Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8878 |
| ensemblid | ENSG00000161011.20 |
| hgncid | 11280 |
| symbol | SQSTM1 |
| name | sequestosome 1 |
| refseq_nuc | NM_003900.5 |
| refseq_prot | NP_003891.1 |
| ensembl_nuc | ENST00000389805.9 |
| ensembl_prot | ENSP00000374455.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 179820905 |
| end | 179838078 |
| strand | + |
| ver | v1.2 |
| region | chr5:179820905-179838078 |
| region5000 | chr5:179815905-179843078 |
| regionname0 | SQSTM1_chr5_179820905_179838078 |
| regionname5000 | SQSTM1_chr5_179815905_179843078 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 440 | 446 | 89 | 82 | 205 | 18 | 50 | 156 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | MASLT others(435): Show |
chr5 | 179815905 | 179843078 |
| a0002 | 0/0 | 440 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | MASLT others(435): Show |
chr5 | 179815905 | 179843078 |
| a0003 | 0/0 | 440 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | MASLT others(435): Show |
chr5 | 179815905 | 179843078 |
| a0004 | 0/0 | 440 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | MASLT others(435): Show |
chr5 | 179815905 | 179843078 |
| a0005 | 0/0 | 440 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | MASLT others(435): Show |
chr5 | 179815905 | 179843078 |
| a0006 | 0/0 | 440 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | MASLT others(435): Show |
chr5 | 179815905 | 179843078 |
| a0007 | 0/0 | 440 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | MASLT others(435): Show |
chr5 | 179815905 | 179843078 |
| a0008 | 0/0 | 440 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | MASLT others(435): Show |
chr5 | 179815905 | 179843078 |
| a0009 | 0/0 | 440 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | MASLT others(435): Show |
chr5 | 179815905 | 179843078 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1320 | 279 | 24 | 56 | 154 | 8 | 36 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0001c0002 | 1/0 | 1320 | 85 | 16 | 22 | 25 | 10 | 11 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0001c0003 | 0/0 | 1320 | 41 | 21 | 2 | 16 | 0 | 2 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0001c0004 | 0/0 | 1320 | 8 | 8 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0001c0005 | 0/0 | 1320 | 7 | 6 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0001c0006 | 0/0 | 1320 | 6 | 6 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0001c0008 | 0/0 | 1320 | 5 | 2 | 0 | 2 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0001c0009 | 0/0 | 1320 | 4 | 4 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0001c0010 | 0/0 | 1320 | 3 | 0 | 0 | 3 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0001c0011 | 0/0 | 1320 | 3 | 0 | 0 | 3 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0001c0015 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0001c0017 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0001c0018 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0001c0020 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0001c0021 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0002c0007 | 0/0 | 1320 | 6 | 6 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0003c0012 | 0/0 | 1320 | 2 | 0 | 2 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0004c0014 | 0/0 | 1320 | 2 | 0 | 2 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0005c0013 | 0/0 | 1320 | 2 | 1 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0006c0022 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0007c0016 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0008c0019 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 | ||
| a0009c0023 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ATGGC others(1315): Show |
chr5 | 179815905 | 179843078 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2840 | 252 | 21 | 49 | 141 | 6 | 34 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0001t0002 | 0/0 | 2840 | 4 | 0 | 0 | 4 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0001t0003 | 0/0 | 2842 | 12 | 2 | 5 | 2 | 2 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2837): Show |
chr5 | 179815905 | 179843078 |
| a0001c0001t0008 | 0/0 | 2840 | 5 | 0 | 0 | 5 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0001t0011 | 0/0 | 2842 | 2 | 0 | 2 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2837): Show |
chr5 | 179815905 | 179843078 |
| a0001c0001t0012 | 0/0 | 2840 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0001t0013 | 0/0 | 2906 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2901): Show |
chr5 | 179815905 | 179843078 |
| a0001c0001t0015 | 0/0 | 2840 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0001t0017 | 0/0 | 2840 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0002t0001 | 0/0 | 2840 | 7 | 7 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0002t0002 | 1/0 | 2840 | 73 | 4 | 22 | 25 | 10 | 11 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0002t0005 | 0/0 | 2840 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0002t0006 | 0/0 | 2840 | 3 | 3 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0002t0014 | 0/0 | 2840 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0003t0001 | 0/0 | 2840 | 10 | 8 | 1 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0003t0002 | 0/0 | 2840 | 18 | 0 | 1 | 15 | 0 | 2 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0003t0003 | 0/0 | 2842 | 3 | 3 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2837): Show |
chr5 | 179815905 | 179843078 |
| a0001c0003t0005 | 0/0 | 2840 | 4 | 4 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0003t0006 | 0/0 | 2840 | 2 | 2 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0003t0010 | 0/0 | 2825 | 3 | 3 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2820): Show |
chr5 | 179815905 | 179843078 |
| a0001c0003t0016 | 0/0 | 2840 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0004t0001 | 0/0 | 2840 | 8 | 8 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0005t0001 | 0/0 | 2840 | 7 | 6 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0006t0004 | 0/0 | 2840 | 3 | 3 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0006t0009 | 0/0 | 2840 | 3 | 3 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0008t0001 | 0/0 | 2840 | 2 | 2 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0008t0002 | 0/0 | 2840 | 3 | 0 | 0 | 2 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0009t0004 | 0/0 | 2840 | 4 | 4 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0010t0002 | 0/0 | 2840 | 3 | 0 | 0 | 3 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0011t0001 | 0/0 | 2840 | 3 | 0 | 0 | 3 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0015t0002 | 0/0 | 2840 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0017t0002 | 0/0 | 2840 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0018t0005 | 0/0 | 2840 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0020t0001 | 0/0 | 2840 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0001c0021t0001 | 0/0 | 2840 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0002c0007t0002 | 0/0 | 2840 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0002c0007t0007 | 0/0 | 2840 | 5 | 5 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0003c0012t0002 | 0/0 | 2840 | 2 | 0 | 2 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0004c0014t0002 | 0/0 | 2840 | 2 | 0 | 2 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0005c0013t0001 | 0/0 | 2840 | 2 | 1 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0006c0022t0001 | 0/0 | 2840 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0007c0016t0005 | 0/0 | 2840 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0008c0019t0001 | 0/0 | 2840 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| a0009c0023t0006 | 0/0 | 2840 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | ACGGC others(2835): Show |
chr5 | 179815905 | 179843078 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 1 | 0 | 13 | 0 | 2 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 3 | 3 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0007 | 0/0 | 5 | 1 | 1 | 2 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0031 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0032 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0033 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0062 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0065 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0066 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0296 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0008g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0008g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0008g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0011g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0012g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0013g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0015g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0001t0017g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0005 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0020 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0023 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0024 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0055 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0002t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0005g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0010g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0010g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0010g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0003t0016g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0004t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0004t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0004t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0005t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0005t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0005t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0005t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0006t0004g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0006t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0006t0009g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0006t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0008t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0008t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0008t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0008t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0008t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0009t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0009t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0009t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0009t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0010t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0010t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0011t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0011t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0011t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0015t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0017t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0018t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0020t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0001c0021t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0002c0007t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0002c0007t0007g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0002c0007t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0002c0007t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0003c0012t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0004c0014t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0004c0014t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0005c0013t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0006c0022t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0007c0016t0005g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0008c0019t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| a0009c0023t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0039 | EUR | GBR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0020 | EUR | GBR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | GBR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0156 | EUR | GBR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0067 | EUR | FIN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0013 | EUR | FIN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | FIN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00423 | hp1 | a0001 | c0015 | t0002 | g0034 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00558 | hp2 | a0001 | c0010 | t0002 | g0038 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00609 | hp1 | a0006 | c0022 | t0001 | g0008 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0055 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0020 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00733 | hp2 | a0001 | c0001 | t0011 | g0040 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0194 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0068 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0104 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0069 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0109 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0035 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01069 | hp2 | a0003 | c0012 | t0002 | g0005 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0035 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01071 | hp2 | a0003 | c0012 | t0002 | g0005 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01074 | hp1 | a0001 | c0001 | t0011 | g0040 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0107 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01167 | hp2 | a0001 | c0005 | t0001 | g0012 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0039 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01175 | hp1 | a0004 | c0014 | t0002 | g0110 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0221 | AMR | PUR | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0111 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01346 | hp2 | a0004 | c0014 | t0002 | g0128 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01361 | hp1 | a0001 | c0017 | t0002 | g0004 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01433 | hp1 | a0007 | c0016 | t0005 | g0099 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0105 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0055 | EUR | IBS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0195 | EUR | IBS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0023 | EUR | IBS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0192 | EUR | IBS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0119 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01884 | hp2 | a0005 | c0013 | t0001 | g0015 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01891 | hp1 | a0002 | c0007 | t0007 | g0081 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0070 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0096 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0019 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0270 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02055 | hp1 | a0001 | c0003 | t0005 | g0137 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02071 | hp1 | a0001 | c0011 | t0001 | g0210 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02071 | hp2 | a0001 | c0003 | t0002 | g0050 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02080 | hp1 | a0001 | c0003 | t0002 | g0183 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02132 | hp1 | a0001 | c0003 | t0002 | g0050 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02145 | hp2 | a0001 | c0003 | t0016 | g0144 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | CDX | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CDX | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CDX | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02258 | hp1 | a0002 | c0007 | t0007 | g0018 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02280 | hp2 | a0001 | c0018 | t0005 | g0140 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02300 | hp1 | a0005 | c0013 | t0001 | g0015 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02451 | hp1 | a0002 | c0007 | t0007 | g0018 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02572 | hp1 | a0001 | c0003 | t0006 | g0146 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0189 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02615 | hp1 | a0001 | c0020 | t0001 | g0043 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0088 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0217 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02630 | hp2 | a0001 | c0009 | t0004 | g0092 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02647 | hp2 | a0001 | c0002 | t0014 | g0080 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0171 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0213 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02723 | hp1 | a0001 | c0004 | t0001 | g0043 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02723 | hp2 | a0001 | c0006 | t0009 | g0142 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0108 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0141 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02809 | hp2 | a0002 | c0007 | t0007 | g0158 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0012 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0044 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02896 | hp1 | a0001 | c0001 | t0017 | g0075 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02896 | hp2 | a0001 | c0003 | t0005 | g0041 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02897 | hp1 | a0001 | c0003 | t0005 | g0041 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02897 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02922 | hp1 | a0001 | c0003 | t0010 | g0130 | AFR | ESN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02922 | hp2 | a0001 | c0006 | t0004 | g0091 | AFR | ESN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02965 | hp1 | a0001 | c0003 | t0010 | g0073 | AFR | ESN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02965 | hp2 | a0008 | c0019 | t0001 | g0180 | AFR | ESN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02970 | hp1 | a0001 | c0008 | t0001 | g0093 | AFR | ESN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02970 | hp2 | a0001 | c0005 | t0001 | g0012 | AFR | ESN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02976 | hp1 | a0001 | c0005 | t0001 | g0136 | AFR | ESN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | ESN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0019 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03041 | hp2 | a0001 | c0002 | t0006 | g0084 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0219 | AFR | MSL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03098 | hp2 | a0001 | c0006 | t0009 | g0037 | AFR | MSL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0112 | AFR | ESN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03139 | hp2 | a0001 | c0006 | t0004 | g0045 | AFR | ESN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ESN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03209 | hp1 | a0001 | c0003 | t0003 | g0150 | AFR | MSL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03209 | hp2 | a0001 | c0005 | t0001 | g0100 | AFR | MSL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03225 | hp2 | a0001 | c0009 | t0004 | g0090 | AFR | MSL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03453 | hp1 | a0001 | c0003 | t0003 | g0149 | AFR | MSL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0220 | AFR | MSL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | MSL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0012 | AFR | MSL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0036 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03516 | hp1 | a0001 | c0003 | t0006 | g0143 | AFR | ESN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0025 | AFR | ESN | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03540 | hp2 | a0009 | c0023 | t0006 | g0131 | AFR | GWD | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0086 | AFR | MSL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03654 | hp2 | a0001 | c0008 | t0002 | g0054 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0193 | SAS | STU | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0024 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0125 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03710 | hp2 | a0001 | c0001 | t0013 | g0295 | SAS | PJL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03927 | hp1 | a0001 | c0003 | t0002 | g0169 | SAS | BEB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0024 | SAS | BEB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03942 | hp2 | a0001 | c0003 | t0002 | g0148 | SAS | BEB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0147 | SAS | STU | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0188 | SAS | STU | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | STU | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18522 | hp1 | a0001 | c0003 | t0003 | g0135 | AFR | YRI | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18522 | hp2 | a0001 | c0009 | t0004 | g0089 | AFR | YRI | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0151 | EAS | CHB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18906 | hp1 | a0001 | c0006 | t0004 | g0045 | AFR | YRI | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18906 | hp2 | a0001 | c0003 | t0010 | g0083 | AFR | YRI | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18945 | hp1 | a0001 | c0010 | t0002 | g0103 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18946 | hp2 | a0001 | c0003 | t0002 | g0187 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18957 | hp1 | a0001 | c0003 | t0002 | g0314 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18961 | hp1 | a0001 | c0008 | t0002 | g0287 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18972 | hp2 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18973 | hp2 | a0001 | c0011 | t0001 | g0281 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18975 | hp1 | a0001 | c0003 | t0002 | g0297 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18979 | hp2 | a0001 | c0003 | t0002 | g0315 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18982 | hp1 | a0001 | c0001 | t0012 | g0009 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18988 | hp1 | a0001 | c0001 | t0008 | g0289 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18991 | hp1 | a0001 | c0003 | t0002 | g0185 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18995 | hp1 | a0001 | c0003 | t0002 | g0186 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19003 | hp1 | a0001 | c0003 | t0002 | g0316 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19006 | hp2 | a0001 | c0003 | t0002 | g0129 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19007 | hp1 | a0001 | c0001 | t0008 | g0063 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19010 | hp1 | a0001 | c0010 | t0002 | g0038 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19030 | hp1 | a0001 | c0002 | t0006 | g0145 | AFR | LWK | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19030 | hp2 | a0001 | c0002 | t0005 | g0078 | AFR | LWK | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19043 | hp1 | a0001 | c0004 | t0001 | g0047 | AFR | LWK | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19043 | hp2 | a0001 | c0003 | t0005 | g0076 | AFR | LWK | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19056 | hp2 | a0001 | c0001 | t0015 | g0027 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19060 | hp1 | a0001 | c0003 | t0002 | g0161 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19062 | hp1 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19063 | hp1 | a0001 | c0003 | t0002 | g0313 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19064 | hp1 | a0001 | c0008 | t0002 | g0004 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19067 | hp2 | a0001 | c0011 | t0001 | g0282 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19079 | hp2 | a0001 | c0003 | t0002 | g0034 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19084 | hp1 | a0001 | c0021 | t0001 | g0266 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19086 | hp2 | a0001 | c0003 | t0002 | g0034 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19088 | hp2 | a0001 | c0001 | t0008 | g0063 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19240 | hp1 | a0002 | c0007 | t0007 | g0018 | AFR | YRI | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | YRI | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | ASW | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA20129 | hp2 | a0001 | c0002 | t0006 | g0085 | AFR | ASW | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0215 | EUR | TSI | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0155 | EUR | TSI | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0293 | EUR | TSI | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0117 | EUR | TSI | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | GIH | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | GIH | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0019 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02109 | hp1 | a0001 | c0004 | t0001 | g0047 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02486 | hp2 | a0002 | c0007 | t0002 | g0214 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG03471 | hp2 | a0001 | c0008 | t0001 | g0077 | AFR | MSL | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG06807 | hp1 | a0001 | c0006 | t0009 | g0037 | AFR | USA | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | USA | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | USA | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | LWK | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| NA21309 | hp2 | a0001 | c0009 | t0004 | g0074 | AFR | LWK | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0296 | REF | REF | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0127 | REF | REF | SQSTM1_chr5_179815905_179843078 | SQSTM1 | chr5 | 179815905 | 179843078 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179823003 | C | T | 1 | a0009 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.251C>T | p.Thr84Ile | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/8 | 283/2840 | 251/1323 | 84/440 | chr5 | 179823003 | |||
| chr5:179825146 | C | T | 1 | a0006 | 1 | HG00609.hp1 | missense_variant&splice_region_variant | MODERATE | c.674C>T | p.Ala225Val | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/8 | 706/2840 | 674/1323 | 225/440 | chr5 | 179825146 | |||
| chr5:179825184 | A | G | 1 | a0004 | 2 | HG01175.hp1 HG01346.hp2 |
missense_variant | MODERATE | c.712A>G | p.Lys238Glu | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/8 | 744/2840 | 712/1323 | 238/440 | chr5 | 179825184 | |||
| chr5:179833099 | G | C | 1 | a0007 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.822G>C | p.Glu274Asp | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/8 | 854/2840 | 822/1323 | 274/440 | chr5 | 179833099 | |||
| chr5:179833211 | A | G | 1 | a0008 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.934A>G | p.Arg312Gly | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/8 | 966/2840 | 934/1323 | 312/440 | chr5 | 179833211 | |||
| chr5:179833232 | G | A | 1 | a0002 | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp1 others(3): Show |
missense_variant | MODERATE | c.955G>A | p.Glu319Lys | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/8 | 987/2840 | 955/1323 | 319/440 | chr5 | 179833232 | |||
| chr5:179833238 | C | T | 1 | a0005 | 2 | HG01884.hp2 HG02300.hp1 |
missense_variant | MODERATE | c.961C>T | p.Arg321Cys | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/8 | 993/2840 | 961/1323 | 321/440 | chr5 | 179833238 | |||
| chr5:179836445 | C | T | 1 | a0003 | 2 | HG01069.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.1175C>T | p.Pro392Leu | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 1207/2840 | 1175/1323 | 392/440 | chr5 | 179836445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179833066 | G | A | 1 | a0001c0015 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.789G>A | p.Gly263Gly | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/8 | 821/2840 | 789/1323 | 263/440 | chr5 | 179833066 | |||
| chr5:179833096 | A | G | 1 | a0001c0021 | 1 | NA19084.hp1 | synonymous_variant | LOW | c.819A>G | p.Pro273Pro | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/8 | 851/2840 | 819/1323 | 273/440 | chr5 | 179833096 | |||
| chr5:179833153 | C | T | 15 | a0001c0001 a0001c0003 a0001c0004 others(12): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
synonymous_variant | LOW | c.876C>T | p.Asp292Asp | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/8 | 908/2840 | 876/1323 | 292/440 | chr5 | 179833153 | |||
| chr5:179833183 | C | T | 2 | a0001c0004 a0001c0020 |
9 | HG02109.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
synonymous_variant | LOW | c.906C>T | p.Gly302Gly | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/8 | 938/2840 | 906/1323 | 302/440 | chr5 | 179833183 | |||
