Search by Gene
| Item | Value |
|---|---|
| geneid | 221302 |
| ensemblid | ENSG00000153975.10 |
| hgncid | 21224 |
| symbol | ZUP1 |
| name | zinc finger containing ubiquitin peptidase 1 |
| refseq_nuc | NM_145062.3 |
| refseq_prot | NP_659499.2 |
| ensembl_nuc | ENST00000368576.8 |
| ensembl_prot | ENSP00000357565.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 116635618 |
| end | 116668766 |
| strand | - |
| ver | v1.2 |
| region | chr6:116635618-116668766 |
| region5000 | chr6:116630618-116673766 |
| regionname0 | ZUP1_chr6_116635618_116668766 |
| regionname5000 | ZUP1_chr6_116630618_116673766 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 578 | 210 | 45 | 27 | 105 | 11 | 20 | ZUP1_chr6_116630618_116673766 | ZUP1 | MLSCN others(573): Show |
chr6 | 116630618 | 116673766 |
| a0002 | 0/0 | 578 | 165 | 42 | 30 | 62 | 7 | 24 | ZUP1_chr6_116630618_116673766 | ZUP1 | MLSCN others(573): Show |
chr6 | 116630618 | 116673766 |
| a0003 | 0/0 | 578 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | MLSCN others(573): Show |
chr6 | 116630618 | 116673766 |
| a0004 | 0/0 | 578 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | MLSCN others(573): Show |
chr6 | 116630618 | 116673766 |
| a0005 | 0/0 | 578 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | MLSCN others(573): Show |
chr6 | 116630618 | 116673766 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1734 | 208 | 44 | 27 | 104 | 11 | 20 | ZUP1_chr6_116630618_116673766 | ZUP1 | ATGCT others(1729): Show |
chr6 | 116630618 | 116673766 | ||
| a0001c0004 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | ATGCT others(1729): Show |
chr6 | 116630618 | 116673766 | ||
| a0001c0006 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | ATGCT others(1729): Show |
chr6 | 116630618 | 116673766 | ||
| a0002c0002 | 0/0 | 1734 | 164 | 41 | 30 | 62 | 7 | 24 | ZUP1_chr6_116630618_116673766 | ZUP1 | ATGCT others(1729): Show |
chr6 | 116630618 | 116673766 | ||
| a0002c0003 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | ATGCT others(1729): Show |
chr6 | 116630618 | 116673766 | ||
| a0003c0005 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | ATGCT others(1729): Show |
chr6 | 116630618 | 116673766 | ||
| a0004c0008 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | ATGCT others(1729): Show |
chr6 | 116630618 | 116673766 | ||
| a0005c0007 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | ATGCT others(1729): Show |
chr6 | 116630618 | 116673766 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2167 | 208 | 44 | 27 | 104 | 11 | 20 | ZUP1_chr6_116630618_116673766 | ZUP1 | GAATG others(2162): Show |
chr6 | 116630618 | 116673766 |
| a0001c0004t0001 | 0/0 | 2167 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | GAATG others(2162): Show |
chr6 | 116630618 | 116673766 |
| a0001c0006t0001 | 0/0 | 2167 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | GAATG others(2162): Show |
chr6 | 116630618 | 116673766 |
| a0002c0002t0001 | 0/0 | 2167 | 152 | 35 | 29 | 61 | 7 | 20 | ZUP1_chr6_116630618_116673766 | ZUP1 | GAATG others(2162): Show |
chr6 | 116630618 | 116673766 |
| a0002c0002t0002 | 0/0 | 2167 | 11 | 6 | 0 | 1 | 0 | 4 | ZUP1_chr6_116630618_116673766 | ZUP1 | GAATG others(2162): Show |
chr6 | 116630618 | 116673766 |
| a0002c0002t0003 | 0/0 | 2167 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | GAATG others(2162): Show |
chr6 | 116630618 | 116673766 |
| a0002c0003t0001 | 0/0 | 2167 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | GAATG others(2162): Show |
chr6 | 116630618 | 116673766 |
| a0003c0005t0001 | 0/0 | 2167 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | GAATG others(2162): Show |
chr6 | 116630618 | 116673766 |
| a0004c0008t0001 | 0/0 | 2167 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | GAATG others(2162): Show |
chr6 | 116630618 | 116673766 |
| a0005c0007t0001 | 0/0 | 2167 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | GAATG others(2162): Show |
chr6 | 116630618 | 116673766 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0002 | 0/0 | 16 | 0 | 3 | 9 | 0 | 4 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0005 | 0/0 | 12 | 0 | 2 | 8 | 1 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0009 | 0/0 | 7 | 5 | 0 | 0 | 1 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0028 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0030 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0001c0006t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0003 | 0/0 | 15 | 0 | 2 | 10 | 0 | 3 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0004 | 0/0 | 12 | 0 | 4 | 3 | 4 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0016 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0026 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0040 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0002c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0003c0005t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0004c0008t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| a0005c0007t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | GBR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | GBR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0004 | EUR | FIN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0100 | EUR | FIN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00544 | hp2 | a0001 | c0006 | t0001 | g0168 | EAS | CHS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | CHS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00609 | hp1 | a0003 | c0005 | t0001 | g0140 | EAS | CHS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | CHS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | CHS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0102 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | PUR | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0033 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01358 | hp2 | a0002 | c0002 | t0003 | g0055 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | IBS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0084 | EUR | IBS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0004 | EUR | IBS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | PEL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | PEL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0107 | AMR | PEL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02148 | hp1 | a0004 | c0008 | t0001 | g0113 | AMR | PEL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0033 | AMR | PEL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CDX | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0023 | AMR | PEL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0122 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | KHV | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0121 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0145 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0073 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0074 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0115 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0026 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0067 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0060 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02895 | hp1 | a0005 | c0007 | t0001 | g0203 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0041 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0041 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0116 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0032 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0063 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | MSL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0059 | AFR | MSL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0101 | AFR | MSL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0025 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0026 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0114 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0039 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0064 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0097 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0065 | SAS | STU | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0032 | SAS | BEB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | BEB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0058 | SAS | BEB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0099 | SAS | BEB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0184 | SAS | STU | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0110 | SAS | STU | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0040 | SAS | STU | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0094 | SAS | STU | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0104 | SAS | STU | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | CHB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | YRI | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0108 | AFR | LWK | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0061 | AFR | LWK | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0112 | AFR | YRI | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0093 | AFR | YRI | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ASW | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0085 | EUR | TSI | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | TSI | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0016 | SAS | GIH | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | CLM | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0068 | AFR | MSL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0056 | AFR | MSL | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | USA | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | USA | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | USA | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | LWK | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0159 | REF | REF | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0166 | REF | REF | ZUP1_chr6_116630618_116673766 | ZUP1 | chr6 | 116630618 | 116673766 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116645895 | T | G | 1 | a0003 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.1508A>C | p.Asn503Thr | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/10 | 1724/2167 | 1508/1737 | 503/578 | chr6 | 116645895 | |||
| chr6:116652019 | T | C | 2 | a0002a0004 | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
missense_variant | MODERATE | c.1135A>G | p.Asn379Asp | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 6/10 | 1351/2167 | 1135/1737 | 379/578 | chr6 | 116652019 | |||
| chr6:116666958 | T | G | 1 | a0005 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.235A>C | p.Asn79His | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/10 | 451/2167 | 235/1737 | 79/578 | chr6 | 116666958 | |||
| chr6:116666963 | T | A | 1 | a0005 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.230A>T | p.Lys77Ile | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/10 | 446/2167 | 230/1737 | 77/578 | chr6 | 116666963 | |||
| chr6:116666964 | T | A | 1 | a0005 | 1 | HG02895.hp1 | stop_gained | HIGH | c.229A>T | p.Lys77* | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/10 | 445/2167 | 229/1737 | 77/578 | chr6 | 116666964 | |||
| chr6:116666972 | T | C | 1 | a0004 | 1 | HG02148.hp1 | missense_variant | MODERATE | c.221A>G | p.Asp74Gly | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/10 | 437/2167 | 221/1737 | 74/578 | chr6 | 116666972 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116645729 | A | T | 1 | a0001c0004 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.1674T>A | p.Ser558Ser | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/10 | 1890/2167 | 1674/1737 | 558/578 | chr6 | 116645729 | |||
