Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1829 |
| ensemblid | ENSG00000046604.14 |
| hgncid | 3049 |
| symbol | DSG2 |
| name | desmoglein 2 |
| refseq_nuc | NM_001943.5 |
| refseq_prot | NP_001934.2 |
| ensembl_nuc | ENST00000261590.13 |
| ensembl_prot | ENSP00000261590.8 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 31498177 |
| end | 31549008 |
| strand | + |
| ver | v1.2 |
| region | chr18:31498177-31549008 |
| region5000 | chr18:31493177-31554008 |
| regionname0 | DSG2_chr18_31498177_31549008 |
| regionname5000 | DSG2_chr18_31493177_31554008 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1118 | 220 | 80 | 36 | 79 | 6 | 18 | 55 | DSG2_chr18_31493177_31554008 | DSG2 | MARSP others(1113): Show |
chr18 | 31493177 | 31554008 |
| a0002 | 0/1 | 1118 | 104 | 5 | 16 | 64 | 5 | 13 | 45 | DSG2_chr18_31493177_31554008 | DSG2 | MARSP others(1113): Show |
chr18 | 31493177 | 31554008 |
| a0003 | 0/0 | 1118 | 8 | 0 | 6 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | MARSP others(1113): Show |
chr18 | 31493177 | 31554008 |
| a0004 | 0/0 | 1118 | 6 | 0 | 1 | 5 | 0 | 0 | 5 | DSG2_chr18_31493177_31554008 | DSG2 | MARSP others(1113): Show |
chr18 | 31493177 | 31554008 |
| a0005 | 0/0 | 1118 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | MARSP others(1113): Show |
chr18 | 31493177 | 31554008 |
| a0006 | 0/0 | 1118 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | MARSP others(1113): Show |
chr18 | 31493177 | 31554008 |
| a0007 | 0/0 | 1118 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | MARSP others(1113): Show |
chr18 | 31493177 | 31554008 |
| a0008 | 0/0 | 1118 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | MARSP others(1113): Show |
chr18 | 31493177 | 31554008 |
| a0009 | 0/0 | 1118 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | MARSP others(1113): Show |
chr18 | 31493177 | 31554008 |
| a0010 | 0/0 | 1118 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | MARSP others(1113): Show |
chr18 | 31493177 | 31554008 |
| a0011 | 0/0 | 1118 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | MARSP others(1113): Show |
chr18 | 31493177 | 31554008 |
| a0012 | 0/0 | 1118 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | MARSP others(1113): Show |
chr18 | 31493177 | 31554008 |
| a0013 | 0/0 | 1118 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | MARSP others(1113): Show |
chr18 | 31493177 | 31554008 |
| a0014 | 0/0 | 1118 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | MARSP others(1113): Show |
chr18 | 31493177 | 31554008 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3354 | 98 | 10 | 26 | 42 | 5 | 14 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0001c0003 | 0/0 | 3354 | 72 | 32 | 4 | 31 | 1 | 4 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0001c0005 | 0/0 | 3354 | 17 | 17 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0001c0006 | 0/0 | 3354 | 15 | 13 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0001c0008 | 0/0 | 3354 | 6 | 0 | 0 | 6 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0001c0010 | 0/0 | 3354 | 5 | 4 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0001c0011 | 0/0 | 3354 | 3 | 0 | 3 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0001c0014 | 0/0 | 3354 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0001c0023 | 0/0 | 3354 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0001c0025 | 0/0 | 3354 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0002c0002 | 0/1 | 3354 | 79 | 5 | 16 | 43 | 5 | 9 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0002c0004 | 0/0 | 3354 | 22 | 0 | 0 | 21 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0002c0016 | 0/0 | 3354 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0002c0027 | 0/0 | 3354 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0003c0007 | 0/0 | 3354 | 8 | 0 | 6 | 0 | 2 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0004c0009 | 0/0 | 3354 | 6 | 0 | 1 | 5 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0005c0012 | 0/0 | 3354 | 3 | 3 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0005c0021 | 0/0 | 3354 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0006c0013 | 0/0 | 3354 | 3 | 3 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0007c0015 | 0/0 | 3354 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0008c0019 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0009c0024 | 0/0 | 3354 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0010c0026 | 0/0 | 3354 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0011c0018 | 0/0 | 3354 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0012c0022 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0013c0017 | 0/0 | 3354 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 | ||
| a0014c0020 | 0/0 | 3354 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | ATGGC others(3349): Show |
chr18 | 31493177 | 31554008 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5697 | 95 | 10 | 26 | 39 | 5 | 14 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5692): Show |
chr18 | 31493177 | 31554008 |
| a0001c0001t0009 | 0/0 | 5695 | 3 | 0 | 0 | 3 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5690): Show |
chr18 | 31493177 | 31554008 |
| a0001c0003t0003 | 0/0 | 5696 | 33 | 11 | 1 | 21 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5691): Show |
chr18 | 31493177 | 31554008 |
| a0001c0003t0004 | 0/0 | 5696 | 35 | 17 | 3 | 10 | 1 | 4 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5691): Show |
chr18 | 31493177 | 31554008 |
| a0001c0003t0008 | 0/0 | 5696 | 3 | 3 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5691): Show |
chr18 | 31493177 | 31554008 |
| a0001c0003t0015 | 0/0 | 5696 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5691): Show |
chr18 | 31493177 | 31554008 |
| a0001c0005t0001 | 0/0 | 5697 | 17 | 17 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5692): Show |
chr18 | 31493177 | 31554008 |
| a0001c0006t0005 | 0/0 | 5696 | 6 | 6 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5691): Show |
chr18 | 31493177 | 31554008 |
| a0001c0006t0006 | 0/0 | 5699 | 6 | 4 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5694): Show |
chr18 | 31493177 | 31554008 |
| a0001c0006t0016 | 0/0 | 5700 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5695): Show |
chr18 | 31493177 | 31554008 |
| a0001c0006t0017 | 0/0 | 5699 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5694): Show |
chr18 | 31493177 | 31554008 |
| a0001c0006t0020 | 0/0 | 5695 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5690): Show |
chr18 | 31493177 | 31554008 |
| a0001c0008t0002 | 0/0 | 5699 | 6 | 0 | 0 | 6 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5694): Show |
chr18 | 31493177 | 31554008 |
| a0001c0010t0007 | 0/0 | 5700 | 5 | 4 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5695): Show |
chr18 | 31493177 | 31554008 |
| a0001c0011t0003 | 0/0 | 5696 | 3 | 0 | 3 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5691): Show |
chr18 | 31493177 | 31554008 |
| a0001c0014t0001 | 0/0 | 5697 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5692): Show |
chr18 | 31493177 | 31554008 |
| a0001c0023t0004 | 0/0 | 5696 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5691): Show |
chr18 | 31493177 | 31554008 |
| a0001c0025t0001 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5692): Show |
chr18 | 31493177 | 31554008 |
| a0002c0002t0002 | 0/1 | 5699 | 77 | 5 | 16 | 43 | 5 | 7 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5694): Show |
chr18 | 31493177 | 31554008 |
| a0002c0002t0014 | 0/0 | 5699 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5694): Show |
chr18 | 31493177 | 31554008 |
| a0002c0004t0002 | 0/0 | 5699 | 22 | 0 | 0 | 21 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5694): Show |
chr18 | 31493177 | 31554008 |
| a0002c0016t0010 | 0/0 | 5699 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5694): Show |
chr18 | 31493177 | 31554008 |
| a0002c0027t0002 | 0/0 | 5699 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5694): Show |
chr18 | 31493177 | 31554008 |
| a0003c0007t0002 | 0/0 | 5699 | 8 | 0 | 6 | 0 | 2 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5694): Show |
chr18 | 31493177 | 31554008 |
| a0004c0009t0003 | 0/0 | 5696 | 6 | 0 | 1 | 5 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5691): Show |
chr18 | 31493177 | 31554008 |
| a0005c0012t0006 | 0/0 | 5699 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5694): Show |
chr18 | 31493177 | 31554008 |
| a0005c0012t0013 | 0/0 | 5695 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5690): Show |
chr18 | 31493177 | 31554008 |
| a0005c0021t0019 | 0/0 | 5699 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5694): Show |
chr18 | 31493177 | 31554008 |
| a0006c0013t0012 | 0/0 | 5699 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5694): Show |
chr18 | 31493177 | 31554008 |
| a0006c0013t0021 | 0/0 | 5699 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5694): Show |
chr18 | 31493177 | 31554008 |
| a0007c0015t0011 | 0/0 | 5695 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5690): Show |
chr18 | 31493177 | 31554008 |
| a0008c0019t0001 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5692): Show |
chr18 | 31493177 | 31554008 |
| a0009c0024t0018 | 0/0 | 5697 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5692): Show |
chr18 | 31493177 | 31554008 |
| a0010c0026t0005 | 0/0 | 5696 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5691): Show |
chr18 | 31493177 | 31554008 |
| a0011c0018t0001 | 0/0 | 5697 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5692): Show |
chr18 | 31493177 | 31554008 |
| a0012c0022t0004 | 0/0 | 5696 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5691): Show |
chr18 | 31493177 | 31554008 |
| a0013c0017t0001 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5692): Show |
chr18 | 31493177 | 31554008 |
| a0014c0020t0001 | 0/0 | 5697 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | GAGGA others(5692): Show |
chr18 | 31493177 | 31554008 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 0 | 4 | 4 | 1 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0009g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0001t0009g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0002 | 0/0 | 7 | 2 | 1 | 4 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0008g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0003t0015g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0005t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0005t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0005t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0005t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0005t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0005t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0005t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0005t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0005t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0005t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0005t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0005t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0006t0005g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0006t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0006t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0006t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0006t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0006t0006g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0006t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0006t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0006t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0006t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0006t0016g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0006t0017g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0006t0020g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0008t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0008t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0008t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0008t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0008t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0008t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0010t0007g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0010t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0010t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0010t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0010t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0011t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0011t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0011t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0014t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0014t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0023t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0001c0025t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0017 