| chr5:179833213 | G | A | 10 | a0001c0001 a0001c0005 a0001c0008 others(7): Show |
300 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(297): Show |
synonymous_variant | LOW | c.936G>A | p.Arg312Arg | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/8 | 968/2840 | 936/1323 | 312/440 | chr5 | 179833213 | |||
| chr5:179833231 | C | T | 3 | a0001c0005 a0007c0016 a0008c0019 |
9 | HG01167.hp2 HG01433.hp1 HG02886.hp2 others(6): Show |
synonymous_variant | LOW | c.954C>T | p.Ser318Ser | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/8 | 986/2840 | 954/1323 | 318/440 | chr5 | 179833231 | |||
| chr5:179833601 | G | A | 1 | a0001c0017 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.984G>A | p.Ser328Ser | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/8 | 1016/2840 | 984/1323 | 328/440 | chr5 | 179833601 | |||
| chr5:179833661 | G | A | 4 | a0001c0006 a0001c0009 a0001c0018 others(1): Show |
12 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(9): Show |
synonymous_variant | LOW | c.1044G>A | p.Pro348Pro | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/8 | 1076/2840 | 1044/1323 | 348/440 | chr5 | 179833661 | |||
| chr5:179836446 | G | A | 1 | a0001c0010 | 3 | HG00558.hp2 NA18945.hp1 NA19010.hp1 |
synonymous_variant | LOW | c.1176G>A | p.Pro392Pro | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 1208/2840 | 1176/1323 | 392/440 | chr5 | 179836446 | |||
| chr5:179836515 | G | A | 1 | a0001c0011 | 3 | HG02071.hp1 NA18973.hp2 NA19067.hp2 |
synonymous_variant | LOW | c.1245G>A | p.Arg415Arg | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 1277/2840 | 1245/1323 | 415/440 | chr5 | 179836515 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179820912 | G | A | 2 | a0001c0006t0004 a0001c0009t0004 |
7 | HG02630.hp2 HG02922.hp2 HG03139.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-25G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/8 | 25 | chr5 | 179820912 | ||||||
| chr5:179836606 | ACCTCTTC others(8): Show |
A | 1 | a0001c0003t0010 | 3 | HG02922.hp1 HG02965.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*23_*37delCGTGCCCC others(7): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 23 | INFO_REALIGN_3_PRIME | chr5 | 179836606 | |||||
| chr5:179836652 | G | A | 1 | a0001c0001t0012 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*59G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 59 | chr5 | 179836652 | ||||||
| chr5:179836659 | A | C | 1 | a0001c0001t0008 | 5 | NA18972.hp2 NA18988.hp1 NA19007.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*66A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 66 | chr5 | 179836659 | ||||||
| chr5:179836676 | G | A | 1 | a0001c0001t0011 | 2 | HG00733.hp2 HG01074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*83G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 83 | chr5 | 179836676 | ||||||
| chr5:179836767 | C | CTG | 3 | a0001c0001t0003 a0001c0001t0011 a0001c0003t0003 |
17 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*187_*188dupTG | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 189 | INFO_REALIGN_3_PRIME | chr5 | 179836767 | |||||
| chr5:179836849 | A | AGCGCGCT others(59): Show |
1 | a0001c0001t0013 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*257_*322dupGCGCGC others(60): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 323 | INFO_REALIGN_3_PRIME | chr5 | 179836849 | |||||
| chr5:179836853 | C | T | 1 | a0001c0001t0017 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*260C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 260 | chr5 | 179836853 | ||||||
| chr5:179836872 | C | G | 4 | a0001c0002t0006 a0001c0003t0006 a0001c0003t0016 others(1): Show |
7 | HG02145.hp2 HG02572.hp1 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*279C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 279 | chr5 | 179836872 | ||||||
| chr5:179836980 | A | G | 1 | a0001c0001t0015 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*387A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 387 | chr5 | 179836980 | ||||||
| chr5:179837132 | T | G | 4 | a0001c0002t0005 a0001c0003t0005 a0001c0018t0005 others(1): Show |
7 | HG01433.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*539T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 539 | chr5 | 179837132 | ||||||
| chr5:179837200 | C | A | 1 | a0001c0003t0016 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*607C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 607 | chr5 | 179837200 | ||||||
| chr5:179837379 | G | A | 1 | a0002c0007t0007 | 5 | HG01891.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*786G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 786 | chr5 | 179837379 | ||||||
| chr5:179837666 | C | T | 1 | a0001c0002t0014 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1073C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 1073 | chr5 | 179837666 | ||||||
| chr5:179837731 | T | C | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(27): Show |
338 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*1138T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 1138 | chr5 | 179837731 | ||||||
| chr5:179837915 | G | T | 34 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(31): Show |
353 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(350): Show |
3_prime_UTR_variant | MODIFIER | c.*1322G>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 8/8 | 1322 | chr5 | 179837915 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179821257 | G | A | 7 | a0001c0001t0003g0071 a0001c0002t0002g0035 a0001c0002t0002g0036 others(4): Show |
9 | HG00280.hp1 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.205+116G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179821257 | |||||||
| chr5:179821314 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.205+173C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179821314 | |||||||
| chr5:179821502 | T | C | 1 | a0001c0003t0010g0073 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.205+361T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179821502 | |||||||
| chr5:179821516 | G | A | 1 | a0001c0009t0004g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.205+375G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179821516 | |||||||
| chr5:179821608 | G | C | 1 | a0001c0001t0017g0075 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.205+467G>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179821608 | |||||||
| chr5:179821629 | G | A | 1 | a0001c0002t0002g0067 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.205+488G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179821629 | |||||||
| chr5:179821636 | C | T | 1 | a0001c0001t0001g0317 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.205+495C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179821636 | |||||||
| chr5:179821642 | A | G | 6 | a0001c0003t0002g0034 a0001c0003t0002g0313 a0001c0003t0002g0314 others(3): Show |
7 | HG00423.hp1 NA18957.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.205+501A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179821642 | |||||||
| chr5:179821662 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.205+521C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179821662 | |||||||
| chr5:179821774 | A | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(192): Show |
278 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.205+633A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179821774 | |||||||
| chr5:179821782 | C | CCTAA | 8 | a0001c0001t0001g0082 a0001c0001t0003g0079 a0001c0002t0005g0078 others(5): Show |
10 | HG01891.hp1 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.205+643_205+644ins others(4): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 179821782 | ||||||
| chr5:179821798 | CTGGTG | C | 3 | a0001c0002t0006g0084 a0001c0002t0006g0085 a0001c0003t0010g0083 |
3 | HG03041.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.205+660_205+664del others(5): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 179821798 | ||||||
| chr5:179821926 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0176 a0001c0001t0001g0311 |
4 | HG02683.hp2 HG04115.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.205+785A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179821926 | |||||||
| chr5:179821946 | T | TA | 14 | a0001c0001t0001g0087 a0001c0001t0001g0177 a0001c0002t0005g0078 others(11): Show |
15 | HG02615.hp2 HG02630.hp2 HG02922.hp2 others(12): Show |
intron_variant | MODIFIER | c.205+818dupA | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 179821946 | ||||||
| chr5:179821946 | TA | T | 59 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0029 others(56): Show |
82 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.205+818delA | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 179821946 | ||||||
| chr5:179822073 | A | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(176): Show |
247 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.206-885A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822073 | |||||||
| chr5:179822073 | A | T | 1 | a0001c0001t0001g0283 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.206-885A>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822073 | |||||||
| chr5:179822090 | A | G | 3 | a0002c0007t0007g0018 a0002c0007t0007g0081 a0002c0007t0007g0158 |
5 | HG01891.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.206-868A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822090 | |||||||
| chr5:179822099 | T | A | 132 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0022 others(129): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.206-859T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822099 | |||||||
| chr5:179822110 | T | C | 21 | a0001c0001t0001g0094 a0001c0001t0001g0132 a0001c0001t0001g0133 others(18): Show |
24 | HG01123.hp1 HG01943.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.206-848T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822110 | |||||||
| chr5:179822179 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(115): Show |
176 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.206-779A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822179 | |||||||
| chr5:179822221 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.206-737C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822221 | |||||||
| chr5:179822323 | A | C | 32 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0133 others(29): Show |
37 | HG00733.hp2 HG01074.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.206-635A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822323 | |||||||
| chr5:179822353 | T | A | 1 | a0001c0003t0005g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.206-605T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822353 | |||||||
| chr5:179822376 | C | G | 9 | a0001c0001t0001g0118 a0001c0001t0001g0132 a0001c0003t0005g0041 others(6): Show |
12 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.206-582C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822376 | |||||||
| chr5:179822433 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
325 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.206-525T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822433 | |||||||
| chr5:179822445 | A | G | 4 | a0001c0001t0001g0062 a0001c0001t0001g0280 a0001c0011t0001g0281 others(1): Show |
5 | NA18954.hp1 NA18966.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.206-513A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822445 | |||||||
| chr5:179822531 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.206-427C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822531 | |||||||
| chr5:179822601 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.206-357C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822601 | |||||||
| chr5:179822614 | G | A | 1 | a0001c0005t0001g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.206-344G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822614 | |||||||
| chr5:179822636 | G | A | 1 | a0001c0001t0001g0288 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.206-322G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822636 | |||||||
| chr5:179822827 | T | C | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.206-131T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822827 | |||||||
| chr5:179822832 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.206-126C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822832 | |||||||
| chr5:179822903 | T | A | 6 | a0001c0003t0002g0034 a0001c0003t0002g0313 a0001c0003t0002g0314 others(3): Show |
7 | HG00423.hp1 NA18957.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.206-55T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 1/7 | chr5 | 179822903 | |||||||
| chr5:179823065 | C | G | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | NA19065.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.301+12C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823065 | |||||||
| chr5:179823093 | C | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0269 a0001c0001t0001g0271 others(11): Show |
17 | HG01256.hp1 HG01361.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.301+40C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823093 | |||||||
| chr5:179823130 | C | T | 13 | a0001c0001t0003g0071 a0001c0001t0003g0079 a0001c0001t0003g0117 others(10): Show |
14 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.301+77C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823130 | |||||||
| chr5:179823204 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0232 a0001c0001t0001g0233 |
7 | HG00639.hp2 HG01123.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.301+151G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823204 | |||||||
| chr5:179823214 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0065 a0001c0001t0001g0160 |
7 | HG00323.hp2 HG01109.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.301+161C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823214 | |||||||
| chr5:179823298 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.301+245G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823298 | |||||||
| chr5:179823392 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
303 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(300): Show |
intron_variant | MODIFIER | c.301+339G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823392 | |||||||
| chr5:179823416 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
270 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.301+363A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823416 | |||||||
| chr5:179823439 | A | C | 1 | a0001c0001t0001g0267 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.301+386A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823439 | |||||||