| chr6:116647514 | T | C | 1 | a0001c0006 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.1413A>G | p.Glu471Glu | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 8/10 | 1629/2167 | 1413/1737 | 471/578 | chr6 | 116647514 | |||
| chr6:116656703 | A | G | 1 | a0002c0003 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.942T>C | p.Asp314Asp | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/10 | 1158/2167 | 942/1737 | 314/578 | chr6 | 116656703 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116668604 | A | G | 1 | a0002c0002t0002 | 11 | HG02129.hp2 HG02572.hp2 HG02886.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-54T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 1/10 | 1412 | chr6 | 116668604 | ||||||
| chr6:116668740 | A | G | 1 | a0002c0002t0003 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-190T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 1/10 | 1548 | chr6 | 116668740 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116635981 | A | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0119a0001c0001t0001g0126others(3): Show | 9 | NA18939.hp2 NA18954.hp2 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.1690-102T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116635981 | |||||||
| chr6:116636229 | T | C | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1690-350A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116636229 | |||||||
| chr6:116636266 | C | T | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1690-387G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116636266 | |||||||
| chr6:116636332 | T | A | 1 | a0001c0001t0001g0177 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1690-453A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116636332 | |||||||
| chr6:116636341 | G | A | 1 | a0002c0002t0001g0090 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1690-462C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116636341 | |||||||
| chr6:116636383 | G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0188 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1690-504C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116636383 | |||||||
| chr6:116636425 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1690-546T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116636425 | |||||||
| chr6:116636443 | GAATT | G | 44 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(41): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1690-568_1690-565d others(6): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116636443 | |||||||
| chr6:116636536 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1690-657T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116636536 | |||||||
| chr6:116636649 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1690-770T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116636649 | |||||||
| chr6:116636764 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1690-885T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116636764 | |||||||
| chr6:116636808 | C | G | 33 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0021others(30): Show | 52 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.1690-929G>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116636808 | |||||||
| chr6:116636842 | A | G | 5 | a0002c0002t0001g0042a0002c0002t0001g0043a0002c0002t0001g0044others(2): Show | 8 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1690-963T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116636842 | |||||||
| chr6:116636850 | A | T | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1690-971T>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116636850 | |||||||
| chr6:116636887 | G | A | 10 | a0002c0002t0002g0032a0002c0002t0002g0056a0002c0002t0002g0057others(7): Show | 11 | HG02129.hp2 HG02572.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1690-1008C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116636887 | |||||||
| chr6:116637028 | TA | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0047others(10): Show | 24 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1690-1150delT | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116637028 | |||||||
| chr6:116637084 | A | G | 1 | a0002c0002t0001g0101 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1690-1205T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116637084 | |||||||
| chr6:116637098 | A | C | 44 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(41): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1690-1219T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116637098 | |||||||
| chr6:116637489 | C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0125 | 3 | HG01168.hp1 HG01169.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1690-1610G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116637489 | |||||||
| chr6:116637490 | G | A | 45 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(42): Show | 91 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1690-1611C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116637490 | |||||||
| chr6:116637679 | G | A | 4 | a0002c0002t0001g0042a0002c0002t0001g0043a0002c0002t0001g0044others(1): Show | 7 | HG01243.hp2 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1690-1800C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116637679 | |||||||
| chr6:116637790 | C | T | 1 | a0002c0002t0001g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1690-1911G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116637790 | |||||||
| chr6:116637934 | C | A | 10 | a0002c0002t0002g0032a0002c0002t0002g0056a0002c0002t0002g0057others(7): Show | 11 | HG02129.hp2 HG02572.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1690-2055G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116637934 | |||||||
| chr6:116637934 | C | T | 1 | a0001c0001t0001g0049 | 2 | HG01261.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1690-2055G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116637934 | |||||||
| chr6:116637988 | G | A | 1 | a0002c0002t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1690-2109C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116637988 | |||||||
| chr6:116638066 | C | CA | 96 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0029others(93): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1690-2188dupT | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638066 | |||||||
| chr6:116638066 | C | CAA | 17 | a0001c0001t0001g0131a0001c0001t0001g0132a0002c0002t0001g0007others(14): Show | 28 | HG00544.hp1 HG01106.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1690-2189_1690-218 others(6): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638066 | |||||||
| chr6:116638134 | C | G | 1 | a0002c0002t0001g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1690-2255G>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638134 | |||||||
| chr6:116638249 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1690-2370T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638249 | |||||||
| chr6:116638390 | G | A | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1690-2511C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638390 | |||||||
| chr6:116638427 | A | C | 1 | a0001c0001t0001g0167 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1690-2548T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638427 | |||||||
| chr6:116638509 | C | A | 1 | a0002c0002t0001g0082 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1690-2630G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638509 | |||||||
| chr6:116638526 | T | C | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1690-2647A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638526 | |||||||
| chr6:116638717 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1690-2838G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638717 | |||||||
| chr6:116638759 | C | T | 1 | a0002c0002t0001g0138 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1690-2880G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638759 | |||||||
| chr6:116638806 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1690-2927T>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638806 | |||||||
| chr6:116638853 | C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0047others(11): Show | 25 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1690-2974G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638853 | |||||||
| chr6:116638862 | C | T | 2 | a0002c0002t0001g0010a0002c0002t0001g0020 | 8 | HG00609.hp2 HG02040.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-2983G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638862 | |||||||
| chr6:116638899 | G | T | 1 | a0001c0001t0001g0135 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1690-3020C>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638899 | |||||||
| chr6:116638904 | G | A | 3 | a0002c0002t0002g0061a0002c0002t0002g0062a0002c0002t0002g0063 | 3 | HG02572.hp2 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1690-3025C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116638904 | |||||||
| chr6:116639001 | G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0119a0001c0001t0001g0126others(3): Show | 9 | NA18939.hp2 NA18954.hp2 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.1690-3122C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639001 | |||||||
| chr6:116639132 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1690-3253C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639132 | |||||||
| chr6:116639187 | G | A | 3 | a0002c0002t0001g0041a0002c0002t0001g0114a0002c0002t0001g0115 | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690-3308C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639187 | |||||||
| chr6:116639269 | A | C | 1 | a0002c0002t0001g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1690-3390T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639269 | |||||||
| chr6:116639414 | G | A | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1690-3535C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639414 | |||||||
| chr6:116639448 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1690-3569C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639448 | |||||||
| chr6:116639492 | CT | C | 3 | a0002c0002t0001g0024a0002c0002t0001g0108a0002c0002t0001g0109 | 5 | HG02572.hp1 HG02630.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1690-3614delA | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639492 | |||||||
| chr6:116639505 | G | A | 1 | a0002c0002t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1690-3626C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639505 | |||||||
| chr6:116639516 | A | G | 10 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 20 | HG00544.hp1 HG01106.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.1690-3637T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639516 | |||||||
| chr6:116639524 | C | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(33): Show | 59 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1690-3645G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639524 | |||||||
| chr6:116639532 | G | A | 10 | a0002c0002t0002g0032a0002c0002t0002g0056a0002c0002t0002g0057others(7): Show | 11 | HG02129.hp2 HG02572.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1690-3653C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639532 | |||||||
| chr6:116639539 | C | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(33): Show | 59 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1690-3660G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639539 | |||||||
| chr6:116639560 | A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(183): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1690-3681T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639560 | |||||||
