Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23279 |
| ensemblid | ENSG00000030066.14 |
| hgncid | 18017 |
| symbol | NUP160 |
| name | nucleoporin 160 |
| refseq_nuc | NM_015231.3 |
| refseq_prot | NP_056046.2 |
| ensembl_nuc | ENST00000378460.7 |
| ensembl_prot | ENSP00000367721.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 47778118 |
| end | 47848350 |
| strand | - |
| ver | v1.2 |
| region | chr11:47778118-47848350 |
| region5000 | chr11:47773118-47853350 |
| regionname0 | NUP160_chr11_47778118_47848350 |
| regionname5000 | NUP160_chr11_47773118_47853350 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1402 | 232 | 76 | 31 | 94 | 7 | 22 | 77 | NUP160_chr11_47773118_47853350 | NUP160 | MAAAG others(1397): Show |
chr11 | 47773118 | 47853350 |
| a0002 | 0/0 | 1402 | 84 | 8 | 27 | 26 | 5 | 18 | 21 | NUP160_chr11_47773118_47853350 | NUP160 | MAAAG others(1397): Show |
chr11 | 47773118 | 47853350 |
| a0003 | 0/0 | 1402 | 14 | 0 | 0 | 14 | 0 | 0 | 8 | NUP160_chr11_47773118_47853350 | NUP160 | MAAAG others(1397): Show |
chr11 | 47773118 | 47853350 |
| a0004 | 0/0 | 1402 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | MAAAG others(1397): Show |
chr11 | 47773118 | 47853350 |
| a0005 | 0/0 | 1402 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NUP160_chr11_47773118_47853350 | NUP160 | MAAAG others(1397): Show |
chr11 | 47773118 | 47853350 |
| a0006 | 0/0 | 1402 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | MAAAG others(1397): Show |
chr11 | 47773118 | 47853350 |
| a0007 | 0/0 | 1402 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | MAAAG others(1397): Show |
chr11 | 47773118 | 47853350 |
| a0008 | 0/0 | 359 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | MAAAG others(354): Show |
chr11 | 47773118 | 47853350 |
| a0009 | 0/0 | 1402 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | MAAAG others(1397): Show |
chr11 | 47773118 | 47853350 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4206 | 217 | 67 | 31 | 90 | 6 | 22 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4201): Show |
chr11 | 47773118 | 47853350 | ||
| a0001c0004 | 1/0 | 4206 | 5 | 4 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4201): Show |
chr11 | 47773118 | 47853350 | ||
| a0001c0005 | 0/0 | 4206 | 5 | 0 | 0 | 4 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4201): Show |
chr11 | 47773118 | 47853350 | ||
| a0001c0006 | 0/0 | 4206 | 4 | 4 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4201): Show |
chr11 | 47773118 | 47853350 | ||
| a0001c0015 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4201): Show |
chr11 | 47773118 | 47853350 | ||
| a0002c0002 | 0/0 | 4206 | 82 | 8 | 27 | 25 | 4 | 18 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4201): Show |
chr11 | 47773118 | 47853350 | ||
| a0002c0013 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4201): Show |
chr11 | 47773118 | 47853350 | ||
| a0002c0014 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4201): Show |
chr11 | 47773118 | 47853350 | ||
| a0003c0003 | 0/0 | 4206 | 14 | 0 | 0 | 14 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4201): Show |
chr11 | 47773118 | 47853350 | ||
| a0004c0007 | 0/0 | 4206 | 2 | 0 | 2 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4201): Show |
chr11 | 47773118 | 47853350 | ||
| a0005c0008 | 0/0 | 4206 | 2 | 0 | 0 | 2 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4201): Show |
chr11 | 47773118 | 47853350 | ||
| a0006c0012 | 0/0 | 4206 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4201): Show |
chr11 | 47773118 | 47853350 | ||
| a0007c0010 | 0/0 | 4206 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4201): Show |
chr11 | 47773118 | 47853350 | ||
| a0008c0011 | 0/0 | 4108 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4103): Show |
chr11 | 47773118 | 47853350 | ||
| a0009c0009 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | ATGGC others(4201): Show |
chr11 | 47773118 | 47853350 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5228 | 127 | 60 | 13 | 45 | 1 | 7 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0001c0001t0002 | 0/0 | 5228 | 83 | 7 | 15 | 45 | 4 | 12 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0001c0001t0003 | 0/0 | 5228 | 6 | 0 | 3 | 0 | 1 | 2 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0001c0001t0004 | 0/0 | 5228 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0001c0004t0001 | 1/0 | 5228 | 5 | 4 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0001c0005t0001 | 0/0 | 5228 | 5 | 0 | 0 | 4 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0001c0006t0001 | 0/0 | 5228 | 4 | 4 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0001c0015t0001 | 0/0 | 5228 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0002c0002t0001 | 0/0 | 5228 | 82 | 8 | 27 | 25 | 4 | 18 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0002c0013t0001 | 0/0 | 5228 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0002c0014t0001 | 0/0 | 5228 | 1 | 0 | 0 | 0 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0003c0003t0001 | 0/0 | 5228 | 14 | 0 | 0 | 14 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0004c0007t0001 | 0/0 | 5228 | 2 | 0 | 2 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0005c0008t0002 | 0/0 | 5228 | 2 | 0 | 0 | 2 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0006c0012t0001 | 0/0 | 5228 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0007c0010t0001 | 0/0 | 5228 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| a0008c0011t0001 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5125): Show |
chr11 | 47773118 | 47853350 |
| a0009c0009t0002 | 0/0 | 5228 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | GTTCC others(5223): Show |
chr11 | 47773118 | 47853350 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0004t0001g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0004t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0005t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0005t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0005t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0005t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0006t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0006t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0006t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0006t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0001c0015t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0013t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0002c0014t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0003c0003t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0003c0003t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0003c0003t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0003c0003t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0003c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0003c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0003c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0003c0003t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0003c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0003c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0003c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0003c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0003c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0003c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0004c0007t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0004c0007t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0005c0008t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0005c0008t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0006c0012t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0007c0010t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0008c0011t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| a0009c0009t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0186 | EUR | GBR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0188 | EUR | GBR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | FIN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0046 | EUR | FIN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0283 | EUR | FIN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0105 | EUR | FIN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00408 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | CHS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | CHS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | CHS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | CHS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | CHS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00609 | hp1 | a0001 | c0005 | t0001 | g0125 | EAS | CHS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | CHS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | CHS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00673 | hp2 | a0003 | c0003 | t0001 | g0015 | EAS | CHS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0107 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0102 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0216 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0323 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0327 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0113 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01257 | hp1 | a0004 | c0007 | t0001 | g0044 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0092 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01258 | hp2 | a0004 | c0007 | t0001 | g0114 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0075 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0095 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | IBS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01515 | hp2 | a0002 | c0014 | t0001 | g0048 | EUR | IBS | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PEL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0111 | AMR | PEL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PEL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01978 | hp2 | a0006 | c0012 | t0001 | g0078 | AMR | PEL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0079 | AMR | PEL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0103 | AMR | PEL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | KHV | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02071 | hp1 | a0002 | c0013 | t0001 | g0115 | EAS | KHV | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02083 | hp1 | a0003 | c0003 | t0001 | g0014 | EAS | KHV | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | KHV | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02155 | hp2 | a0003 | c0003 | t0001 | g0008 | EAS | CDX | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02257 | hp1 | a0001 | c0006 | t0001 | g0322 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02293 | hp1 | a0007 | c0010 | t0001 | g0259 | AMR | PEL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | PEL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02523 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | KHV | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0104 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0219 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0037 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0110 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0098 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | ESN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0220 | AFR | ESN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | ESN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02965 | hp2 | a0001 | c0015 | t0001 | g0273 | AFR | ESN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ESN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0043 | AFR | ESN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0172 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ESN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ESN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | ESN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0032 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0221 | AFR | MSL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03579 | hp2 | a0001 | c0006 | t0001 | g0264 | AFR | MSL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0108 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0285 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0304 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0018 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0077 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0106 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | BEB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | BEB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0100 | SAS | BEB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0328 | SAS | BEB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0085 | SAS | BEB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | STU | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0033 | SAS | STU | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | STU | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0101 | SAS | STU | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | STU | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0099 | SAS | STU | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0305 | SAS | STU | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | CHB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | YRI | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | YRI | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18940 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18942 | hp2 | a0003 | c0003 | t0001 | g0016 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18943 | hp2 | a0001 | c0005 | t0001 | g0123 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18944 | hp2 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18949 | hp2 | a0008 | c0011 | t0001 | g0175 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18961 | hp1 | a0005 | c0008 | t0002 | g0309 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18968 | hp2 | a0001 | c0005 | t0001 | g0050 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18977 | hp1 | a0005 | c0008 | t0002 | g0280 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18977 | hp2 | a0001 | c0005 | t0001 | g0128 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18981 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18983 | hp1 | a0009 | c0009 | t0002 | g0284 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19007 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19009 | hp2 | a0003 | c0003 | t0001 | g0013 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19011 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19088 | hp1 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19240 | hp1 | a0001 | c0006 | t0001 | g0267 | AFR | YRI | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ASW | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | ASW | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA20752 | hp1 | a0001 | c0005 | t0001 | g0224 | EUR | TSI | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0171 | EUR | TSI | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0027 | EUR | TSI | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0039 | EUR | TSI | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | GIH | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0118 | SAS | GIH | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0090 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0112 | AMR | CLM | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02559 | hp1 | a0001 | c0006 | t0001 | g0170 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0222 | AFR | MSL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | USA | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | USA | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | LWK | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | LWK | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0165 | REF | REF | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0001 | g0122 | REF | REF | NUP160_chr11_47773118_47853350 | NUP160 | chr11 | 47773118 | 47853350 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47780345 | C | T | 1 | a0004 | 2 | HG01257.hp1 HG01258.hp2 |
missense_variant&splice_region_variant | MODERATE | c.4117G>A | p.Ala1373Thr | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 35/36 | 4149/5228 | 4117/4209 | 1373/1402 | chr11 | 47780345 | |||
| chr11:47819572 | CTTCATCA others(2364): Show |
C | 1 | a0008 | 1 | NA18949.hp2 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.1078-122_1176-115d others(2): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/36 | chr11 | 47819572 | |||||||
| chr11:47822127 | C | T | 1 | a0006 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.1037G>A | p.Arg346His | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 8/36 | 1069/5228 | 1037/4209 | 346/1402 | chr11 | 47822127 | |||
| chr11:47835701 | T | C | 4 | a0002 a0003 a0004 others(1): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
missense_variant | MODERATE | c.949A>G | p.Thr317Ala | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/36 | 981/5228 | 949/4209 | 317/1402 | chr11 | 47835701 | |||
| chr11:47835770 | C | T | 1 | a0007 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.880G>A | p.Val294Ile | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/36 | 912/5228 | 880/4209 | 294/1402 | chr11 | 47835770 | |||
| chr11:47839881 | C | G | 1 | a0009 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.608G>C | p.Gly203Ala | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/36 | 640/5228 | 608/4209 | 203/1402 | chr11 | 47839881 | |||
| chr11:47840035 | T | C | 1 | a0005 | 2 | NA18961.hp1 NA18977.hp1 |
missense_variant | MODERATE | c.454A>G | p.Ile152Val | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/36 | 486/5228 | 454/4209 | 152/1402 | chr11 | 47840035 | |||
| chr11:47848303 | C | T | 1 | a0003 | 14 | HG00408.hp2 HG00673.hp2 HG02083.hp1 others(11): Show |
missense_variant | MODERATE | c.16G>A | p.Ala6Thr | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 1/36 | 48/5228 | 16/4209 | 6/1402 | chr11 | 47848303 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47779171 | T | C | 1 | a0001c0006 | 4 | HG02257.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
synonymous_variant | LOW | c.4143A>G | p.Lys1381Lys | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 36/36 | 4175/5228 | 4143/4209 | 1381/1402 | chr11 | 47779171 | |||
| chr11:47808401 | G | A | 1 | a0002c0013 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.2268C>T | p.Asp756Asp | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/36 | 2300/5228 | 2268/4209 | 756/1402 | chr11 | 47808401 | |||
| chr11:47812384 | C | T | 1 | a0001c0005 | 5 | HG00609.hp1 NA18943.hp2 NA18968.hp2 others(2): Show |
synonymous_variant | LOW | c.1896G>A | p.Arg632Arg | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 16/36 | 1928/5228 | 1896/4209 | 632/1402 | chr11 | 47812384 | |||
| chr11:47813040 | G | A | 14 | a0001c0001 a0001c0005 a0001c0006 others(11): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
synonymous_variant | LOW | c.1692C>T | p.Asp564Asp | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 15/36 | 1724/5228 | 1692/4209 | 564/1402 | chr11 | 47813040 | |||
| chr11:47835702 | G | A | 1 | a0002c0014 | 1 | HG01515.hp2 | synonymous_variant | LOW | c.948C>T | p.Pro316Pro | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/36 | 980/5228 | 948/4209 | 316/1402 | chr11 | 47835702 | |||
| chr11:47839910 | G | C | 1 | a0001c0015 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.579C>G | p.Ala193Ala | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/36 | 611/5228 | 579/4209 | 193/1402 | chr11 | 47839910 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47778223 | C | G | 4 | a0001c0001t0002 a0001c0001t0004 a0005c0008t0002 others(1): Show |
87 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*882G>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 36/36 | 882 | chr11 | 47778223 | ||||||
| chr11:47778522 | T | C | 1 | a0001c0001t0004 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*583A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 36/36 | 583 | chr11 | 47778522 | ||||||
| chr11:47779076 | C | T | 1 | a0001c0001t0003 | 6 | HG01071.hp2 HG01099.hp1 HG01257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*29G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 36/36 | 29 | chr11 | 47779076 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47779352 | T | C | 28 | a0002c0002t0001g0039 a0002c0002t0001g0040 a0002c0002t0001g0041 others(25): Show |
28 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.4120-158A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 35/35 | chr11 | 47779352 | |||||||
| chr11:47779364 | T | A | 1 | a0001c0001t0002g0192 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.4120-170A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 35/35 | chr11 | 47779364 | |||||||
| chr11:47779400 | T | G | 1 | a0001c0001t0002g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4120-206A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 35/35 | chr11 | 47779400 | |||||||
| chr11:47779458 | G | A | 11 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.4120-264C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 35/35 | chr11 | 47779458 | |||||||
| chr11:47779506 | C | G | 3 | a0001c0001t0002g0198 a0001c0001t0002g0300 a0001c0001t0002g0308 |
3 | NA18747.hp1 NA18998.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.4120-312G>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 35/35 | chr11 | 47779506 | |||||||
| chr11:47779549 | A | G | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.4120-355T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 35/35 | chr11 | 47779549 | |||||||
| chr11:47779621 | A | G | 1 | a0001c0001t0002g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4120-427T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 35/35 | chr11 | 47779621 | |||||||
| chr11:47780010 | G | A | 1 | a0001c0001t0002g0308 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4119+333C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 35/35 | chr11 | 47780010 | |||||||
| chr11:47780109 | C | A | 1 | a0001c0001t0002g0327 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4119+234G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 35/35 | chr11 | 47780109 | |||||||
| chr11:47780256 | A | T | 3 | a0002c0002t0001g0033 a0002c0002t0001g0077 a0002c0002t0001g0100 |
3 | HG03704.hp2 HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.4119+87T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 35/35 | chr11 | 47780256 | |||||||
| chr11:47780519 | G | A | 9 | a0002c0002t0001g0046 a0002c0002t0001g0110 a0002c0002t0001g0111 others(6): Show |
9 | HG00280.hp2 HG01123.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.4015-72C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47780519 | |||||||
| chr11:47780540 | CT | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(221): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.4015-94delA | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47780540 | |||||||
| chr11:47780540 | CTT | C | 100 | a0001c0001t0001g0149 a0001c0001t0002g0062 a0002c0002t0001g0001 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.4015-95_4015-94del others(2): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47780540 | |||||||
| chr11:47780840 | T | G | 1 | a0001c0001t0002g0068 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4015-393A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47780840 | |||||||