| chr5:179823442 | C | T | 1 | a0001c0002t0002g0196 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.301+389C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823442 | |||||||
| chr5:179823445 | C | CA | 30 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0061 others(27): Show |
34 | HG00438.hp1 HG00621.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.302-378dupA | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0173 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.302-389_302-378dup others(12): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CA | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(50): Show |
70 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.302-378delA | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CAA | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(41): Show |
64 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.302-379_302-378del others(2): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CAAA | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0049 others(18): Show |
24 | HG00323.hp2 HG00733.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.302-380_302-378del others(3): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CAAAA | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0029 others(20): Show |
30 | HG00597.hp2 HG01361.hp1 HG01516.hp1 others(27): Show |
intron_variant | MODIFIER | c.302-381_302-378del others(4): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CAAAAA | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(48): Show |
64 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.302-382_302-378del others(5): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CAAAAAA | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0164 a0001c0001t0001g0172 others(6): Show |
9 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-383_302-378del others(6): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CAAAAAAA | C | 28 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0133 others(25): Show |
32 | HG01243.hp2 HG02071.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.302-384_302-378del others(7): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CAAAAAAA others(3): Show |
C | 1 | a0001c0003t0006g0143 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.302-387_302-378del others(10): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CAAAAAAA others(4): Show |
C | 8 | a0001c0003t0005g0041 a0001c0003t0005g0137 a0001c0003t0006g0146 others(5): Show |
9 | HG02055.hp1 HG02145.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-388_302-378del others(11): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0198 a0001c0002t0002g0020 |
2 | HG01891.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.302-389_302-378del others(12): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CAAAAAAA others(6): Show |
C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0051 others(14): Show |
18 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.302-390_302-378del others(13): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CAAAAAAA others(7): Show |
C | 3 | a0001c0002t0002g0055 a0001c0002t0002g0192 a0001c0002t0002g0195 |
4 | HG00639.hp1 HG01515.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-391_302-378del others(14): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CAAAAAAA others(8): Show |
C | 1 | a0001c0003t0003g0135 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.302-392_302-378del others(15): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CAAAAAAA others(11): Show |
C | 1 | a0001c0002t0002g0188 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.302-395_302-378del others(18): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823445 | CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0001g0008 a0001c0002t0006g0145 |
2 | NA19030.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.302-396_302-378del others(19): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823445 | ||||||
| chr5:179823453 | A | C | 1 | a0001c0002t0005g0078 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.301+400A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823453 | |||||||
| chr5:179823454 | A | C | 1 | a0001c0003t0005g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.301+401A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823454 | |||||||
| chr5:179823500 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
269 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.302-358C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823500 | |||||||
| chr5:179823531 | C | CTAGGGAT others(26): Show |
1 | a0001c0003t0006g0146 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.302-302_302-270dup others(33): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 179823531 | ||||||
| chr5:179823589 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0293 a0001c0001t0001g0294 others(1): Show |
6 | HG02683.hp1 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.302-269C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823589 | |||||||
| chr5:179823680 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.302-178C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823680 | |||||||
| chr5:179823762 | C | T | 6 | a0001c0001t0001g0124 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG01243.hp1 HG02145.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.302-96C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823762 | |||||||
| chr5:179823800 | C | T | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.302-58C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823800 | |||||||
| chr5:179823853 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA18971.hp2 | splice_region_variant&intron_variant | LOW | c.302-5T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 2/7 | chr5 | 179823853 | |||||||
| chr5:179824143 | C | T | 1 | a0001c0003t0010g0073 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.532-39C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 3/7 | chr5 | 179824143 | |||||||
| chr5:179824159 | C | T | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.532-23C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 3/7 | chr5 | 179824159 | |||||||
| chr5:179824450 | A | G | 2 | a0001c0003t0003g0149 a0001c0003t0003g0150 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.673+127A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179824450 | |||||||
| chr5:179824455 | C | G | 2 | a0001c0003t0005g0041 a0001c0003t0005g0137 |
3 | HG02055.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.673+132C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179824455 | |||||||
| chr5:179824475 | T | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
300 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.673+152T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179824475 | |||||||
| chr5:179824480 | T | A | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.673+157T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179824480 | |||||||
| chr5:179824490 | C | G | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.673+167C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179824490 | |||||||
| chr5:179824560 | T | G | 3 | a0001c0001t0001g0293 a0001c0003t0005g0041 a0001c0003t0005g0137 |
4 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.673+237T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179824560 | |||||||
| chr5:179824598 | C | T | 3 | a0001c0002t0006g0084 a0001c0002t0006g0085 a0001c0002t0014g0080 |
3 | HG02647.hp2 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.673+275C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179824598 | |||||||
| chr5:179824600 | G | A | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.673+277G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179824600 | |||||||
| chr5:179824610 | C | T | 1 | a0001c0006t0009g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.673+287C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179824610 | |||||||
| chr5:179824664 | A | C | 1 | a0002c0007t0002g0214 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.673+341A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179824664 | |||||||
| chr5:179824704 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.673+381T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179824704 | |||||||
| chr5:179824756 | C | T | 1 | a0001c0002t0006g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.674-390C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179824756 | |||||||
| chr5:179824772 | T | G | 1 | a0001c0001t0001g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.674-374T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179824772 | |||||||
| chr5:179824791 | C | T | 8 | a0001c0001t0001g0133 a0001c0004t0001g0043 a0001c0004t0001g0044 others(5): Show |
10 | HG02109.hp1 HG02615.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.674-355C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179824791 | |||||||
| chr5:179825052 | G | A | 12 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0002t0006g0084 others(9): Show |
15 | HG01167.hp2 HG01433.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.674-94G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179825052 | |||||||
| chr5:179825075 | A | G | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.674-71A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 4/7 | chr5 | 179825075 | |||||||
| chr5:179825256 | C | T | 1 | a0001c0003t0002g0316 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.754+30C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179825256 | |||||||
| chr5:179825265 | C | A | 1 | a0007c0016t0005g0099 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.754+39C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179825265 | |||||||
| chr5:179825360 | C | T | 3 | a0002c0007t0007g0018 a0002c0007t0007g0081 a0002c0007t0007g0158 |
5 | HG01891.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.754+134C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179825360 | |||||||
| chr5:179825439 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.754+213C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179825439 | |||||||
| chr5:179825440 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0062 a0001c0001t0001g0280 |
5 | NA18942.hp1 NA18954.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+214G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179825440 | |||||||
| chr5:179825537 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
307 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(304): Show |
intron_variant | MODIFIER | c.754+311A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179825537 | |||||||
| chr5:179825760 | G | T | 1 | a0001c0001t0003g0171 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.754+534G>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179825760 | |||||||
| chr5:179825827 | T | C | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.754+601T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179825827 | |||||||
| chr5:179825854 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.754+628G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179825854 | |||||||
| chr5:179825962 | G | C | 2 | a0001c0001t0008g0063 a0001c0001t0008g0289 |
3 | NA18988.hp1 NA19007.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.754+736G>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179825962 | |||||||
| chr5:179826045 | C | G | 3 | a0002c0007t0007g0018 a0002c0007t0007g0081 a0002c0007t0007g0158 |
5 | HG01891.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.754+819C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179826045 | |||||||
| chr5:179826167 | A | AT | 6 | a0001c0001t0001g0123 a0001c0001t0001g0170 a0001c0001t0001g0233 others(3): Show |
6 | HG01106.hp2 NA18951.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.754+956dupT | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179826167 | ||||||
| chr5:179826251 | CCCTCCTG others(2202): Show |
C | 1 | a0001c0003t0001g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.754+1031_754+3239d others(2): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179826251 | ||||||
| chr5:179826285 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0177 |
2 | HG00621.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.754+1059C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179826285 | |||||||
| chr5:179826458 | C | A | 1 | a0001c0002t0002g0052 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.754+1232C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179826458 | |||||||
| chr5:179826478 | A | G | 1 | a0001c0001t0001g0302 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.754+1252A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179826478 | |||||||
| chr5:179826487 | C | T | 2 | a0001c0001t0001g0290 a0001c0001t0001g0299 |
2 | NA18953.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.754+1261C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179826487 | |||||||
| chr5:179826496 | C | T | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.754+1270C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179826496 | |||||||
| chr5:179826562 | T | C | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.754+1336T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179826562 | |||||||
| chr5:179826598 | G | GTT | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
289 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.754+1386_754+1387d others(4): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179826598 | ||||||
| chr5:179826598 | GT | G | 9 | a0001c0002t0006g0145 a0001c0003t0003g0150 a0001c0003t0006g0143 others(6): Show |
9 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.754+1387delT | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179826598 | ||||||
| chr5:179826640 | G | A | 1 | a0001c0002t0014g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.754+1414G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179826640 | |||||||
| chr5:179826669 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.754+1443C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179826669 | |||||||
| chr5:179826704 | G | A | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.754+1478G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179826704 | |||||||
| chr5:179826754 | C | T | 11 | a0001c0001t0003g0071 a0001c0001t0003g0079 a0001c0001t0003g0117 others(8): Show |
12 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.754+1528C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179826754 | |||||||
| chr5:179826875 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
273 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.754+1649C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179826875 | |||||||