| chr6:116639726 | C | A | 1 | a0002c0002t0001g0091 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1690-3847G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639726 | |||||||
| chr6:116639834 | C | T | 6 | a0002c0002t0002g0032a0002c0002t0002g0057a0002c0002t0002g0058others(3): Show | 7 | HG02129.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1690-3955G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639834 | |||||||
| chr6:116639851 | A | G | 37 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(34): Show | 60 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1690-3972T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639851 | |||||||
| chr6:116639890 | G | A | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1690-4011C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639890 | |||||||
| chr6:116639896 | C | G | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1690-4017G>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639896 | |||||||
| chr6:116639930 | A | C | 1 | a0002c0002t0001g0043 | 2 | HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1690-4051T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639930 | |||||||
| chr6:116639952 | C | T | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1690-4073G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116639952 | |||||||
| chr6:116640023 | G | A | 5 | a0002c0002t0001g0042a0002c0002t0001g0043a0002c0002t0001g0044others(2): Show | 8 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1690-4144C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640023 | |||||||
| chr6:116640057 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1690-4178G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640057 | |||||||
| chr6:116640119 | G | A | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1690-4240C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640119 | |||||||
| chr6:116640156 | T | C | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1690-4277A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640156 | |||||||
| chr6:116640165 | C | T | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1690-4286G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640165 | |||||||
| chr6:116640166 | CT | C | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1690-4288delA | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640166 | |||||||
| chr6:116640241 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1690-4362C>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640241 | |||||||
| chr6:116640242 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1690-4363C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640242 | |||||||
| chr6:116640250 | T | A | 1 | a0002c0002t0001g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1690-4371A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640250 | |||||||
| chr6:116640293 | A | G | 1 | a0002c0002t0001g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1690-4414T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640293 | |||||||
| chr6:116640310 | A | G | 1 | a0002c0002t0001g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1690-4431T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640310 | |||||||
| chr6:116640397 | A | T | 3 | a0002c0002t0001g0041a0002c0002t0001g0114a0002c0002t0001g0115 | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690-4518T>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640397 | |||||||
| chr6:116640421 | T | A | 44 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(41): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1690-4542A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640421 | |||||||
| chr6:116640445 | C | T | 10 | a0002c0002t0002g0032a0002c0002t0002g0056a0002c0002t0002g0057others(7): Show | 11 | HG02129.hp2 HG02572.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1690-4566G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640445 | |||||||
| chr6:116640473 | G | C | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1690-4594C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640473 | |||||||
| chr6:116640482 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1690-4603G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640482 | |||||||
| chr6:116640483 | G | A | 1 | a0002c0002t0001g0010 | 5 | NA18965.hp2 NA18973.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.1690-4604C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640483 | |||||||
| chr6:116640492 | A | G | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1690-4613T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640492 | |||||||
| chr6:116640501 | T | C | 1 | a0002c0002t0001g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1690-4622A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640501 | |||||||
| chr6:116640553 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1690-4674T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640553 | |||||||
| chr6:116640670 | A | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0072others(3): Show | 9 | HG00099.hp2 HG01081.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1690-4791T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640670 | |||||||
| chr6:116640723 | A | G | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1690-4844T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640723 | |||||||
| chr6:116640831 | C | G | 44 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(41): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1689+4883G>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640831 | |||||||
| chr6:116640833 | C | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 7 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1689+4881G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640833 | |||||||
| chr6:116640870 | T | C | 1 | a0002c0002t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1689+4844A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640870 | |||||||
| chr6:116640903 | A | C | 1 | a0002c0003t0001g0122 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1689+4811T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640903 | |||||||
| chr6:116640951 | G | A | 10 | a0002c0002t0002g0032a0002c0002t0002g0056a0002c0002t0002g0057others(7): Show | 11 | HG02129.hp2 HG02572.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1689+4763C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116640951 | |||||||
| chr6:116641015 | G | C | 1 | a0002c0002t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1689+4699C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641015 | |||||||
| chr6:116641027 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1689+4687C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641027 | |||||||
| chr6:116641080 | A | G | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1689+4634T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641080 | |||||||
| chr6:116641086 | CAAA | C | 10 | a0002c0002t0002g0032a0002c0002t0002g0056a0002c0002t0002g0057others(7): Show | 11 | HG02129.hp2 HG02572.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1689+4625_1689+462 others(7): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641086 | |||||||
| chr6:116641091 | G | A | 130 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(127): Show | 225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1689+4623C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641091 | |||||||
| chr6:116641224 | C | A | 44 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(41): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1689+4490G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641224 | |||||||
| chr6:116641255 | C | G | 4 | a0002c0002t0002g0032a0002c0002t0002g0057a0002c0002t0002g0058others(1): Show | 5 | HG02129.hp2 HG03017.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1689+4459G>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641255 | |||||||
| chr6:116641280 | C | T | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1689+4434G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641280 | |||||||
| chr6:116641329 | C | T | 1 | a0002c0002t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1689+4385G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641329 | |||||||
| chr6:116641335 | G | A | 24 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0021others(21): Show | 42 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.1689+4379C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641335 | |||||||
| chr6:116641375 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1689+4339C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641375 | |||||||
| chr6:116641386 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1689+4328A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641386 | |||||||
| chr6:116641389 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1689+4325A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641389 | |||||||
| chr6:116641398 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1689+4316T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641398 | |||||||
| chr6:116641460 | G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0125 | 3 | HG01168.hp1 HG01169.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1689+4254C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641460 | |||||||
| chr6:116641508 | G | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(33): Show | 59 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1689+4206C>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641508 | |||||||
| chr6:116641510 | A | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(33): Show | 59 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1689+4204T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641510 | |||||||
| chr6:116641569 | C | G | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1689+4145G>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641569 | |||||||
| chr6:116641572 | C | A | 10 | a0002c0002t0002g0032a0002c0002t0002g0056a0002c0002t0002g0057others(7): Show | 11 | HG02129.hp2 HG02572.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1689+4142G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641572 | |||||||
| chr6:116641642 | G | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(33): Show | 59 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1689+4072C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641642 | |||||||
| chr6:116641647 | C | G | 1 | a0001c0001t0001g0174 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1689+4067G>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641647 | |||||||
| chr6:116641725 | C | T | 42 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0021others(39): Show | 65 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.1689+3989G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641725 | |||||||
| chr6:116641810 | G | C | 1 | a0002c0002t0001g0066 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1689+3904C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641810 | |||||||
| chr6:116641979 | C | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(33): Show | 59 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1689+3735G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641979 | |||||||
| chr6:116641985 | A | G | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1689+3729T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116641985 | |||||||
| chr6:116642013 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1689+3701C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642013 | |||||||
| chr6:116642099 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1689+3615T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642099 | |||||||
| chr6:116642105 | C | T | 1 | a0002c0002t0002g0063 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1689+3609G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642105 | |||||||