| chr11:47781218 | G | A | 5 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0227 others(2): Show |
5 | HG01255.hp2 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.4015-771C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47781218 | |||||||
| chr11:47781250 | A | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0312 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4015-803T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47781250 | |||||||
| chr11:47781577 | T | C | 1 | a0001c0001t0001g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4015-1130A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47781577 | |||||||
| chr11:47781584 | T | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0312 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4015-1137A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47781584 | |||||||
| chr11:47781685 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4015-1238A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47781685 | |||||||
| chr11:47781834 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4014+1239C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47781834 | |||||||
| chr11:47781954 | T | G | 1 | a0001c0001t0002g0290 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.4014+1119A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47781954 | |||||||
| chr11:47782054 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4014+1019C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782054 | |||||||
| chr11:47782274 | A | T | 1 | a0003c0003t0001g0003 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4014+799T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782274 | |||||||
| chr11:47782289 | T | TAAAAAAA others(3): Show |
1 | a0001c0001t0001g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4014+774_4014+783d others(12): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782289 | |||||||
| chr11:47782289 | T | TAAAAAAA others(7): Show |
1 | a0001c0001t0003g0323 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4014+770_4014+783d others(16): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782289 | |||||||
| chr11:47782289 | T | TAAAAAAA others(8): Show |
1 | a0001c0001t0003g0171 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4014+769_4014+783d others(17): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782289 | |||||||
| chr11:47782296 | AAAAAAAA others(16): Show |
A | 2 | a0002c0002t0001g0030 a0002c0002t0001g0094 |
2 | NA18956.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.4014+754_4014+776d others(25): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782296 | |||||||
| chr11:47782297 | A | T | 1 | a0002c0002t0001g0076 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.4014+776T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782297 | |||||||
| chr11:47782298 | AAAAAAAT others(4): Show |
A | 7 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0052 others(4): Show |
7 | HG00438.hp1 HG01358.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.4014+764_4014+774d others(13): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782298 | |||||||
| chr11:47782298 | AAAAAAAT others(6): Show |
A | 1 | a0002c0002t0001g0076 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.4014+762_4014+774d others(15): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782298 | |||||||
| chr11:47782298 | AAAAAAAT others(12): Show |
A | 1 | a0002c0002t0001g0034 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.4014+756_4014+774d others(21): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782298 | |||||||
| chr11:47782298 | AAAAAAAT others(14): Show |
A | 2 | a0002c0002t0001g0033 a0002c0002t0001g0099 |
2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.4014+754_4014+774d others(23): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782298 | |||||||
| chr11:47782298 | AAAAAAAT others(16): Show |
A | 5 | a0002c0002t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0077 others(2): Show |
5 | HG01433.hp2 HG02738.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.4014+752_4014+774d others(25): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782298 | |||||||
| chr11:47782298 | AAAAAAAT others(18): Show |
A | 1 | a0002c0002t0001g0038 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4014+750_4014+774d others(27): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782298 | |||||||
| chr11:47782299 | A | T | 1 | a0002c0002t0001g0075 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4014+774T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782299 | |||||||
| chr11:47782300 | AAAAATAT others(4): Show |
A | 1 | a0002c0002t0001g0088 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.4014+762_4014+772d others(13): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782300 | |||||||
| chr11:47782300 | AAAAATAT others(6): Show |
A | 1 | a0002c0002t0001g0053 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4014+760_4014+772d others(15): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782300 | |||||||
| chr11:47782300 | AAAAATAT others(12): Show |
A | 1 | a0003c0003t0001g0014 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4014+754_4014+772d others(21): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782300 | |||||||
| chr11:47782300 | AAAAATAT others(16): Show |
A | 2 | a0002c0002t0001g0018 a0002c0002t0001g0118 |
2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4014+750_4014+772d others(25): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782300 | |||||||
| chr11:47782300 | AAAAATAT others(20): Show |
A | 2 | a0001c0001t0002g0061 a0001c0001t0002g0302 |
2 | NA18940.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.4014+746_4014+772d others(29): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782300 | |||||||
| chr11:47782301 | A | T | 9 | a0002c0002t0001g0017 a0002c0002t0001g0025 a0002c0002t0001g0037 others(6): Show |
9 | HG00735.hp1 HG01123.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.4014+772T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782301 | |||||||
| chr11:47782301 | AAAATATA others(19): Show |
A | 8 | a0001c0001t0002g0067 a0001c0001t0002g0070 a0001c0001t0002g0205 others(5): Show |
8 | NA18952.hp1 NA18983.hp1 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.4014+746_4014+771d others(28): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782301 | |||||||
| chr11:47782302 | AAATATAT others(12): Show |
A | 1 | a0006c0012t0001g0078 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4014+752_4014+770d others(21): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782302 | |||||||
| chr11:47782302 | AAATATAT others(14): Show |
A | 2 | a0002c0002t0001g0096 a0002c0002t0001g0097 |
2 | HG00544.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.4014+750_4014+770d others(23): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782302 | |||||||
| chr11:47782302 | AAATATAT others(16): Show |
A | 2 | a0001c0001t0001g0316 a0002c0002t0001g0100 |
2 | HG02145.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.4014+748_4014+770d others(25): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782302 | |||||||
| chr11:47782302 | AAATATAT others(18): Show |
A | 2 | a0001c0001t0002g0065 a0001c0001t0002g0289 |
2 | HG02148.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.4014+746_4014+770d others(27): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782302 | |||||||
| chr11:47782302 | AAATATAT others(20): Show |
A | 1 | a0001c0001t0002g0195 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.4014+744_4014+770d others(29): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782302 | |||||||
| chr11:47782303 | A | T | 16 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0025 others(13): Show |
17 | HG00735.hp1 HG01123.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.4014+770T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782303 | |||||||
| chr11:47782303 | AATATATA others(1): Show |
A | 6 | a0001c0001t0001g0325 a0001c0001t0001g0332 a0001c0006t0001g0170 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.4014+762_4014+769d others(10): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782303 | |||||||
| chr11:47782303 | AATATATA others(3): Show |
A | 7 | a0001c0001t0001g0074 a0001c0001t0001g0121 a0001c0001t0001g0182 others(4): Show |
7 | HG01884.hp2 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4014+760_4014+769d others(12): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782303 | |||||||
| chr11:47782303 | AATATATA others(5): Show |
A | 9 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(6): Show |
9 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.4014+758_4014+769d others(14): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782303 | |||||||
| chr11:47782303 | AATATATA others(7): Show |
A | 9 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0218 others(6): Show |
9 | HG01257.hp2 HG02451.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.4014+756_4014+769d others(16): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782303 | |||||||
| chr11:47782303 | AATATATA others(9): Show |
A | 4 | a0001c0001t0001g0138 a0001c0001t0001g0234 a0001c0001t0001g0237 others(1): Show |
4 | HG01109.hp2 HG06807.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.4014+754_4014+769d others(18): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782303 | |||||||
| chr11:47782303 | AATATATA others(11): Show |
A | 1 | a0001c0001t0001g0152 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.4014+752_4014+769d others(20): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782303 | |||||||
| chr11:47782303 | AATATATA others(13): Show |
A | 6 | a0001c0001t0001g0140 a0001c0001t0001g0244 a0001c0001t0001g0266 others(3): Show |
6 | HG01099.hp2 HG02293.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.4014+750_4014+769d others(22): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782303 | |||||||
| chr11:47782303 | AATATATA others(15): Show |
A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0129 a0001c0001t0001g0132 others(67): Show |
71 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.4014+748_4014+769d others(24): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782303 | |||||||
| chr11:47782303 | AATATATA others(17): Show |
A | 4 | a0001c0001t0002g0068 a0001c0001t0002g0277 a0001c0001t0002g0327 others(1): Show |
4 | HG01192.hp2 HG03471.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.4014+746_4014+769d others(26): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782303 | |||||||
| chr11:47782303 | AATATATA others(19): Show |
A | 56 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0059 others(53): Show |
56 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.4014+744_4014+769d others(28): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782303 | |||||||
| chr11:47782304 | ATATATAT others(2): Show |
A | 7 | a0001c0001t0001g0213 a0001c0001t0001g0333 a0002c0002t0001g0040 others(4): Show |
7 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.4014+760_4014+768d others(11): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782304 | |||||||
| chr11:47782304 | ATATATAT others(4): Show |
A | 8 | a0001c0001t0001g0312 a0002c0002t0001g0022 a0002c0002t0001g0045 others(5): Show |
8 | HG00438.hp2 HG02071.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4014+758_4014+768d others(13): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782304 | |||||||
| chr11:47782304 | ATATATAT others(6): Show |
A | 12 | a0001c0001t0001g0183 a0001c0001t0001g0229 a0001c0001t0001g0230 others(9): Show |
12 | HG00323.hp2 HG00741.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.4014+756_4014+768d others(15): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782304 | |||||||
| chr11:47782304 | ATATATAT others(8): Show |
A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0228 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.4014+754_4014+768d others(17): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782304 | |||||||
| chr11:47782304 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0239 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4014+752_4014+768d others(19): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782304 | |||||||
| chr11:47782304 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0225 |
2 | HG02056.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.4014+750_4014+768d others(21): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782304 | |||||||
| chr11:47782304 | ATATATAT others(14): Show |
A | 12 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0139 others(9): Show |
12 | HG00558.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.4014+748_4014+768d others(23): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782304 | |||||||
| chr11:47782304 | ATATATAT others(16): Show |
A | 10 | a0001c0001t0001g0141 a0001c0001t0001g0164 a0001c0001t0001g0249 others(7): Show |
10 | HG00280.hp2 HG01081.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.4014+746_4014+768d others(25): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782304 | |||||||
| chr11:47782304 | ATATATAT others(18): Show |
A | 8 | a0001c0001t0002g0062 a0001c0001t0002g0069 a0001c0001t0002g0199 others(5): Show |
8 | HG01433.hp1 NA18944.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.4014+744_4014+768d others(27): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782304 | |||||||
| chr11:47782304 | ATATATAT others(20): Show |
A | 2 | a0001c0001t0002g0204 a0001c0001t0002g0210 |
2 | NA19003.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4014+742_4014+768d others(29): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782304 | |||||||
| chr11:47782305 | T | A | 7 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0335 others(4): Show |
7 | HG01099.hp1 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4014+768A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782305 | |||||||
| chr11:47782307 | T | A | 5 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0334 others(2): Show |
5 | HG02896.hp2 HG02965.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.4014+766A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782307 | |||||||
| chr11:47782309 | T | A | 4 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0334 others(1): Show |
4 | HG02896.hp2 HG03017.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4014+764A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782309 | |||||||
| chr11:47782311 | T | A | 3 | a0001c0001t0001g0176 a0001c0001t0001g0179 a0001c0001t0003g0172 |
3 | HG02280.hp1 HG03017.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4014+762A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782311 | |||||||
| chr11:47782313 | T | A | 9 | a0001c0001t0001g0176 a0001c0001t0001g0325 a0001c0001t0001g0332 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.4014+760A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782313 | |||||||
| chr11:47782315 | T | A | 21 | a0001c0001t0001g0074 a0001c0001t0001g0121 a0001c0001t0001g0176 others(18): Show |
21 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.4014+758A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782315 | |||||||
| chr11:47782317 | T | A | 32 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0074 others(29): Show |
32 | HG00438.hp2 HG00642.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.4014+756A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782317 | |||||||
| chr11:47782319 | T | A | 46 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0074 others(43): Show |
46 | HG00323.hp2 HG00438.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.4014+754A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782319 | |||||||
| chr11:47782321 | T | A | 47 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0121 others(44): Show |
47 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.4014+752A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782321 | |||||||
| chr11:47782323 | T | A | 43 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0121 others(40): Show |
43 | HG01071.hp2 HG01109.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.4014+750A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782323 | |||||||
| chr11:47782325 | T | A | 38 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0121 others(35): Show |
38 | HG01071.hp2 HG01099.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.4014+748A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782325 | |||||||
| chr11:47782327 | T | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0129 a0001c0001t0001g0132 others(89): Show |
93 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.4014+746A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782327 | |||||||
| chr11:47782329 | T | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0129 a0001c0001t0001g0134 others(41): Show |
45 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.4014+744A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782329 | |||||||
| chr11:47782331 | T | A | 29 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0143 others(26): Show |
29 | HG00323.hp1 HG00733.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.4014+742A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782331 | |||||||
| chr11:47782333 | T | A | 5 | a0001c0001t0002g0191 a0001c0001t0002g0283 a0001c0001t0003g0173 others(2): Show |
5 | HG00323.hp1 HG01071.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.4014+740A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782333 | |||||||
| chr11:47782335 | T | A | 3 | a0001c0001t0003g0173 a0001c0001t0003g0174 a0001c0001t0003g0268 |
3 | HG01071.hp2 HG01257.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.4014+738A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782335 | |||||||
| chr11:47782337 | T | A | 1 | a0001c0001t0003g0268 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4014+736A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782337 | |||||||
| chr11:47782355 | T | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(88): Show |
92 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.4014+718A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782355 | |||||||
| chr11:47782359 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4014+714G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782359 | |||||||
| chr11:47782373 | T | C | 1 | a0006c0012t0001g0078 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4014+700A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782373 | |||||||
| chr11:47782389 | G | A | 11 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.4014+684C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782389 | |||||||
| chr11:47782510 | C | T | 1 | a0001c0001t0002g0274 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.4014+563G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782510 | |||||||
| chr11:47782585 | G | A | 4 | a0001c0006t0001g0170 a0001c0006t0001g0264 a0001c0006t0001g0267 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4014+488C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782585 | |||||||
| chr11:47782771 | G | A | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4014+302C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782771 | |||||||
| chr11:47782805 | C | T | 6 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG00544.hp1 HG02300.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.4014+268G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782805 | |||||||
| chr11:47782819 | T | C | 18 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0136 others(15): Show |
18 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.4014+254A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782819 | |||||||
| chr11:47782861 | G | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0311 a0001c0001t0001g0313 |
3 | HG02451.hp2 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.4014+212C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782861 | |||||||
| chr11:47782942 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4014+131T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782942 | |||||||
| chr11:47782947 | C | T | 3 | a0002c0002t0001g0102 a0002c0002t0001g0107 a0002c0002t0001g0216 |
3 | HG00741.hp1 HG01070.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.4014+126G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47782947 | |||||||
| chr11:47783042 | T | C | 1 | a0002c0002t0001g0026 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4014+31A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 34/35 | chr11 | 47783042 | |||||||
| chr11:47783310 | A | C | 1 | a0001c0001t0004g0285 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3889-112T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 33/35 | chr11 | 47783310 | |||||||
| chr11:47783376 | G | GA | 10 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3889-179dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 33/35 | chr11 | 47783376 | |||||||
| chr11:47783668 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3889-470T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 33/35 | chr11 | 47783668 | |||||||
| chr11:47783866 | G | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(207): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.3889-668C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 33/35 | chr11 | 47783866 | |||||||
| chr11:47783926 | T | C | 87 | a0001c0001t0001g0185 a0001c0001t0002g0056 a0001c0001t0002g0057 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.3889-728A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 33/35 | chr11 | 47783926 | |||||||
| chr11:47783974 | G | A | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | NA19056.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.3889-776C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 33/35 | chr11 | 47783974 | |||||||
| chr11:47784006 | TA | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(306): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.3889-809delT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 33/35 | chr11 | 47784006 | |||||||
| chr11:47784062 | C | A | 85 | a0001c0001t0001g0153 a0001c0001t0001g0185 a0001c0001t0002g0056 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.3888+860G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 33/35 | chr11 | 47784062 | |||||||
| chr11:47784255 | G | A | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG02723.hp1 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3888+667C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 33/35 | chr11 | 47784255 | |||||||
| chr11:47784304 | G | A | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.3888+618C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 33/35 | chr11 | 47784304 | |||||||
| chr11:47784654 | G | A | 20 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(17): Show |
20 | HG00733.hp2 HG01081.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.3888+268C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 33/35 | chr11 | 47784654 | |||||||
| chr11:47784659 | T | G | 2 | a0002c0002t0001g0023 a0002c0002t0001g0081 |
2 | NA18971.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.3888+263A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 33/35 | chr11 | 47784659 | |||||||
| chr11:47784786 | C | T | 1 | a0001c0001t0002g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3888+136G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 33/35 | chr11 | 47784786 | |||||||
| chr11:47784791 | G | A | 1 | a0001c0005t0001g0224 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3888+131C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 33/35 | chr11 | 47784791 | |||||||
