | A | 1 | a0001c0001t0005g0287 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.508+1740G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757431 | |||||||
| chr2:135757496 | T | C | 3 | a0001c0001t0005g0281 a0001c0001t0005g0283 a0001c0001t0005g0288 |
3 | HG03017.hp2 HG03654.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.508+1805T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757496 | |||||||
| chr2:135757700 | A | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.508+2009A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757700 | |||||||
| chr2:135757785 | A | AT | 6 | a0001c0001t0001g0178 a0001c0001t0001g0218 a0001c0001t0003g0072 others(3): Show |
6 | HG01261.hp2 HG02055.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.508+2109dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135757785 | ||||||
| chr2:135757785 | A | T | 9 | a0001c0001t0003g0086 a0001c0002t0002g0005 a0001c0002t0002g0232 others(6): Show |
14 | HG00738.hp1 HG01496.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2094A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757785 | |||||||
| chr2:135757888 | G | A | 49 | a0001c0001t0002g0231 a0001c0001t0002g0274 a0001c0002t0002g0004 others(46): Show |
67 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.508+2197G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757888 | |||||||
| chr2:135757972 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.508+2281A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757972 | |||||||
| chr2:135758014 | A | G | 6 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0155 others(3): Show |
6 | HG02895.hp1 HG02897.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.508+2323A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758014 | |||||||
| chr2:135758075 | A | AT | 88 | a0001c0001t0001g0134 a0001c0001t0001g0141 a0001c0001t0001g0142 others(85): Show |
95 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(92): Show |
intron_variant | MODIFIER | c.508+2400dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135758075 | ||||||
| chr2:135758075 | A | ATT | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(146): Show |
192 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.508+2399_508+2400d others(4): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135758075 | ||||||
| chr2:135758151 | C | T | 30 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(27): Show |
36 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.508+2460C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758151 | |||||||
| chr2:135758231 | T | C | 30 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(27): Show |
36 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.508+2540T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758231 | |||||||
| chr2:135758289 | G | A | 76 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(73): Show |
82 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(79): Show |
intron_variant | MODIFIER | c.508+2598G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758289 | |||||||
| chr2:135758354 | A | G | 76 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(73): Show |
82 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(79): Show |
intron_variant | MODIFIER | c.508+2663A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758354 | |||||||
| chr2:135758366 | G | A | 1 | a0001c0001t0003g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.508+2675G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758366 | |||||||
| chr2:135758441 | T | A | 19 | a0001c0001t0004g0003 a0001c0001t0004g0030 a0001c0001t0004g0116 others(16): Show |
25 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.508+2750T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758441 | |||||||
| chr2:135758558 | C | T | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(290): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.508+2867C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758558 | |||||||
| chr2:135758738 | A | T | 66 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0067 others(63): Show |
68 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(65): Show |
intron_variant | MODIFIER | c.508+3047A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758738 | |||||||
| chr2:135758764 | A | ATTTTTTT others(29): Show |
1 | a0001c0001t0002g0230 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.509-3042_509-3041i others(38): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135758764 | ||||||
| chr2:135758782 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.509-3036A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758782 | |||||||
| chr2:135758806 | T | C | 1 | a0001c0001t0003g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.509-3012T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758806 | |||||||
| chr2:135758808 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0223 |
2 | HG02129.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.509-3010C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758808 | |||||||
| chr2:135758846 | C | T | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(4): Show |
7 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.509-2972C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758846 | |||||||
| chr2:135758903 | C | T | 21 | a0001c0001t0004g0003 a0001c0001t0004g0030 a0001c0001t0004g0116 others(18): Show |
27 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.509-2915C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758903 | |||||||
| chr2:135758938 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.509-2880T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758938 | |||||||
| chr2:135758978 | C | T | 1 | a0001c0001t0011g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.509-2840C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758978 | |||||||
| chr2:135759178 | A | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(113): Show |
158 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.509-2640A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759178 | |||||||
| chr2:135759190 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.509-2628A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759190 | |||||||
| chr2:135759324 | T | TA | 10 | a0001c0001t0003g0008 a0001c0001t0003g0034 a0001c0001t0003g0036 others(7): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.509-2492dupA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135759324 | ||||||
| chr2:135759400 | G | A | 50 | a0001c0001t0002g0231 a0001c0001t0002g0274 a0001c0001t0004g0126 others(47): Show |
68 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.509-2418G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759400 | |||||||
| chr2:135759451 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.509-2367C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759451 | |||||||
| chr2:135759577 | G | C | 1 | a0001c0001t0001g0010 | 3 | HG00621.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.509-2241G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759577 | |||||||
| chr2:135759607 | A | G | 10 | a0001c0001t0003g0008 a0001c0001t0003g0034 a0001c0001t0003g0036 others(7): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.509-2211A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759607 | |||||||