| chr6:116642108 | A | C | 1 | a0002c0002t0002g0063 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1689+3606T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642108 | |||||||
| chr6:116642116 | T | C | 130 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(127): Show | 225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1689+3598A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642116 | |||||||
| chr6:116642117 | T | C | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1689+3597A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642117 | |||||||
| chr6:116642143 | T | C | 42 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0021others(39): Show | 65 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.1689+3571A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642143 | |||||||
| chr6:116642188 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1689+3526A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642188 | |||||||
| chr6:116642365 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1689+3349G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642365 | |||||||
| chr6:116642366 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1689+3348A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642366 | |||||||
| chr6:116642367 | T | G | 91 | a0001c0001t0001g0148a0002c0002t0001g0003a0002c0002t0001g0004others(88): Show | 161 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1689+3347A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642367 | |||||||
| chr6:116642374 | A | C | 46 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0021others(43): Show | 70 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(67): Show |
intron_variant | MODIFIER | c.1689+3340T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642374 | |||||||
| chr6:116642420 | T | G | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1689+3294A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642420 | |||||||
| chr6:116642499 | A | G | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1689+3215T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642499 | |||||||
| chr6:116642569 | G | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0047others(11): Show | 25 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1689+3145C>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642569 | |||||||
| chr6:116642585 | C | A | 10 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 20 | HG00544.hp1 HG01106.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.1689+3129G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642585 | |||||||
| chr6:116642715 | C | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(33): Show | 59 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1689+2999G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642715 | |||||||
| chr6:116642790 | C | T | 43 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(40): Show | 89 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1689+2924G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642790 | |||||||
| chr6:116642949 | G | A | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1689+2765C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642949 | |||||||
| chr6:116642955 | A | C | 1 | a0002c0002t0002g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1689+2759T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642955 | |||||||
| chr6:116642975 | C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0151 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1689+2739G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116642975 | |||||||
| chr6:116643009 | G | A | 24 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0021others(21): Show | 42 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.1689+2705C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643009 | |||||||
| chr6:116643038 | C | T | 44 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(41): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1689+2676G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643038 | |||||||
| chr6:116643119 | C | A | 1 | a0001c0001t0001g0129 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1689+2595G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643119 | |||||||
| chr6:116643134 | C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0124a0001c0001t0001g0150 | 7 | HG00738.hp1 HG01074.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+2580G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643134 | |||||||
| chr6:116643135 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1689+2579C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643135 | |||||||
| chr6:116643169 | C | A | 1 | a0001c0001t0001g0181 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1689+2545G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643169 | |||||||
| chr6:116643169 | C | T | 8 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0045others(5): Show | 17 | HG00544.hp1 HG00741.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.1689+2545G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643169 | |||||||
| chr6:116643170 | G | A | 3 | a0002c0002t0001g0041a0002c0002t0001g0114a0002c0002t0001g0115 | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+2544C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643170 | |||||||
| chr6:116643176 | T | G | 4 | a0002c0002t0001g0015a0002c0002t0001g0033a0002c0002t0001g0067others(1): Show | 8 | HG00741.hp2 HG01255.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1689+2538A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643176 | |||||||
| chr6:116643191 | T | G | 6 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0045others(3): Show | 12 | HG00544.hp1 HG02132.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.1689+2523A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643191 | |||||||
| chr6:116643226 | T | G | 1 | a0002c0002t0001g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1689+2488A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643226 | |||||||
| chr6:116643298 | A | G | 24 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0021others(21): Show | 42 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.1689+2416T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643298 | |||||||
| chr6:116643374 | C | T | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1689+2340G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643374 | |||||||
| chr6:116643438 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1689+2276A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643438 | |||||||
| chr6:116643448 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1689+2266A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643448 | |||||||
| chr6:116643619 | A | G | 42 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0021others(39): Show | 65 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.1689+2095T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643619 | |||||||
| chr6:116643690 | T | A | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1689+2024A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643690 | |||||||
| chr6:116643907 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1689+1807G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116643907 | |||||||
| chr6:116644013 | G | C | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1689+1701C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644013 | |||||||
| chr6:116644158 | A | G | 1 | a0002c0002t0002g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1689+1556T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644158 | |||||||
| chr6:116644164 | T | G | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1689+1550A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644164 | |||||||
| chr6:116644246 | A | G | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1689+1468T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644246 | |||||||
| chr6:116644338 | G | A | 1 | a0002c0002t0001g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1689+1376C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644338 | |||||||
| chr6:116644385 | C | A | 3 | a0002c0002t0001g0041a0002c0002t0001g0114a0002c0002t0001g0115 | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+1329G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644385 | |||||||
| chr6:116644390 | G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(68): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1689+1324C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644390 | |||||||
| chr6:116644497 | T | C | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1689+1217A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644497 | |||||||
| chr6:116644545 | T | G | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1689+1169A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644545 | |||||||
| chr6:116644595 | C | A | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1689+1119G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644595 | |||||||
| chr6:116644631 | T | C | 1 | a0002c0002t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1689+1083A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644631 | |||||||
| chr6:116644662 | G | C | 1 | a0002c0002t0001g0021 | 3 | HG00639.hp2 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1689+1052C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644662 | |||||||
| chr6:116644695 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1689+1019C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644695 | |||||||
| chr6:116644695 | G | T | 1 | a0003c0005t0001g0140 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1689+1019C>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644695 | |||||||
| chr6:116644745 | C | T | 44 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(41): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1689+969G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644745 | |||||||
| chr6:116644756 | G | T | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1689+958C>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644756 | |||||||
| chr6:116644816 | G | A | 1 | a0002c0002t0001g0099 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1689+898C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644816 | |||||||
| chr6:116644903 | A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(196): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1689+811T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644903 | |||||||
| chr6:116644917 | G | C | 1 | a0002c0002t0001g0068 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1689+797C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116644917 | |||||||
| chr6:116645105 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1689+609C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116645105 | |||||||
| chr6:116645149 | TTAAAC | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(33): Show | 59 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1689+560_1689+564d others(7): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116645149 | |||||||
| chr6:116645287 | GA | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0125 | 3 | HG01168.hp1 HG01169.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1689+426delT | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116645287 | |||||||
| chr6:116645360 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1689+354G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116645360 | |||||||
| chr6:116645387 | C | T | 1 | a0002c0002t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1689+327G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116645387 | |||||||
| chr6:116645568 | G | A | 1 | a0002c0002t0002g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1689+146C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116645568 | |||||||