| chr11:47785088 | T | C | 1 | a0001c0001t0002g0198 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3747-25A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47785088 | |||||||
| chr11:47785088 | T | TGAGTTTC others(285): Show |
69 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(66): Show |
70 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.3747-26_3747-25ins others(292): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47785088 | |||||||
| chr11:47785088 | T | TGAGTTTC others(299): Show |
2 | a0002c0002t0001g0041 a0004c0007t0001g0044 |
2 | HG01175.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.3747-26_3747-25ins others(306): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47785088 | |||||||
| chr11:47785088 | T | TGAGTTTC others(300): Show |
15 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0102 others(12): Show |
15 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(12): Show |
intron_variant | MODIFIER | c.3747-26_3747-25ins others(307): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47785088 | |||||||
| chr11:47785088 | T | TGAGTTTC others(301): Show |
6 | a0002c0002t0001g0039 a0002c0002t0001g0045 a0002c0002t0001g0049 others(3): Show |
6 | HG01123.hp2 HG01169.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.3747-26_3747-25ins others(308): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47785088 | |||||||
| chr11:47785088 | T | TGAGTTTC others(302): Show |
4 | a0002c0002t0001g0040 a0002c0002t0001g0043 a0002c0002t0001g0110 others(1): Show |
4 | HG01167.hp2 HG01192.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.3747-26_3747-25ins others(309): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47785088 | |||||||
| chr11:47785088 | T | TGAGTTTC others(303): Show |
2 | a0002c0002t0001g0042 a0002c0002t0001g0109 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3747-26_3747-25ins others(310): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47785088 | |||||||
| chr11:47785088 | T | TGAGTTTC others(304): Show |
2 | a0002c0002t0001g0108 a0002c0002t0001g0120 |
2 | HG00642.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.3747-26_3747-25ins others(311): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47785088 | |||||||
| chr11:47785238 | T | C | 1 | a0001c0006t0001g0264 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3747-175A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47785238 | |||||||
| chr11:47785446 | T | C | 1 | a0002c0002t0001g0120 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3747-383A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47785446 | |||||||
| chr11:47785515 | T | C | 1 | a0001c0001t0001g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3747-452A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47785515 | |||||||
| chr11:47785638 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3747-575T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47785638 | |||||||
| chr11:47785685 | T | A | 1 | a0001c0001t0004g0285 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3747-622A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47785685 | |||||||
| chr11:47786032 | A | C | 1 | a0001c0001t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3746+421T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47786032 | |||||||
| chr11:47786222 | T | C | 86 | a0001c0001t0001g0185 a0001c0001t0002g0056 a0001c0001t0002g0057 others(83): Show |
86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.3746+231A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47786222 | |||||||
| chr11:47786223 | C | A | 1 | a0001c0001t0001g0255 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3746+230G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 32/35 | chr11 | 47786223 | |||||||
| chr11:47786625 | T | G | 1 | a0001c0001t0001g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3645-71A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47786625 | |||||||
| chr11:47786758 | C | T | 4 | a0001c0006t0001g0170 a0001c0006t0001g0264 a0001c0006t0001g0267 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3645-204G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47786758 | |||||||
| chr11:47786917 | T | C | 1 | a0002c0002t0001g0041 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3645-363A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47786917 | |||||||
| chr11:47787089 | C | CTTTTT | 111 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(108): Show |
112 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.3645-540_3645-536d others(7): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787089 | |||||||
| chr11:47787089 | C | CTTTTTT | 204 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0074 others(201): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.3645-541_3645-536d others(8): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787089 | |||||||
| chr11:47787089 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3645-535G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787089 | |||||||
| chr11:47787101 | A | T | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.3645-547T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787101 | |||||||
| chr11:47787148 | C | T | 1 | a0002c0002t0001g0026 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3645-594G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787148 | |||||||
| chr11:47787284 | C | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(207): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.3645-730G>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787284 | |||||||
| chr11:47787297 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3645-743C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787297 | |||||||
| chr11:47787428 | C | CT | 91 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(88): Show |
92 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.3644+753dupA | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787428 | |||||||
| chr11:47787428 | CT | C | 6 | a0001c0001t0001g0218 a0001c0001t0001g0312 a0001c0001t0002g0056 others(3): Show |
6 | HG02451.hp2 HG02738.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3644+753delA | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787428 | |||||||
| chr11:47787428 | CTT | C | 97 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(94): Show |
98 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.3644+752_3644+753d others(4): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787428 | |||||||
| chr11:47787448 | G | T | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3644+734C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787448 | |||||||
| chr11:47787491 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3644+691C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787491 | |||||||
| chr11:47787507 | G | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0311 a0001c0001t0001g0313 |
3 | HG02451.hp2 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3644+675C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787507 | |||||||
| chr11:47787786 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3644+396G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787786 | |||||||
| chr11:47787819 | G | A | 4 | a0001c0001t0002g0192 a0001c0001t0002g0208 a0001c0001t0002g0209 others(1): Show |
4 | NA18943.hp1 NA19003.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.3644+363C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47787819 | |||||||
| chr11:47788075 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3644+107G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 31/35 | chr11 | 47788075 | |||||||
| chr11:47788674 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0312 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3410-63C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47788674 | |||||||
| chr11:47788851 | A | G | 2 | a0005c0008t0002g0280 a0005c0008t0002g0309 |
2 | NA18961.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.3410-240T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47788851 | |||||||
| chr11:47789065 | C | T | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.3410-454G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47789065 | |||||||
| chr11:47789183 | A | T | 1 | a0001c0001t0001g0263 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3410-572T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47789183 | |||||||
| chr11:47789359 | A | T | 1 | a0002c0002t0001g0026 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3410-748T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47789359 | |||||||
| chr11:47789423 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3410-812C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47789423 | |||||||
| chr11:47789757 | A | C | 69 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(66): Show |
70 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.3410-1146T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47789757 | |||||||
| chr11:47789866 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3410-1255T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47789866 | |||||||
| chr11:47789944 | CT | C | 104 | a0001c0001t0001g0121 a0001c0001t0001g0153 a0001c0001t0001g0332 others(101): Show |
105 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.3410-1334delA | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47789944 | |||||||
| chr11:47789967 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3410-1356G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47789967 | |||||||
| chr11:47789975 | C | T | 5 | a0001c0001t0001g0160 a0001c0001t0001g0248 a0001c0001t0001g0250 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3410-1364G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47789975 | |||||||
| chr11:47790211 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3410-1600C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47790211 | |||||||
| chr11:47790371 | T | C | 1 | a0001c0001t0002g0070 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3409+1559A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47790371 | |||||||
| chr11:47790381 | A | G | 102 | a0001c0001t0001g0121 a0001c0001t0001g0312 a0002c0002t0001g0001 others(99): Show |
103 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.3409+1549T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47790381 | |||||||
| chr11:47790419 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3409+1511G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47790419 | |||||||
| chr11:47790601 | T | C | 2 | a0001c0001t0002g0187 a0001c0001t0002g0330 |
2 | NA18968.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.3409+1329A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47790601 | |||||||
| chr11:47790759 | C | T | 88 | a0001c0001t0001g0185 a0001c0001t0002g0056 a0001c0001t0002g0057 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.3409+1171G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47790759 | |||||||
| chr11:47791158 | C | CT | 188 | a0001c0001t0001g0185 a0001c0001t0002g0056 a0001c0001t0002g0057 others(185): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.3409+771dupA | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47791158 | |||||||
| chr11:47791158 | CT | C | 10 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3409+771delA | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47791158 | |||||||
| chr11:47791244 | C | T | 3 | a0003c0003t0001g0007 a0003c0003t0001g0011 a0003c0003t0001g0014 |
3 | HG02083.hp1 NA18944.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.3409+686G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47791244 | |||||||
| chr11:47791413 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3409+517G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47791413 | |||||||
| chr11:47791669 | A | T | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3409+261T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47791669 | |||||||
| chr11:47791731 | T | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0312 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3409+199A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47791731 | |||||||
| chr11:47791852 | T | G | 1 | a0001c0001t0002g0286 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3409+78A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47791852 | |||||||
| chr11:47791870 | A | G | 1 | a0002c0002t0001g0040 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3409+60T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47791870 | |||||||
| chr11:47791884 | C | T | 330 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(327): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.3409+46G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 29/35 | chr11 | 47791884 | |||||||
| chr11:47792053 | G | A | 8 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0234 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.3349-63C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 28/35 | chr11 | 47792053 | |||||||
| chr11:47792228 | T | C | 2 | a0002c0002t0001g0045 a0002c0002t0001g0117 |
2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3349-238A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 28/35 | chr11 | 47792228 | |||||||
| chr11:47792268 | A | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(95): Show |
99 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.3349-278T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 28/35 | chr11 | 47792268 | |||||||
| chr11:47792439 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3348+347G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 28/35 | chr11 | 47792439 | |||||||
| chr11:47792660 | A | C | 1 | a0001c0001t0002g0305 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3348+126T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 28/35 | chr11 | 47792660 | |||||||
| chr11:47792728 | A | G | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.3348+58T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 28/35 | chr11 | 47792728 | |||||||
| chr11:47793096 | C | T | 15 | a0001c0001t0001g0074 a0001c0001t0001g0213 a0001c0001t0001g0214 others(12): Show |
15 | HG01071.hp2 HG01099.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.3188-150G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793096 | |||||||
| chr11:47793385 | C | A | 2 | a0002c0002t0001g0049 a0002c0002t0001g0119 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3188-439G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793385 | |||||||
| chr11:47793722 | GT | G | 16 | a0001c0001t0001g0311 a0001c0004t0001g0221 a0001c0004t0001g0222 others(13): Show |
16 | HG00438.hp2 HG00741.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.3188-777delA | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793722 | |||||||
| chr11:47793722 | GTT | G | 16 | a0001c0004t0001g0219 a0002c0002t0001g0021 a0002c0002t0001g0022 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.3188-778_3188-777d others(4): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793722 | |||||||
| chr11:47793722 | GTTT | G | 26 | a0001c0001t0001g0179 a0001c0001t0001g0334 a0001c0004t0001g0220 others(23): Show |
26 | HG00280.hp2 HG00544.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.3188-779_3188-777d others(5): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793722 | |||||||
| chr11:47793722 | GTTTT | G | 22 | a0001c0001t0001g0178 a0001c0001t0001g0335 a0001c0001t0001g0336 others(19): Show |
22 | HG00438.hp1 HG01258.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.3188-780_3188-777d others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793722 | |||||||
| chr11:47793722 | GTTTTT | G | 29 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(26): Show |
30 | HG00408.hp2 HG00609.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.3188-781_3188-777d others(7): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793722 | |||||||
| chr11:47793722 | GTTTTTT | G | 20 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0127 others(17): Show |
20 | HG01167.hp1 HG01496.hp2 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.3188-782_3188-777d others(8): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793722 | |||||||
| chr11:47793722 | GTTTTTTT | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(84): Show |
88 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.3188-783_3188-777d others(9): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793722 | |||||||
| chr11:47793722 | GTTTTTTT others(1): Show |
G | 106 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(103): Show |
106 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.3188-784_3188-777d others(10): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793722 | |||||||
| chr11:47793722 | GTTTTTTT others(5): Show |
G | 1 | a0003c0003t0001g0005 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3188-788_3188-777d others(14): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793722 | |||||||
| chr11:47793722 | GTTTTTTT others(10): Show |
G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0312 a0002c0002t0001g0084 |
3 | HG00639.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3188-793_3188-777d others(19): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793722 | |||||||
| chr11:47793722 | GTTTTTTT others(12): Show |
G | 1 | a0002c0002t0001g0032 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3188-795_3188-777d others(21): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793722 | |||||||
| chr11:47793722 | GTTTTTTT others(13): Show |
G | 1 | a0002c0002t0001g0081 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3188-796_3188-777d others(22): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793722 | |||||||
| chr11:47793732 | T | G | 2 | a0001c0001t0001g0248 a0001c0001t0001g0316 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3188-786A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793732 | |||||||
| chr11:47793733 | T | G | 11 | a0001c0001t0001g0127 a0001c0001t0001g0139 a0001c0001t0001g0141 others(8): Show |
11 | HG01496.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.3188-787A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793733 | |||||||
| chr11:47793734 | T | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(81): Show |
85 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.3188-788A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793734 | |||||||
| chr11:47793735 | T | G | 99 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(96): Show |
99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.3188-789A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793735 | |||||||
| chr11:47793736 | T | G | 1 | a0001c0001t0001g0238 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3188-790A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793736 | |||||||
| chr11:47793743 | T | G | 84 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0059 others(81): Show |
84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.3188-797A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793743 | |||||||
| chr11:47793886 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0279 |
3 | HG01891.hp1 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3188-940C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47793886 | |||||||
| chr11:47794074 | G | A | 1 | a0001c0001t0002g0298 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3188-1128C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47794074 | |||||||
| chr11:47794150 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(206): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.3188-1204C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47794150 | |||||||
| chr11:47794221 | C | T | 10 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3188-1275G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47794221 | |||||||
| chr11:47794461 | C | A | 1 | a0002c0002t0001g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3188-1515G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47794461 | |||||||
| chr11:47794500 | G | A | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.3188-1554C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47794500 | |||||||
| chr11:47794540 | G | T | 1 | a0002c0002t0001g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3188-1594C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47794540 | |||||||
| chr11:47794794 | C | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3188-1848G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47794794 | |||||||
| chr11:47794886 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0312 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3188-1940G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47794886 | |||||||
| chr11:47794893 | A | G | 5 | a0001c0001t0002g0189 a0001c0001t0002g0197 a0001c0001t0002g0211 others(2): Show |
5 | NA18953.hp2 NA18971.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.3188-1947T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47794893 | |||||||
| chr11:47795355 | A | G | 1 | a0002c0002t0001g0081 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3188-2409T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47795355 | |||||||
| chr11:47795458 | T | G | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.3187+2321A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47795458 | |||||||
| chr11:47795630 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3187+2149G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47795630 | |||||||
| chr11:47795738 | A | G | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.3187+2041T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47795738 | |||||||
| chr11:47795852 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3187+1927C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47795852 | |||||||
| chr11:47795889 | C | T | 88 | a0001c0001t0001g0185 a0001c0001t0002g0056 a0001c0001t0002g0057 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.3187+1890G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47795889 | |||||||
| chr11:47796152 | T | TA | 204 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(201): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.3187+1626dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47796152 | |||||||
| chr11:47796152 | T | TAA | 12 | a0001c0001t0001g0074 a0001c0001t0001g0127 a0001c0001t0001g0140 others(9): Show |
12 | HG01081.hp1 HG01109.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.3187+1625_3187+162 others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47796152 | |||||||
| chr11:47796346 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3187+1433G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47796346 | |||||||
| chr11:47796628 | T | C | 1 | a0003c0003t0001g0016 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.3187+1151A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47796628 | |||||||
| chr11:47796758 | C | T | 3 | a0002c0002t0001g0041 a0002c0002t0001g0045 a0002c0002t0001g0117 |
3 | HG01175.hp1 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3187+1021G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47796758 | |||||||
| chr11:47796961 | G | C | 10 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3187+818C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47796961 | |||||||
| chr11:47797079 | A | G | 1 | a0002c0002t0001g0215 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3187+700T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47797079 | |||||||
| chr11:47797149 | A | AAATTCAC others(2): Show |