| chr2:135759621 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.509-2197G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759621 | |||||||
| chr2:135759766 | A | AT | 26 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(23): Show |
26 | HG00639.hp1 HG00673.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.509-2030dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135759766 | ||||||
| chr2:135759766 | A | ATT | 157 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(154): Show |
203 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.509-2031_509-2030d others(4): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135759766 | ||||||
| chr2:135759766 | A | ATTT | 30 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(27): Show |
50 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.509-2032_509-2030d others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135759766 | ||||||
| chr2:135759766 | ATT | A | 60 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0067 others(57): Show |
62 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(59): Show |
intron_variant | MODIFIER | c.509-2031_509-2030d others(4): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135759766 | ||||||
| chr2:135759799 | C | T | 23 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(20): Show |
24 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.509-2019C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759799 | |||||||
| chr2:135759901 | C | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(281): Show |
352 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(349): Show |
intron_variant | MODIFIER | c.509-1917C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759901 | |||||||
| chr2:135760062 | C | A | 1 | a0001c0007t0020g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.509-1756C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135760062 | |||||||
| chr2:135760122 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.509-1696C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135760122 | |||||||
| chr2:135760201 | G | T | 1 | a0001c0003t0001g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.509-1617G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135760201 | |||||||
| chr2:135760533 | T | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(83): Show |
122 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.509-1285T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135760533 | |||||||
| chr2:135760603 | C | CA | 3 | a0001c0001t0001g0158 a0001c0001t0001g0167 a0001c0001t0001g0191 |
3 | NA18952.hp1 NA19070.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.509-1215_509-1214i others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135760603 | |||||||
| chr2:135760691 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02896.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.509-1127A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135760691 | |||||||
| chr2:135761411 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.509-407C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135761411 | |||||||
| chr2:135761430 | TG | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
202 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.509-386delG | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135761430 | ||||||
| chr2:135761547 | C | T | 1 | a0001c0001t0003g0086 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.509-271C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135761547 | |||||||
| chr2:135761936 | C | A | 5 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0187 others(2): Show |
5 | NA18939.hp2 NA18941.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.602+25C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135761936 | |||||||
| chr2:135761937 | A | G | 1 | a0001c0007t0020g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.602+26A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135761937 | |||||||
| chr2:135762143 | C | A | 1 | a0001c0001t0003g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.602+232C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762143 | |||||||
| chr2:135762292 | C | T | 54 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0067 others(51): Show |
56 | HG01261.hp2 HG01346.hp1 HG01952.hp2 others(53): Show |
intron_variant | MODIFIER | c.602+381C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762292 | |||||||
| chr2:135762473 | C | T | 60 | a0001c0001t0001g0209 a0001c0001t0002g0006 a0001c0001t0002g0225 others(57): Show |
82 | HG00280.hp1 HG00642.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.602+562C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762473 | |||||||
| chr2:135762487 | A | G | 2 | a0001c0002t0002g0241 a0001c0002t0002g0262 |
2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.602+576A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762487 | |||||||
| chr2:135762530 | T | A | 66 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0067 others(63): Show |
68 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(65): Show |
intron_variant | MODIFIER | c.602+619T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762530 | |||||||
| chr2:135762531 | A | T | 1 | a0001c0001t0012g0150 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.602+620A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762531 | |||||||
| chr2:135762578 | T | A | 3 | a0001c0001t0003g0076 a0001c0001t0003g0144 a0001c0001t0003g0145 |
3 | HG02451.hp1 HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.602+667T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762578 | |||||||
| chr2:135762616 | T | G | 76 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(73): Show |
82 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(79): Show |
intron_variant | MODIFIER | c.602+705T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762616 | |||||||
| chr2:135762625 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG03491.hp2 HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.602+714G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762625 | |||||||
| chr2:135762648 | TC | T | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.602+738delC | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762648 | |||||||
| chr2:135762665 | A | C | 2 | a0001c0003t0001g0044 a0001c0003t0001g0054 |
2 | NA18988.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.602+754A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762665 | |||||||
| chr2:135762735 | G | A | 10 | a0001c0001t0003g0008 a0001c0001t0003g0034 a0001c0001t0003g0036 others(7): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.602+824G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762735 | |||||||
| chr2:135763134 | C | T | 1 | a0001c0001t0003g0089 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602+1223C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763134 | |||||||
| chr2:135763341 | TACTA | T | 10 | a0001c0001t0003g0008 a0001c0001t0003g0034 a0001c0001t0003g0036 others(7): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.602+1431_602+1434d others(6): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763341 | |||||||
| chr2:135763669 | T | A | 1 | a0001c0002t0002g0234 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.602+1758T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763669 | |||||||