| chr6:116645583 | C | CA | 22 | a0001c0001t0001g0150a0001c0001t0001g0161a0002c0002t0001g0021others(19): Show | 30 | HG00639.hp2 HG01243.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.1689+130dupT | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116645583 | |||||||
| chr6:116645596 | A | G | 1 | a0002c0002t0001g0096 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1689+118T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 9/9 | chr6 | 116645596 | |||||||
| chr6:116646420 | A | G | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1469-486T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 8/9 | chr6 | 116646420 | |||||||
| chr6:116646494 | T | C | 10 | a0002c0002t0002g0032a0002c0002t0002g0056a0002c0002t0002g0057others(7): Show | 11 | HG02129.hp2 HG02572.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1469-560A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 8/9 | chr6 | 116646494 | |||||||
| chr6:116646694 | C | A | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1469-760G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 8/9 | chr6 | 116646694 | |||||||
| chr6:116646698 | C | G | 1 | a0002c0002t0002g0063 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1468+761G>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 8/9 | chr6 | 116646698 | |||||||
| chr6:116646730 | A | G | 1 | a0002c0002t0001g0086 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1468+729T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 8/9 | chr6 | 116646730 | |||||||
| chr6:116646945 | C | A | 1 | a0002c0002t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1468+514G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 8/9 | chr6 | 116646945 | |||||||
| chr6:116646970 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1468+489T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 8/9 | chr6 | 116646970 | |||||||
| chr6:116647050 | T | C | 130 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(127): Show | 225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1468+409A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 8/9 | chr6 | 116647050 | |||||||
| chr6:116647107 | G | A | 12 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0194others(9): Show | 15 | HG02055.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1468+352C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 8/9 | chr6 | 116647107 | |||||||
| chr6:116647218 | G | A | 4 | a0002c0002t0001g0014a0002c0002t0001g0068a0002c0002t0001g0093others(1): Show | 7 | HG02145.hp1 HG02280.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1468+241C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 8/9 | chr6 | 116647218 | |||||||
| chr6:116647302 | C | T | 3 | a0002c0002t0001g0041a0002c0002t0001g0114a0002c0002t0001g0115 | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+157G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 8/9 | chr6 | 116647302 | |||||||
| chr6:116647350 | T | C | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1468+109A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 8/9 | chr6 | 116647350 | |||||||
| chr6:116647383 | AC | A | 24 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0065others(21): Show | 42 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1468+75delG | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 8/9 | chr6 | 116647383 | |||||||
| chr6:116648018 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1317-408G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116648018 | |||||||
| chr6:116648193 | G | A | 1 | a0002c0002t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1317-583C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116648193 | |||||||
| chr6:116648350 | G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0052 | 7 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1317-740C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116648350 | |||||||
| chr6:116648450 | T | G | 1 | a0002c0002t0002g0060 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1317-840A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116648450 | |||||||
| chr6:116648520 | T | C | 1 | a0002c0002t0001g0036 | 2 | NA19003.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1317-910A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116648520 | |||||||
| chr6:116648555 | G | A | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1317-945C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116648555 | |||||||
| chr6:116648556 | A | G | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1317-946T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116648556 | |||||||
| chr6:116648610 | T | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(33): Show | 59 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1317-1000A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116648610 | |||||||
| chr6:116648656 | A | G | 24 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0021others(21): Show | 42 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.1317-1046T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116648656 | |||||||
| chr6:116648783 | G | A | 90 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(87): Show | 160 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1317-1173C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116648783 | |||||||
| chr6:116648958 | G | C | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1317-1348C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116648958 | |||||||
| chr6:116649061 | C | G | 108 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0047others(105): Show | 191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1317-1451G>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116649061 | |||||||
| chr6:116649196 | T | A | 45 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(42): Show | 91 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1317-1586A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116649196 | |||||||
| chr6:116649261 | A | T | 1 | a0001c0001t0001g0163 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1317-1651T>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116649261 | |||||||
| chr6:116649296 | C | T | 1 | a0002c0002t0001g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1317-1686G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116649296 | |||||||
| chr6:116649320 | C | G | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1317-1710G>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116649320 | |||||||
| chr6:116649370 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1317-1760T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116649370 | |||||||
| chr6:116649495 | C | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0118a0001c0001t0001g0134 | 4 | NA18942.hp2 NA18977.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1317-1885G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116649495 | |||||||
| chr6:116649497 | G | A | 2 | a0002c0002t0002g0059a0002c0002t0002g0060 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1317-1887C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116649497 | |||||||
| chr6:116649517 | G | A | 1 | a0002c0002t0001g0104 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1317-1907C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116649517 | |||||||
| chr6:116649658 | C | A | 4 | a0002c0002t0001g0015a0002c0002t0001g0023a0002c0002t0001g0106others(1): Show | 9 | HG00741.hp2 HG01255.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+1914G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116649658 | |||||||
| chr6:116649700 | C | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(10): Show | 38 | HG00408.hp2 HG02015.hp1 HG02027.hp1 others(35): Show |
intron_variant | MODIFIER | c.1316+1872G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116649700 | |||||||
| chr6:116649869 | A | C | 34 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0021others(31): Show | 53 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.1316+1703T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116649869 | |||||||
| chr6:116649880 | C | T | 1 | a0002c0002t0002g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1316+1692G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116649880 | |||||||
| chr6:116650113 | C | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0191 | 8 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1316+1459G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650113 | |||||||
| chr6:116650151 | C | T | 4 | a0002c0002t0001g0015a0002c0002t0001g0023a0002c0002t0001g0106others(1): Show | 9 | HG00741.hp2 HG01255.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+1421G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650151 | |||||||
| chr6:116650167 | A | G | 2 | a0002c0002t0001g0014a0002c0002t0001g0093 | 5 | HG02145.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316+1405T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650167 | |||||||
| chr6:116650178 | T | G | 93 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(90): Show | 164 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1316+1394A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650178 | |||||||
| chr6:116650283 | G | A | 1 | a0002c0002t0001g0066 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1316+1289C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650283 | |||||||
| chr6:116650373 | G | C | 1 | a0001c0001t0001g0048 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1316+1199C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650373 | |||||||
| chr6:116650379 | G | T | 1 | a0003c0005t0001g0140 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1316+1193C>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650379 | |||||||
| chr6:116650415 | T | TCCG | 1 | a0001c0001t0001g0019 | 4 | NA18943.hp1 NA18947.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.1316+1154_1316+115 others(7): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650415 | |||||||
| chr6:116650422 | C | CA | 9 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0171others(6): Show | 9 | HG00544.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+1149dupT | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650422 | |||||||
| chr6:116650422 | C | CAA | 25 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0021others(22): Show | 44 | HG00639.hp2 HG00741.hp2 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.1316+1148_1316+114 others(6): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650422 | |||||||
| chr6:116650422 | C | CAAA | 51 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(48): Show | 99 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1316+1147_1316+114 others(7): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650422 | |||||||
| chr6:116650422 | C | CAAAA | 11 | a0002c0002t0001g0042a0002c0002t0001g0043a0002c0002t0001g0044others(8): Show | 14 | HG00597.hp1 HG01175.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1316+1146_1316+114 others(8): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650422 | |||||||
| chr6:116650512 | A | G | 10 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 20 | HG00544.hp1 HG01106.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.1316+1060T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650512 | |||||||
| chr6:116650641 | A | G | 10 | a0002c0002t0002g0032a0002c0002t0002g0056a0002c0002t0002g0057others(7): Show | 11 | HG02129.hp2 HG02572.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1316+931T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650641 | |||||||
| chr6:116650786 | A | G | 1 | a0002c0003t0001g0122 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1316+786T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650786 | |||||||
| chr6:116650805 | C | T | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1316+767G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650805 | |||||||