209 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(206): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.3187+629_3187+630i others(11): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47797149 | |||||||
| chr11:47797152 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(206): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.3187+627C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47797152 | |||||||
| chr11:47797153 | G | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(206): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.3187+626C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47797153 | |||||||
| chr11:47797155 | A | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(206): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.3187+624T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47797155 | |||||||
| chr11:47797323 | C | T | 2 | a0001c0005t0001g0125 a0001c0005t0001g0224 |
2 | HG00609.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3187+456G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47797323 | |||||||
| chr11:47797627 | G | C | 1 | a0001c0005t0001g0224 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3187+152C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 27/35 | chr11 | 47797627 | |||||||
| chr11:47798560 | C | T | 10 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2794-97G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47798560 | |||||||
| chr11:47798675 | T | A | 322 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(319): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.2794-212A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47798675 | |||||||
| chr11:47798689 | G | A | 15 | a0002c0002t0001g0021 a0002c0002t0001g0025 a0002c0002t0001g0026 others(12): Show |
15 | HG00639.hp1 HG00735.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.2794-226C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47798689 | |||||||
| chr11:47798691 | G | A | 2 | a0002c0002t0001g0098 a0002c0002t0001g0118 |
2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2794-228C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47798691 | |||||||
| chr11:47798941 | T | TA | 21 | a0001c0001t0001g0074 a0001c0001t0001g0213 a0001c0001t0001g0214 others(18): Show |
21 | HG01071.hp2 HG01099.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.2794-479dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47798941 | |||||||
| chr11:47799154 | C | T | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2794-691G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47799154 | |||||||
| chr11:47799162 | T | G | 1 | a0008c0011t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2794-699A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47799162 | |||||||
| chr11:47799184 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2794-721G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47799184 | |||||||
| chr11:47799418 | C | T | 5 | a0001c0001t0002g0186 a0001c0001t0002g0211 a0001c0001t0002g0281 others(2): Show |
5 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(2): Show |
intron_variant | MODIFIER | c.2794-955G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47799418 | |||||||
| chr11:47799601 | A | G | 330 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(327): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.2794-1138T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47799601 | |||||||
| chr11:47799966 | C | T | 310 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(307): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.2794-1503G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47799966 | |||||||
| chr11:47800014 | G | C | 1 | a0001c0001t0002g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2794-1551C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47800014 | |||||||
| chr11:47800168 | C | T | 1 | a0002c0002t0001g0108 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2793+1643G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47800168 | |||||||
| chr11:47800240 | C | CA | 91 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(88): Show |
92 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.2793+1570dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47800240 | |||||||
| chr11:47800252 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2793+1559C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47800252 | |||||||
| chr11:47800277 | C | T | 1 | a0002c0002t0001g0217 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2793+1534G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47800277 | |||||||
| chr11:47800290 | C | G | 10 | a0001c0001t0001g0140 a0001c0001t0001g0160 a0001c0001t0001g0248 others(7): Show |
10 | HG01261.hp1 HG02258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.2793+1521G>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47800290 | |||||||
| chr11:47800359 | A | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0312 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2793+1452T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47800359 | |||||||
| chr11:47800527 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2793+1284C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47800527 | |||||||
| chr11:47800611 | C | T | 17 | a0002c0002t0001g0018 a0002c0002t0001g0030 a0002c0002t0001g0031 others(14): Show |
17 | HG00544.hp2 HG01433.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.2793+1200G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47800611 | |||||||
| chr11:47800665 | C | T | 69 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(66): Show |
70 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.2793+1146G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47800665 | |||||||
| chr11:47800824 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2793+987A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47800824 | |||||||
| chr11:47800883 | A | C | 5 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0227 others(2): Show |
5 | HG02809.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2793+928T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47800883 | |||||||
| chr11:47801028 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2793+783G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47801028 | |||||||
| chr11:47801504 | C | T | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.2793+307G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47801504 | |||||||
| chr11:47801506 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2793+305G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 23/35 | chr11 | 47801506 | |||||||
| chr11:47801997 | G | T | 1 | a0002c0002t0001g0098 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2674-67C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47801997 | |||||||
| chr11:47802079 | T | C | 1 | a0001c0001t0002g0070 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2674-149A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47802079 | |||||||
| chr11:47802122 | T | G | 15 | a0001c0001t0001g0074 a0001c0001t0001g0213 a0001c0001t0001g0214 others(12): Show |
15 | HG01071.hp2 HG01099.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.2674-192A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47802122 | |||||||
| chr11:47802224 | A | C | 1 | a0003c0003t0001g0010 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2674-294T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47802224 | |||||||
| chr11:47802231 | G | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0213 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.2674-301C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47802231 | |||||||
| chr11:47802255 | A | C | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2674-325T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47802255 | |||||||
| chr11:47802260 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA18964.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2674-330T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47802260 | |||||||
| chr11:47802462 | ATAAGATG others(8): Show |
A | 1 | a0001c0001t0002g0211 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2674-547_2674-533d others(17): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47802462 | |||||||
| chr11:47802639 | C | T | 330 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(327): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.2674-709G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47802639 | |||||||
| chr11:47802911 | G | A | 1 | a0003c0003t0001g0012 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2673+527C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47802911 | |||||||
| chr11:47803142 | A | AAAT | 116 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0129 others(113): Show |
116 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2673+293_2673+295d others(5): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47803142 | |||||||
| chr11:47803142 | A | AAATAAT | 28 | a0001c0001t0001g0137 a0001c0001t0001g0152 a0001c0001t0001g0183 others(25): Show |
28 | HG00280.hp2 HG00673.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.2673+290_2673+295d others(8): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47803142 | |||||||
| chr11:47803142 | A | AAATAATA others(2): Show |
72 | a0001c0001t0001g0074 a0001c0001t0001g0130 a0001c0001t0001g0131 others(69): Show |
72 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.2673+287_2673+295d others(11): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47803142 | |||||||
| chr11:47803142 | A | AAATAATA others(5): Show |
11 | a0001c0001t0001g0230 a0001c0001t0002g0186 a0001c0001t0002g0188 others(8): Show |
11 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.2673+284_2673+295d others(14): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47803142 | |||||||
| chr11:47803142 | A | AAATAATA others(8): Show |
7 | a0002c0002t0001g0001 a0002c0002t0001g0021 a0002c0002t0001g0095 others(4): Show |
8 | HG01433.hp2 HG02083.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2673+281_2673+295d others(17): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47803142 | |||||||
| chr11:47803142 | AAAT | A | 10 | a0001c0001t0002g0056 a0001c0001t0002g0070 a0001c0001t0002g0198 others(7): Show |
10 | HG01192.hp2 HG02056.hp2 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.2673+293_2673+295d others(5): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47803142 | |||||||
| chr11:47803142 | AAATAAT | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0176 a0001c0001t0001g0312 |
3 | HG02280.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2673+290_2673+295d others(8): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47803142 | |||||||
| chr11:47803270 | T | TAGTC | 4 | a0001c0006t0001g0170 a0001c0006t0001g0264 a0001c0006t0001g0267 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2673+164_2673+167d others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47803270 | |||||||
| chr11:47803275 | C | T | 1 | a0001c0001t0003g0171 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2673+163G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 22/35 | chr11 | 47803275 | |||||||
| chr11:47803551 | A | G | 1 | a0001c0001t0002g0211 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2575-15T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47803551 | |||||||
| chr11:47803553 | G | T | 1 | a0001c0001t0002g0211 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2575-17C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47803553 | |||||||
| chr11:47803554 | T | A | 1 | a0001c0001t0002g0211 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2575-18A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47803554 | |||||||
| chr11:47803576 | T | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2575-40A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47803576 | |||||||
| chr11:47803685 | CCT | C | 13 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2575-151_2575-150d others(4): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47803685 | |||||||
| chr11:47803781 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(207): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2575-245T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47803781 | |||||||
| chr11:47803868 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2575-332G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47803868 | |||||||
| chr11:47803963 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2575-427G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47803963 | |||||||
| chr11:47804038 | G | A | 103 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 others(100): Show |
104 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2575-502C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47804038 | |||||||
| chr11:47804044 | G | T | 1 | a0001c0001t0002g0211 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2574+505C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47804044 | |||||||
| chr11:47804172 | C | T | 1 | a0002c0002t0001g0104 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2574+377G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47804172 | |||||||
| chr11:47804183 | G | GA | 88 | a0001c0001t0001g0150 a0001c0001t0001g0225 a0001c0001t0002g0056 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2574+365dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47804183 | |||||||
| chr11:47804319 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2574+230T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47804319 | |||||||
| chr11:47804420 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(91): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2574+129T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47804420 | |||||||
| chr11:47804421 | T | C | 1 | a0001c0001t0002g0197 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2574+128A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47804421 | |||||||
| chr11:47804538 | A | C | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.2574+11T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 21/35 | chr11 | 47804538 | |||||||
| chr11:47804864 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2505-246G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 20/35 | chr11 | 47804864 | |||||||
| chr11:47805042 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2505-424G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 20/35 | chr11 | 47805042 | |||||||
| chr11:47805113 | T | TA | 10 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2505-496dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 20/35 | chr11 | 47805113 | |||||||
| chr11:47805447 | C | CTTT | 184 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(181): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.2504+703_2504+705d others(5): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 20/35 | chr11 | 47805447 | |||||||
| chr11:47805447 | C | CTTTT | 23 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0136 others(20): Show |
23 | HG01109.hp2 HG01175.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.2504+702_2504+705d others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 20/35 | chr11 | 47805447 | |||||||
| chr11:47805632 | G | A | 1 | a0001c0001t0002g0276 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2504+521C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 20/35 | chr11 | 47805632 | |||||||
| chr11:47805746 | G | A | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG02723.hp1 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2504+407C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 20/35 | chr11 | 47805746 | |||||||
| chr11:47805860 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2504+293C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 20/35 | chr11 | 47805860 | |||||||
| chr11:47806342 | T | C | 1 | a0001c0001t0002g0274 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2345-30A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806342 | |||||||
| chr11:47806562 | C | T | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG02723.hp1 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2345-250G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806562 | |||||||
| chr11:47806787 | CTA | C | 9 | a0001c0001t0002g0059 a0001c0001t0002g0062 a0001c0001t0002g0065 others(6): Show |
9 | HG01109.hp1 HG01192.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.2344+281_2344+282d others(4): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806787 | |||||||
| chr11:47806788 | TATAC | T | 15 | a0001c0001t0001g0185 a0001c0001t0002g0057 a0001c0001t0002g0187 others(12): Show |
15 | HG00642.hp2 HG00673.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.2344+278_2344+281d others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806788 | |||||||
| chr11:47806788 | TATACAC | T | 9 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0063 others(6): Show |
9 | HG00741.hp2 HG01515.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.2344+276_2344+281d others(8): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806788 | |||||||
| chr11:47806788 | TATACACA others(1): Show |
T | 11 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0186 others(8): Show |
11 | HG00140.hp1 HG00323.hp1 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.2344+274_2344+281d others(10): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806788 | |||||||
| chr11:47806788 | TATACACA others(3): Show |
T | 11 | a0001c0001t0002g0188 a0001c0001t0002g0193 a0001c0001t0002g0202 others(8): Show |
11 | HG00140.hp2 HG03017.hp2 HG03834.hp1 others(8): Show |
intron_variant | MODIFIER | c.2344+272_2344+281d others(12): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806788 | |||||||
| chr11:47806788 | TATACACA others(5): Show |
T | 3 | a0001c0001t0002g0192 a0001c0001t0002g0282 a0001c0001t0003g0323 |
3 | HG01099.hp1 HG01433.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2344+270_2344+281d others(14): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806788 | |||||||
| chr11:47806788 | TATACACA others(7): Show |
T | 4 | a0001c0001t0002g0073 a0001c0001t0002g0212 a0001c0001t0003g0173 others(1): Show |
4 | HG01257.hp2 HG02602.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.2344+268_2344+281d others(16): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806788 | |||||||
| chr11:47806788 | TATACACA others(9): Show |
T | 3 | a0001c0001t0002g0066 a0001c0001t0002g0307 a0001c0001t0002g0310 |
3 | HG04204.hp1 NA18987.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2344+266_2344+281d others(18): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806788 | |||||||
| chr11:47806788 | TATACACA others(11): Show |
T | 1 | a0001c0001t0003g0268 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2344+264_2344+281d others(20): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806788 | |||||||
| chr11:47806790 | T | C | 25 | a0001c0001t0002g0056 a0001c0001t0002g0068 a0001c0001t0002g0069 others(22): Show |
25 | HG00597.hp1 HG00639.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.2344+280A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806790 | |||||||
| chr11:47806790 | T | TAC | 3 | a0001c0004t0001g0221 a0001c0004t0001g0222 a0001c0006t0001g0322 |
3 | HG02257.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2344+278_2344+279d others(4): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806790 | |||||||
| chr11:47806790 | TAC | T | 15 | a0001c0001t0001g0121 a0001c0001t0001g0177 a0001c0001t0001g0272 others(12): Show |
15 | HG00438.hp1 HG01123.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.2344+278_2344+279d others(4): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806790 | |||||||
| chr11:47806790 | TACAC | T | 21 | a0001c0001t0001g0252 a0001c0001t0001g0271 a0001c0001t0001g0313 others(18): Show |
21 | HG01243.hp1 HG01358.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.2344+276_2344+279d others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806790 | |||||||
| chr11:47806790 | TACACAC | T | 21 | a0001c0001t0001g0148 a0001c0001t0001g0176 a0001c0001t0001g0242 others(18): Show |
21 | HG00544.hp1 HG00639.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.2344+274_2344+279d others(8): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806790 | |||||||
| chr11:47806790 | TACACACA others(1): Show |
T | 20 | a0001c0001t0001g0168 a0001c0001t0001g0237 a0002c0002t0001g0017 others(17): Show |
20 | HG00408.hp2 HG00544.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.2344+272_2344+279d others(10): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806790 | |||||||
| chr11:47806790 | TACACACA others(3): Show |
T | 19 | a0001c0001t0001g0135 a0001c0001t0001g0141 a0001c0001t0001g0152 others(16): Show |
19 | HG00609.hp2 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2344+270_2344+279d others(12): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806790 | |||||||
| chr11:47806790 | TACACACA others(5): Show |
T | 31 | a0001c0001t0001g0138 a0001c0001t0001g0149 a0001c0001t0001g0151 others(28): Show |
32 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.2344+268_2344+279d others(14): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806790 | |||||||
| chr11:47806790 | TACACACA others(7): Show |
T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0132 others(33): Show |
37 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.2344+266_2344+279d others(16): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806790 | |||||||
| chr11:47806790 | TACACACA others(9): Show |
T | 20 | a0001c0001t0001g0054 a0001c0001t0001g0124 a0001c0001t0001g0126 others(17): Show |
20 | HG00280.hp1 HG00558.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.2344+264_2344+279d others(18): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806790 | |||||||
| chr11:47806790 | TACACACA others(11): Show |
T | 7 | a0001c0001t0001g0055 a0001c0001t0001g0136 a0001c0001t0001g0144 others(4): Show |
7 | HG02698.hp2 HG02818.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2344+262_2344+279d others(20): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806790 | |||||||
| chr11:47806790 | TACACACA others(13): Show |
T | 9 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0001g0164 others(6): Show |
9 | HG00733.hp2 HG01081.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.2344+260_2344+279d others(22): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806790 | |||||||
| chr11:47806790 | TACACACA others(15): Show |
T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0263 a0001c0001t0001g0325 |
3 | HG02630.hp2 HG02717.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.2344+258_2344+279d others(24): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806790 | |||||||
| chr11:47806790 | TACACACA others(17): Show |
T | 1 | a0002c0002t0001g0021 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2344+256_2344+279d others(26): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806790 | |||||||
| chr11:47806792 | C | T | 5 | a0002c0002t0001g0030 a0002c0002t0001g0033 a0002c0002t0001g0075 others(2): Show |
5 | HG01261.hp2 HG02523.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.2344+278G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806792 | |||||||
| chr11:47806794 | C | T | 7 | a0002c0002t0001g0028 a0002c0002t0001g0052 a0002c0002t0001g0095 others(4): Show |
7 | HG00438.hp1 HG01346.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.2344+276G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806794 | |||||||
| chr11:47806796 | C | T | 13 | a0002c0002t0001g0026 a0002c0002t0001g0032 a0002c0002t0001g0035 others(10): Show |