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0014g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0002t0014g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0004t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0016t0010g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0002c0027t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0003c0007t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0003c0007t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0003c0007t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0003c0007t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0003c0007t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0003c0007t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0003c0007t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0004c0009t0003g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0004c0009t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0004c0009t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0004c0009t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0005c0012t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0005c0012t0013g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0005c0012t0013g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0005c0021t0019g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0006c0013t0012g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0006c0013t0021g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0007c0015t0011g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0007c0015t0011g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0008c0019t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0009c0024t0018g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0010c0026t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0011c0018t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0012c0022t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0013c0017t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| a0014c0020t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0021 | EUR | GBR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00140 | hp2 | a0001 | c0003 | t0004 | g0031 | EUR | GBR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0068 | EUR | FIN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00280 | hp2 | a0003 | c0007 | t0002 | g0066 | EUR | FIN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0017 | EUR | FIN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00423 | hp1 | a0001 | c0003 | t0003 | g0078 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00438 | hp1 | a0002 | c0004 | t0002 | g0016 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00544 | hp1 | a0008 | c0019 | t0001 | g0269 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00544 | hp2 | a0001 | c0003 | t0003 | g0076 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0277 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00609 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00609 | hp2 | a0002 | c0004 | t0002 | g0053 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00673 | hp2 | a0002 | c0004 | t0002 | g0134 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0022 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0282 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00741 | hp1 | a0001 | c0010 | t0007 | g0059 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG00741 | hp2 | a0003 | c0007 | t0002 | g0200 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01069 | hp2 | a0001 | c0003 | t0004 | g0030 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01070 | hp1 | a0003 | c0007 | t0002 | g0244 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01071 | hp1 | a0003 | c0007 | t0002 | g0206 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01071 | hp2 | a0001 | c0003 | t0004 | g0030 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0285 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01167 | hp1 | a0001 | c0006 | t0006 | g0027 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01168 | hp1 | a0001 | c0003 | t0004 | g0172 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01169 | hp2 | a0001 | c0006 | t0006 | g0027 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0279 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01243 | hp1 | a0009 | c0024 | t0018 | g0174 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01255 | hp1 | a0003 | c0007 | t0002 | g0230 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01261 | hp1 | a0004 | c0009 | t0003 | g0008 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0137 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0122 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0074 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01433 | hp2 | a0003 | c0007 | t0002 | g0038 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01496 | hp1 | a0001 | c0011 | t0003 | g0071 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0123 | EUR | IBS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0228 | EUR | IBS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01516 | hp2 | a0003 | c0007 | t0002 | g0231 | EUR | IBS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01884 | hp1 | a0001 | c0003 | t0004 | g0209 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01884 | hp2 | a0001 | c0006 | t0020 | g0181 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01891 | hp2 | a0001 | c0005 | t0001 | g0145 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0024 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0128 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01975 | hp2 | a0001 | c0003 | t0003 | g0002 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0129 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01978 | hp2 | a0003 | c0007 | t0002 | g0038 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0130 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG01993 | hp2 | a0001 | c0011 | t0003 | g0225 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02015 | hp1 | a0001 | c0003 | t0003 | g0267 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02015 | hp2 | a0001 | c0008 | t0002 | g0063 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02027 | hp2 | a0001 | c0003 | t0003 | g0264 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0092 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02040 | hp2 | a0001 | c0003 | t0003 | g0268 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02055 | hp1 | a0001 | c0006 | t0005 | g0252 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02055 | hp2 | a0010 | c0026 | t0005 | g0173 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02056 | hp2 | a0002 | c0004 | t0002 | g0054 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02074 | hp1 | a0001 | c0003 | t0004 | g0151 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02080 | hp1 | a0001 | c0008 | t0002 | g0080 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02083 | hp2 | a0002 | c0004 | t0002 | g0070 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02129 | hp1 | a0002 | c0004 | t0002 | g0023 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02132 | hp1 | a0001 | c0003 | t0003 | g0266 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02135 | hp2 | a0001 | c0008 | t0002 | g0111 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02145 | hp1 | a0001 | c0003 | t0003 | g0189 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0120 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0024 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02155 | hp2 | a0002 | c0004 | t0002 | g0223 | EAS | CDX | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02165 | hp2 | a0001 | c0003 | t0004 | g0026 | EAS | CDX | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02257 | hp1 | a0005 | c0012 | t0013 | g0251 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02257 | hp2 | a0001 | c0003 | t0004 | g0215 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0283 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02273 | hp2 | a0001 | c0011 | t0003 | g0072 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0135 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02451 | hp1 | a0001 | c0006 | t0006 | g0179 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02451 | hp2 | a0001 | c0003 | t0004 | g0175 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02523 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02572 | hp1 | a0001 | c0010 | t0007 | g0276 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02572 | hp2 | a0001 | c0003 | t0004 | g0249 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02615 | hp1 | a0001 | c0005 | t0001 | g0186 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02615 | hp2 | a0001 | c0010 | t0007 | g0284 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02622 | hp1 | a0001 | c0003 | t0004 | g0190 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0168 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02630 | hp1 | a0001 | c0003 | t0004 | g0232 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02630 | hp2 | a0001 | c0003 | t0003 | g0192 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02647 | hp1 | a0001 | c0006 | t0017 | g0162 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02647 | hp2 | a0001 | c0006 | t0016 | g0079 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02723 | hp1 | a0001 | c0003 | t0003 | g0002 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02723 | hp2 | a0001 | c0003 | t0004 | g0025 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02735 | hp2 | a0001 | c0003 | t0004 | g0031 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0211 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02809 | hp2 | a0001 | c0014 | t0001 | g0213 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02818 | hp1 | a0001 | c0003 | t0004 | g0165 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02886 | hp1 | a0001 | c0006 | t0005 | g0255 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0170 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02895 | hp1 | a0001 | c0003 | t0004 | g0035 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02896 | hp1 | a0001 | c0005 | t0001 | g0006 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02897 | hp1 | a0001 | c0003 | t0004 | g0035 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02897 | hp2 | a0001 | c0005 | t0001 | g0182 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02922 | hp1 | a0006 | c0013 | t0021 | g0262 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02922 | hp2 | a0007 | c0015 | t0011 | g0260 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02965 | hp2 | a0001 | c0005 | t0001 | g0212 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02970 | hp1 | a0001 | c0005 | t0001 | g0166 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02970 | hp2 | a0001 | c0003 | t0015 | g0160 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02976 | hp1 | a0005 | c0012 | t0013 | g0254 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02976 | hp2 | a0001 | c0003 | t0004 | g0210 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03017 | hp1 | a0002 | c0016 | t0010 | g0011 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0148 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03041 | hp2 | a0001 | c0003 | t0004 | g0025 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03098 | hp1 | a0001 | c0006 | t0005 | g0039 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03098 | hp2 | a0001 | c0005 | t0001 | g0183 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03130 | hp1 | a0001 | c0003 | t0003 | g0032 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03130 | hp2 | a0001 | c0003 | t0008 | g0253 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03139 | hp1 | a0001 | c0006 | t0005 | g0258 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03139 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03195 | hp1 | a0001 | c0010 | t0007 | g0286 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03195 | hp2 | a0001 | c0014 | t0001 | g0227 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03209 | hp1 | a0006 | c0013 | t0012 | g0029 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03209 | hp2 | a0001 | c0003 | t0003 | g0280 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03225 | hp1 | a0006 | c0013 | t0012 | g0029 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03453 | hp1 | a0001 | c0003 | t0003 | g0184 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03453 | hp2 | a0001 | c0006 | t0006 | g0169 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03486 | hp1 | a0001 | c0003 | t0004 | g0241 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03486 | hp2 | a0001 | c0003 | t0004 | g0208 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0018 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0018 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03516 | hp1 | a0001 | c0005 | t0001 | g0193 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03516 | hp2 | a0001 | c0003 | t0003 | g0032 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03540 | hp1 | a0001 | c0010 | t0007 | g0281 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0106 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03579 | hp1 | a0001 | c0006 | t0006 | g0250 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03579 | hp2 | a0001 | c0003 | t0003 | g0246 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0139 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03669 | hp1 | a0011 | c0018 | t0001 | g0157 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0041 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0040 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03831 | hp1 | a0002 | c0004 | t0002 | g0045 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03927 | hp1 | a0001 | c0003 | t0004 | g0176 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03942 | hp1 | a0002 | c0002 | t0014 | g0098 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03942 | hp2 | a0002 | c0027 | t0002 | g0085 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG04115 | hp1 | a0002 | c0016 | t0010 | g0011 | SAS | STU | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG04184 | hp1 | a0001 | c0003 | t0004 | g0158 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0103 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0099 | SAS | STU | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG04228 | hp2 | a0001 | c0003 | t0004 | g0115 | SAS | STU | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18522 | hp1 | a0001 | c0006 | t0005 | g0259 | AFR | YRI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18522 | hp2 | a0001 | c0003 | t0004 | g0152 | AFR | YRI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18612 | hp1 | a0002 | c0004 | t0002 | g0012 | EAS | CHB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18612 | hp2 | a0002 | c0004 | t0002 | g0036 | EAS | CHB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18906 | hp1 | a0001 | c0023 | t0004 | g0167 | AFR | YRI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18906 | hp2 | a0001 | c0003 | t0004 | g0187 | AFR | YRI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18941 | hp1 | a0002 | c0004 | t0002 | g0077 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18944 | hp1 | a0001 | c0001 | t0009 | g0033 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18946 | hp1 | a0001 | c0008 | t0002 | g0073 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18951 | hp2 | a0001 | c0003 | t0003 | g0140 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18957 | hp2 | a0002 | c0004 | t0002 | g0275 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18960 | hp2 | a0004 | c0009 | t0003 | g0049 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18961 | hp2 | a0001 | c0003 | t0004 | g0095 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18967 | hp1 | a0001 | c0001 | t0009 | g0247 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18967 | hp2 | a0001 | c0003 | t0003 | g0141 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18968 | hp2 | a0004 | c0009 | t0003 | g0008 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18969 | hp1 | a0001 | c0003 | t0003 | g0125 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18971 | hp1 | a0001 | c0003 | t0003 | g0105 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18972 | hp1 | a0012 | c0022 | t0004 | g0146 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18973 | hp2 | a0002 | c0004 | t0002 | g0278 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18974 | hp1 | a0002 | c0004 | t0002 | g0023 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18977 | hp2 | a0001 | c0001 | t0009 | g0033 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18978 | hp2 | a0001 | c0003 | t0004 | g0154 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18985 | hp1 | a0002 | c0004 | t0002 | g0037 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18985 | hp2 | a0001 | c0003 | t0004 | g0150 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18987 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18995 | hp1 | a0002 | c0004 | t0002 | g0201 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18995 | hp2 | a0001 | c0008 | t0002 | g0086 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18998 | hp1 | a0001 | c0003 | t0003 | g0088 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18999 | hp1 | a0001 | c0008 | t0002 | g0082 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA18999 | hp2 | a0001 | c0003 | t0003 | g0273 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19000 | hp1 | a0001 | c0003 | t0004 | g0149 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19000 | hp2 | a0002 | c0004 | t0002 | g0016 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19005 | hp1 | a0001 | c0003 | t0003 | g0217 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19010 | hp1 | a0001 | c0003 | t0003 | g0271 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19011 | hp1 | a0002 | c0004 | t0002 | g0037 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19012 | hp1 | a0004 | c0009 | t0003 | g0008 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19030 | hp1 | a0001 | c0003 | t0003 | g0245 | AFR | LWK | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19030 | hp2 | a0001 | c0006 | t0005 | g0039 | AFR | LWK | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0185 | AFR | LWK | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19043 | hp2 | a0001 | c0025 | t0001 | g0261 | AFR | LWK | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19054 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19058 | hp2 | a0001 | c0003 | t0004 | g0026 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19060 | hp1 | a0002 | c0004 | t0002 | g0075 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19062 | hp2 | a0001 | c0003 | t0003 | g0265 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19064 | hp2 | a0001 | c0003 | t0004 | g0057 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19067 | hp2 | a0001 | c0003 | t0004 | g0147 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19070 | hp1 | a0001 | c0003 | t0003 | g0116 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19074 | hp1 | a0002 | c0004 | t0002 | g0036 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19074 | hp2 | a0004 | c0009 | t0003 | g0091 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19079 | hp2 | a0001 | c0003 | t0003 | g0274 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19083 | hp2 | a0004 | c0009 | t0003 | g0084 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19085 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19085 | hp2 | a0002 | c0004 | t0002 | g0235 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19088 | hp1 | a0001 | c0003 | t0004 | g0159 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19088 | hp2 | a0002 | c0004 | t0002 | g0012 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19240 | hp1 | a0001 | c0003 | t0008 | g0256 | AFR | YRI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA19240 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | YRI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA20129 | hp2 | a0005 | c0021 | t0019 | g0163 | AFR | ASW | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA20752 | hp1 | a0014 | c0020 | t0001 | g0044 | EUR | TSI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | GIH | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA20905 | hp2 | a0002 | c0002 | t0014 | g0089 | SAS | GIH | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02109 | hp1 | a0001 | c0003 | t0008 | g0257 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0144 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02559 | hp1 | a0001 | c0006 | t0006 | g0178 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG03471 | hp2 | a0007 | c0015 | t0011 | g0263 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG06807 | hp1 | a0001 | c0003 | t0003 | g0002 | AFR | USA | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| HG06807 | hp2 | a0001 | c0003 | t0004 | g0067 | AFR | USA | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA20300 | hp1 | a0013 | c0017 | t0001 | g0028 | AFR | USA | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0047 | AFR | USA | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA21309 | hp1 | a0005 | c0012 | t0006 | g0132 | AFR | LWK | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| NA21309 | hp2 | a0001 | c0003 | t0003 | g0214 | AFR | LWK | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0097 | REF | REF | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0056 | REF | REF | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:31524751 | A | G | 1 | a0014 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.877A>G | p.Ile293Val | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/15 | 952/5697 | 877/3357 | 293/1118 | chr18 | 31524751 | |||
| chr18:31536321 | G | A | 1 | a0005 | 4 | HG02257.hp1 HG02976.hp1 NA20129.hp2 others(1): Show |
missense_variant | MODERATE | c.1543G>A | p.Val515Ile | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/15 | 1618/5697 | 1543/3357 | 515/1118 | chr18 | 31536321 | |||
| chr18:31536328 | C | T | 1 | a0010 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1550C>T | p.Ala517Val | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/15 | 1625/5697 | 1550/3357 | 517/1118 | chr18 | 31536328 | |||
| chr18:31536375 | G | A | 1 | a0012 | 1 | NA18972.hp1 | missense_variant | MODERATE | c.1597G>A | p.Val533Ile | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/15 | 1672/5697 | 1597/3357 | 533/1118 | chr18 | 31536375 | |||
| chr18:31542655 | G | A | 1 | a0003 | 8 | HG00280.hp2 HG00741.hp2 HG01070.hp1 others(5): Show |
missense_variant | MODERATE | c.2137G>A | p.Glu713Lys | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/15 | 2212/5697 | 2137/3357 | 713/1118 | chr18 | 31542655 | |||
| chr18:31542791 | C | T | 1 | a0008 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.2273C>T | p.Ala758Val | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/15 | 2348/5697 | 2273/3357 | 758/1118 | chr18 | 31542791 | |||
| chr18:31542836 | G | A | 2 | a0002 a0003 |