| chr5:179826926 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
355 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(352): Show |
intron_variant | MODIFIER | c.754+1700A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179826926 | |||||||
| chr5:179827206 | TCA | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
296 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.754+1984_754+1985d others(4): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179827206 | ||||||
| chr5:179827225 | A | C | 1 | a0001c0001t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.754+1999A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827225 | |||||||
| chr5:179827247 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
304 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(301): Show |
intron_variant | MODIFIER | c.754+2021G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827247 | |||||||
| chr5:179827340 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
355 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(352): Show |
intron_variant | MODIFIER | c.754+2114T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827340 | |||||||
| chr5:179827351 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.754+2125G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827351 | |||||||
| chr5:179827363 | A | G | 1 | a0001c0002t0002g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.754+2137A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827363 | |||||||
| chr5:179827365 | G | C | 5 | a0001c0004t0001g0043 a0001c0004t0001g0044 a0001c0004t0001g0047 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+2139G>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827365 | |||||||
| chr5:179827519 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0240 a0006c0022t0001g0008 |
5 | HG00609.hp1 HG02015.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+2293C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827519 | |||||||
| chr5:179827589 | A | G | 1 | a0009c0023t0006g0131 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.754+2363A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827589 | |||||||
| chr5:179827604 | A | G | 15 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0002t0006g0084 others(12): Show |
20 | HG01167.hp2 HG01433.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.754+2378A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827604 | |||||||
| chr5:179827604 | A | T | 12 | a0001c0001t0003g0071 a0001c0001t0003g0079 a0001c0001t0003g0134 others(9): Show |
13 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.754+2378A>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827604 | |||||||
| chr5:179827643 | G | A | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.754+2417G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827643 | |||||||
| chr5:179827657 | C | A | 1 | a0001c0002t0002g0102 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.754+2431C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827657 | |||||||
| chr5:179827711 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.754+2485C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827711 | |||||||
| chr5:179827753 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.754+2527G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827753 | |||||||
| chr5:179827763 | GTTTC | G | 15 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0002t0006g0084 others(12): Show |
20 | HG01167.hp2 HG01433.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.754+2545_754+2548d others(6): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179827763 | ||||||
| chr5:179827783 | C | G | 1 | a0001c0001t0003g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.754+2557C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827783 | |||||||
| chr5:179827796 | G | A | 2 | a0001c0003t0005g0041 a0001c0003t0005g0137 |
3 | HG02055.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.754+2570G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827796 | |||||||
| chr5:179827846 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
271 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.754+2620A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827846 | |||||||
| chr5:179827938 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.754+2712G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827938 | |||||||
| chr5:179827964 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.754+2738C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827964 | |||||||
| chr5:179827967 | A | C | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.754+2741A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179827967 | |||||||
| chr5:179828094 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.754+2868G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828094 | |||||||
| chr5:179828103 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.754+2877T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828103 | |||||||
| chr5:179828106 | T | C | 1 | a0002c0007t0007g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.754+2880T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828106 | |||||||
| chr5:179828189 | C | T | 1 | a0002c0007t0002g0214 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.754+2963C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828189 | |||||||
| chr5:179828249 | T | A | 1 | a0001c0003t0005g0041 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.754+3023T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828249 | |||||||
| chr5:179828275 | C | T | 3 | a0002c0007t0007g0018 a0002c0007t0007g0081 a0002c0007t0007g0158 |
5 | HG01891.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.754+3049C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828275 | |||||||
| chr5:179828353 | CT | C | 11 | a0001c0001t0003g0071 a0001c0001t0003g0079 a0001c0001t0003g0117 others(8): Show |
12 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.754+3137delT | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179828353 | ||||||
| chr5:179828362 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.754+3136T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828362 | |||||||
| chr5:179828364 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.754+3138C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828364 | |||||||
| chr5:179828366 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.754+3140T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828366 | |||||||
| chr5:179828367 | A | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.754+3141A>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828367 | |||||||
| chr5:179828369 | C | CT | 44 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(41): Show |
53 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.754+3164dupT | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179828369 | ||||||
| chr5:179828369 | C | CTTTT | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.754+3161_754+3164d others(6): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179828369 | ||||||
| chr5:179828369 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.754+3143C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828369 | |||||||
| chr5:179828369 | CT | C | 22 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0042 others(19): Show |
24 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.754+3164delT | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179828369 | ||||||
| chr5:179828369 | CTTTTTT | C | 7 | a0001c0005t0001g0012 a0001c0005t0001g0086 a0001c0005t0001g0100 others(4): Show |
10 | HG01167.hp2 HG01433.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.754+3159_754+3164d others(8): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179828369 | ||||||
| chr5:179828371 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.754+3145T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828371 | |||||||
| chr5:179828408 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0201 |
2 | HG02056.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.754+3182T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828408 | |||||||
| chr5:179828431 | T | C | 13 | a0001c0001t0003g0071 a0001c0001t0003g0079 a0001c0001t0003g0117 others(10): Show |
14 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.754+3205T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828431 | |||||||
| chr5:179828488 | C | A | 1 | a0001c0001t0001g0235 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.754+3262C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828488 | |||||||
| chr5:179828819 | C | CA | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
272 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.754+3599dupA | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179828819 | ||||||
| chr5:179828878 | G | T | 1 | a0001c0001t0001g0211 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.754+3652G>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828878 | |||||||
| chr5:179828970 | G | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
304 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(301): Show |
intron_variant | MODIFIER | c.754+3744G>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179828970 | |||||||
| chr5:179829000 | C | T | 1 | a0001c0003t0003g0135 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.754+3774C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829000 | |||||||
| chr5:179829164 | T | C | 3 | a0001c0003t0010g0073 a0001c0003t0010g0083 a0001c0003t0010g0130 |
3 | HG02922.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.755-3868T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829164 | |||||||
| chr5:179829165 | T | G | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.755-3867T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829165 | |||||||
| chr5:179829202 | C | T | 1 | a0001c0008t0001g0093 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.755-3830C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829202 | |||||||
| chr5:179829206 | C | G | 1 | a0001c0008t0001g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.755-3826C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829206 | |||||||
| chr5:179829234 | T | A | 32 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0133 others(29): Show |
38 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.755-3798T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829234 | |||||||
| chr5:179829277 | T | A | 1 | a0001c0001t0001g0236 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.755-3755T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829277 | |||||||
| chr5:179829324 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.755-3708C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829324 | |||||||
| chr5:179829387 | A | G | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.755-3645A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829387 | |||||||
| chr5:179829388 | A | C | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.755-3644A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829388 | |||||||
| chr5:179829684 | T | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.755-3348T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829684 | |||||||
| chr5:179829685 | T | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.755-3347T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829685 | |||||||
| chr5:179829686 | T | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.755-3346T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829686 | |||||||
| chr5:179829687 | T | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.755-3345T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829687 | |||||||
| chr5:179829688 | T | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
355 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(352): Show |
intron_variant | MODIFIER | c.755-3344T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829688 | |||||||
| chr5:179829688 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.755-3344T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829688 | |||||||
| chr5:179829689 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.755-3343T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829689 | |||||||
| chr5:179829689 | T | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
355 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(352): Show |
intron_variant | MODIFIER | c.755-3343T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829689 | |||||||
| chr5:179829690 | T | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
355 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(352): Show |
intron_variant | MODIFIER | c.755-3342T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829690 | |||||||
| chr5:179829690 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.755-3342T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829690 | |||||||
| chr5:179829691 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
355 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(352): Show |
intron_variant | MODIFIER | c.755-3341A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829691 | |||||||
| chr5:179829692 | T | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.755-3340T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829692 | |||||||
| chr5:179829693 | C | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
355 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(352): Show |
intron_variant | MODIFIER | c.755-3339C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829693 | |||||||
| chr5:179829693 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.755-3339C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829693 | |||||||
| chr5:179829694 | T | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.755-3338T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829694 | |||||||
| chr5:179829695 | T | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.755-3337T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829695 | |||||||
| chr5:179829696 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.755-3336T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829696 | |||||||
| chr5:179829696 | T | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
355 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(352): Show |
intron_variant | MODIFIER | c.755-3336T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829696 | |||||||
| chr5:179829697 | C | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
355 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(352): Show |
intron_variant | MODIFIER | c.755-3335C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829697 | |||||||
| chr5:179829697 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.755-3335C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829697 | |||||||