| chr2:135763671 | C | A | 1 | a0001c0002t0002g0234 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.602+1760C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763671 | |||||||
| chr2:135763673 | A | G | 10 | a0001c0001t0003g0008 a0001c0001t0003g0034 a0001c0001t0003g0036 others(7): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.602+1762A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763673 | |||||||
| chr2:135763862 | C | T | 1 | a0001c0001t0003g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.602+1951C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763862 | |||||||
| chr2:135763925 | G | A | 1 | a0001c0001t0003g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.602+2014G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763925 | |||||||
| chr2:135763944 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(72): Show |
111 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.602+2033G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763944 | |||||||
| chr2:135764025 | G | A | 66 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0067 others(63): Show |
68 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(65): Show |
intron_variant | MODIFIER | c.602+2114G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764025 | |||||||
| chr2:135764128 | TAAATA | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(126): Show |
167 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.602+2236_602+2240d others(7): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 135764128 | ||||||
| chr2:135764134 | A | C | 5 | a0001c0001t0003g0073 a0001c0001t0003g0087 a0001c0001t0003g0093 others(2): Show |
5 | NA18947.hp2 NA18970.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.602+2223A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764134 | |||||||
| chr2:135764160 | A | G | 2 | a0001c0003t0001g0049 a0001c0003t0001g0061 |
2 | HG00558.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.602+2249A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764160 | |||||||
| chr2:135764218 | G | C | 1 | a0001c0001t0004g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.602+2307G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764218 | |||||||
| chr2:135764293 | C | G | 1 | a0001c0003t0001g0048 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.602+2382C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764293 | |||||||
| chr2:135764431 | A | T | 10 | a0001c0001t0003g0008 a0001c0001t0003g0034 a0001c0001t0003g0036 others(7): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.602+2520A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764431 | |||||||
| chr2:135764465 | A | G | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.602+2554A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764465 | |||||||
| chr2:135764564 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0143 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.602+2653A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764564 | |||||||
| chr2:135764620 | A | G | 1 | a0001c0001t0011g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.602+2709A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764620 | |||||||
| chr2:135764726 | G | A | 2 | a0001c0001t0003g0108 a0001c0001t0022g0090 |
2 | NA18954.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.602+2815G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764726 | |||||||
| chr2:135764806 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.602+2895T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764806 | |||||||
| chr2:135764807 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.602+2896G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764807 | |||||||
| chr2:135764824 | G | T | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.602+2913G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764824 | |||||||
| chr2:135765033 | C | T | 1 | a0001c0003t0001g0048 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.602+3122C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765033 | |||||||
| chr2:135765067 | GCTT | G | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG01433.hp2 HG03491.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.602+3161_602+3163d others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 135765067 | ||||||
| chr2:135765087 | T | G | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.602+3176T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765087 | |||||||
| chr2:135765105 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(82): Show |
121 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.602+3194C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765105 | |||||||
| chr2:135765140 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(113): Show |
158 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.602+3229A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765140 | |||||||
| chr2:135765187 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.602+3276T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765187 | |||||||
| chr2:135765208 | G | GT | 8 | a0001c0001t0001g0166 a0001c0001t0004g0118 a0001c0001t0004g0122 others(5): Show |
8 | HG00408.hp2 HG00639.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.602+3311dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 135765208 | ||||||
| chr2:135765213 | T | G | 93 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(90): Show |
100 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(97): Show |
intron_variant | MODIFIER | c.602+3302T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765213 | |||||||
| chr2:135765222 | T | C | 1 | a0001c0001t0002g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.602+3311T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765222 | |||||||
| chr2:135765254 | A | G | 41 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0067 others(38): Show |
43 | HG01346.hp1 HG01952.hp2 HG01978.hp1 others(40): Show |
intron_variant | MODIFIER | c.602+3343A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765254 | |||||||
| chr2:135765370 | C | T | 1 | a0001c0001t0003g0085 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.602+3459C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765370 | |||||||
| chr2:135765371 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(76): Show |
115 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.602+3460G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765371 | |||||||
| chr2:135765433 | A | G | 1 | a0001c0004t0003g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.602+3522A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765433 | |||||||
| chr2:135765475 | T | C | 66 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0067 others(63): Show |
68 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(65): Show |
intron_variant | MODIFIER | c.602+3564T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765475 | |||||||
| chr2:135765487 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG01433.hp2 HG03491.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.602+3576G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765487 | |||||||
| chr2:135765648 | CT | C | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(7): Show |
10 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.602+3748delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 135765648 | ||||||