111 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
missense_variant | MODERATE | c.2318G>A | p.Arg773Lys | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/15 | 2393/5697 | 2318/3357 | 773/1118 | chr18 | 31542836 | |||
| chr18:31545973 | A | C | 1 | a0006 | 3 | HG02922.hp1 HG03209.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.2587A>C | p.Met863Leu | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2662/5697 | 2587/3357 | 863/1118 | chr18 | 31545973 | |||
| chr18:31546033 | T | C | 2 | a0009 a0013 |
2 | HG01243.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.2647T>C | p.Ser883Pro | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2722/5697 | 2647/3357 | 883/1118 | chr18 | 31546033 | |||
| chr18:31546094 | C | T | 1 | a0009 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.2708C>T | p.Thr903Ile | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2783/5697 | 2708/3357 | 903/1118 | chr18 | 31546094 | |||
| chr18:31546272 | T | G | 1 | a0007 | 2 | HG02922.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.2886T>G | p.Ile962Met | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2961/5697 | 2886/3357 | 962/1118 | chr18 | 31546272 | |||
| chr18:31546292 | C | T | 1 | a0011 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.2906C>T | p.Ala969Val | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2981/5697 | 2906/3357 | 969/1118 | chr18 | 31546292 | |||
| chr18:31546595 | C | T | 1 | a0004 | 6 | HG01261.hp1 NA18960.hp2 NA18968.hp2 others(3): Show |
missense_variant | MODERATE | c.3209C>T | p.Thr1070Met | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 3284/5697 | 3209/3357 | 1070/1118 | chr18 | 31546595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:31520859 | A | G | 1 | a0002c0027 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.273A>G | p.Gly91Gly | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 4/15 | 348/5697 | 273/3357 | 91/1118 | chr18 | 31520859 | |||
| chr18:31524735 | C | T | 18 | a0001c0003 a0001c0005 a0001c0006 others(15): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
synonymous_variant | LOW | c.861C>T | p.Asn287Asn | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/15 | 936/5697 | 861/3357 | 287/1118 | chr18 | 31524735 | |||
| chr18:31538974 | G | C | 1 | a0001c0023 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.1875G>C | p.Leu625Leu | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/15 | 1950/5697 | 1875/3357 | 625/1118 | chr18 | 31538974 | |||
| chr18:31541224 | C | T | 1 | a0002c0016 | 2 | HG03017.hp1 HG04115.hp1 |
synonymous_variant | LOW | c.1911C>T | p.Cys637Cys | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/15 | 1986/5697 | 1911/3357 | 637/1118 | chr18 | 31541224 | |||
| chr18:31541227 | A | G | 1 | a0002c0016 | 2 | HG03017.hp1 HG04115.hp1 |
synonymous_variant | LOW | c.1914A>G | p.Gly638Gly | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/15 | 1989/5697 | 1914/3357 | 638/1118 | chr18 | 31541227 | |||
| chr18:31542729 | C | T | 1 | a0007c0015 | 2 | HG02922.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.2211C>T | p.Gly737Gly | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/15 | 2286/5697 | 2211/3357 | 737/1118 | chr18 | 31542729 | |||
| chr18:31545870 | T | C | 1 | a0010c0026 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.2484T>C | p.Asp828Asp | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2559/5697 | 2484/3357 | 828/1118 | chr18 | 31545870 | |||
| chr18:31545891 | A | G | 6 | a0001c0003 a0001c0011 a0001c0023 others(3): Show |
85 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
synonymous_variant | LOW | c.2505A>G | p.Thr835Thr | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2580/5697 | 2505/3357 | 835/1118 | chr18 | 31545891 | |||
| chr18:31545972 | T | C | 1 | a0007c0015 | 2 | HG02922.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.2586T>C | p.Ser862Ser | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2661/5697 | 2586/3357 | 862/1118 | chr18 | 31545972 | |||
| chr18:31546089 | A | G | 1 | a0001c0025 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.2703A>G | p.Lys901Lys | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2778/5697 | 2703/3357 | 901/1118 | chr18 | 31546089 | |||
| chr18:31546521 | A | C | 1 | a0001c0014 | 2 | HG02809.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.3135A>C | p.Thr1045Thr | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 3210/5697 | 3135/3357 | 1045/1118 | chr18 | 31546521 | |||
| chr18:31546629 | C | T | 1 | a0001c0010 | 5 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
synonymous_variant | LOW | c.3243C>T | p.Val1081Val | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 3318/5697 | 3243/3357 | 1081/1118 | chr18 | 31546629 | |||
| chr18:31546707 | T | C | 19 | a0001c0003 a0001c0006 a0001c0008 others(16): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
synonymous_variant | LOW | c.3321T>C | p.Val1107Val | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 3396/5697 | 3321/3357 | 1107/1118 | chr18 | 31546707 | |||
| chr18:31546719 | C | T | 1 | a0005c0021 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.3333C>T | p.Ser1111Ser | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 3408/5697 | 3333/3357 | 1111/1118 | chr18 | 31546719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:31546874 | C | T | 1 | a0006c0013t0021 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*131C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 131 | chr18 | 31546874 | ||||||
| chr18:31546981 | T | G | 1 | a0002c0016t0010 | 2 | HG03017.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*238T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 238 | chr18 | 31546981 | ||||||
| chr18:31547190 | A | G | 1 | a0001c0006t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*447A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 447 | chr18 | 31547190 | ||||||
| chr18:31547308 | A | G | 6 | a0001c0008t0002 a0002c0002t0002 a0002c0002t0014 others(3): Show |
115 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*565A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 565 | chr18 | 31547308 | ||||||
| chr18:31547341 | CAG | C | 1 | a0001c0001t0009 | 3 | NA18944.hp1 NA18967.hp1 NA18977.hp2 |
3_prime_UTR_variant | MODIFIER | c.*599_*600delAG | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 599 | chr18 | 31547341 | ||||||
| chr18:31547342 | A | AGT | 5 | a0001c0003t0004 a0001c0006t0016 a0001c0010t0007 others(2): Show |
42 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*611_*612dupTG | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 613 | INFO_REALIGN_3_PRIME | chr18 | 31547342 | |||||
| chr18:31547420 | T | C | 1 | a0001c0003t0008 | 3 | HG02109.hp1 HG03130.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*677T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 677 | chr18 | 31547420 | ||||||
| chr18:31547448 | G | A | 1 | a0007c0015t0011 | 2 | HG02922.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*705G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 705 | chr18 | 31547448 | ||||||
| chr18:31547550 | G | A | 1 | a0007c0015t0011 | 2 | HG02922.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*807G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 807 | chr18 | 31547550 | ||||||
| chr18:31547676 | C | CA | 10 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0008 others(7): Show |
89 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*944dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 945 | INFO_REALIGN_3_PRIME | chr18 | 31547676 | |||||
| chr18:31547694 | G | GA | 2 | a0001c0006t0005 a0010c0026t0005 |
7 | HG02055.hp1 HG02055.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*960dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 961 | INFO_REALIGN_3_PRIME | chr18 | 31547694 | |||||
| chr18:31547732 | C | T | 1 | a0001c0006t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*989C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 989 | chr18 | 31547732 | ||||||
| chr18:31547779 | C | G | 1 | a0001c0006t0016 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1036C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1036 | chr18 | 31547779 | ||||||
| chr18:31547794 | T | C | 1 | a0001c0006t0017 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1051T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1051 | chr18 | 31547794 | ||||||
| chr18:31547814 | T | C | 1 | a0002c0002t0014 | 2 | HG03942.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1071T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1071 | chr18 | 31547814 | ||||||
| chr18:31548007 | G | A | 1 | a0009c0024t0018 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1264G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1264 | chr18 | 31548007 | ||||||
| chr18:31548007 | G | C | 1 | a0001c0003t0015 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1264G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1264 | chr18 | 31548007 | ||||||
| chr18:31548082 | G | A | 7 | a0001c0003t0004 a0001c0006t0016 a0001c0010t0007 others(4): Show |
46 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1339G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1339 | chr18 | 31548082 | ||||||
| chr18:31548128 | C | T | 2 | a0001c0006t0020 a0005c0012t0013 |
3 | HG01884.hp2 HG02257.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1385C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1385 | chr18 | 31548128 | ||||||
| chr18:31548132 | A | T | 1 | a0001c0006t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1389A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1389 | chr18 | 31548132 | ||||||
| chr18:31548214 | T | C | 1 | a0002c0016t0010 | 2 | HG03017.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1471T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1471 | chr18 | 31548214 | ||||||
| chr18:31548417 | G | A | 1 | a0005c0021t0019 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1674G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1674 | chr18 | 31548417 | ||||||
| chr18:31548455 | C | CTG | 28 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0008 others(25): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*1714_*1715dupGT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1716 | INFO_REALIGN_3_PRIME | chr18 | 31548455 | |||||
| chr18:31548587 | A | G | 2 | a0006c0013t0012 a0006c0013t0021 |
3 | HG02922.hp1 HG03209.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1844A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1844 | chr18 | 31548587 | ||||||
| chr18:31548609 | T | C | 29 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0008 others(26): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*1866T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1866 | chr18 | 31548609 | ||||||
| chr18:31548703 | C | T | 1 | a0007c0015t0011 | 2 | HG02922.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1960C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1960 | chr18 | 31548703 | ||||||
| chr18:31548905 | CAGTT | C | 13 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0008 others(10): Show |
95 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2163_*2166delAGTT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2163 | chr18 | 31548905 | ||||||
| chr18:31548916 | G | A | 13 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0008 others(10): Show |
95 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2173G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2173 | chr18 | 31548916 | ||||||
| chr18:31548988 | G | A | 29 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0008 others(26): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*2245G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2245 | chr18 | 31548988 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:31498370 | C | G | 8 | a0001c0003t0003g0280 a0001c0005t0001g0283 a0001c0010t0007g0281 others(5): Show |
8 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+74C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498370 | |||||||