| chr5:179829698 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.755-3334C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829698 | |||||||
| chr5:179829698 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
355 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(352): Show |
intron_variant | MODIFIER | c.755-3334C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829698 | |||||||
| chr5:179829699 | T | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
355 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(352): Show |
intron_variant | MODIFIER | c.755-3333T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829699 | |||||||
| chr5:179829700 | C | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.755-3332C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829700 | |||||||
| chr5:179829701 | T | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.755-3331T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829701 | |||||||
| chr5:179829702 | C | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.755-3330C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829702 | |||||||
| chr5:179829703 | C | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.755-3329C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829703 | |||||||
| chr5:179829704 | T | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.755-3328T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829704 | |||||||
| chr5:179829705 | C | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.755-3327C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829705 | |||||||
| chr5:179829728 | A | G | 13 | a0001c0001t0003g0071 a0001c0001t0003g0079 a0001c0001t0003g0117 others(10): Show |
14 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.755-3304A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829728 | |||||||
| chr5:179829790 | A | G | 1 | a0001c0001t0001g0276 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.755-3242A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829790 | |||||||
| chr5:179829887 | C | T | 1 | a0001c0001t0001g0061 | 2 | NA18947.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.755-3145C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829887 | |||||||
| chr5:179829923 | C | A | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(34): Show |
51 | HG00609.hp1 HG00621.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.755-3109C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829923 | |||||||
| chr5:179829988 | T | C | 6 | a0001c0005t0001g0012 a0001c0005t0001g0086 a0001c0005t0001g0100 others(3): Show |
9 | HG01167.hp2 HG01433.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.755-3044T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829988 | |||||||
| chr5:179829996 | G | C | 2 | a0001c0001t0001g0290 a0001c0001t0001g0299 |
2 | NA18953.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.755-3036G>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179829996 | |||||||
| chr5:179830001 | G | A | 3 | a0001c0003t0010g0073 a0001c0003t0010g0083 a0001c0003t0010g0130 |
3 | HG02922.hp1 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.755-3031G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830001 | |||||||
| chr5:179830060 | G | T | 1 | a0001c0021t0001g0266 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.755-2972G>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830060 | |||||||
| chr5:179830108 | C | A | 1 | a0001c0001t0001g0294 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.755-2924C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830108 | |||||||
| chr5:179830131 | AC | A | 51 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0133 others(48): Show |
60 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.755-2900delC | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830131 | |||||||
| chr5:179830135 | A | AAAAC | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
288 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.755-2893_755-2890d others(6): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179830135 | ||||||
| chr5:179830135 | A | C | 51 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0133 others(48): Show |
60 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.755-2897A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830135 | |||||||
| chr5:179830171 | C | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.755-2861C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830171 | |||||||
| chr5:179830312 | A | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0017g0075 |
3 | HG02896.hp1 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.755-2720A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830312 | |||||||
| chr5:179830384 | A | G | 3 | a0001c0002t0006g0084 a0001c0002t0006g0085 a0001c0002t0014g0080 |
3 | HG02647.hp2 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.755-2648A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830384 | |||||||
| chr5:179830393 | G | A | 3 | a0002c0007t0007g0018 a0002c0007t0007g0081 a0002c0007t0007g0158 |
5 | HG01891.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.755-2639G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830393 | |||||||
| chr5:179830473 | G | A | 25 | a0001c0001t0001g0133 a0001c0002t0001g0095 a0001c0002t0001g0218 others(22): Show |
31 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.755-2559G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830473 | |||||||
| chr5:179830555 | TTTTC | T | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.755-2473_755-2470d others(6): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179830555 | ||||||
| chr5:179830578 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0229 |
2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.755-2454C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830578 | |||||||
| chr5:179830616 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.755-2416C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830616 | |||||||
| chr5:179830620 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.755-2412G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830620 | |||||||
| chr5:179830630 | CTCACTGC others(2): Show |
C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0264 a0001c0001t0001g0265 |
5 | NA18952.hp1 NA18969.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.755-2400_755-2392d others(11): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179830630 | ||||||
| chr5:179830682 | C | T | 1 | a0001c0002t0002g0195 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.755-2350C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830682 | |||||||
| chr5:179830793 | T | C | 33 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0133 others(30): Show |
39 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.755-2239T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830793 | |||||||
| chr5:179830809 | GTCTCCCA others(139): Show |
G | 1 | a0001c0003t0010g0073 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.755-2210_755-2065d others(2): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179830809 | ||||||
| chr5:179830823 | T | C | 25 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0133 others(22): Show |
29 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.755-2209T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830823 | |||||||
| chr5:179830850 | C | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0060 |
4 | HG02165.hp1 NA18944.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.755-2182C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179830850 | |||||||
| chr5:179831001 | C | T | 9 | a0001c0002t0001g0095 a0001c0002t0001g0218 a0001c0003t0001g0025 others(6): Show |
11 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.755-2031C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831001 | |||||||
| chr5:179831009 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.755-2023G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831009 | |||||||
| chr5:179831176 | C | A | 61 | a0001c0001t0001g0021 a0001c0001t0001g0060 a0001c0001t0001g0064 others(58): Show |
70 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.755-1856C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831176 | |||||||
| chr5:179831184 | G | C | 96 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
132 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.755-1848G>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831184 | |||||||
| chr5:179831212 | C | T | 1 | a0001c0002t0001g0114 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.755-1820C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831212 | |||||||
| chr5:179831232 | G | C | 1 | a0001c0001t0001g0087 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.755-1800G>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831232 | |||||||
| chr5:179831292 | G | C | 1 | a0001c0001t0001g0311 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.755-1740G>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831292 | |||||||
| chr5:179831348 | T | C | 4 | a0001c0003t0006g0143 a0001c0003t0006g0146 a0001c0003t0010g0083 others(1): Show |
4 | HG02145.hp2 HG02572.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.755-1684T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831348 | |||||||
| chr5:179831395 | C | T | 1 | a0001c0018t0005g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.755-1637C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831395 | |||||||
| chr5:179831399 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.755-1633T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831399 | |||||||
| chr5:179831411 | A | C | 3 | a0001c0003t0003g0135 a0001c0003t0003g0149 a0001c0003t0003g0150 |
3 | HG03209.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.755-1621A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831411 | |||||||
| chr5:179831428 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.755-1604A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831428 | |||||||
| chr5:179831491 | G | A | 8 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0017g0075 others(5): Show |
8 | HG02055.hp2 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.755-1541G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831491 | |||||||
| chr5:179831498 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.755-1534C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831498 | |||||||
| chr5:179831523 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
306 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(303): Show |
intron_variant | MODIFIER | c.755-1509G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831523 | |||||||
| chr5:179831555 | G | A | 7 | a0001c0005t0001g0012 a0001c0005t0001g0086 a0001c0005t0001g0100 others(4): Show |
10 | HG01167.hp2 HG01433.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.755-1477G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831555 | |||||||
| chr5:179831589 | T | A | 1 | a0001c0001t0001g0248 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.755-1443T>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831589 | |||||||
| chr5:179831590 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.755-1442G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831590 | |||||||
| chr5:179831611 | G | A | 1 | a0001c0018t0005g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.755-1421G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831611 | |||||||
| chr5:179831621 | G | A | 1 | a0001c0002t0001g0095 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.755-1411G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831621 | |||||||
| chr5:179831622 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.755-1410G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831622 | |||||||
| chr5:179831651 | G | A | 2 | a0001c0002t0005g0078 a0001c0003t0005g0076 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.755-1381G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831651 | |||||||
| chr5:179831790 | C | CT | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
298 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.755-1230dupT | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 179831790 | ||||||
| chr5:179831901 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
348 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(345): Show |
intron_variant | MODIFIER | c.755-1131G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831901 | |||||||
| chr5:179831908 | C | T | 5 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.755-1124C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831908 | |||||||
| chr5:179831940 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.755-1092C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831940 | |||||||
| chr5:179831973 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0230 |
2 | HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.755-1059C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831973 | |||||||
| chr5:179831977 | G | A | 7 | a0001c0005t0001g0012 a0001c0005t0001g0086 a0001c0005t0001g0100 others(4): Show |
10 | HG01167.hp2 HG01433.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.755-1055G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179831977 | |||||||
| chr5:179832026 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.755-1006G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832026 | |||||||
| chr5:179832030 | G | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
327 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(324): Show |
intron_variant | MODIFIER | c.755-1002G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832030 | |||||||
| chr5:179832034 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.755-998C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832034 | |||||||
| chr5:179832167 | G | A | 7 | a0001c0006t0004g0045 a0001c0006t0004g0091 a0001c0006t0009g0037 others(4): Show |
9 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.755-865G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832167 | |||||||
| chr5:179832448 | G | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0223 others(4): Show |
11 | HG01081.hp1 HG01256.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.755-584G>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832448 | |||||||
| chr5:179832459 | C | T | 1 | a0001c0002t0001g0218 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.755-573C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832459 | |||||||
| chr5:179832463 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.755-569G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832463 | |||||||