| chr2:135765711 | C | A | 10 | a0001c0001t0003g0008 a0001c0001t0003g0034 a0001c0001t0003g0036 others(7): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.602+3800C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765711 | |||||||
| chr2:135765780 | G | A | 2 | a0001c0003t0001g0042 a0001c0003t0001g0043 |
2 | HG00423.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.602+3869G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765780 | |||||||
| chr2:135765824 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.602+3913C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765824 | |||||||
| chr2:135766104 | G | A | 1 | a0001c0002t0002g0226 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.603-3665G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766104 | |||||||
| chr2:135766126 | G | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.603-3643G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766126 | |||||||
| chr2:135766304 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.603-3465G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766304 | |||||||
| chr2:135766306 | T | G | 1 | a0001c0007t0020g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.603-3463T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766306 | |||||||
| chr2:135766341 | T | C | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.603-3428T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766341 | |||||||
| chr2:135766352 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.603-3417T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766352 | |||||||
| chr2:135766409 | C | T | 6 | a0001c0002t0002g0007 a0001c0002t0002g0234 a0001c0002t0002g0240 others(3): Show |
9 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.603-3360C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766409 | |||||||
| chr2:135766653 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.603-3116G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766653 | |||||||
| chr2:135766796 | A | G | 2 | a0001c0002t0002g0244 a0001c0002t0002g0245 |
2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.603-2973A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766796 | |||||||
| chr2:135767177 | A | G | 29 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(26): Show |
35 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.603-2592A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135767177 | |||||||
| chr2:135767196 | A | G | 76 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(73): Show |
82 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(79): Show |
intron_variant | MODIFIER | c.603-2573A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135767196 | |||||||
| chr2:135767520 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.603-2249T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135767520 | |||||||
| chr2:135767739 | G | T | 49 | a0001c0001t0002g0231 a0001c0001t0002g0274 a0001c0002t0002g0004 others(46): Show |
67 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.603-2030G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135767739 | |||||||
| chr2:135767893 | A | G | 29 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(26): Show |
35 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.603-1876A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135767893 | |||||||
| chr2:135768176 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.603-1593T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768176 | |||||||
| chr2:135768286 | C | A | 2 | a0001c0002t0002g0011 a0001c0002t0002g0257 |
4 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.603-1483C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768286 | |||||||
| chr2:135768290 | C | T | 1 | a0001c0001t0011g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.603-1479C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768290 | |||||||
| chr2:135768357 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.603-1412C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768357 | |||||||
| chr2:135768511 | T | G | 3 | a0001c0001t0003g0076 a0001c0001t0003g0144 a0001c0001t0003g0145 |
3 | HG02451.hp1 HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.603-1258T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768511 | |||||||
| chr2:135768603 | G | A | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.603-1166G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768603 | |||||||
| chr2:135768617 | A | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.603-1152A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768617 | |||||||
| chr2:135768732 | T | C | 8 | a0001c0001t0005g0025 a0001c0001t0005g0281 a0001c0001t0005g0283 others(5): Show |
9 | HG03017.hp2 HG03654.hp2 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.603-1037T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768732 | |||||||
| chr2:135768754 | C | G | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.603-1015C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768754 | |||||||
| chr2:135768861 | C | A | 1 | a0001c0002t0002g0237 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.603-908C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768861 | |||||||
| chr2:135768910 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.603-859C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768910 | |||||||
| chr2:135769041 | C | T | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.603-728C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135769041 | |||||||
| chr2:135769202 | A | G | 8 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(5): Show |
8 | HG01433.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.603-567A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135769202 | |||||||
| chr2:135769397 | G | GT | 61 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(58): Show |
83 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.603-358dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 135769397 | ||||||
| chr2:135769397 | GT | G | 12 | a0001c0001t0001g0175 a0001c0001t0003g0008 a0001c0001t0003g0034 others(9): Show |
13 | HG01257.hp1 HG02258.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.603-358delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 135769397 | ||||||
| chr2:135769411 | T | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(84): Show |
123 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.603-358T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135769411 | |||||||
| chr2:135769550 | G | C | 59 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(56): Show |
81 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.603-219G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135769550 | |||||||
| chr2:135769748 | G | T | 1 | a0001c0001t0005g0285 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.603-21G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135769748 | |||||||
| chr2:135769748 | GT | G | 25 | a0001c0001t0003g0073 a0001c0003t0001g0013 a0001c0003t0001g0042 others(22): Show |
26 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(23): Show |
splice_region_variant&intron_variant | LOW | c.603-8delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 135769748 | ||||||
| chr2:135769873 | G | GTGAT | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(82): Show |