13 | HG01358.hp2 HG02083.hp1 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.2344+274G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806796 | |||||||
| chr11:47806798 | C | T | 13 | a0002c0002t0001g0025 a0002c0002t0001g0027 a0002c0002t0001g0031 others(10): Show |
13 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.2344+272G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806798 | |||||||
| chr11:47806800 | C | T | 14 | a0002c0002t0001g0017 a0002c0002t0001g0019 a0002c0002t0001g0029 others(11): Show |
14 | HG00408.hp2 HG00544.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.2344+270G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806800 | |||||||
| chr11:47806802 | C | T | 8 | a0002c0002t0001g0024 a0002c0002t0001g0038 a0002c0002t0001g0081 others(5): Show |
8 | HG00609.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2344+268G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806802 | |||||||
| chr11:47806804 | C | T | 4 | a0002c0002t0001g0001 a0002c0002t0001g0020 a0002c0002t0001g0022 others(1): Show |
5 | HG03017.hp1 HG03491.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.2344+266G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806804 | |||||||
| chr11:47806808 | C | T | 3 | a0002c0002t0001g0041 a0002c0002t0001g0045 a0002c0002t0001g0117 |
3 | HG01175.hp1 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2344+262G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806808 | |||||||
| chr11:47806816 | C | T | 1 | a0002c0002t0001g0021 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2344+254G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806816 | |||||||
| chr11:47806846 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2344+224G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806846 | |||||||
| chr11:47806848 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2344+222G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806848 | |||||||
| chr11:47806850 | C | CATATATA others(3): Show |
3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0227 |
3 | HG02809.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2344+219_2344+220i others(12): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806850 | |||||||
| chr11:47806850 | C | T | 11 | a0001c0001t0001g0152 a0001c0001t0001g0176 a0001c0001t0001g0231 others(8): Show |
11 | HG02273.hp2 HG02280.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.2344+220G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806850 | |||||||
| chr11:47806852 | C | CACACACA others(3): Show |
2 | a0001c0001t0001g0317 a0001c0001t0002g0206 |
2 | HG03130.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2344+217_2344+218i others(12): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806852 | |||||||
| chr11:47806852 | C | CACAT | 6 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0002g0194 others(3): Show |
6 | HG00733.hp1 HG01261.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.2344+217_2344+218i others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806852 | |||||||
| chr11:47806852 | C | CAT | 19 | a0001c0001t0001g0140 a0001c0001t0001g0160 a0001c0001t0001g0179 others(16): Show |
19 | HG01175.hp2 HG01943.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.2344+216_2344+217d others(4): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806852 | |||||||
| chr11:47806852 | C | CATATATA others(5): Show |
1 | a0001c0001t0001g0228 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2344+217_2344+218i others(14): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806852 | |||||||
| chr11:47806852 | C | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(171): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.2344+218G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47806852 | |||||||
| chr11:47807003 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2344+67T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47807003 | |||||||
| chr11:47807006 | A | G | 31 | a0002c0002t0001g0039 a0002c0002t0001g0040 a0002c0002t0001g0041 others(28): Show |
31 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.2344+64T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47807006 | |||||||
| chr11:47807016 | A | T | 1 | a0002c0002t0001g0001 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2344+54T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 19/35 | chr11 | 47807016 | |||||||
| chr11:47807213 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2274-73C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47807213 | |||||||
| chr11:47807270 | A | C | 1 | a0001c0001t0002g0294 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2274-130T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47807270 | |||||||
| chr11:47807358 | T | C | 8 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0262 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.2274-218A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47807358 | |||||||
| chr11:47807436 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(206): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.2274-296G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47807436 | |||||||
| chr11:47807469 | C | A | 1 | a0001c0001t0002g0211 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2274-329G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47807469 | |||||||
| chr11:47807470 | A | G | 1 | a0001c0001t0002g0211 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2274-330T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47807470 | |||||||
| chr11:47807471 | G | C | 1 | a0001c0001t0002g0211 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2274-331C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47807471 | |||||||
| chr11:47807793 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(91): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2273+603A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47807793 | |||||||
| chr11:47807835 | G | GTATAA | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.2273+556_2273+560d others(7): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47807835 | |||||||
| chr11:47807919 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2273+477G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47807919 | |||||||
| chr11:47808001 | C | T | 3 | a0002c0002t0001g0041 a0002c0002t0001g0045 a0002c0002t0001g0117 |
3 | HG01175.hp1 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2273+395G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47808001 | |||||||
| chr11:47808014 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0324 |
2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2273+382C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47808014 | |||||||
| chr11:47808100 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(91): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2273+296A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47808100 | |||||||
| chr11:47808168 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2273+228G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47808168 | |||||||
| chr11:47808216 | G | A | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG02723.hp1 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2273+180C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47808216 | |||||||
| chr11:47808251 | G | A | 6 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 others(3): Show |
6 | HG01071.hp2 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2273+145C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47808251 | |||||||
| chr11:47808263 | A | T | 1 | a0005c0008t0002g0309 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2273+133T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 18/35 | chr11 | 47808263 | |||||||
| chr11:47808668 | C | T | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2140-139G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47808668 | |||||||
| chr11:47808740 | C | T | 21 | a0002c0002t0001g0017 a0002c0002t0001g0019 a0002c0002t0001g0020 others(18): Show |
21 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.2140-211G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47808740 | |||||||
| chr11:47808897 | C | A | 1 | a0001c0005t0001g0224 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2140-368G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47808897 | |||||||
| chr11:47809036 | T | C | 330 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(327): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.2140-507A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809036 | |||||||
| chr11:47809038 | T | C | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.2140-509A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809038 | |||||||
| chr11:47809046 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2140-517T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809046 | |||||||
| chr11:47809058 | G | A | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2140-529C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809058 | |||||||
| chr11:47809084 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2140-555C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809084 | |||||||
| chr11:47809095 | C | G | 1 | a0001c0001t0002g0072 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2140-566G>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809095 | |||||||
| chr11:47809256 | C | CA | 283 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(280): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.2140-728dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809256 | |||||||
| chr11:47809256 | C | CAA | 23 | a0001c0001t0001g0121 a0001c0001t0001g0137 a0001c0001t0001g0138 others(20): Show |
23 | HG01109.hp2 HG01192.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.2140-729_2140-728d others(4): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809256 | |||||||
| chr11:47809444 | ATAAT | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0311 a0001c0001t0001g0313 |
3 | HG02451.hp2 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2140-919_2140-916d others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809444 | |||||||
| chr11:47809521 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2140-992C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809521 | |||||||
| chr11:47809569 | C | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0142 a0001c0001t0001g0143 others(9): Show |
13 | HG00558.hp2 HG02071.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.2140-1040G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809569 | |||||||
| chr11:47809718 | T | TACAGAGC others(3): Show |
1 | a0001c0001t0002g0211 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2140-1199_2140-119 others(14): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809718 | |||||||
| chr11:47809734 | C | CA | 111 | a0001c0001t0001g0121 a0001c0001t0001g0147 a0001c0001t0001g0153 others(108): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.2140-1206dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809734 | |||||||
| chr11:47809734 | C | CAA | 121 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(118): Show |
122 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.2140-1207_2140-120 others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809734 | |||||||
| chr11:47809734 | C | CAAA | 6 | a0001c0001t0001g0135 a0001c0001t0001g0231 a0001c0001t0001g0249 others(3): Show |
6 | HG00597.hp2 HG02615.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.2140-1208_2140-120 others(7): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809734 | |||||||
| chr11:47809757 | AAG | A | 33 | a0002c0002t0001g0001 a0002c0002t0001g0022 a0002c0002t0001g0023 others(30): Show |
34 | HG00544.hp2 HG00609.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.2140-1230_2140-122 others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809757 | |||||||
| chr11:47809758 | AG | A | 31 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0019 others(28): Show |
31 | HG00408.hp2 HG00639.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.2140-1230delC | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809758 | |||||||
| chr11:47809759 | G | A | 2 | a0002c0002t0001g0052 a0002c0002t0001g0053 |
2 | HG00438.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.2140-1230C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809759 | |||||||
| chr11:47809780 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0121 others(209): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.2140-1251T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809780 | |||||||
| chr11:47809861 | C | T | 6 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 others(3): Show |
6 | HG01071.hp2 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2140-1332G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47809861 | |||||||
| chr11:47810238 | T | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2140-1709A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47810238 | |||||||
| chr11:47810566 | A | T | 7 | a0001c0001t0002g0057 a0001c0001t0002g0063 a0001c0001t0002g0064 others(4): Show |
7 | HG00741.hp2 HG01346.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.2139+1498T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47810566 | |||||||
| chr11:47810708 | C | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(119): Show |
123 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.2139+1356G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47810708 | |||||||
| chr11:47810889 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2139+1175G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47810889 | |||||||
| chr11:47811019 | T | C | 330 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(327): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.2139+1045A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47811019 | |||||||
| chr11:47811241 | G | A | 83 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0059 others(80): Show |
83 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.2139+823C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47811241 | |||||||
| chr11:47811256 | C | T | 5 | a0002c0002t0001g0027 a0002c0002t0001g0089 a0002c0002t0001g0091 others(2): Show |
5 | HG01167.hp1 HG01258.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.2139+808G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47811256 | |||||||
| chr11:47811419 | G | T | 1 | a0002c0002t0001g0001 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2139+645C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47811419 | |||||||
| chr11:47811484 | GA | G | 9 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(6): Show |
9 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2139+579delT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47811484 | |||||||
| chr11:47811512 | A | G | 1 | a0002c0002t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2139+552T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47811512 | |||||||
| chr11:47811676 | A | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(306): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.2139+388T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47811676 | |||||||
| chr11:47811826 | C | T | 1 | a0002c0002t0001g0026 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2139+238G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47811826 | |||||||
| chr11:47811839 | C | T | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2139+225G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47811839 | |||||||
| chr11:47811846 | A | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(206): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.2139+218T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 17/35 | chr11 | 47811846 | |||||||
| chr11:47812544 | T | C | 1 | a0001c0001t0001g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1851-115A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 15/35 | chr11 | 47812544 | |||||||
| chr11:47812571 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1851-142G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 15/35 | chr11 | 47812571 | |||||||
| chr11:47812794 | G | A | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1850+88C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 15/35 | chr11 | 47812794 | |||||||
| chr11:47813136 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0244 |
2 | NA18970.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1685-89G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 14/35 | chr11 | 47813136 | |||||||
| chr11:47813872 | C | T | 1 | a0003c0003t0001g0003 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1585-457G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47813872 | |||||||
| chr11:47813930 | G | A | 1 | a0002c0002t0001g0090 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1585-515C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47813930 | |||||||
| chr11:47814070 | C | CA | 258 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(255): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1585-656dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814070 | |||||||
| chr11:47814070 | C | CAA | 37 | a0001c0001t0001g0133 a0001c0001t0001g0142 a0001c0001t0001g0146 others(34): Show |
37 | HG00408.hp1 HG00642.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1585-657_1585-656d others(4): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814070 | |||||||
| chr11:47814070 | CAAAAAAA others(4): Show |
C | 10 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1585-666_1585-656d others(13): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814070 | |||||||
| chr11:47814140 | T | TCAAA | 215 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(212): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1585-729_1585-726d others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814140 | |||||||
| chr11:47814169 | A | C | 66 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(63): Show |
67 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1585-754T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814169 | |||||||
| chr11:47814229 | A | G | 1 | a0001c0001t0002g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1585-814T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814229 | |||||||
| chr11:47814255 | G | C | 2 | a0001c0001t0002g0066 a0001c0001t0002g0307 |
2 | NA18987.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1585-840C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814255 | |||||||
| chr11:47814419 | A | G | 310 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(307): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1585-1004T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814419 | |||||||
| chr11:47814474 | G | A | 69 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(66): Show |
70 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1584+1005C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814474 | |||||||
| chr11:47814510 | T | C | 88 | a0001c0001t0001g0185 a0001c0001t0002g0056 a0001c0001t0002g0057 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1584+969A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814510 | |||||||
| chr11:47814538 | C | CA | 49 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0002g0056 others(46): Show |
49 | HG00673.hp1 HG00673.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1584+940dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814538 | |||||||
| chr11:47814545 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1584+934T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814545 | |||||||
| chr11:47814613 | C | CTATA | 7 | a0001c0001t0002g0062 a0001c0001t0002g0069 a0001c0001t0002g0199 others(4): Show |
7 | NA18944.hp1 NA18945.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.1584+862_1584+865d others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814613 | |||||||
| chr11:47814682 | A | C | 2 | a0001c0001t0002g0212 a0001c0001t0002g0310 |
2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1584+797T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814682 | |||||||
| chr11:47814750 | T | A | 69 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(66): Show |
70 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1584+729A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814750 | |||||||
| chr11:47814994 | G | A | 1 | a0002c0002t0001g0097 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1584+485C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47814994 | |||||||
| chr11:47815004 | G | T | 28 | a0002c0002t0001g0039 a0002c0002t0001g0040 a0002c0002t0001g0041 others(25): Show |
28 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1584+475C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47815004 | |||||||
| chr11:47815149 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1584+330G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47815149 | |||||||
| chr11:47815262 | A | C | 4 | a0001c0006t0001g0170 a0001c0006t0001g0264 a0001c0006t0001g0267 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1584+217T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47815262 | |||||||
| chr11:47815357 | G | A | 1 | a0001c0001t0003g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1584+122C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47815357 | |||||||
| chr11:47815377 | A | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1584+102T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 13/35 | chr11 | 47815377 | |||||||
| chr11:47815781 | T | C | 28 | a0002c0002t0001g0039 a0002c0002t0001g0040 a0002c0002t0001g0041 others(25): Show |
28 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1414-132A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 12/35 | chr11 | 47815781 | |||||||
| chr11:47815856 | G | C | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1413+90C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 12/35 | chr11 | 47815856 | |||||||
| chr11:47815879 | G | A | 1 | a0002c0002t0001g0076 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1413+67C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 12/35 | chr11 | 47815879 | |||||||
| chr11:47816042 | G | T | 1 | a0002c0002t0001g0034 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1330-13C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47816042 | |||||||
| chr11:47816058 | A | G | 1 | a0001c0001t0002g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1330-29T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47816058 | |||||||
| chr11:47816086 | G | A | 309 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(306): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1330-57C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47816086 | |||||||
| chr11:47816129 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0312 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1330-100T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47816129 | |||||||
| chr11:47816215 | A | G | 1 | a0001c0015t0001g0273 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1330-186T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47816215 | |||||||
| chr11:47816321 | G | A | 10 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1330-292C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47816321 | |||||||
| chr11:47816426 | A | G | 1 | a0001c0001t0003g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1330-397T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47816426 | |||||||
| chr11:47816612 | T | A | 1 | a0001c0001t0001g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1330-583A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47816612 | |||||||