| chr6:116650814 | T | C | 1 | a0001c0001t0001g0054 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1316+758A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650814 | |||||||
| chr6:116650913 | T | TAC | 32 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(29): Show | 50 | HG00140.hp1 HG00544.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1316+657_1316+658d others(4): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650913 | |||||||
| chr6:116650942 | G | A | 2 | a0002c0002t0002g0059a0002c0002t0002g0060 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1316+630C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650942 | |||||||
| chr6:116650954 | C | T | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1316+618G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116650954 | |||||||
| chr6:116651014 | T | C | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1316+558A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116651014 | |||||||
| chr6:116651436 | T | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1316+136A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 7/9 | chr6 | 116651436 | |||||||
| chr6:116652369 | T | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.962-177A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116652369 | |||||||
| chr6:116652402 | C | A | 130 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(127): Show | 225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.962-210G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116652402 | |||||||
| chr6:116652660 | T | G | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.962-468A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116652660 | |||||||
| chr6:116652694 | C | T | 2 | a0002c0002t0001g0037a0002c0002t0001g0112 | 3 | HG02257.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.962-502G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116652694 | |||||||
| chr6:116652746 | T | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(127): Show | 225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.962-554A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116652746 | |||||||
| chr6:116652764 | C | A | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.962-572G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116652764 | |||||||
| chr6:116652892 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.962-700A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116652892 | |||||||
| chr6:116652920 | T | C | 3 | a0002c0002t0001g0041a0002c0002t0001g0114a0002c0002t0001g0115 | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.962-728A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116652920 | |||||||
| chr6:116652939 | A | C | 1 | a0002c0002t0001g0083 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.962-747T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116652939 | |||||||
| chr6:116653025 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.962-833C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116653025 | |||||||
| chr6:116653071 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.962-879A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116653071 | |||||||
| chr6:116653085 | G | C | 44 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(41): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.962-893C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116653085 | |||||||
| chr6:116653260 | C | A | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.962-1068G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116653260 | |||||||
| chr6:116653376 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.962-1184A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116653376 | |||||||
| chr6:116653767 | A | G | 92 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(89): Show | 164 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.962-1575T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116653767 | |||||||
| chr6:116653923 | G | C | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.962-1731C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116653923 | |||||||
| chr6:116654013 | A | T | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.962-1821T>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116654013 | |||||||
| chr6:116654057 | C | T | 1 | a0002c0002t0001g0082 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.962-1865G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116654057 | |||||||
| chr6:116654071 | C | T | 4 | a0002c0002t0001g0014a0002c0002t0001g0068a0002c0002t0001g0093others(1): Show | 7 | HG02145.hp1 HG02280.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.962-1879G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116654071 | |||||||
| chr6:116654867 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.961+1817A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116654867 | |||||||
| chr6:116655040 | T | C | 1 | a0002c0002t0001g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.961+1644A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116655040 | |||||||
| chr6:116655054 | T | C | 1 | a0002c0002t0001g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.961+1630A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116655054 | |||||||
| chr6:116655163 | A | G | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.961+1521T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116655163 | |||||||
| chr6:116655620 | T | C | 21 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0046others(18): Show | 33 | HG00323.hp1 HG00673.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.961+1064A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116655620 | |||||||
| chr6:116655751 | T | G | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.961+933A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116655751 | |||||||
| chr6:116655936 | T | A | 1 | a0002c0002t0002g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.961+748A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116655936 | |||||||
| chr6:116656068 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0186 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.961+605_961+615del others(11): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656068 | |||||||
| chr6:116656072 | TTTTTG | T | 45 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(42): Show | 91 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.961+607_961+611del others(5): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656072 | |||||||
| chr6:116656077 | GT | G | 45 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0021others(42): Show | 68 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(65): Show |
intron_variant | MODIFIER | c.961+606delA | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656077 | |||||||
| chr6:116656085 | T | G | 45 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(42): Show | 91 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.961+599A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656085 | |||||||
| chr6:116656109 | C | T | 1 | a0002c0002t0002g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.961+575G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656109 | |||||||
| chr6:116656141 | G | A | 1 | a0002c0003t0001g0122 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.961+543C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656141 | |||||||
| chr6:116656143 | A | G | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.961+541T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656143 | |||||||
| chr6:116656156 | C | T | 44 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(41): Show | 88 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.961+528G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656156 | |||||||
| chr6:116656182 | C | T | 5 | a0002c0002t0001g0021a0002c0002t0001g0101a0002c0002t0001g0102others(2): Show | 7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.961+502G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656182 | |||||||
| chr6:116656257 | T | C | 1 | a0002c0002t0001g0095 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.961+427A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656257 | |||||||
| chr6:116656296 | C | A | 49 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(46): Show | 96 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.961+388G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656296 | |||||||
| chr6:116656311 | C | T | 28 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0023others(25): Show | 45 | HG00741.hp2 HG01123.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.961+373G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656311 | |||||||
| chr6:116656401 | A | C | 1 | a0001c0001t0001g0011 | 5 | HG00741.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.961+283T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656401 | |||||||
| chr6:116656462 | C | G | 146 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(143): Show | 249 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.961+222G>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656462 | |||||||
| chr6:116656576 | AT | A | 45 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(42): Show | 91 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.961+107delA | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 5/9 | chr6 | 116656576 | |||||||
| chr6:116656975 | T | A | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.793-123A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116656975 | |||||||
| chr6:116657004 | AAC | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(33): Show | 59 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.793-154_793-153del others(2): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116657004 | |||||||
| chr6:116657004 | AACAC | A | 77 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(74): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.793-156_793-153del others(4): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116657004 | |||||||
| chr6:116657011 | A | T | 1 | a0001c0001t0001g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.793-159T>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116657011 | |||||||
| chr6:116657022 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.793-170G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116657022 | |||||||
| chr6:116657022 | CACAA | C | 16 | a0002c0002t0001g0021a0002c0002t0001g0022a0002c0002t0001g0026others(13): Show | 24 | HG00639.hp2 HG00673.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.793-174_793-171del others(4): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116657022 | |||||||
| chr6:116657024 | C | A | 57 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(54): Show | 84 | HG00280.hp2 HG00323.hp1 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.793-172G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116657024 | |||||||
| chr6:116657026 | A | C | 12 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0027others(9): Show | 27 | HG00544.hp1 HG01106.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.793-174T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116657026 | |||||||
| chr6:116657028 | A | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 20 | HG00544.hp1 HG01106.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.793-176T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116657028 | |||||||
| chr6:116657133 | C | A | 1 | a0002c0002t0001g0096 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.793-281G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116657133 | |||||||
| chr6:116657173 | C | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | NA18966.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.793-321G>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116657173 | |||||||