| chr5:179832548 | G | A | 8 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0017g0075 others(5): Show |
8 | HG02055.hp2 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.755-484G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832548 | |||||||
| chr5:179832561 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.755-471G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832561 | |||||||
| chr5:179832646 | C | T | 8 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.755-386C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832646 | |||||||
| chr5:179832736 | C | A | 6 | a0001c0001t0001g0124 a0001c0002t0001g0174 a0001c0002t0006g0084 others(3): Show |
6 | HG02647.hp2 HG02886.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.755-296C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832736 | |||||||
| chr5:179832835 | T | C | 28 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0124 others(25): Show |
33 | HG01167.hp2 HG01433.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.755-197T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832835 | |||||||
| chr5:179832842 | G | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
351 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(348): Show |
intron_variant | MODIFIER | c.755-190G>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832842 | |||||||
| chr5:179832847 | G | A | 1 | a0001c0003t0002g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.755-185G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832847 | |||||||
| chr5:179832882 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0242 |
5 | HG01081.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.755-150C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832882 | |||||||
| chr5:179832928 | C | T | 2 | a0001c0002t0002g0156 a0001c0002t0014g0080 |
2 | HG00140.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.755-104C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832928 | |||||||
| chr5:179832929 | G | A | 1 | a0001c0001t0001g0048 | 2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.755-103G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832929 | |||||||
| chr5:179832959 | C | A | 2 | a0001c0002t0006g0084 a0001c0002t0006g0085 |
2 | HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.755-73C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179832959 | |||||||
| chr5:179833009 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(140): Show |
217 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.755-23G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 5/7 | chr5 | 179833009 | |||||||
| chr5:179833281 | G | A | 2 | a0001c0002t0001g0218 a0001c0003t0001g0025 |
4 | HG02818.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.969+35G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/7 | chr5 | 179833281 | |||||||
| chr5:179833331 | C | G | 49 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0118 others(46): Show |
60 | HG01167.hp2 HG01243.hp2 HG01433.hp1 others(57): Show |
intron_variant | MODIFIER | c.969+85C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/7 | chr5 | 179833331 | |||||||
| chr5:179833478 | C | G | 69 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(66): Show |
91 | HG00140.hp1 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.970-109C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/7 | chr5 | 179833478 | |||||||
| chr5:179833494 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
318 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.970-93G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/7 | chr5 | 179833494 | |||||||
| chr5:179833509 | C | T | 17 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0139 others(14): Show |
22 | HG01167.hp2 HG02145.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.970-78C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/7 | chr5 | 179833509 | |||||||
| chr5:179833523 | G | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG01243.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.970-64G>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/7 | chr5 | 179833523 | |||||||
| chr5:179833528 | T | C | 65 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0028 others(62): Show |
86 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.970-59T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 6/7 | chr5 | 179833528 | |||||||
| chr5:179833856 | C | T | 1 | a0001c0002t0002g0193 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1165+74C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179833856 | |||||||
| chr5:179833865 | CAGA | C | 19 | a0001c0002t0001g0095 a0001c0005t0001g0012 a0001c0005t0001g0086 others(16): Show |
26 | HG01167.hp2 HG01433.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1165+86_1165+88del others(3): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179833865 | ||||||
| chr5:179833895 | C | A | 23 | a0001c0001t0001g0124 a0001c0002t0006g0145 a0001c0003t0001g0119 others(20): Show |
28 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1165+113C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179833895 | |||||||
| chr5:179833958 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1165+176C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179833958 | |||||||
| chr5:179833959 | G | A | 6 | a0001c0005t0001g0012 a0001c0005t0001g0086 a0001c0005t0001g0100 others(3): Show |
9 | HG01167.hp2 HG01433.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1165+177G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179833959 | |||||||
| chr5:179834001 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
347 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(344): Show |
intron_variant | MODIFIER | c.1165+219G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834001 | |||||||
| chr5:179834027 | A | G | 37 | a0001c0001t0002g0013 a0001c0001t0002g0191 a0001c0001t0002g0231 others(34): Show |
49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1165+245A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834027 | |||||||
| chr5:179834033 | G | A | 1 | a0001c0002t0001g0046 | 2 | HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1165+251G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834033 | |||||||
| chr5:179834034 | G | A | 1 | a0002c0007t0007g0081 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1165+252G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834034 | |||||||
| chr5:179834041 | T | TAAAACTT others(14): Show |
1 | a0001c0001t0001g0250 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1165+260_1165+280d others(23): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179834041 | ||||||
| chr5:179834051 | C | T | 3 | a0001c0009t0004g0074 a0001c0009t0004g0089 a0001c0009t0004g0092 |
3 | HG02630.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1165+269C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834051 | |||||||
| chr5:179834060 | C | T | 6 | a0001c0005t0001g0012 a0001c0005t0001g0086 a0001c0005t0001g0100 others(3): Show |
9 | HG01167.hp2 HG01433.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1165+278C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834060 | |||||||
| chr5:179834083 | C | G | 1 | a0001c0002t0005g0078 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1165+301C>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834083 | |||||||
| chr5:179834132 | C | T | 8 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0017g0075 others(5): Show |
8 | HG02055.hp2 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1165+350C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834132 | |||||||
| chr5:179834154 | A | AG | 16 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(13): Show |
25 | HG00558.hp1 HG00621.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1165+373dupG | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179834154 | ||||||
| chr5:179834154 | A | AGG | 6 | a0001c0001t0011g0040 a0001c0002t0001g0095 a0001c0002t0001g0218 others(3): Show |
6 | HG00733.hp2 HG02818.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165+373_1165+374i others(4): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179834154 | ||||||
| chr5:179834155 | GA | G | 6 | a0001c0001t0001g0049 a0001c0001t0001g0168 a0001c0002t0001g0046 others(3): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1165+374delA | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834155 | |||||||
| chr5:179834156 | A | AG | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1165+384dupG | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179834156 | ||||||
| chr5:179834156 | A | AGG | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(67): Show |
77 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.1165+383_1165+384d others(4): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179834156 | ||||||
| chr5:179834156 | A | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(43): Show |
60 | HG00558.hp1 HG00621.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.1165+374A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834156 | |||||||
| chr5:179834156 | AG | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0116 others(27): Show |
35 | HG01081.hp2 HG01167.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.1165+384delG | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179834156 | ||||||
| chr5:179834166 | G | T | 2 | a0001c0003t0005g0041 a0001c0003t0005g0137 |
3 | HG02055.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1165+384G>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834166 | |||||||
| chr5:179834235 | G | A | 4 | a0001c0001t0001g0165 a0001c0001t0001g0271 a0001c0001t0001g0309 others(1): Show |
4 | HG01361.hp2 HG01975.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165+453G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834235 | |||||||
| chr5:179834236 | T | TG | 67 | a0001c0001t0001g0124 a0001c0001t0001g0201 a0001c0001t0001g0226 others(64): Show |
88 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1165+461dupG | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179834236 | ||||||
| chr5:179834243 | GT | G | 12 | a0001c0001t0001g0009 a0001c0002t0006g0084 a0001c0002t0014g0080 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.1165+462delT | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834243 | |||||||
| chr5:179834244 | T | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0065 others(131): Show |
170 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1165+462T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834244 | |||||||
| chr5:179834251 | T | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0271 a0001c0001t0001g0309 others(1): Show |
4 | HG01361.hp2 HG01975.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165+469T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834251 | |||||||
| chr5:179834337 | G | A | 9 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0124 others(6): Show |
9 | HG02055.hp2 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1165+555G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834337 | |||||||
| chr5:179834344 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1165+562G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834344 | |||||||
| chr5:179834407 | T | TTTTA | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
311 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(308): Show |
intron_variant | MODIFIER | c.1165+628_1165+629i others(6): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179834407 | ||||||
| chr5:179834407 | T | TTTTATTT others(1): Show |
13 | a0001c0001t0003g0071 a0001c0001t0003g0079 a0001c0001t0003g0117 others(10): Show |
14 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1165+628_1165+629i others(10): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179834407 | ||||||
| chr5:179834407 | T | TTTTATTT others(9): Show |
2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG01243.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1165+628_1165+629i others(18): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179834407 | ||||||
| chr5:179834407 | TTTTG | T | 10 | a0001c0001t0001g0208 a0001c0003t0005g0041 a0001c0003t0005g0137 others(7): Show |
14 | HG01167.hp2 HG01433.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1165+629_1165+632d others(6): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179834407 | ||||||
| chr5:179834411 | G | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
339 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(336): Show |
intron_variant | MODIFIER | c.1165+629G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834411 | |||||||
| chr5:179834439 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1165+657C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834439 | |||||||
| chr5:179834457 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1165+675G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834457 | |||||||
| chr5:179834481 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1165+699T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834481 | |||||||
| chr5:179834517 | A | T | 15 | a0001c0001t0001g0118 a0001c0001t0003g0071 a0001c0001t0003g0079 others(12): Show |
16 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1165+735A>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834517 | |||||||
| chr5:179834526 | A | G | 15 | a0001c0001t0001g0118 a0001c0001t0003g0071 a0001c0001t0003g0079 others(12): Show |
16 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1165+744A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834526 | |||||||
| chr5:179834540 | C | T | 5 | a0001c0001t0001g0061 a0001c0001t0001g0237 a0001c0001t0001g0243 others(2): Show |
6 | HG00621.hp1 NA18747.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165+758C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834540 | |||||||
| chr5:179834552 | A | T | 2 | a0001c0002t0005g0078 a0001c0003t0005g0076 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1165+770A>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834552 | |||||||
| chr5:179834566 | C | A | 1 | a0001c0002t0001g0046 | 2 | HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1165+784C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834566 | |||||||
| chr5:179834571 | C | T | 5 | a0001c0001t0001g0168 a0001c0002t0001g0046 a0001c0002t0002g0055 others(2): Show |
7 | HG00639.hp1 HG01358.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1165+789C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834571 | |||||||
| chr5:179834592 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
333 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(330): Show |
intron_variant | MODIFIER | c.1165+810G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834592 | |||||||
| chr5:179834620 | G | C | 1 | a0001c0001t0001g0257 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1165+838G>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834620 | |||||||