| chr18:31498443 | C | T | 1 | a0002c0004t0002g0278 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.45+147C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498443 | |||||||
| chr18:31498471 | G | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.45+175G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498471 | |||||||
| chr18:31498488 | C | T | 1 | a0002c0002t0002g0277 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.45+192C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498488 | |||||||
| chr18:31498553 | A | C | 111 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(108): Show |
136 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.45+257A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498553 | |||||||
| chr18:31498652 | C | G | 7 | a0001c0003t0003g0184 a0001c0003t0004g0187 a0001c0005t0001g0006 others(4): Show |
10 | HG02615.hp1 HG02895.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+356C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498652 | |||||||
| chr18:31498664 | A | G | 165 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(162): Show |
200 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.45+368A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498664 | |||||||
| chr18:31498817 | A | T | 1 | a0001c0006t0020g0181 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.45+521A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498817 | |||||||
| chr18:31498841 | A | G | 4 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0006t0006g0178 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+545A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498841 | |||||||
| chr18:31498859 | C | T | 4 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0006t0006g0178 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+563C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498859 | |||||||
| chr18:31499001 | C | T | 2 | a0001c0003t0004g0031 a0001c0003t0004g0176 |
3 | HG00140.hp2 HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.45+705C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499001 | |||||||
| chr18:31499093 | G | T | 8 | a0001c0003t0003g0184 a0001c0003t0004g0187 a0001c0005t0001g0006 others(5): Show |
11 | HG02572.hp1 HG02615.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+797G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499093 | |||||||
| chr18:31499203 | C | A | 1 | a0002c0002t0002g0040 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.45+907C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499203 | |||||||
| chr18:31499205 | C | T | 14 | a0001c0001t0001g0272 a0001c0003t0003g0002 a0001c0003t0003g0264 others(11): Show |
20 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.45+909C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499205 | |||||||
| chr18:31499237 | T | G | 36 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(33): Show |
43 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.45+941T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499237 | |||||||
| chr18:31499272 | C | G | 4 | a0001c0001t0001g0161 a0001c0006t0006g0027 a0001c0006t0017g0162 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+976C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499272 | |||||||
| chr18:31499306 | C | T | 4 | a0001c0001t0001g0161 a0001c0006t0006g0027 a0001c0006t0017g0162 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+1010C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499306 | |||||||
| chr18:31499357 | C | CGT | 83 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0087 others(80): Show |
103 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.45+1090_45+1091dup others(2): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31499357 | ||||||
| chr18:31499357 | C | CGTGT | 8 | a0001c0001t0001g0142 a0001c0003t0003g0140 a0001c0003t0003g0141 others(5): Show |
9 | HG00140.hp2 HG01884.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+1088_45+1091dup others(4): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31499357 | ||||||
| chr18:31499357 | C | CGTGTGT | 3 | a0001c0003t0004g0175 a0002c0002t0002g0143 a0009c0024t0018g0174 |
3 | HG01243.hp1 HG02080.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.45+1086_45+1091dup others(6): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31499357 | ||||||
| chr18:31499357 | CGT | C | 3 | a0001c0003t0004g0249 a0001c0003t0015g0160 a0014c0020t0001g0044 |
3 | HG02572.hp2 HG02970.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.45+1090_45+1091del others(2): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31499357 | ||||||
| chr18:31499357 | CGTGT | C | 125 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(122): Show |
156 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.45+1088_45+1091del others(4): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31499357 | ||||||
| chr18:31499357 | CGTGTGTG others(3): Show |
C | 1 | a0002c0002t0002g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.45+1082_45+1091del others(10): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31499357 | ||||||
| chr18:31499369 | T | C | 2 | a0001c0003t0004g0249 a0001c0003t0015g0160 |
2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.45+1073T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499369 | |||||||
| chr18:31499371 | T | C | 123 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(120): Show |
154 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.45+1075T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499371 | |||||||
| chr18:31499639 | C | T | 9 | a0001c0003t0003g0280 a0001c0005t0001g0283 a0001c0010t0007g0281 others(6): Show |
9 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+1343C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499639 | |||||||
| chr18:31499641 | T | C | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.45+1345T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499641 | |||||||
| chr18:31499649 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.45+1353T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499649 | |||||||
| chr18:31500036 | T | TA | 43 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0087 others(40): Show |
45 | HG00738.hp2 HG01106.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.45+1763dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31500036 | ||||||
| chr18:31500036 | T | TAA | 11 | a0001c0001t0001g0177 a0001c0003t0008g0253 a0001c0006t0005g0039 others(8): Show |
13 | HG01070.hp1 HG01175.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.45+1762_45+1763dup others(2): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31500036 | ||||||
| chr18:31500036 | T | TAAA | 66 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(63): Show |
86 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.45+1761_45+1763dup others(3): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31500036 | ||||||
| chr18:31500036 | T | TAAAA | 20 | a0001c0001t0001g0191 a0001c0001t0001g0194 a0001c0001t0001g0196 others(17): Show |
24 | HG00741.hp2 HG01069.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.45+1760_45+1763dup others(4): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31500036 | ||||||
| chr18:31500066 | G | A | 1 | a0001c0003t0004g0165 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45+1770G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500066 | |||||||
| chr18:31500122 | A | C | 1 | a0001c0008t0002g0082 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.45+1826A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500122 | |||||||
| chr18:31500132 | G | C | 1 | a0001c0008t0002g0082 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.45+1836G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500132 | |||||||
| chr18:31500170 | T | G | 2 | a0001c0001t0001g0090 a0002c0002t0002g0017 |
3 | HG00323.hp2 HG00642.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.45+1874T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500170 | |||||||
| chr18:31500206 | G | A | 4 | a0001c0001t0001g0161 a0001c0006t0006g0027 a0001c0006t0017g0162 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+1910G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500206 | |||||||
| chr18:31500596 | A | T | 4 | a0001c0001t0001g0161 a0001c0006t0006g0027 a0001c0006t0017g0162 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+2300A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500596 | |||||||
| chr18:31500684 | G | A | 39 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(36): Show |
46 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.45+2388G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500684 | |||||||
| chr18:31500793 | A | G | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.45+2497A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500793 | |||||||
| chr18:31501112 | C | T | 151 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(148): Show |
183 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.45+2816C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31501112 | |||||||
| chr18:31501241 | C | T | 1 | a0006c0013t0021g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.45+2945C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31501241 | |||||||
| chr18:31501497 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.45+3201C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31501497 | |||||||
| chr18:31501685 | G | C | 4 | a0001c0003t0003g0032 a0001c0003t0003g0189 a0001c0003t0003g0245 others(1): Show |
5 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+3389G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31501685 | |||||||
| chr18:31501797 | C | G | 39 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(36): Show |
46 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.45+3501C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31501797 | |||||||
| chr18:31501865 | T | A | 5 | a0002c0002t0002g0092 a0004c0009t0003g0008 a0004c0009t0003g0049 others(2): Show |
7 | HG01261.hp1 HG02040.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+3569T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31501865 | |||||||
| chr18:31501966 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.45+3670G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31501966 | |||||||
| chr18:31502149 | T | G | 3 | a0001c0003t0004g0165 a0001c0005t0001g0166 a0001c0023t0004g0167 |
3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+3853T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502149 | |||||||
| chr18:31502229 | T | G | 1 | a0002c0002t0002g0093 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.45+3933T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502229 | |||||||
| chr18:31502268 | T | C | 36 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(33): Show |
44 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.45+3972T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502268 | |||||||
| chr18:31502409 | T | C | 3 | a0001c0003t0004g0165 a0001c0005t0001g0166 a0001c0023t0004g0167 |
3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+4113T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502409 | |||||||
| chr18:31502531 | C | G | 3 | a0001c0003t0008g0253 a0005c0012t0013g0251 a0005c0012t0013g0254 |
3 | HG02257.hp1 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.45+4235C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502531 | |||||||
| chr18:31502675 | TGGAAGGC others(3): Show |
T | 3 | a0001c0003t0004g0165 a0001c0005t0001g0166 a0001c0023t0004g0167 |
3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+4382_45+4391del others(10): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31502675 | ||||||
| chr18:31502736 | G | A | 1 | a0002c0002t0002g0094 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.45+4440G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502736 | |||||||
| chr18:31502888 | G | T | 1 | a0001c0001t0001g0007 | 4 | NA18963.hp1 NA18968.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+4592G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502888 | |||||||