| chr6:116657201 | C | T | 1 | a0002c0002t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.793-349G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116657201 | |||||||
| chr6:116657254 | A | G | 1 | a0002c0002t0001g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.793-402T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116657254 | |||||||
| chr6:116657426 | CT | C | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.793-575delA | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116657426 | |||||||
| chr6:116657486 | G | A | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.793-634C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116657486 | |||||||
| chr6:116658092 | T | TCAAA | 5 | a0002c0002t0001g0021a0002c0002t0001g0101a0002c0002t0001g0102others(2): Show | 7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.792+707_792+710dup others(4): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116658092 | |||||||
| chr6:116658195 | CA | C | 10 | a0002c0002t0002g0032a0002c0002t0002g0056a0002c0002t0002g0057others(7): Show | 11 | HG02129.hp2 HG02572.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.792+607delT | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116658195 | |||||||
| chr6:116658270 | C | T | 1 | a0002c0002t0001g0079 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.792+533G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116658270 | |||||||
| chr6:116658328 | G | C | 58 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(55): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.792+475C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116658328 | |||||||
| chr6:116658408 | C | A | 1 | a0002c0002t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.792+395G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116658408 | |||||||
| chr6:116658459 | C | T | 1 | a0002c0002t0001g0138 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.792+344G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116658459 | |||||||
| chr6:116658553 | T | C | 1 | a0001c0001t0001g0047 | 2 | HG00642.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.792+250A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116658553 | |||||||
| chr6:116658569 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.792+234C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116658569 | |||||||
| chr6:116658767 | A | G | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.792+36T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 4/9 | chr6 | 116658767 | |||||||
| chr6:116659152 | G | A | 45 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(42): Show | 91 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.671-228C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116659152 | |||||||
| chr6:116659318 | T | C | 146 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(143): Show | 249 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.671-394A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116659318 | |||||||
| chr6:116659326 | C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0162 | 3 | HG01516.hp1 HG01517.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.671-402G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116659326 | |||||||
| chr6:116659376 | A | C | 1 | a0002c0002t0001g0075 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.671-452T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116659376 | |||||||
| chr6:116659508 | T | G | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.671-584A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116659508 | |||||||
| chr6:116659630 | A | AT | 35 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0023others(32): Show | 55 | HG00741.hp2 HG01123.hp1 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.671-707_671-706ins others(1): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116659630 | |||||||
| chr6:116659630 | A | T | 95 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(92): Show | 170 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.671-706T>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116659630 | |||||||
| chr6:116659872 | TG | T | 3 | a0002c0002t0001g0041a0002c0002t0001g0114a0002c0002t0001g0115 | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+863delC | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116659872 | |||||||
| chr6:116659975 | A | G | 1 | a0002c0002t0001g0066 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.670+761T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116659975 | |||||||
| chr6:116660163 | C | T | 1 | a0002c0002t0001g0078 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.670+573G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116660163 | |||||||
| chr6:116660164 | G | A | 28 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0023others(25): Show | 45 | HG00741.hp2 HG01123.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.670+572C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116660164 | |||||||
| chr6:116660190 | T | C | 1 | a0002c0002t0001g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.670+546A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116660190 | |||||||
| chr6:116660228 | C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0129 | 3 | HG00597.hp2 HG02015.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.670+508G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116660228 | |||||||
| chr6:116660295 | G | A | 8 | a0002c0002t0001g0041a0002c0002t0001g0042a0002c0002t0001g0043others(5): Show | 12 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.670+441C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116660295 | |||||||
| chr6:116660383 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.670+353A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116660383 | |||||||
| chr6:116660385 | G | A | 3 | a0002c0002t0001g0041a0002c0002t0001g0114a0002c0002t0001g0115 | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+351C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116660385 | |||||||
| chr6:116660406 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.670+330A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116660406 | |||||||
| chr6:116660415 | A | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(33): Show | 59 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.670+321T>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116660415 | |||||||
| chr6:116660519 | T | C | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.670+217A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116660519 | |||||||
| chr6:116660662 | A | C | 1 | a0001c0001t0001g0142 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.670+74T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116660662 | |||||||
| chr6:116660664 | TC | T | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.670+71delG | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116660664 | |||||||
| chr6:116660703 | A | G | 1 | a0001c0001t0001g0054 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+33T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 3/9 | chr6 | 116660703 | |||||||
| chr6:116660904 | C | CT | 9 | a0001c0001t0001g0054a0001c0001t0001g0171a0001c0001t0001g0195others(6): Show | 12 | HG01106.hp2 HG01109.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.560-59dupA | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116660904 | |||||||
| chr6:116660926 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.560-80C>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116660926 | |||||||
| chr6:116660981 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.560-135G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116660981 | |||||||
| chr6:116661024 | A | G | 46 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(43): Show | 92 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.560-178T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116661024 | |||||||
| chr6:116661077 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.560-231A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116661077 | |||||||
| chr6:116661301 | G | C | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.560-455C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116661301 | |||||||
| chr6:116661323 | A | G | 5 | a0002c0002t0001g0021a0002c0002t0001g0101a0002c0002t0001g0102others(2): Show | 7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.560-477T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116661323 | |||||||
| chr6:116661348 | C | CA | 53 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(50): Show | 100 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.560-503dupT | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116661348 | |||||||
| chr6:116661369 | T | C | 1 | a0002c0002t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.560-523A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116661369 | |||||||
| chr6:116661556 | G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0191 | 8 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.560-710C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116661556 | |||||||
| chr6:116661755 | GA | G | 36 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0023others(33): Show | 57 | HG00741.hp2 HG01123.hp1 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.560-910delT | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116661755 | |||||||
| chr6:116661997 | G | A | 1 | a0002c0002t0001g0033 | 2 | HG01258.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.560-1151C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116661997 | |||||||
| chr6:116662002 | T | G | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.560-1156A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116662002 | |||||||
| chr6:116662170 | A | G | 2 | a0002c0002t0001g0075a0002c0002t0001g0076 | 2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.560-1324T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116662170 | |||||||
| chr6:116662179 | A | G | 1 | a0002c0002t0001g0021 | 3 | HG00639.hp2 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.560-1333T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116662179 | |||||||
| chr6:116662193 | C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0129 | 3 | HG00597.hp2 HG02015.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.560-1347G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116662193 | |||||||
| chr6:116662387 | A | AT | 10 | a0002c0002t0002g0032a0002c0002t0002g0056a0002c0002t0002g0057others(7): Show | 11 | HG02129.hp2 HG02572.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.560-1542dupA | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116662387 | |||||||
| chr6:116662399 | C | G | 4 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0123others(1): Show | 6 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.560-1553G>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116662399 | |||||||
| chr6:116662753 | C | T | 2 | a0002c0002t0001g0033a0002c0002t0001g0067 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.560-1907G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116662753 | |||||||
| chr6:116662865 | G | A | 8 | a0002c0002t0001g0041a0002c0002t0001g0042a0002c0002t0001g0043others(5): Show | 12 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.560-2019C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116662865 | |||||||
| chr6:116662901 | G | C | 1 | a0001c0001t0001g0053 | 2 | HG00099.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.560-2055C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116662901 | |||||||
| chr6:116663085 | C | T | 3 | a0002c0002t0002g0061a0002c0002t0002g0062a0002c0002t0002g0063 | 3 | HG02572.hp2 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.560-2239G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116663085 | |||||||