| chr11:47816739 | G | T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0313 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1330-710C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47816739 | |||||||
| chr11:47816781 | GA | G | 313 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(310): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1330-753delT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47816781 | |||||||
| chr11:47816976 | G | GT | 86 | a0001c0001t0001g0145 a0001c0001t0001g0178 a0001c0001t0001g0179 others(83): Show |
87 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1330-948dupA | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47816976 | |||||||
| chr11:47817342 | C | CT | 32 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0147 others(29): Show |
32 | HG00438.hp1 HG00544.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.1329+713dupA | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47817342 | |||||||
| chr11:47817346 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0223 |
2 | HG00558.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1329+710A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47817346 | |||||||
| chr11:47817351 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1329+705A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47817351 | |||||||
| chr11:47817465 | G | T | 1 | a0001c0001t0002g0304 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1329+591C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47817465 | |||||||
| chr11:47817535 | C | T | 8 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(5): Show |
8 | HG00597.hp2 NA18947.hp2 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.1329+521G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47817535 | |||||||
| chr11:47817627 | G | A | 1 | a0001c0001t0001g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1329+429C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 11/35 | chr11 | 47817627 | |||||||
| chr11:47818164 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1261-40G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47818164 | |||||||
| chr11:47818386 | C | T | 9 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(6): Show |
9 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1261-262G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47818386 | |||||||
| chr11:47818549 | C | CAAA | 31 | a0002c0002t0001g0039 a0002c0002t0001g0040 a0002c0002t0001g0041 others(28): Show |
31 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1261-428_1261-426d others(5): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47818549 | |||||||
| chr11:47818549 | C | CAAAA | 69 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(66): Show |
70 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1261-429_1261-426d others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47818549 | |||||||
| chr11:47818554 | C | A | 31 | a0002c0002t0001g0039 a0002c0002t0001g0040 a0002c0002t0001g0041 others(28): Show |
31 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1261-430G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47818554 | |||||||
| chr11:47818707 | T | G | 1 | a0001c0001t0001g0144 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1261-583A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47818707 | |||||||
| chr11:47818763 | T | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0184 a0001c0001t0001g0325 |
3 | HG02630.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1260+611A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47818763 | |||||||
| chr11:47819070 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(207): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1260+304A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47819070 | |||||||
| chr11:47819080 | G | A | 1 | a0001c0006t0001g0267 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1260+294C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47819080 | |||||||
| chr11:47819082 | G | A | 1 | a0001c0006t0001g0267 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1260+292C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47819082 | |||||||
| chr11:47819170 | G | C | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1260+204C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47819170 | |||||||
| chr11:47819205 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1260+169G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47819205 | |||||||
| chr11:47819312 | C | CA | 86 | a0001c0001t0001g0269 a0001c0001t0001g0311 a0001c0001t0002g0056 others(83): Show |
86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1260+61dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47819312 | |||||||
| chr11:47819312 | C | CAA | 11 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(8): Show |
11 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+60_1260+61dup others(2): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47819312 | |||||||
| chr11:47819333 | A | G | 10 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1260+41T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 10/35 | chr11 | 47819333 | |||||||
| chr11:47819508 | G | C | 1 | a0001c0001t0002g0301 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1176-50C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47819508 | |||||||
| chr11:47819637 | C | G | 7 | a0001c0001t0002g0062 a0001c0001t0002g0069 a0001c0001t0002g0199 others(4): Show |
7 | NA18944.hp1 NA18945.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.1176-179G>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47819637 | |||||||
| chr11:47819775 | T | C | 4 | a0001c0006t0001g0170 a0001c0006t0001g0264 a0001c0006t0001g0267 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176-317A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47819775 | |||||||
| chr11:47819777 | A | T | 4 | a0001c0006t0001g0170 a0001c0006t0001g0264 a0001c0006t0001g0267 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176-319T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47819777 | |||||||
| chr11:47819804 | T | C | 1 | a0001c0001t0002g0282 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1176-346A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47819804 | |||||||
| chr11:47819951 | A | G | 2 | a0005c0008t0002g0280 a0005c0008t0002g0309 |
2 | NA18961.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1176-493T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47819951 | |||||||
| chr11:47820029 | G | A | 88 | a0001c0001t0001g0269 a0001c0001t0002g0056 a0001c0001t0002g0057 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1176-571C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47820029 | |||||||
| chr11:47820031 | C | T | 329 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(326): Show |
331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.1176-573G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47820031 | |||||||
| chr11:47820165 | G | A | 2 | a0002c0002t0001g0075 a0002c0002t0001g0090 |
2 | HG01123.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1176-707C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47820165 | |||||||
| chr11:47820241 | C | T | 2 | a0001c0001t0002g0058 a0001c0001t0002g0190 |
2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1176-783G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47820241 | |||||||
| chr11:47820310 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(206): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1176-852T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47820310 | |||||||
| chr11:47820395 | C | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(306): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1176-937G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47820395 | |||||||
| chr11:47820724 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0312 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1175+1000C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47820724 | |||||||
| chr11:47820736 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1175+988C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47820736 | |||||||
| chr11:47820763 | G | C | 6 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 others(3): Show |
6 | HG01071.hp2 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1175+961C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47820763 | |||||||
| chr11:47820982 | CCT | C | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1175+740_1175+741d others(4): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47820982 | |||||||
| chr11:47821135 | T | G | 3 | a0001c0001t0002g0197 a0001c0001t0002g0296 a0001c0001t0002g0297 |
3 | NA18953.hp2 NA19002.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1175+589A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47821135 | |||||||
| chr11:47821154 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1175+570A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47821154 | |||||||
| chr11:47821336 | T | C | 21 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(18): Show |
21 | HG01243.hp1 HG01261.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.1175+388A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47821336 | |||||||
| chr11:47821352 | C | CT | 61 | a0001c0001t0001g0140 a0001c0001t0001g0149 a0001c0001t0001g0251 others(58): Show |
62 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1175+371dupA | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47821352 | |||||||
| chr11:47821352 | C | CTT | 77 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(74): Show |
78 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1175+370_1175+371d others(4): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47821352 | |||||||
| chr11:47821352 | C | CTTT | 7 | a0001c0001t0001g0139 a0001c0001t0001g0148 a0001c0001t0001g0154 others(4): Show |
7 | HG00597.hp2 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1175+369_1175+371d others(5): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47821352 | |||||||
| chr11:47821388 | T | C | 2 | a0001c0001t0002g0195 a0001c0001t0002g0293 |
2 | HG02273.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1175+336A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47821388 | |||||||
| chr11:47821460 | C | T | 2 | a0002c0002t0001g0024 a0002c0002t0001g0082 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1175+264G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47821460 | |||||||
| chr11:47821565 | G | A | 1 | a0001c0006t0001g0264 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1175+159C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47821565 | |||||||
| chr11:47821581 | A | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(206): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1175+143T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47821581 | |||||||
| chr11:47821663 | C | T | 1 | a0001c0015t0001g0273 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1175+61G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 9/35 | chr11 | 47821663 | |||||||
| chr11:47821878 | G | A | 18 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0136 others(15): Show |
18 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1078-57C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 8/35 | chr11 | 47821878 | |||||||
| chr11:47821944 | T | C | 1 | a0008c0011t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1078-123A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 8/35 | chr11 | 47821944 | |||||||
| chr11:47821945 | T | G | 1 | a0008c0011t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1078-124A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 8/35 | chr11 | 47821945 | |||||||
| chr11:47822015 | A | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0311 a0001c0001t0001g0313 |
3 | HG02451.hp2 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1077+72T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 8/35 | chr11 | 47822015 | |||||||
| chr11:47822176 | C | T | 1 | a0001c0001t0002g0289 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1000-12G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47822176 | |||||||
| chr11:47822261 | A | T | 4 | a0001c0001t0002g0192 a0001c0001t0002g0209 a0001c0001t0002g0287 others(1): Show |
4 | NA18943.hp1 NA19077.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000-97T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47822261 | |||||||
| chr11:47822372 | C | T | 2 | a0002c0002t0001g0018 a0002c0002t0001g0099 |
2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1000-208G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47822372 | |||||||
| chr11:47822801 | T | A | 3 | a0002c0002t0001g0076 a0002c0002t0001g0097 a0006c0012t0001g0078 |
3 | HG00544.hp2 HG01978.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1000-637A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47822801 | |||||||
| chr11:47822816 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(206): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1000-652C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47822816 | |||||||
| chr11:47822935 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1000-771A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47822935 | |||||||
| chr11:47823031 | T | C | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1000-867A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47823031 | |||||||
| chr11:47823198 | T | G | 1 | a0001c0001t0002g0201 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1000-1034A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47823198 | |||||||
| chr11:47823679 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1000-1515G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47823679 | |||||||
| chr11:47823711 | A | G | 1 | a0001c0001t0002g0286 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1000-1547T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47823711 | |||||||
| chr11:47824008 | C | CAT | 8 | a0001c0001t0001g0147 a0001c0001t0001g0168 a0001c0001t0001g0240 others(5): Show |
8 | HG02300.hp2 HG03492.hp1 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.1000-1846_1000-184 others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824008 | |||||||
| chr11:47824008 | C | CATAT | 13 | a0001c0001t0001g0121 a0001c0001t0001g0144 a0001c0001t0001g0145 others(10): Show |
13 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.1000-1848_1000-184 others(8): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824008 | |||||||
| chr11:47824008 | C | CATATATA others(3): Show |
1 | a0001c0001t0001g0124 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1000-1854_1000-184 others(14): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824008 | |||||||
| chr11:47824008 | CAT | C | 19 | a0001c0001t0001g0074 a0001c0001t0001g0135 a0001c0001t0001g0152 others(16): Show |
19 | HG01081.hp1 HG01255.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1000-1846_1000-184 others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824008 | |||||||
| chr11:47824008 | CATAT | C | 40 | a0001c0001t0001g0137 a0001c0001t0001g0141 a0001c0001t0001g0143 others(37): Show |
40 | HG00438.hp1 HG00673.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1000-1848_1000-184 others(8): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824008 | |||||||
| chr11:47824008 | CATATAT | C | 24 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0138 others(21): Show |
24 | HG01243.hp1 HG01257.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.1000-1850_1000-184 others(10): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824008 | |||||||
| chr11:47824008 | CATATATA others(1): Show |
C | 26 | a0001c0001t0001g0139 a0001c0001t0001g0179 a0001c0001t0001g0226 others(23): Show |
27 | HG00544.hp2 HG01109.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.1000-1852_1000-184 others(12): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824008 | |||||||
| chr11:47824008 | CATATATA others(3): Show |
C | 30 | a0001c0001t0001g0136 a0001c0001t0001g0232 a0001c0001t0001g0233 others(27): Show |
30 | HG00609.hp2 HG00639.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1000-1854_1000-184 others(14): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824008 | |||||||
| chr11:47824008 | CATATATA others(5): Show |
C | 5 | a0002c0002t0001g0026 a0002c0002t0001g0046 a0002c0002t0001g0075 others(2): Show |
5 | HG00280.hp2 HG01261.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-1856_1000-184 others(16): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824008 | |||||||
| chr11:47824008 | CATATATA others(7): Show |
C | 3 | a0001c0006t0001g0170 a0001c0006t0001g0267 a0001c0006t0001g0322 |
3 | HG02257.hp1 HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1000-1858_1000-184 others(18): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824008 | |||||||
| chr11:47824019 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1000-1855T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824019 | |||||||
| chr11:47824023 | A | ATATATAT others(11): Show |
1 | a0001c0001t0002g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1000-1860_1000-185 others(22): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824023 | |||||||
| chr11:47824025 | A | ATATATAT others(11): Show |
2 | a0001c0001t0002g0058 a0001c0001t0002g0190 |
2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1000-1862_1000-186 others(22): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824025 | |||||||
| chr11:47824027 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0002g0187 a0001c0001t0002g0330 |
3 | HG02280.hp1 NA18968.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1000-1863T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824027 | |||||||
| chr11:47824036 | TATATATA others(11): Show |
T | 3 | a0001c0001t0001g0311 a0001c0001t0002g0187 a0001c0001t0002g0330 |
3 | NA18968.hp1 NA18970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1000-1890_1000-187 others(22): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824036 | |||||||
| chr11:47824039 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1000-1875T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824039 | |||||||
| chr11:47824041 | A | G | 9 | a0001c0001t0002g0060 a0001c0001t0002g0067 a0001c0001t0002g0069 others(6): Show |
9 | HG01433.hp1 HG01515.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1000-1877T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824041 | |||||||
| chr11:47824042 | TATATATA others(5): Show |
T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0313 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1000-1890_1000-187 others(16): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824042 | |||||||
| chr11:47824043 | A | G | 35 | a0001c0001t0001g0269 a0001c0001t0002g0057 a0001c0001t0002g0061 others(32): Show |
35 | HG00323.hp1 HG00597.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1000-1879T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824043 | |||||||
| chr11:47824045 | A | ATATATAT others(3): Show |
1 | a0005c0008t0002g0280 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1000-1882_1000-188 others(14): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824045 | |||||||
| chr11:47824045 | A | ATATATAT others(1): Show |
3 | a0001c0001t0002g0212 a0001c0001t0002g0304 a0001c0001t0002g0310 |
3 | HG03669.hp1 HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1000-1882_1000-188 others(12): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824045 | |||||||
| chr11:47824045 | A | ATATATG | 7 | a0001c0001t0002g0065 a0001c0001t0002g0071 a0001c0001t0002g0203 others(4): Show |
7 | HG00733.hp1 HG01175.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000-1882_1000-188 others(10): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824045 | |||||||
| chr11:47824045 | A | ATATG | 6 | a0001c0001t0002g0072 a0001c0001t0002g0186 a0001c0001t0002g0198 others(3): Show |
6 | HG00140.hp1 HG00735.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000-1882_1000-188 others(8): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824045 | |||||||
| chr11:47824045 | A | ATG | 10 | a0001c0001t0002g0068 a0001c0001t0002g0204 a0001c0001t0002g0274 others(7): Show |
10 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.1000-1882_1000-188 others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824045 | |||||||
| chr11:47824045 | A | G | 13 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0064 others(10): Show |
13 | HG00140.hp2 HG01109.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.1000-1881T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824045 | |||||||
| chr11:47824048 | TATATAC | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0325 a0001c0001t0002g0056 |
3 | HG02630.hp2 HG03139.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1000-1890_1000-188 others(10): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824048 | |||||||
| chr11:47824050 | T | C | 5 | a0001c0001t0001g0225 a0001c0001t0001g0332 a0001c0001t0001g0333 others(2): Show |
5 | HG00438.hp1 HG02056.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-1886A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824050 | |||||||
| chr11:47824050 | TATAC | T | 10 | a0001c0001t0001g0182 a0001c0001t0002g0060 a0001c0001t0002g0067 others(7): Show |
10 | HG01433.hp1 HG01515.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1000-1890_1000-188 others(8): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824050 | |||||||
| chr11:47824052 | T | C | 106 | a0001c0001t0001g0074 a0001c0001t0001g0136 a0001c0001t0001g0164 others(103): Show |
107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.1000-1888A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824052 | |||||||
| chr11:47824052 | T | TAC | 6 | a0001c0001t0001g0002 a0001c0001t0001g0148 a0001c0001t0001g0149 others(3): Show |
6 | HG00741.hp1 HG02723.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000-1890_1000-188 others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824052 | |||||||
| chr11:47824052 | T | TATAC | 21 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0157 others(18): Show |
21 | HG00323.hp2 HG00642.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1000-1889_1000-188 others(8): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824052 | |||||||
| chr11:47824052 | T | TATATAC | 3 | a0001c0001t0003g0268 a0002c0002t0001g0049 a0002c0002t0001g0119 |
3 | HG01071.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1000-1889_1000-188 others(10): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824052 | |||||||
| chr11:47824052 | TAC | T | 38 | a0001c0001t0001g0054 a0001c0001t0001g0181 a0001c0001t0001g0269 others(35): Show |
38 | HG00323.hp1 HG00597.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1000-1890_1000-188 others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824052 | |||||||
| chr11:47824054 | C | T | 43 | a0001c0001t0001g0121 a0001c0001t0001g0180 a0001c0001t0001g0312 others(40): Show |
43 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.1000-1890G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824054 | |||||||
| chr11:47824069 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0226 a0001c0001t0001g0254 |
3 | HG02895.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1000-1905C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824069 | |||||||
| chr11:47824262 | A | G | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1000-2098T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824262 | |||||||
| chr11:47824306 | T | A | 1 | a0001c0001t0002g0211 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1000-2142A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824306 | |||||||