| chr18:31502996 | G | A | 164 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(161): Show |
199 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.45+4700G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502996 | |||||||
| chr18:31503051 | C | T | 1 | a0001c0006t0006g0027 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.45+4755C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503051 | |||||||
| chr18:31503053 | G | A | 40 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(37): Show |
48 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.45+4757G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503053 | |||||||
| chr18:31503298 | G | A | 1 | a0001c0005t0001g0144 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.45+5002G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503298 | |||||||
| chr18:31503303 | A | G | 8 | a0001c0003t0003g0184 a0001c0003t0004g0187 a0001c0005t0001g0006 others(5): Show |
11 | HG02615.hp1 HG02895.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+5007A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503303 | |||||||
| chr18:31503377 | A | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0242 |
4 | HG00423.hp2 HG02083.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+5081A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503377 | |||||||
| chr18:31503402 | G | C | 1 | a0001c0001t0001g0050 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.45+5106G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503402 | |||||||
| chr18:31503427 | G | C | 1 | a0001c0010t0007g0276 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.45+5131G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503427 | |||||||
| chr18:31503460 | T | C | 1 | a0002c0004t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.45+5164T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503460 | |||||||
| chr18:31503599 | G | A | 40 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(37): Show |
48 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.45+5303G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503599 | |||||||
| chr18:31503657 | A | G | 1 | a0001c0010t0007g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.45+5361A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503657 | |||||||
| chr18:31503667 | G | T | 127 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(124): Show |
154 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.45+5371G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503667 | |||||||
| chr18:31503668 | C | T | 4 | a0001c0003t0003g0032 a0001c0003t0003g0189 a0001c0003t0003g0245 others(1): Show |
5 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+5372C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503668 | |||||||
| chr18:31503820 | G | A | 8 | a0001c0003t0003g0184 a0001c0003t0004g0187 a0001c0005t0001g0006 others(5): Show |
11 | HG02615.hp1 HG02895.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+5524G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503820 | |||||||
| chr18:31503925 | G | A | 164 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(161): Show |
199 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.45+5629G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503925 | |||||||
| chr18:31503979 | G | T | 8 | a0001c0003t0003g0184 a0001c0003t0004g0187 a0001c0005t0001g0006 others(5): Show |
11 | HG02615.hp1 HG02895.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+5683G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503979 | |||||||
| chr18:31504142 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.45+5846G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31504142 | |||||||
| chr18:31504458 | T | A | 152 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(149): Show |
185 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.45+6162T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31504458 | |||||||
| chr18:31504553 | T | TG | 40 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(37): Show |
48 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.45+6260dupG | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31504553 | ||||||
| chr18:31504718 | C | T | 4 | a0001c0001t0001g0161 a0001c0006t0006g0027 a0001c0006t0017g0162 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+6422C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31504718 | |||||||
| chr18:31504878 | C | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.45+6582C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31504878 | |||||||
| chr18:31504925 | A | G | 3 | a0001c0003t0004g0165 a0001c0005t0001g0166 a0001c0023t0004g0167 |
3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+6629A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31504925 | |||||||
| chr18:31504986 | C | T | 1 | a0001c0003t0004g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.45+6690C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31504986 | |||||||
| chr18:31505003 | T | G | 1 | a0001c0003t0004g0095 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.45+6707T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505003 | |||||||
| chr18:31505110 | A | G | 1 | a0002c0002t0002g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.45+6814A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505110 | |||||||
| chr18:31505336 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.45+7040C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505336 | |||||||
| chr18:31505527 | G | A | 1 | a0002c0002t0002g0096 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.45+7231G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505527 | |||||||
| chr18:31505555 | A | G | 2 | a0001c0006t0006g0169 a0010c0026t0005g0173 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.45+7259A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505555 | |||||||
| chr18:31505656 | C | CT | 45 | a0001c0001t0001g0048 a0001c0001t0001g0081 a0001c0001t0001g0136 others(42): Show |
52 | HG00673.hp2 HG01106.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.45+7375dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31505656 | ||||||
| chr18:31505656 | CT | C | 24 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0161 others(21): Show |
28 | HG00140.hp2 HG00609.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.45+7375delT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31505656 | ||||||
| chr18:31505786 | C | T | 3 | a0001c0003t0004g0165 a0001c0005t0001g0166 a0001c0023t0004g0167 |
3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+7490C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505786 | |||||||
| chr18:31505815 | C | G | 33 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(30): Show |
40 | HG01891.hp2 HG02074.hp1 HG02165.hp2 others(37): Show |
intron_variant | MODIFIER | c.45+7519C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505815 | |||||||
| chr18:31505863 | T | C | 1 | a0001c0005t0001g0144 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.45+7567T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505863 | |||||||
| chr18:31505899 | C | T | 3 | a0001c0003t0004g0025 a0002c0002t0002g0148 a0006c0013t0012g0029 |
5 | HG02723.hp2 HG03041.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+7603C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505899 | |||||||
| chr18:31506085 | A | G | 153 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(150): Show |
186 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.45+7789A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506085 | |||||||
| chr18:31506229 | G | A | 3 | a0001c0003t0008g0253 a0005c0012t0013g0251 a0005c0012t0013g0254 |
3 | HG02257.hp1 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.45+7933G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506229 | |||||||
| chr18:31506376 | T | G | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.45+8080T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506376 | |||||||
| chr18:31506413 | C | T | 1 | a0001c0003t0003g0078 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.45+8117C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506413 | |||||||
| chr18:31506486 | A | G | 40 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(37): Show |
48 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.45+8190A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506486 | |||||||
| chr18:31506669 | AGT | A | 3 | a0001c0003t0004g0165 a0001c0005t0001g0166 a0001c0023t0004g0167 |
3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+8375_45+8376del others(2): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31506669 | ||||||
| chr18:31506678 | A | G | 1 | a0001c0003t0003g0273 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.45+8382A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506678 | |||||||
| chr18:31506689 | T | G | 12 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0003t0003g0184 others(9): Show |
15 | HG02451.hp1 HG02559.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.45+8393T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506689 | |||||||
| chr18:31506884 | C | T | 2 | a0001c0006t0006g0169 a0010c0026t0005g0173 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.45+8588C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506884 | |||||||
| chr18:31506893 | G | T | 166 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(163): Show |
201 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.45+8597G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506893 | |||||||
| chr18:31507037 | C | G | 2 | a0001c0005t0001g0166 a0001c0023t0004g0167 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+8741C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31507037 | |||||||
| chr18:31507138 | C | T | 3 | a0001c0003t0004g0165 a0001c0005t0001g0166 a0001c0023t0004g0167 |
3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+8842C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31507138 | |||||||
| chr18:31507198 | T | G | 24 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(21): Show |
28 | HG01891.hp2 HG02074.hp1 HG02165.hp2 others(25): Show |
intron_variant | MODIFIER | c.45+8902T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31507198 | |||||||
| chr18:31507689 | C | A | 3 | a0001c0003t0004g0165 a0001c0005t0001g0166 a0001c0023t0004g0167 |
3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+9393C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31507689 | |||||||
| chr18:31507789 | T | C | 2 | a0002c0002t0002g0099 a0002c0002t0014g0098 |
2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.45+9493T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31507789 | |||||||
| chr18:31508010 | A | G | 153 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(150): Show |
186 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.45+9714A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508010 | |||||||
| chr18:31508015 | G | A | 4 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0006t0006g0178 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+9719G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508015 | |||||||
| chr18:31508100 | T | G | 1 | a0001c0006t0016g0079 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.45+9804T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508100 | |||||||
| chr18:31508145 | G | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0142 |
3 | HG01243.hp2 HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.45+9849G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508145 | |||||||
| chr18:31508185 | G | A | 153 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(150): Show |
186 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.45+9889G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508185 | |||||||
| chr18:31508231 | G | A | 2 | a0001c0005t0001g0144 a0001c0005t0001g0145 |
2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.45+9935G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508231 | |||||||
| chr18:31508289 | T | G | 1 | a0001c0001t0001g0243 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.46-9950T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508289 | |||||||