121 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.657+56_657+59dupGA others(2): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 135769873 | ||||||
| chr2:135770201 | T | C | 3 | a0001c0004t0003g0026 a0001c0004t0003g0027 a0001c0004t0003g0028 |
3 | NA19002.hp1 NA19006.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.658-370T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770201 | |||||||
| chr2:135770231 | A | G | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.658-340A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770231 | |||||||
| chr2:135770416 | T | C | 2 | a0001c0003t0001g0013 a0001c0003t0001g0057 |
3 | HG02074.hp1 HG02129.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.658-155T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770416 | |||||||
| chr2:135770434 | C | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(137): Show |
183 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.658-137C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770434 | |||||||
| chr2:135770436 | A | G | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.658-135A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770436 | |||||||
| chr2:135770464 | C | A | 48 | a0001c0001t0002g0231 a0001c0002t0002g0004 a0001c0002t0002g0005 others(45): Show |
66 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.658-107C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770464 | |||||||
| chr2:135770476 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.658-95T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770476 | |||||||
| chr2:135770489 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.658-82A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770489 | |||||||
| chr2:135770787 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.822+52G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135770787 | |||||||
| chr2:135771021 | T | TACTACTA others(23): Show |
13 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(10): Show |
14 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.822+308_822+337dup others(30): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 135771021 | ||||||
| chr2:135771199 | G | A | 2 | a0001c0001t0003g0108 a0001c0001t0022g0090 |
2 | NA18954.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.822+464G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135771199 | |||||||
| chr2:135771386 | G | T | 1 | a0001c0002t0002g0239 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.822+651G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135771386 | |||||||
| chr2:135771414 | T | G | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.822+679T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135771414 | |||||||
| chr2:135771430 | G | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.822+695G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135771430 | |||||||
| chr2:135771533 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.822+798G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135771533 | |||||||
| chr2:135772116 | A | G | 1 | a0001c0001t0005g0281 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.823-304A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135772116 | |||||||
| chr2:135772183 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.823-237A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135772183 | |||||||
| chr2:135772283 | A | G | 2 | a0001c0003t0001g0042 a0001c0003t0001g0043 |
2 | HG00423.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.823-137A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135772283 | |||||||
| chr2:135772323 | T | G | 1 | a0001c0001t0014g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.823-97T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135772323 | |||||||
| chr2:135772327 | T | TA | 27 | a0001c0001t0001g0179 a0001c0002t0002g0241 a0001c0003t0001g0013 others(24): Show |
28 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.823-81dupA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 135772327 | ||||||
| chr2:135772587 | G | A | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.950+40G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772587 | |||||||
| chr2:135772678 | G | A | 76 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0014 others(73): Show |
79 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(76): Show |
intron_variant | MODIFIER | c.950+131G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772678 | |||||||
| chr2:135772694 | C | G | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.950+147C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772694 | |||||||
| chr2:135772717 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.950+170A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772717 | |||||||
| chr2:135772809 | C | T | 61 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(58): Show |
83 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.950+262C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772809 | |||||||
| chr2:135772821 | G | A | 58 | a0001c0001t0003g0009 a0001c0001t0003g0014 a0001c0001t0003g0067 others(55): Show |
60 | HG01261.hp2 HG01346.hp1 HG01952.hp2 others(57): Show |
intron_variant | MODIFIER | c.950+274G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772821 | |||||||
| chr2:135772873 | C | T | 59 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(56): Show |
81 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.950+326C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772873 | |||||||
| chr2:135772906 | G | A | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.950+359G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772906 | |||||||
| chr2:135772910 | G | A | 4 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0017g0204 others(1): Show |
4 | HG02040.hp1 NA18954.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.950+363G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772910 | |||||||
| chr2:135772968 | C | T | 1 | a0001c0001t0002g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.950+421C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772968 | |||||||
| chr2:135772986 | G | A | 76 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0014 others(73): Show |
79 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(76): Show |
intron_variant | MODIFIER | c.950+439G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772986 | |||||||
| chr2:135773037 | C | CA | 27 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(24): Show |
28 | HG00544.hp2 HG01175.hp1 HG01978.hp2 others(25): Show |
intron_variant | MODIFIER | c.950+511dupA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 135773037 | ||||||
| chr2:135773037 | C | CAAA | 48 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(45): Show |
68 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.950+509_950+511dup others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 135773037 | ||||||
| chr2:135773037 | C | CAAAA | 11 | a0001c0001t0002g0267 a0001c0001t0011g0147 a0001c0002t0002g0011 others(8): Show |
13 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.950+508_950+511dup others(4): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 135773037 | ||||||
| chr2:135773037 | CA | C | 11 | a0001c0001t0001g0137 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.950+511delA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 135773037 | ||||||