| chr11:47824322 | T | A | 3 | a0002c0002t0001g0042 a0002c0002t0001g0043 a0002c0002t0001g0109 |
3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1000-2158A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824322 | |||||||
| chr11:47824399 | A | G | 1 | a0002c0002t0001g0039 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1000-2235T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824399 | |||||||
| chr11:47824532 | C | G | 18 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0136 others(15): Show |
18 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1000-2368G>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824532 | |||||||
| chr11:47824612 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1000-2448T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824612 | |||||||
| chr11:47824650 | T | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(64): Show |
68 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1000-2486A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824650 | |||||||
| chr11:47824715 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1000-2551G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824715 | |||||||
| chr11:47824814 | GT | G | 99 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(96): Show |
100 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1000-2651delA | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824814 | |||||||
| chr11:47824904 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1000-2740G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47824904 | |||||||
| chr11:47825135 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1000-2971G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825135 | |||||||
| chr11:47825159 | G | A | 86 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(83): Show |
86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1000-2995C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825159 | |||||||
| chr11:47825218 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1000-3054G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825218 | |||||||
| chr11:47825295 | T | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1000-3131A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825295 | |||||||
| chr11:47825302 | G | A | 1 | a0002c0002t0001g0029 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1000-3138C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825302 | |||||||
| chr11:47825307 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1000-3143C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825307 | |||||||
| chr11:47825454 | C | CTT | 84 | a0001c0001t0001g0002 a0001c0001t0001g0126 a0001c0001t0001g0127 others(81): Show |
85 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1000-3292_1000-329 others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825454 | |||||||
| chr11:47825454 | C | CTTT | 7 | a0001c0001t0001g0124 a0001c0001t0001g0178 a0001c0001t0001g0179 others(4): Show |
7 | HG01891.hp1 HG02293.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1000-3293_1000-329 others(7): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825454 | |||||||
| chr11:47825476 | G | A | 8 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0234 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1000-3312C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825476 | |||||||
| chr11:47825524 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1000-3360G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825524 | |||||||
| chr11:47825587 | G | T | 1 | a0001c0001t0002g0189 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1000-3423C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825587 | |||||||
| chr11:47825596 | G | A | 2 | a0002c0002t0001g0087 a0002c0002t0001g0088 |
2 | NA18990.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1000-3432C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825596 | |||||||
| chr11:47825635 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1000-3471A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825635 | |||||||
| chr11:47825876 | G | A | 87 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1000-3712C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825876 | |||||||
| chr11:47825946 | T | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0272 |
2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1000-3782A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47825946 | |||||||
| chr11:47826171 | A | C | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1000-4007T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47826171 | |||||||
| chr11:47826242 | G | C | 1 | a0002c0002t0001g0108 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1000-4078C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47826242 | |||||||
| chr11:47826313 | T | C | 320 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(317): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1000-4149A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47826313 | |||||||
| chr11:47826392 | G | A | 1 | a0001c0001t0002g0301 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1000-4228C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47826392 | |||||||
| chr11:47826528 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1000-4364C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47826528 | |||||||
| chr11:47826560 | T | TC | 80 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(77): Show |
81 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1000-4397dupG | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47826560 | |||||||
| chr11:47826560 | TC | T | 106 | a0001c0001t0001g0312 a0001c0001t0002g0186 a0001c0001t0002g0281 others(103): Show |
107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1000-4397delG | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47826560 | |||||||
| chr11:47826570 | C | T | 10 | a0001c0001t0001g0121 a0001c0001t0001g0178 a0001c0001t0001g0179 others(7): Show |
10 | HG02451.hp2 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1000-4406G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47826570 | |||||||
| chr11:47826755 | G | T | 8 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0234 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1000-4591C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47826755 | |||||||
| chr11:47826780 | C | T | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG02723.hp1 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1000-4616G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47826780 | |||||||
| chr11:47826890 | T | G | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1000-4726A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47826890 | |||||||
| chr11:47826957 | T | C | 5 | a0002c0002t0001g0027 a0002c0002t0001g0089 a0002c0002t0001g0091 others(2): Show |
5 | HG01167.hp1 HG01258.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000-4793A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47826957 | |||||||
| chr11:47827183 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0279 |
3 | HG01891.hp1 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1000-5019C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47827183 | |||||||
| chr11:47827256 | T | C | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0279 |
3 | HG01891.hp1 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1000-5092A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47827256 | |||||||
| chr11:47827363 | C | CA | 51 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0155 others(48): Show |
51 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1000-5200dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47827363 | |||||||
| chr11:47827585 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1000-5421G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47827585 | |||||||
| chr11:47827710 | G | A | 1 | a0002c0002t0001g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1000-5546C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47827710 | |||||||
| chr11:47827723 | C | T | 330 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(327): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.1000-5559G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47827723 | |||||||
| chr11:47827880 | C | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(86): Show |
90 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1000-5716G>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47827880 | |||||||
| chr11:47827918 | T | G | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1000-5754A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47827918 | |||||||
| chr11:47828279 | A | ATATACAA others(10): Show |
3 | a0001c0006t0001g0170 a0001c0006t0001g0267 a0001c0006t0001g0322 |
3 | HG02257.hp1 HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1000-6132_1000-611 others(21): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47828279 | |||||||
| chr11:47828289 | A | G | 1 | a0001c0001t0001g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1000-6125T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47828289 | |||||||
| chr11:47828360 | T | C | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0279 |
3 | HG01891.hp1 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1000-6196A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47828360 | |||||||
| chr11:47828597 | CAT | C | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1000-6435_1000-643 others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47828597 | |||||||
| chr11:47828812 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1000-6648C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47828812 | |||||||
| chr11:47828831 | T | C | 1 | a0002c0002t0001g0108 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1000-6667A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47828831 | |||||||
| chr11:47828939 | A | C | 26 | a0001c0001t0001g0074 a0001c0001t0001g0136 a0001c0001t0001g0137 others(23): Show |
26 | HG01071.hp2 HG01099.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.999+6712T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47828939 | |||||||
| chr11:47829018 | G | A | 1 | a0001c0001t0001g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.999+6633C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47829018 | |||||||
| chr11:47829184 | G | GC | 122 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(119): Show |
123 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.999+6466dupG | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47829184 | |||||||
| chr11:47829452 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(85): Show |
89 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.999+6199G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47829452 | |||||||
| chr11:47829481 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.999+6170T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47829481 | |||||||
| chr11:47829699 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.999+5952G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47829699 | |||||||
| chr11:47829747 | C | T | 3 | a0002c0002t0001g0030 a0002c0002t0001g0031 a0002c0002t0001g0094 |
3 | NA18956.hp2 NA18967.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.999+5904G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47829747 | |||||||
| chr11:47829802 | C | T | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.999+5849G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47829802 | |||||||
| chr11:47829824 | C | T | 86 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(83): Show |
86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.999+5827G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47829824 | |||||||
| chr11:47830284 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.999+5367A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47830284 | |||||||
| chr11:47830505 | T | C | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.999+5146A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47830505 | |||||||
| chr11:47830879 | A | G | 309 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(306): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.999+4772T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47830879 | |||||||
| chr11:47830890 | G | A | 1 | a0001c0001t0001g0314 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.999+4761C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47830890 | |||||||
| chr11:47830926 | A | G | 309 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(306): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.999+4725T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47830926 | |||||||
| chr11:47831061 | A | G | 330 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(327): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.999+4590T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831061 | |||||||
| chr11:47831161 | T | TCAA | 102 | a0001c0001t0001g0177 a0001c0001t0001g0272 a0002c0002t0001g0001 others(99): Show |
103 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.999+4487_999+4489d others(5): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831161 | |||||||
| chr11:47831247 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.999+4404G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831247 | |||||||
| chr11:47831525 | A | G | 1 | a0001c0001t0002g0326 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.999+4126T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831525 | |||||||
| chr11:47831609 | C | T | 1 | a0002c0002t0001g0038 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.999+4042G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831609 | |||||||
| chr11:47831800 | G | A | 4 | a0001c0006t0001g0170 a0001c0006t0001g0264 a0001c0006t0001g0267 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+3851C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831800 | |||||||
| chr11:47831829 | C | T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0313 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.999+3822G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831829 | |||||||
| chr11:47831830 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.999+3821C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831830 | |||||||
| chr11:47831842 | C | CA | 7 | a0001c0001t0001g0121 a0001c0001t0001g0239 a0001c0001t0001g0312 others(4): Show |
7 | HG02056.hp2 HG02723.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.999+3808dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831842 | |||||||
| chr11:47831842 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.999+3799_999+3808d others(12): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831842 | |||||||
| chr11:47831842 | C | CAAAAAAA others(14): Show |
2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.999+3788_999+3808d others(23): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831842 | |||||||
| chr11:47831842 | CA | C | 26 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0178 others(23): Show |
26 | HG00733.hp1 HG00735.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.999+3808delT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831842 | |||||||
| chr11:47831842 | CAA | C | 83 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(80): Show |
83 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.999+3807_999+3808d others(4): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831842 | |||||||
| chr11:47831842 | CAAAA | C | 7 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG02056.hp1 NA18972.hp1 NA18986.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+3805_999+3808d others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831842 | |||||||
| chr11:47831842 | CAAAAA | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(75): Show |
79 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.999+3804_999+3808d others(7): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831842 | |||||||
| chr11:47831842 | CAAAAAA | C | 7 | a0001c0001t0001g0132 a0001c0001t0001g0177 a0001c0001t0001g0272 others(4): Show |
7 | HG00438.hp2 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+3803_999+3808d others(8): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831842 | |||||||
| chr11:47831842 | CAAAAAAA | C | 46 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 others(43): Show |
46 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.999+3802_999+3808d others(9): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831842 | |||||||
| chr11:47831842 | CAAAAAAA others(1): Show |
C | 6 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0042 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+3801_999+3808d others(10): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831842 | |||||||
| chr11:47831842 | CAAAAAAA others(2): Show |
C | 51 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0019 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.999+3800_999+3808d others(11): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831842 | |||||||
| chr11:47831883 | C | T | 1 | a0006c0012t0001g0078 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.999+3768G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831883 | |||||||
| chr11:47831894 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0334 a0001c0001t0001g0335 |
2 | HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.999+3742_999+3756d others(17): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831894 | |||||||
| chr11:47831894 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0336 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.999+3741_999+3756d others(18): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831894 | |||||||
| chr11:47831894 | C | CTTTTTTT others(13): Show |
2 | a0001c0001t0001g0121 a0001c0001t0001g0312 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.999+3737_999+3756d others(22): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831894 | |||||||
| chr11:47831894 | CT | C | 9 | a0002c0002t0001g0022 a0002c0002t0001g0031 a0002c0002t0001g0033 others(6): Show |
9 | HG01978.hp2 HG03017.hp1 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.999+3756delA | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831894 | |||||||
| chr11:47831894 | CTT | C | 60 | a0001c0001t0001g0181 a0002c0002t0001g0001 a0002c0002t0001g0017 others(57): Show |
61 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.999+3755_999+3756d others(4): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831894 | |||||||
| chr11:47831894 | CTTT | C | 9 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(6): Show |
9 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.999+3754_999+3756d others(5): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831894 | |||||||
| chr11:47831894 | CTTTTTTT | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(93): Show |
97 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.999+3750_999+3756d others(9): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831894 | |||||||
| chr11:47831894 | CTTTTTTT others(1): Show |
C | 103 | a0001c0001t0001g0074 a0001c0001t0001g0130 a0001c0001t0001g0131 others(100): Show |
103 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.999+3749_999+3756d others(10): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831894 | |||||||
| chr11:47831894 | CTTTTTTT others(2): Show |
C | 35 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 others(32): Show |
35 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.999+3748_999+3756d others(11): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831894 | |||||||
| chr11:47831894 | CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0001g0111 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.999+3747_999+3756d others(12): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47831894 | |||||||
| chr11:47832059 | G | A | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | NA19056.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.999+3592C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47832059 | |||||||
| chr11:47832122 | G | A | 3 | a0002c0002t0001g0042 a0002c0002t0001g0043 a0002c0002t0001g0109 |
3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.999+3529C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47832122 | |||||||
| chr11:47832241 | C | T | 2 | a0001c0001t0002g0188 a0001c0001t0004g0285 |
2 | HG00140.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.999+3410G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47832241 | |||||||
| chr11:47832243 | T | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(64): Show |
68 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.999+3408A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47832243 | |||||||
| chr11:47832252 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.999+3399T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47832252 | |||||||
| chr11:47832326 | C | T | 1 | a0002c0002t0001g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.999+3325G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47832326 | |||||||
| chr11:47832718 | A | G | 1 | a0001c0001t0002g0282 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.999+2933T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47832718 | |||||||
| chr11:47832723 | C | T | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.999+2928G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47832723 | |||||||
| chr11:47832903 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.999+2748A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47832903 | |||||||
| chr11:47832920 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.999+2731T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47832920 | |||||||
| chr11:47832973 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.999+2678C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47832973 | |||||||
| chr11:47833423 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(85): Show |
89 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.999+2228G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47833423 | |||||||
| chr11:47833462 | G | GA | 304 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(301): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.999+2188dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47833462 | |||||||
| chr11:47833729 | C | T | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG02723.hp1 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.999+1922G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47833729 | |||||||
| chr11:47833810 | TG | T | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.999+1840delC | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47833810 | |||||||
| chr11:47833837 | CA | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(64): Show |
68 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.999+1813delT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47833837 | |||||||
| chr11:47833956 | G | A | 1 | a0002c0002t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.999+1695C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47833956 | |||||||
| chr11:47833975 | T | C | 3 | a0001c0001t0003g0173 a0001c0001t0003g0174 a0001c0001t0003g0268 |
3 | HG01071.hp2 HG01257.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.999+1676A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47833975 | |||||||
| chr11:47834154 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.999+1497C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47834154 | |||||||