| chr18:31508353 | A | ATTTAT | 15 | a0001c0001t0001g0164 a0001c0001t0001g0188 a0001c0001t0001g0233 others(12): Show |
16 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.46-9838_46-9834dup others(5): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31508353 | ||||||
| chr18:31508353 | A | ATTTATTT others(3): Show |
1 | a0001c0003t0003g0246 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-9843_46-9834dup others(10): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31508353 | ||||||
| chr18:31508353 | A | ATTTATTT others(8): Show |
1 | a0001c0001t0001g0237 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.46-9848_46-9834dup others(15): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31508353 | ||||||
| chr18:31508353 | ATTTAT | A | 24 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0042 others(21): Show |
27 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.46-9838_46-9834del others(5): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31508353 | ||||||
| chr18:31508353 | ATTTATTT others(3): Show |
A | 60 | a0001c0001t0001g0101 a0001c0001t0001g0153 a0001c0001t0001g0155 others(57): Show |
71 | HG00140.hp2 HG00738.hp2 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.46-9843_46-9834del others(10): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31508353 | ||||||
| chr18:31508353 | ATTTATTT others(8): Show |
A | 8 | a0001c0001t0001g0051 a0001c0001t0001g0161 a0001c0003t0004g0165 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-9848_46-9834del others(15): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31508353 | ||||||
| chr18:31508353 | ATTTATTT others(18): Show |
A | 12 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0003t0003g0184 others(9): Show |
15 | HG02451.hp1 HG02559.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.46-9858_46-9834del others(25): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31508353 | ||||||
| chr18:31508429 | C | T | 1 | a0006c0013t0012g0029 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.46-9810C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508429 | |||||||
| chr18:31508463 | G | A | 3 | a0001c0003t0004g0165 a0001c0005t0001g0166 a0001c0023t0004g0167 |
3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.46-9776G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508463 | |||||||
| chr18:31508746 | G | C | 165 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(162): Show |
200 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.46-9493G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508746 | |||||||
| chr18:31508913 | T | G | 2 | a0001c0001t0009g0033 a0001c0001t0009g0247 |
3 | NA18944.hp1 NA18967.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.46-9326T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508913 | |||||||
| chr18:31508995 | C | T | 37 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(34): Show |
45 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.46-9244C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508995 | |||||||
| chr18:31509056 | AAAG | A | 9 | a0001c0003t0003g0280 a0001c0005t0001g0283 a0001c0010t0007g0281 others(6): Show |
9 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.46-9178_46-9176del others(3): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31509056 | ||||||
| chr18:31509246 | T | C | 1 | a0001c0003t0004g0165 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.46-8993T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509246 | |||||||
| chr18:31509264 | A | G | 5 | a0002c0002t0002g0024 a0002c0002t0002g0128 a0002c0002t0002g0129 others(2): Show |
6 | HG01928.hp1 HG01943.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-8975A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509264 | |||||||
| chr18:31509389 | G | C | 4 | a0001c0001t0001g0191 a0001c0001t0001g0207 a0002c0002t0002g0034 others(1): Show |
5 | HG02148.hp2 NA18946.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-8850G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509389 | |||||||
| chr18:31509402 | G | A | 8 | a0001c0003t0008g0256 a0001c0003t0008g0257 a0001c0006t0005g0039 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-8837G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509402 | |||||||
| chr18:31509421 | A | G | 1 | a0007c0015t0011g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46-8818A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509421 | |||||||
| chr18:31509432 | C | CT | 130 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(127): Show |
165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.46-8798dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31509432 | ||||||
| chr18:31509432 | C | CTT | 154 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(151): Show |
186 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.46-8799_46-8798dup others(2): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31509432 | ||||||
| chr18:31509598 | T | C | 4 | a0001c0003t0008g0253 a0001c0006t0006g0250 a0005c0012t0013g0251 others(1): Show |
4 | HG02257.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-8641T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509598 | |||||||
| chr18:31509922 | T | A | 12 | a0001c0001t0001g0171 a0001c0003t0004g0030 a0001c0003t0004g0031 others(9): Show |
14 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.46-8317T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509922 | |||||||
| chr18:31509975 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.46-8264G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509975 | |||||||
| chr18:31510175 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.46-8064G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510175 | |||||||
| chr18:31510226 | C | T | 8 | a0001c0005t0001g0283 a0001c0010t0007g0281 a0001c0010t0007g0284 others(5): Show |
8 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-8013C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510226 | |||||||
| chr18:31510227 | G | A | 1 | a0001c0003t0004g0057 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.46-8012G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510227 | |||||||
| chr18:31510259 | T | G | 4 | a0001c0003t0008g0253 a0001c0006t0006g0250 a0005c0012t0013g0251 others(1): Show |
4 | HG02257.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-7980T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510259 | |||||||
| chr18:31510513 | C | A | 1 | a0001c0003t0004g0208 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.46-7726C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510513 | |||||||
| chr18:31510590 | G | GA | 4 | a0001c0005t0001g0006 a0001c0005t0001g0182 a0001c0025t0001g0261 others(1): Show |
7 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-7636dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31510590 | ||||||
| chr18:31510606 | T | C | 3 | a0001c0003t0004g0165 a0001c0005t0001g0166 a0001c0023t0004g0167 |
3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.46-7633T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510606 | |||||||
| chr18:31510671 | T | G | 6 | a0001c0003t0003g0192 a0001c0003t0004g0035 a0001c0003t0004g0190 others(3): Show |
7 | HG01884.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-7568T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510671 | |||||||
| chr18:31510711 | C | A | 12 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0003t0003g0184 others(9): Show |
15 | HG02451.hp1 HG02559.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.46-7528C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510711 | |||||||
| chr18:31510771 | A | G | 126 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(123): Show |
153 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.46-7468A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510771 | |||||||
| chr18:31510854 | C | T | 1 | a0002c0002t0002g0126 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.46-7385C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510854 | |||||||
| chr18:31510930 | C | T | 15 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0180 others(12): Show |
19 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.46-7309C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510930 | |||||||
| chr18:31510954 | A | G | 2 | a0001c0010t0007g0276 a0007c0015t0011g0260 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.46-7285A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510954 | |||||||
| chr18:31511060 | G | T | 4 | a0001c0003t0004g0152 a0001c0003t0015g0160 a0002c0002t0002g0148 others(1): Show |
5 | HG02970.hp2 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-7179G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511060 | |||||||
| chr18:31511068 | A | G | 16 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(13): Show |
17 | HG01891.hp2 HG02074.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.46-7171A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511068 | |||||||
| chr18:31511322 | G | T | 1 | a0001c0001t0001g0237 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.46-6917G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511322 | |||||||
| chr18:31511400 | G | A | 1 | a0007c0015t0011g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46-6839G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511400 | |||||||
| chr18:31511412 | C | T | 12 | a0001c0008t0002g0073 a0001c0011t0003g0071 a0001c0011t0003g0072 others(9): Show |
14 | HG00438.hp1 HG00597.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-6827C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511412 | |||||||
| chr18:31511551 | A | T | 1 | a0002c0004t0002g0134 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.46-6688A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511551 | |||||||
| chr18:31511620 | A | G | 1 | a0001c0003t0004g0151 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.46-6619A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511620 | |||||||
| chr18:31511938 | G | A | 64 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(61): Show |
73 | HG00738.hp2 HG01106.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.46-6301G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511938 | |||||||
| chr18:31512053 | G | A | 2 | a0001c0003t0003g0214 a0001c0014t0001g0213 |
2 | HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.46-6186G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512053 | |||||||
| chr18:31512080 | C | T | 1 | a0001c0003t0003g0271 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.46-6159C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512080 | |||||||
| chr18:31512326 | A | G | 1 | a0001c0003t0015g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.46-5913A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512326 | |||||||
| chr18:31512447 | G | A | 3 | a0001c0003t0004g0025 a0002c0002t0002g0148 a0006c0013t0012g0029 |
5 | HG02723.hp2 HG03041.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-5792G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512447 | |||||||
| chr18:31512452 | A | G | 1 | a0005c0012t0006g0132 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.46-5787A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512452 | |||||||
| chr18:31512656 | A | G | 159 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(156): Show |
194 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.46-5583A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512656 | |||||||
| chr18:31512661 | T | C | 1 | a0001c0005t0001g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.46-5578T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512661 | |||||||
| chr18:31512798 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.46-5441T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512798 | |||||||
| chr18:31512837 | C | T | 1 | a0002c0004t0002g0075 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.46-5402C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512837 | |||||||