| chr2:135773038 | A | C | 1 | a0001c0001t0003g0092 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.950+491A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773038 | |||||||
| chr2:135773045 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.950+498A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773045 | |||||||
| chr2:135773070 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.950+523A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773070 | |||||||
| chr2:135773169 | C | T | 4 | a0001c0001t0006g0277 a0001c0001t0006g0278 a0001c0001t0006g0279 others(1): Show |
4 | HG02258.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.950+622C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773169 | |||||||
| chr2:135773645 | T | A | 1 | a0001c0001t0009g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.950+1098T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773645 | |||||||
| chr2:135773649 | G | A | 1 | a0001c0002t0002g0252 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.950+1102G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773649 | |||||||
| chr2:135773657 | A | C | 1 | a0001c0001t0001g0195 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.950+1110A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773657 | |||||||
| chr2:135773682 | C | A | 76 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0014 others(73): Show |
79 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(76): Show |
intron_variant | MODIFIER | c.950+1135C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773682 | |||||||
| chr2:135774233 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.950+1686G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774233 | |||||||
| chr2:135774477 | G | A | 1 | a0001c0001t0004g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.951-1772G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774477 | |||||||
| chr2:135774480 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.951-1769A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774480 | |||||||
| chr2:135774501 | A | G | 2 | a0001c0002t0002g0250 a0001c0002t0002g0251 |
2 | NA18968.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.951-1748A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774501 | |||||||
| chr2:135774632 | G | T | 1 | a0001c0002t0002g0024 | 2 | HG02083.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.951-1617G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774632 | |||||||
| chr2:135774655 | G | A | 50 | a0001c0001t0002g0231 a0001c0001t0002g0274 a0001c0002t0002g0004 others(47): Show |
68 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.951-1594G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774655 | |||||||
| chr2:135774674 | G | A | 1 | a0001c0002t0002g0248 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.951-1575G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774674 | |||||||
| chr2:135774801 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.951-1448C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774801 | |||||||
| chr2:135774824 | G | A | 8 | a0001c0004t0003g0026 a0001c0004t0003g0027 a0001c0004t0003g0028 others(5): Show |
8 | HG01358.hp1 HG01993.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.951-1425G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774824 | |||||||
| chr2:135774844 | C | CA | 25 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(22): Show |
26 | HG01433.hp2 HG01978.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.951-1390dupA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 135774844 | ||||||
| chr2:135774948 | T | G | 30 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(27): Show |
36 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.951-1301T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774948 | |||||||
| chr2:135774958 | A | G | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.951-1291A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774958 | |||||||
| chr2:135775018 | T | C | 1 | a0001c0001t0002g0267 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.951-1231T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775018 | |||||||
| chr2:135775185 | G | T | 1 | a0001c0001t0011g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.951-1064G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775185 | |||||||
| chr2:135775243 | C | T | 18 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(15): Show |
19 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.951-1006C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775243 | |||||||
| chr2:135775347 | C | G | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.951-902C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775347 | |||||||
| chr2:135775540 | G | A | 1 | a0001c0002t0002g0241 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.951-709G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775540 | |||||||
| chr2:135775591 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.951-658G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775591 | |||||||
| chr2:135775625 | G | A | 76 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0014 others(73): Show |
79 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(76): Show |
intron_variant | MODIFIER | c.951-624G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775625 | |||||||
| chr2:135775761 | A | G | 1 | a0001c0001t0015g0295 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.951-488A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775761 | |||||||
| chr2:135775798 | G | A | 8 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(5): Show |
8 | HG01433.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.951-451G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775798 | |||||||
| chr2:135775858 | C | A | 2 | a0001c0001t0003g0083 a0001c0001t0003g0113 |
2 | NA19058.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.951-391C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775858 | |||||||
| chr2:135775859 | C | T | 1 | a0001c0001t0004g0033 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.951-390C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775859 | |||||||
| chr2:135775917 | A | G | 1 | a0001c0001t0003g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.951-332A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775917 | |||||||
| chr2:135776015 | C | G | 10 | a0001c0001t0003g0008 a0001c0001t0003g0034 a0001c0001t0003g0036 others(7): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.951-234C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135776015 | |||||||
| chr2:135776217 | A | G | 1 | a0001c0001t0015g0295 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.951-32A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135776217 | |||||||
| chr2:135776423 | A | G | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1053+72A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135776423 | |||||||
| chr2:135776431 | G | T | 1 | a0001c0001t0005g0284 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1053+80G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135776431 | |||||||
| chr2:135776598 | T | C | 10 | a0001c0001t0003g0008 a0001c0001t0003g0034 a0001c0001t0003g0036 others(7): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1053+247T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135776598 | |||||||