| chr11:47834331 | C | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0312 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.999+1320G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47834331 | |||||||
| chr11:47834451 | T | C | 1 | a0001c0001t0002g0274 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.999+1200A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47834451 | |||||||
| chr11:47834562 | A | G | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.999+1089T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47834562 | |||||||
| chr11:47834605 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.999+1046C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47834605 | |||||||
| chr11:47834735 | G | T | 1 | a0001c0001t0002g0330 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.999+916C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47834735 | |||||||
| chr11:47834830 | C | G | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.999+821G>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47834830 | |||||||
| chr11:47834932 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.999+719A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47834932 | |||||||
| chr11:47835181 | C | T | 31 | a0002c0002t0001g0039 a0002c0002t0001g0040 a0002c0002t0001g0041 others(28): Show |
31 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.999+470G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47835181 | |||||||
| chr11:47835481 | AC | A | 28 | a0002c0002t0001g0039 a0002c0002t0001g0040 a0002c0002t0001g0041 others(25): Show |
28 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.999+169delG | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47835481 | |||||||
| chr11:47835616 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(86): Show |
90 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.999+35T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 7/35 | chr11 | 47835616 | |||||||
| chr11:47835823 | T | TAG | 4 | a0001c0006t0001g0170 a0001c0006t0001g0264 a0001c0006t0001g0267 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.841-16_841-15dupCT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 6/35 | chr11 | 47835823 | |||||||
| chr11:47835968 | C | T | 87 | a0001c0001t0001g0185 a0001c0001t0002g0056 a0001c0001t0002g0057 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.841-159G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 6/35 | chr11 | 47835968 | |||||||
| chr11:47835969 | G | A | 1 | a0003c0003t0001g0015 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.841-160C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 6/35 | chr11 | 47835969 | |||||||
| chr11:47835972 | C | T | 1 | a0001c0001t0002g0275 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.841-163G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 6/35 | chr11 | 47835972 | |||||||
| chr11:47836460 | T | A | 329 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0055 others(326): Show |
331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.840+427A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 6/35 | chr11 | 47836460 | |||||||
| chr11:47836465 | T | A | 1 | a0003c0003t0001g0003 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.840+422A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 6/35 | chr11 | 47836465 | |||||||
| chr11:47836522 | G | A | 2 | a0001c0001t0002g0187 a0001c0001t0002g0330 |
2 | NA18968.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.840+365C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 6/35 | chr11 | 47836522 | |||||||
| chr11:47836610 | C | A | 1 | a0001c0001t0002g0276 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.840+277G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 6/35 | chr11 | 47836610 | |||||||
| chr11:47836713 | T | G | 1 | a0001c0001t0002g0308 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.840+174A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 6/35 | chr11 | 47836713 | |||||||
| chr11:47837164 | C | T | 1 | a0002c0002t0001g0041 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.726-163G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 5/35 | chr11 | 47837164 | |||||||
| chr11:47837194 | T | C | 18 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0136 others(15): Show |
18 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.726-193A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 5/35 | chr11 | 47837194 | |||||||
| chr11:47837203 | C | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(119): Show |
123 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.726-202G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 5/35 | chr11 | 47837203 | |||||||
| chr11:47837815 | T | C | 1 | a0002c0002t0001g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.647-192A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47837815 | |||||||
| chr11:47837816 | A | C | 4 | a0001c0006t0001g0170 a0001c0006t0001g0264 a0001c0006t0001g0267 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.647-193T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47837816 | |||||||
| chr11:47837958 | T | C | 4 | a0001c0006t0001g0170 a0001c0006t0001g0264 a0001c0006t0001g0267 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.647-335A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47837958 | |||||||
| chr11:47838142 | A | T | 1 | a0003c0003t0001g0003 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.647-519T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47838142 | |||||||
| chr11:47838230 | T | C | 1 | a0002c0002t0001g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.647-607A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47838230 | |||||||
| chr11:47838320 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.647-697C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47838320 | |||||||
| chr11:47838514 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.647-891G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47838514 | |||||||
| chr11:47838632 | T | TG | 87 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(84): Show |
88 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.647-1010dupC | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47838632 | |||||||
| chr11:47838641 | C | T | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.647-1018G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47838641 | |||||||
| chr11:47838708 | A | G | 1 | a0001c0001t0001g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.647-1085T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47838708 | |||||||
| chr11:47838931 | G | T | 2 | a0005c0008t0002g0280 a0005c0008t0002g0309 |
2 | NA18961.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.646+912C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47838931 | |||||||
| chr11:47839003 | C | CA | 98 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(95): Show |
99 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.646+839dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47839003 | |||||||
| chr11:47839014 | AAAG | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(120): Show |
124 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.646+826_646+828del others(3): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47839014 | |||||||
| chr11:47839194 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(85): Show |
89 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.646+649G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47839194 | |||||||
| chr11:47839195 | G | A | 7 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0227 others(4): Show |
7 | HG02109.hp2 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.646+648C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47839195 | |||||||
| chr11:47839402 | A | C | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.646+441T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47839402 | |||||||
| chr11:47839429 | T | C | 1 | a0001c0006t0001g0264 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.646+414A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47839429 | |||||||
| chr11:47839572 | G | C | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | NA19004.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.646+271C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 4/35 | chr11 | 47839572 | |||||||
| chr11:47840091 | C | A | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.424-26G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 3/35 | chr11 | 47840091 | |||||||
| chr11:47840108 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0312 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.424-43G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 3/35 | chr11 | 47840108 | |||||||
| chr11:47840221 | T | G | 1 | a0002c0002t0001g0038 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.424-156A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 3/35 | chr11 | 47840221 | |||||||
| chr11:47840239 | G | A | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG02723.hp1 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.423+139C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 3/35 | chr11 | 47840239 | |||||||
| chr11:47840305 | A | G | 10 | a0002c0002t0001g0039 a0002c0002t0001g0040 a0002c0002t0001g0102 others(7): Show |
10 | HG00323.hp2 HG00741.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.423+73T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 3/35 | chr11 | 47840305 | |||||||
| chr11:47840327 | G | A | 8 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0234 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.423+51C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 3/35 | chr11 | 47840327 | |||||||
| chr11:47840846 | A | G | 1 | a0001c0001t0002g0187 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.213-258T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47840846 | |||||||
| chr11:47840920 | A | G | 9 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(6): Show |
9 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.213-332T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47840920 | |||||||
| chr11:47840961 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.213-373C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47840961 | |||||||
| chr11:47841017 | T | TAC | 74 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(71): Show |
75 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.213-431_213-430dup others(2): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47841017 | |||||||
| chr11:47841017 | T | TACACAC | 15 | a0001c0001t0001g0129 a0001c0001t0001g0161 a0001c0001t0001g0162 others(12): Show |
15 | HG00280.hp1 HG00733.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.213-435_213-430dup others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47841017 | |||||||
| chr11:47841017 | TAC | T | 15 | a0001c0001t0001g0074 a0001c0001t0001g0213 a0001c0001t0001g0214 others(12): Show |
15 | HG01071.hp2 HG01099.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.213-431_213-430del others(2): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47841017 | |||||||
| chr11:47841061 | T | C | 4 | a0001c0006t0001g0170 a0001c0006t0001g0264 a0001c0006t0001g0267 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.213-473A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47841061 | |||||||
| chr11:47841074 | A | T | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG00323.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.213-486T>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47841074 | |||||||
| chr11:47841088 | A | G | 2 | a0001c0001t0002g0186 a0001c0001t0002g0281 |
2 | HG00140.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.213-500T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47841088 | |||||||
| chr11:47841374 | T | A | 1 | a0002c0002t0001g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.213-786A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47841374 | |||||||
| chr11:47841399 | A | G | 18 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0136 others(15): Show |
18 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.213-811T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47841399 | |||||||
| chr11:47841567 | G | A | 86 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(83): Show |
86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.213-979C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47841567 | |||||||
| chr11:47841683 | TTTTG | T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0005c0008t0002g0280 |
3 | HG01243.hp2 HG02451.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.213-1099_213-1096d others(6): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47841683 | |||||||
| chr11:47841699 | G | T | 1 | a0001c0001t0001g0232 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.213-1111C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47841699 | |||||||
| chr11:47841703 | T | G | 39 | a0001c0001t0002g0208 a0001c0001t0003g0171 a0001c0001t0003g0172 others(36): Show |
39 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.213-1115A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47841703 | |||||||
| chr11:47841918 | G | A | 309 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(306): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.213-1330C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47841918 | |||||||
| chr11:47842109 | T | C | 1 | a0002c0002t0001g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.213-1521A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47842109 | |||||||
| chr11:47842408 | C | T | 2 | a0001c0001t0002g0057 a0001c0001t0002g0278 |
2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.213-1820G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47842408 | |||||||
| chr11:47842423 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.213-1835G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47842423 | |||||||
| chr11:47842461 | G | A | 3 | a0002c0002t0001g0049 a0002c0002t0001g0119 a0002c0002t0001g0120 |
3 | HG00642.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.213-1873C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47842461 | |||||||
| chr11:47842509 | A | C | 1 | a0001c0006t0001g0264 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213-1921T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47842509 | |||||||
| chr11:47842535 | C | T | 1 | a0002c0002t0001g0076 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.213-1947G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47842535 | |||||||
| chr11:47842622 | C | T | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
4 | HG02155.hp1 NA18942.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.213-2034G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47842622 | |||||||
| chr11:47842717 | C | T | 1 | a0002c0002t0001g0017 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.213-2129G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47842717 | |||||||
| chr11:47842780 | A | C | 7 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0227 others(4): Show |
7 | HG02109.hp2 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.213-2192T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47842780 | |||||||
| chr11:47842840 | T | A | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.213-2252A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47842840 | |||||||
| chr11:47842951 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.213-2363A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47842951 | |||||||
| chr11:47843240 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.213-2652G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47843240 | |||||||
| chr11:47843290 | C | T | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.213-2702G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47843290 | |||||||
| chr11:47843338 | T | A | 1 | a0001c0001t0002g0209 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.213-2750A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47843338 | |||||||
| chr11:47843444 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.213-2856G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47843444 | |||||||
| chr11:47843608 | G | T | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.213-3020C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47843608 | |||||||
| chr11:47843927 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.213-3339T>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47843927 | |||||||
| chr11:47844008 | C | T | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.213-3420G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47844008 | |||||||
| chr11:47844220 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.212+3628C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47844220 | |||||||
| chr11:47845088 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.212+2760T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47845088 | |||||||
| chr11:47845107 | C | T | 1 | a0002c0002t0001g0075 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.212+2741G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47845107 | |||||||
| chr11:47845108 | G | A | 1 | a0001c0001t0002g0276 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.212+2740C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47845108 | |||||||
| chr11:47845109 | G | T | 1 | a0001c0001t0002g0276 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.212+2739C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47845109 | |||||||
| chr11:47845439 | T | C | 310 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(307): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.212+2409A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47845439 | |||||||
| chr11:47845507 | C | T | 100 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.212+2341G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47845507 | |||||||
| chr11:47845868 | T | C | 1 | a0001c0001t0002g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.212+1980A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47845868 | |||||||
| chr11:47845901 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.212+1947C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47845901 | |||||||
| chr11:47846020 | C | T | 1 | a0001c0001t0002g0274 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.212+1828G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47846020 | |||||||
| chr11:47846110 | T | C | 1 | a0001c0001t0002g0211 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.212+1738A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47846110 | |||||||
| chr11:47846111 | G | C | 1 | a0002c0002t0001g0051 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.212+1737C>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47846111 | |||||||
| chr11:47846141 | G | GA | 22 | a0001c0001t0001g0074 a0001c0001t0001g0169 a0001c0001t0001g0213 others(19): Show |
22 | HG01071.hp2 HG01099.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.212+1706dupT | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47846141 | |||||||
| chr11:47846193 | TC | T | 3 | a0001c0001t0002g0056 a0001c0001t0002g0274 a0001c0001t0002g0275 |
3 | NA18990.hp2 NA19090.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.212+1654delG | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47846193 | |||||||
| chr11:47846222 | C | A | 1 | a0002c0002t0001g0052 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.212+1626G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47846222 | |||||||
| chr11:47846375 | G | A | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0008c0011t0001g0175 |
3 | NA18945.hp1 NA18949.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.212+1473C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47846375 | |||||||
| chr11:47846422 | A | G | 1 | a0001c0001t0001g0311 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.212+1426T>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47846422 | |||||||
| chr11:47846431 | C | A | 1 | a0001c0001t0001g0271 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.212+1417G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47846431 | |||||||
| chr11:47846623 | C | T | 8 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0127 others(5): Show |
8 | HG00558.hp1 HG00609.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.212+1225G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47846623 | |||||||
| chr11:47846757 | T | A | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.212+1091A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47846757 | |||||||
| chr11:47846888 | G | T | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG02723.hp1 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.212+960C>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47846888 | |||||||
| chr11:47846922 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0124 others(117): Show |
121 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.212+926A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47846922 | |||||||
| chr11:47847162 | G | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0272 |
2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.212+686C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47847162 | |||||||
| chr11:47847243 | C | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.212+605G>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47847243 | |||||||
| chr11:47847301 | C | G | 88 | a0001c0001t0001g0185 a0001c0001t0002g0056 a0001c0001t0002g0057 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.212+547G>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47847301 | |||||||
| chr11:47847332 | C | T | 10 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0180 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.212+516G>A | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47847332 | |||||||
| chr11:47847496 | T | C | 1 | a0002c0002t0001g0053 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.212+352A>G | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47847496 | |||||||
| chr11:47847644 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.212+204C>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47847644 | |||||||
| chr11:47847648 | T | G | 8 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0001t0001g0331 others(5): Show |
8 | HG01192.hp2 HG01978.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.212+200A>C | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47847648 | |||||||
| chr11:47847648 | T | TG | 98 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(95): Show |
98 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.212+199dupC | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47847648 | |||||||
| chr11:47847648 | T | TGG | 51 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 others(48): Show |
51 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.212+198_212+199dup others(2): Show |
NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47847648 | |||||||
| chr11:47847648 | TG | T | 45 | a0001c0005t0001g0050 a0002c0002t0001g0001 a0002c0002t0001g0017 others(42): Show |
46 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.212+199delC | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47847648 | |||||||
| chr11:47847831 | C | A | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.212+17G>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 2/35 | chr11 | 47847831 | |||||||
| chr11:47848164 | T | A | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG02723.hp1 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100+55A>T | NUP160 | ENSG00000030066.14 | transcript | ENST00000378460.7 | protein_coding | 1/35 | chr11 | 47848164 |