| chr6:116663251 | AC | A | 18 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0023others(15): Show | 34 | HG00741.hp2 HG01123.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.560-2406delG | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116663251 | |||||||
| chr6:116663322 | T | A | 94 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0007others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.560-2476A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116663322 | |||||||
| chr6:116663466 | A | C | 1 | a0002c0002t0001g0099 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.560-2620T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116663466 | |||||||
| chr6:116663785 | TA | T | 5 | a0002c0002t0001g0021a0002c0002t0001g0101a0002c0002t0001g0102others(2): Show | 7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.559+2848delT | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116663785 | |||||||
| chr6:116663806 | G | A | 1 | a0002c0002t0001g0103 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.559+2828C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116663806 | |||||||
| chr6:116663921 | T | C | 1 | a0001c0001t0001g0029 | 3 | HG02132.hp1 NA18612.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.559+2713A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116663921 | |||||||
| chr6:116663954 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.559+2680T>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116663954 | |||||||
| chr6:116664016 | T | C | 1 | a0002c0002t0001g0098 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.559+2618A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664016 | |||||||
| chr6:116664027 | T | C | 5 | a0002c0002t0001g0042a0002c0002t0001g0043a0002c0002t0001g0044others(2): Show | 8 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.559+2607A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664027 | |||||||
| chr6:116664157 | G | A | 5 | a0002c0002t0001g0021a0002c0002t0001g0101a0002c0002t0001g0102others(2): Show | 7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.559+2477C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664157 | |||||||
| chr6:116664159 | G | C | 1 | a0002c0002t0002g0058 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.559+2475C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664159 | |||||||
| chr6:116664182 | G | A | 3 | a0002c0002t0001g0033a0002c0002t0001g0065a0002c0002t0001g0067 | 4 | HG01258.hp2 HG02148.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.559+2452C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664182 | |||||||
| chr6:116664210 | C | A | 1 | a0002c0002t0001g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.559+2424G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664210 | |||||||
| chr6:116664275 | A | ACAAAAAT others(8): Show |
9 | a0002c0002t0001g0026a0002c0002t0001g0042a0002c0002t0001g0043others(6): Show | 14 | HG01106.hp2 HG01109.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.559+2344_559+2358d others(17): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664275 | |||||||
| chr6:116664406 | G | C | 1 | a0002c0002t0001g0115 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.559+2228C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664406 | |||||||
| chr6:116664428 | CA | C | 64 | a0001c0001t0001g0072a0002c0002t0001g0003a0002c0002t0001g0004others(61): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.559+2205delT | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664428 | |||||||
| chr6:116664441 | A | AC | 5 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0124others(2): Show | 10 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.559+2192_559+2193i others(3): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664441 | |||||||
| chr6:116664441 | A | C | 7 | a0001c0001t0001g0141a0002c0002t0001g0033a0002c0002t0001g0041others(4): Show | 9 | HG01258.hp2 HG02148.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.559+2193T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664441 | |||||||
| chr6:116664813 | T | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(27): Show | 75 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(72): Show |
intron_variant | MODIFIER | c.559+1821A>C | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664813 | |||||||
| chr6:116664879 | G | GAC | 6 | a0001c0001t0001g0008a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 15 | HG00408.hp2 HG02015.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.559+1753_559+1754d others(4): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664879 | |||||||
| chr6:116664879 | G | GACAC | 9 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 19 | HG00544.hp1 HG01106.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.559+1751_559+1754d others(6): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664879 | |||||||
| chr6:116664879 | GAC | G | 68 | a0001c0001t0001g0072a0002c0002t0001g0003a0002c0002t0001g0004others(65): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.559+1753_559+1754d others(4): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664879 | |||||||
| chr6:116664879 | GACAC | G | 3 | a0001c0001t0001g0193a0002c0002t0002g0056a0003c0005t0001g0140 | 3 | HG00609.hp1 HG03471.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.559+1751_559+1754d others(6): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664879 | |||||||
| chr6:116664949 | G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0195 | 3 | HG02055.hp1 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.559+1685C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116664949 | |||||||
| chr6:116665018 | A | T | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.559+1616T>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665018 | |||||||
| chr6:116665038 | T | C | 94 | a0001c0001t0001g0072a0002c0002t0001g0003a0002c0002t0001g0004others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.559+1596A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665038 | |||||||
| chr6:116665058 | T | A | 5 | a0002c0002t0001g0021a0002c0002t0001g0101a0002c0002t0001g0102others(2): Show | 7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.559+1576A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665058 | |||||||
| chr6:116665073 | G | A | 1 | a0002c0002t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.559+1561C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665073 | |||||||
| chr6:116665342 | A | C | 1 | a0001c0001t0001g0011 | 5 | HG00741.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.559+1292T>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665342 | |||||||
| chr6:116665389 | C | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0191 | 8 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.559+1245G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665389 | |||||||
| chr6:116665515 | C | T | 94 | a0001c0001t0001g0072a0002c0002t0001g0003a0002c0002t0001g0004others(91): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.559+1119G>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665515 | |||||||
| chr6:116665569 | C | CT | 9 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0136others(6): Show | 11 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.559+1064dupA | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665569 | |||||||
| chr6:116665569 | CT | C | 57 | a0001c0001t0001g0054a0001c0001t0001g0134a0001c0001t0001g0188others(54): Show | 105 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.559+1064delA | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665569 | |||||||
| chr6:116665576 | T | C | 1 | a0002c0002t0001g0100 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.559+1058A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665576 | |||||||
| chr6:116665620 | T | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0191 | 8 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.559+1014A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665620 | |||||||
| chr6:116665662 | G | A | 1 | a0002c0002t0001g0112 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.559+972C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665662 | |||||||
| chr6:116665725 | G | A | 5 | a0002c0002t0001g0021a0002c0002t0001g0101a0002c0002t0001g0102others(2): Show | 7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.559+909C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665725 | |||||||
| chr6:116665734 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.559+900A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665734 | |||||||
| chr6:116665754 | G | GT | 64 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0028others(61): Show | 98 | HG00544.hp1 HG00639.hp1 HG00673.hp1 others(95): Show |
intron_variant | MODIFIER | c.559+879dupA | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665754 | |||||||
| chr6:116665754 | G | GTT | 5 | a0001c0001t0001g0118a0002c0002t0001g0041a0002c0002t0001g0104others(2): Show | 6 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.559+878_559+879dup others(2): Show |
ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665754 | |||||||
| chr6:116665885 | C | A | 1 | a0002c0002t0001g0022 | 3 | HG00673.hp2 NA18982.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.559+749G>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116665885 | |||||||
| chr6:116666073 | G | C | 18 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0023others(15): Show | 34 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.559+561C>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116666073 | |||||||
| chr6:116666180 | T | C | 1 | a0001c0001t0001g0053 | 2 | HG00099.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.559+454A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116666180 | |||||||
| chr6:116666185 | T | C | 1 | a0002c0002t0002g0063 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.559+449A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 2/9 | chr6 | 116666185 | |||||||
| chr6:116667229 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-15-22C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 1/9 | chr6 | 116667229 | |||||||
| chr6:116667296 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-15-89C>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 1/9 | chr6 | 116667296 | |||||||
| chr6:116667480 | T | A | 3 | a0002c0002t0002g0061a0002c0002t0002g0062a0002c0002t0002g0063 | 3 | HG02572.hp2 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-15-273A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 1/9 | chr6 | 116667480 | |||||||
| chr6:116667563 | T | A | 1 | a0002c0002t0002g0064 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-15-356A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 1/9 | chr6 | 116667563 | |||||||
| chr6:116667711 | T | C | 3 | a0002c0002t0001g0041a0002c0002t0001g0114a0002c0002t0001g0115 | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-504A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 1/9 | chr6 | 116667711 | |||||||
| chr6:116667787 | T | C | 1 | a0002c0002t0001g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-15-580A>G | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 1/9 | chr6 | 116667787 | |||||||
| chr6:116667934 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-16+632T>A | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 1/9 | chr6 | 116667934 | |||||||
| chr6:116668014 | TA | T | 85 | a0001c0001t0001g0072a0002c0002t0001g0003a0002c0002t0001g0004others(82): Show | 152 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.-16+551delT | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 1/9 | chr6 | 116668014 | |||||||
| chr6:116668028 | T | A | 12 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0194others(9): Show | 15 | HG02055.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-16+538A>T | ZUP1 | ENSG00000153975.10 | transcript | ENST00000368576.8 | protein_coding | 1/9 | chr6 | 116668028 |