| chr2:135776696 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1053+345C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135776696 | |||||||
| chr2:135776733 | T | TA | 8 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(5): Show |
8 | HG01433.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1053+383dupA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 135776733 | ||||||
| chr2:135777064 | A | G | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1053+713A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777064 | |||||||
| chr2:135777183 | G | A | 1 | a0001c0001t0003g0096 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1053+832G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777183 | |||||||
| chr2:135777205 | T | C | 1 | a0001c0001t0003g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1053+854T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777205 | |||||||
| chr2:135777349 | C | T | 1 | a0001c0007t0020g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1053+998C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777349 | |||||||
| chr2:135777379 | T | G | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1053+1028T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777379 | |||||||
| chr2:135777665 | T | A | 51 | a0001c0001t0002g0231 a0001c0001t0002g0274 a0001c0001t0011g0147 others(48): Show |
69 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1054-1283T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777665 | |||||||
| chr2:135777712 | A | G | 4 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0071 others(1): Show |
4 | HG01261.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054-1236A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777712 | |||||||
| chr2:135777719 | C | G | 1 | a0001c0001t0011g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1054-1229C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777719 | |||||||
| chr2:135777775 | C | T | 1 | a0001c0001t0011g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1054-1173C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777775 | |||||||
| chr2:135777794 | A | C | 76 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(73): Show |
82 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(79): Show |
intron_variant | MODIFIER | c.1054-1154A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777794 | |||||||
| chr2:135777840 | G | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(83): Show |
122 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1054-1108G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777840 | |||||||
| chr2:135777888 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1054-1060A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777888 | |||||||
| chr2:135778137 | A | C | 2 | a0001c0001t0011g0147 a0001c0007t0020g0041 |
2 | HG00639.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1054-811A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778137 | |||||||
| chr2:135778156 | G | A | 4 | a0001c0001t0006g0277 a0001c0001t0006g0278 a0001c0001t0006g0279 others(1): Show |
4 | HG02258.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054-792G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778156 | |||||||
| chr2:135778174 | C | CA | 49 | a0001c0001t0001g0132 a0001c0001t0001g0141 a0001c0001t0001g0142 others(46): Show |
51 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.1054-760dupA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 135778174 | ||||||
| chr2:135778180 | A | C | 5 | a0001c0001t0005g0025 a0001c0001t0005g0284 a0001c0001t0005g0285 others(2): Show |
6 | NA18947.hp1 NA18952.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054-768A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778180 | |||||||
| chr2:135778188 | AC | A | 39 | a0001c0001t0002g0274 a0001c0002t0002g0004 a0001c0002t0002g0005 others(36): Show |
53 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.1054-759delC | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778188 | |||||||
| chr2:135778189 | C | A | 11 | a0001c0001t0008g0120 a0001c0002t0002g0004 a0001c0002t0002g0005 others(8): Show |
12 | HG01175.hp2 HG01192.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1054-759C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778189 | |||||||
| chr2:135778202 | A | C | 1 | a0001c0001t0001g0173 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1054-746A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778202 | |||||||
| chr2:135778306 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(231): Show |
284 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.1054-642G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778306 | |||||||
| chr2:135778321 | C | T | 1 | a0001c0002t0002g0229 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1054-627C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778321 | |||||||
| chr2:135778525 | G | A | 49 | a0001c0001t0002g0231 a0001c0001t0002g0274 a0001c0002t0002g0004 others(46): Show |
67 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1054-423G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778525 | |||||||
| chr2:135778543 | C | G | 76 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(73): Show |
82 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(79): Show |
intron_variant | MODIFIER | c.1054-405C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778543 | |||||||
| chr2:135778861 | A | G | 1 | a0001c0001t0011g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1054-87A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778861 | |||||||
| chr2:135779322 | CA | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.1185+251delA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 135779322 | ||||||
| chr2:135779375 | A | T | 1 | a0001c0001t0003g0080 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1185+296A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135779375 | |||||||
| chr2:135779487 | G | A | 86 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(83): Show |
93 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(90): Show |
intron_variant | MODIFIER | c.1185+408G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135779487 | |||||||
| chr2:135779536 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1185+457A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135779536 | |||||||
| chr2:135779595 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0179 |
2 | HG00544.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1185+516G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135779595 | |||||||
| chr2:135779633 | A | G | 1 | a0001c0001t0002g0268 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1186-550A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135779633 | |||||||
| chr2:135779689 | A | G | 1 | a0001c0002t0002g0262 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1186-494A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135779689 | |||||||
| chr2:135779819 | CAAT | C | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1186-362_1186-360d others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 135779819 | ||||||
| chr2:135779843 | TATTATAT others(6): Show |
T | 1 | a0001c0003t0001g0063 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1186-323_1186-311d others(15): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 135779843 | ||||||