| chr5:179834620 | G | T | 16 | a0001c0001t0001g0118 a0001c0001t0001g0230 a0001c0001t0003g0071 others(13): Show |
17 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1165+838G>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834620 | |||||||
| chr5:179834624 | C | A | 16 | a0001c0001t0001g0118 a0001c0001t0001g0230 a0001c0001t0003g0071 others(13): Show |
17 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1165+842C>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834624 | |||||||
| chr5:179834660 | C | T | 1 | a0001c0003t0002g0129 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1165+878C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834660 | |||||||
| chr5:179834664 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
248 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.1165+882C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834664 | |||||||
| chr5:179834668 | G | A | 5 | a0001c0002t0006g0145 a0001c0003t0001g0217 a0001c0003t0001g0219 others(2): Show |
5 | HG01243.hp2 HG02622.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1165+886G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834668 | |||||||
| chr5:179834670 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1165+888C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834670 | |||||||
| chr5:179834676 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1165+894T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834676 | |||||||
| chr5:179834682 | T | G | 1 | a0001c0001t0011g0040 | 2 | HG00733.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1165+900T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834682 | |||||||
| chr5:179834703 | CAT | C | 2 | a0001c0001t0011g0040 a0001c0002t0002g0108 |
3 | HG00733.hp2 HG01074.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1165+922_1165+923d others(4): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834703 | |||||||
| chr5:179834720 | G | A | 1 | a0004c0014t0002g0110 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1165+938G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834720 | |||||||
| chr5:179834814 | G | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0179 a0001c0001t0001g0206 others(5): Show |
10 | HG02155.hp2 NA18943.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.1165+1032G>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834814 | |||||||
| chr5:179834819 | G | A | 1 | a0001c0003t0010g0130 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1165+1037G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834819 | |||||||
| chr5:179834849 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1165+1067C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834849 | |||||||
| chr5:179834856 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1165+1074C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834856 | |||||||
| chr5:179834879 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1165+1097C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834879 | |||||||
| chr5:179834929 | AGACGGGG others(70): Show |
A | 1 | a0001c0001t0002g0191 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1165+1158_1165+123 others(81): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179834929 | ||||||
| chr5:179834953 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0164 |
2 | HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1165+1171G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834953 | |||||||
| chr5:179834970 | G | A | 2 | a0001c0003t0005g0041 a0001c0003t0005g0137 |
3 | HG02055.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1165+1188G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179834970 | |||||||
| chr5:179834990 | G | GCGCCCCT others(70): Show |
1 | a0001c0002t0002g0014 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1165+1212_1165+128 others(81): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179834990 | ||||||
| chr5:179835005 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1165+1223C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835005 | |||||||
| chr5:179835006 | G | A | 3 | a0001c0002t0001g0095 a0001c0002t0002g0189 a0001c0002t0002g0193 |
3 | HG02602.hp1 HG03688.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1165+1224G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835006 | |||||||
| chr5:179835032 | T | G | 1 | a0001c0001t0001g0227 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1165+1250T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835032 | |||||||
| chr5:179835032 | TCTCCTCA others(70): Show |
T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0176 |
3 | HG02683.hp2 HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1165+1259_1166-131 others(81): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179835032 | ||||||
| chr5:179835086 | T | C | 1 | a0001c0003t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1165+1304T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835086 | |||||||
| chr5:179835092 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1165+1310C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835092 | |||||||
| chr5:179835093 | G | A | 12 | a0001c0001t0003g0071 a0001c0001t0003g0079 a0001c0001t0003g0117 others(9): Show |
13 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1165+1311G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835093 | |||||||
| chr5:179835095 | G | A | 9 | a0001c0002t0005g0078 a0001c0003t0005g0076 a0001c0005t0001g0012 others(6): Show |
12 | HG01167.hp2 HG01433.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1165+1313G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835095 | |||||||
| chr5:179835108 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
324 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(321): Show |
intron_variant | MODIFIER | c.1165+1326C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835108 | |||||||
| chr5:179835131 | C | T | 8 | a0001c0006t0004g0045 a0001c0006t0004g0091 a0001c0006t0009g0037 others(5): Show |
10 | HG02630.hp2 HG02723.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1166-1305C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835131 | |||||||
| chr5:179835132 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
279 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.1166-1304G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835132 | |||||||
| chr5:179835156 | T | G | 1 | a0001c0003t0005g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1166-1280T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835156 | |||||||
| chr5:179835163 | C | T | 1 | a0008c0019t0001g0180 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1166-1273C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835163 | |||||||
| chr5:179835187 | T | C | 10 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0124 others(7): Show |
11 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1166-1249T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835187 | |||||||
| chr5:179835205 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1166-1231G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835205 | |||||||
| chr5:179835229 | A | C | 16 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0033 others(13): Show |
24 | HG00673.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1166-1207A>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835229 | |||||||
| chr5:179835233 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
353 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(350): Show |
intron_variant | MODIFIER | c.1166-1203T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835233 | |||||||
| chr5:179835278 | C | CG | 17 | a0001c0001t0001g0097 a0001c0001t0001g0138 a0001c0001t0001g0201 others(14): Show |
17 | HG00597.hp2 HG00741.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1166-1154dupG | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179835278 | ||||||
| chr5:179835286 | C | T | 2 | a0001c0003t0003g0149 a0001c0003t0003g0150 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1166-1150C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835286 | |||||||
| chr5:179835291 | G | A | 20 | a0001c0002t0005g0078 a0001c0002t0006g0145 a0001c0003t0001g0119 others(17): Show |
24 | HG01167.hp2 HG01433.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1166-1145G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835291 | |||||||
| chr5:179835335 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
349 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(346): Show |
intron_variant | MODIFIER | c.1166-1101A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835335 | |||||||
| chr5:179835388 | T | C | 1 | a0001c0001t0001g0048 | 2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1166-1048T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835388 | |||||||
| chr5:179835450 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1166-986G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835450 | |||||||
| chr5:179835491 | C | T | 1 | a0001c0001t0003g0268 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1166-945C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835491 | |||||||
| chr5:179835492 | C | T | 1 | a0001c0005t0001g0136 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1166-944C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835492 | |||||||
| chr5:179835493 | G | A | 9 | a0001c0002t0006g0145 a0001c0003t0001g0119 a0001c0003t0006g0143 others(6): Show |
9 | HG01884.hp1 HG02145.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1166-943G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835493 | |||||||
| chr5:179835497 | A | G | 1 | a0001c0008t0001g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1166-939A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835497 | |||||||
| chr5:179835500 | A | G | 3 | a0002c0007t0007g0018 a0002c0007t0007g0081 a0002c0007t0007g0158 |
5 | HG01891.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1166-936A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835500 | |||||||
| chr5:179835513 | G | A | 5 | a0001c0002t0006g0145 a0001c0003t0006g0143 a0001c0003t0006g0146 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1166-923G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835513 | |||||||
| chr5:179835551 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0278 |
2 | HG02280.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1166-885C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835551 | |||||||
| chr5:179835555 | G | A | 3 | a0002c0007t0007g0018 a0002c0007t0007g0081 a0002c0007t0007g0158 |
5 | HG01891.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1166-881G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835555 | |||||||
| chr5:179835579 | G | C | 1 | a0001c0003t0001g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1166-857G>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835579 | |||||||
| chr5:179835605 | A | G | 1 | a0001c0001t0001g0292 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1166-831A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835605 | |||||||
| chr5:179835623 | C | T | 1 | a0001c0002t0002g0188 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1166-813C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835623 | |||||||
| chr5:179835655 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1166-781C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835655 | |||||||
| chr5:179835673 | G | A | 4 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0001g0283 others(1): Show |
4 | HG01256.hp1 HG01928.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1166-763G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835673 | |||||||
| chr5:179835675 | GGAGAAA | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
279 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.1166-757_1166-752d others(8): Show |
SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 179835675 | ||||||
| chr5:179835679 | A | G | 40 | a0001c0001t0001g0118 a0001c0001t0003g0071 a0001c0001t0003g0079 others(37): Show |
49 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.1166-757A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835679 | |||||||
| chr5:179835680 | A | G | 40 | a0001c0001t0001g0118 a0001c0001t0003g0071 a0001c0001t0003g0079 others(37): Show |
49 | HG00733.hp2 HG01074.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.1166-756A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835680 | |||||||
| chr5:179835733 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
330 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(327): Show |
intron_variant | MODIFIER | c.1166-703A>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835733 | |||||||
| chr5:179835741 | C | T | 11 | a0001c0002t0002g0052 a0001c0002t0002g0054 a0001c0002t0002g0212 others(8): Show |
13 | HG00423.hp1 HG00438.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1166-695C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835741 | |||||||
| chr5:179835843 | C | T | 1 | a0001c0002t0001g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1166-593C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835843 | |||||||
| chr5:179835928 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1166-508T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835928 | |||||||
| chr5:179835987 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1166-449T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179835987 | |||||||
| chr5:179836065 | T | G | 1 | a0001c0001t0001g0094 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1166-371T>G | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179836065 | |||||||
| chr5:179836129 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1166-307C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179836129 | |||||||
| chr5:179836141 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1166-295T>C | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179836141 | |||||||
| chr5:179836287 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1166-149G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179836287 | |||||||
| chr5:179836318 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1166-118G>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179836318 | |||||||
| chr5:179836342 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0253 |
2 | HG03490.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1166-94C>T | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179836342 | |||||||
| chr5:179836381 | G | A | 1 | a0001c0004t0001g0088 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1166-55G>A | SQSTM1 | ENSG00000161011.20 | transcript | ENST00000389805.9 | protein_coding | 7/7 | chr5 | 179836381 |