| chr2:135779872 | TTTATAA | T | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1186-303_1186-298d others(8): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 135779872 | ||||||
| chr2:135779880 | TATA | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(75): Show |
114 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1186-299_1186-297d others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 135779880 | ||||||
| chr2:135779902 | AATAT | A | 86 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(83): Show |
93 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(90): Show |
intron_variant | MODIFIER | c.1186-275_1186-272d others(6): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 135779902 | ||||||
| chr2:135779947 | GTTA | G | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(7): Show |
10 | HG02109.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1186-231_1186-229d others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 135779947 | ||||||
| chr2:135780051 | T | C | 1 | a0001c0001t0003g0221 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1186-132T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135780051 | |||||||
| chr2:135780089 | C | T | 3 | a0001c0001t0003g0083 a0001c0001t0003g0091 a0001c0001t0003g0113 |
3 | NA19058.hp2 NA19078.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1186-94C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135780089 | |||||||
| chr2:135780427 | A | T | 1 | a0001c0001t0003g0091 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1388+42A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135780427 | |||||||
| chr2:135780479 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1388+94T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135780479 | |||||||
| chr2:135780547 | A | T | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1388+162A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135780547 | |||||||
| chr2:135781092 | G | A | 1 | a0001c0001t0002g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1388+707G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781092 | |||||||
| chr2:135781170 | G | A | 4 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1388+785G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781170 | |||||||
| chr2:135781206 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(290): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.1388+821A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781206 | |||||||
| chr2:135781303 | C | A | 1 | a0001c0002t0002g0227 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1388+918C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781303 | |||||||
| chr2:135781317 | G | T | 1 | a0001c0001t0004g0033 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1388+932G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781317 | |||||||
| chr2:135781323 | A | G | 3 | a0001c0001t0003g0097 a0001c0001t0003g0111 a0001c0001t0018g0009 |
3 | NA18939.hp1 NA18959.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1388+938A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781323 | |||||||
| chr2:135781369 | T | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(222): Show |
271 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(268): Show |
intron_variant | MODIFIER | c.1388+984T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781369 | |||||||
| chr2:135781374 | G | A | 1 | a0001c0002t0002g0227 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1388+989G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781374 | |||||||
| chr2:135781375 | C | G | 1 | a0001c0002t0002g0227 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1388+990C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781375 | |||||||
| chr2:135781406 | T | C | 1 | a0001c0001t0003g0108 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1388+1021T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781406 | |||||||
| chr2:135781472 | A | T | 1 | a0001c0001t0003g0079 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1388+1087A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781472 | |||||||
| chr2:135781552 | G | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(84): Show |
123 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1388+1167G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781552 | |||||||
| chr2:135781583 | G | A | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1389-1166G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781583 | |||||||
| chr2:135781760 | C | T | 59 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(56): Show |
81 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.1389-989C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781760 | |||||||
| chr2:135781763 | G | A | 2 | a0001c0001t0001g0159 a0001c0007t0020g0041 |
2 | HG00639.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1389-986G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781763 | |||||||
| chr2:135781843 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(282): Show |
353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.1389-906T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781843 | |||||||
| chr2:135781922 | T | C | 1 | a0001c0001t0002g0265 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1389-827T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781922 | |||||||
| chr2:135781924 | G | A | 1 | a0001c0001t0004g0128 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1389-825G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781924 | |||||||
| chr2:135781943 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(138): Show |
184 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.1389-806G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781943 | |||||||
| chr2:135781972 | G | C | 2 | a0001c0003t0001g0049 a0001c0003t0001g0061 |
2 | HG00558.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.1389-777G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781972 | |||||||
| chr2:135782006 | T | C | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1389-743T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135782006 | |||||||
| chr2:135782100 | T | G | 59 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(56): Show |
81 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.1389-649T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135782100 | |||||||
| chr2:135782144 | TA | T | 4 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0134 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389-601delA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 135782144 | ||||||
| chr2:135782245 | A | G | 1 | a0001c0001t0011g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1389-504A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135782245 | |||||||
| chr2:135782327 | C | T | 24 | a0001c0003t0001g0013 a0001c0003t0001g0042 a0001c0003t0001g0043 others(21): Show |
25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1389-422C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135782327 | |||||||
| chr2:135782513 | A | G | 59 | a0001c0001t0002g0006 a0001c0001t0002g0225 a0001c0001t0002g0230 others(56): Show |
81 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.1389-236A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135782513 |