| chr18:31512881 | A | G | 6 | a0001c0003t0004g0025 a0001c0003t0004g0152 a0001c0003t0015g0160 others(3): Show |
8 | HG01884.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-5358A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512881 | |||||||
| chr18:31513129 | C | A | 6 | a0001c0003t0004g0025 a0001c0003t0004g0152 a0001c0003t0015g0160 others(3): Show |
8 | HG01884.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-5110C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513129 | |||||||
| chr18:31513130 | C | T | 4 | a0001c0005t0001g0168 a0001c0006t0006g0169 a0009c0024t0018g0174 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-5109C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513130 | |||||||
| chr18:31513140 | T | C | 1 | a0001c0006t0006g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-5099T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513140 | |||||||
| chr18:31513181 | A | G | 2 | a0002c0016t0010g0011 a0005c0012t0006g0132 |
3 | HG03017.hp1 HG04115.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.46-5058A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513181 | |||||||
| chr18:31513191 | G | A | 1 | a0002c0002t0002g0138 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.46-5048G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513191 | |||||||
| chr18:31513211 | A | G | 1 | a0001c0006t0006g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-5028A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513211 | |||||||
| chr18:31513354 | A | G | 158 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(155): Show |
193 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.46-4885A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513354 | |||||||
| chr18:31513563 | G | C | 1 | a0001c0003t0004g0176 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.46-4676G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513563 | |||||||
| chr18:31513683 | T | A | 134 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(131): Show |
162 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.46-4556T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513683 | |||||||
| chr18:31513698 | C | T | 5 | a0001c0003t0004g0165 a0001c0005t0001g0166 a0001c0005t0001g0211 others(2): Show |
5 | HG02809.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-4541C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513698 | |||||||
| chr18:31513908 | A | T | 14 | a0001c0003t0004g0025 a0001c0003t0004g0152 a0001c0003t0008g0256 others(11): Show |
17 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.46-4331A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513908 | |||||||
| chr18:31514071 | T | C | 1 | a0002c0002t0002g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.46-4168T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514071 | |||||||
| chr18:31514146 | T | G | 10 | a0001c0003t0003g0184 a0001c0003t0004g0187 a0001c0005t0001g0006 others(7): Show |
14 | HG01167.hp1 HG01169.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-4093T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514146 | |||||||
| chr18:31514371 | G | A | 9 | a0001c0003t0003g0184 a0001c0003t0004g0187 a0001c0005t0001g0006 others(6): Show |
13 | HG01167.hp1 HG01169.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.46-3868G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514371 | |||||||
| chr18:31514388 | T | C | 1 | a0006c0013t0012g0029 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.46-3851T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514388 | |||||||
| chr18:31514462 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.46-3777T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514462 | |||||||
| chr18:31514471 | C | T | 1 | a0002c0002t0002g0094 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.46-3768C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514471 | |||||||
| chr18:31514472 | G | A | 8 | a0001c0005t0001g0283 a0001c0010t0007g0281 a0001c0010t0007g0284 others(5): Show |
8 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-3767G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514472 | |||||||
| chr18:31514501 | T | C | 1 | a0001c0006t0020g0181 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.46-3738T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514501 | |||||||
| chr18:31514657 | T | C | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.46-3582T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514657 | |||||||
| chr18:31514805 | C | T | 14 | a0001c0003t0004g0025 a0001c0003t0004g0152 a0001c0003t0008g0256 others(11): Show |
17 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.46-3434C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514805 | |||||||
| chr18:31514847 | A | G | 16 | a0001c0001t0001g0272 a0001c0003t0003g0002 a0001c0003t0003g0264 others(13): Show |
22 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.46-3392A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514847 | |||||||
| chr18:31515126 | A | G | 164 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(161): Show |
199 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.46-3113A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515126 | |||||||
| chr18:31515133 | C | T | 2 | a0002c0002t0002g0100 a0002c0002t0002g0104 |
2 | HG02523.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.46-3106C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515133 | |||||||
| chr18:31515269 | A | C | 2 | a0001c0003t0004g0232 a0001c0003t0004g0241 |
2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.46-2970A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515269 | |||||||
| chr18:31515317 | G | C | 1 | a0001c0003t0004g0154 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.46-2922G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515317 | |||||||
| chr18:31515357 | G | A | 7 | a0001c0005t0001g0283 a0001c0010t0007g0281 a0001c0010t0007g0284 others(4): Show |
7 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-2882G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515357 | |||||||
| chr18:31515452 | G | A | 4 | a0001c0003t0008g0253 a0001c0006t0006g0250 a0005c0012t0013g0251 others(1): Show |
4 | HG02257.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-2787G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515452 | |||||||
| chr18:31515471 | C | G | 133 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(130): Show |
160 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.46-2768C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515471 | |||||||
| chr18:31515561 | G | A | 14 | a0001c0003t0004g0025 a0001c0003t0004g0152 a0001c0003t0008g0256 others(11): Show |
17 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.46-2678G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515561 | |||||||
| chr18:31515822 | A | C | 139 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(136): Show |
169 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.46-2417A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515822 | |||||||
| chr18:31515925 | A | G | 140 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(137): Show |
167 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.46-2314A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515925 | |||||||
| chr18:31516030 | G | A | 4 | a0001c0003t0003g0032 a0001c0003t0003g0189 a0001c0003t0003g0245 others(1): Show |
5 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-2209G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516030 | |||||||
| chr18:31516058 | T | C | 95 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(92): Show |
121 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.46-2181T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516058 | |||||||
| chr18:31516080 | A | C | 4 | a0001c0003t0003g0032 a0001c0003t0003g0189 a0001c0003t0003g0245 others(1): Show |
5 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-2159A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516080 | |||||||
| chr18:31516126 | CAA | C | 7 | a0001c0003t0008g0256 a0001c0003t0008g0257 a0001c0006t0005g0039 others(4): Show |
8 | HG02055.hp1 HG02109.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-2112_46-2111del others(2): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516126 | |||||||
| chr18:31516141 | G | GT | 16 | a0001c0003t0003g0184 a0001c0003t0004g0165 a0001c0003t0004g0187 others(13): Show |
20 | HG01167.hp1 HG01169.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.46-2088dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31516141 | ||||||
| chr18:31516309 | A | G | 1 | a0002c0004t0002g0053 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.46-1930A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516309 | |||||||
| chr18:31516310 | C | T | 12 | a0001c0003t0003g0184 a0001c0003t0004g0165 a0001c0003t0004g0187 others(9): Show |
17 | HG01167.hp1 HG01169.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.46-1929C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516310 | |||||||
| chr18:31516375 | G | A | 7 | a0001c0005t0001g0283 a0001c0010t0007g0281 a0001c0010t0007g0286 others(4): Show |
7 | HG00280.hp1 HG00738.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-1864G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516375 | |||||||
| chr18:31516421 | G | C | 1 | a0005c0012t0006g0132 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.46-1818G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516421 | |||||||
| chr18:31516427 | A | G | 2 | a0002c0002t0002g0122 a0002c0002t0002g0123 |
2 | HG01346.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.46-1812A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516427 | |||||||
| chr18:31516516 | C | T | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.46-1723C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516516 | |||||||
| chr18:31516520 | A | G | 1 | a0001c0003t0003g0267 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.46-1719A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516520 | |||||||
| chr18:31516553 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.46-1686A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516553 | |||||||
| chr18:31516646 | G | A | 5 | a0001c0001t0009g0033 a0001c0001t0009g0247 a0001c0003t0004g0025 others(2): Show |
7 | HG02723.hp2 HG03041.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-1593G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516646 | |||||||
| chr18:31516647 | C | A | 1 | a0006c0013t0021g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.46-1592C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516647 | |||||||
| chr18:31516724 | G | A | 26 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0108 others(23): Show |
33 | HG00609.hp1 HG00673.hp1 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.46-1515G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516724 | |||||||
| chr18:31516858 | C | T | 1 | a0003c0007t0002g0231 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.46-1381C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516858 | |||||||
| chr18:31516879 | G | T | 1 | a0001c0003t0004g0025 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.46-1360G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516879 | |||||||
| chr18:31516887 | T | G | 1 | a0001c0006t0006g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.46-1352T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516887 | |||||||
| chr18:31516956 | G | T | 143 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(140): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.46-1283G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516956 | |||||||
| chr18:31516989 | G | A | 1 | a0001c0006t0020g0181 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.46-1250G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516989 | |||||||
| chr18:31517132 | T | G | 48 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0004g0025 others(45): Show |
54 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.46-1107T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517132 | |||||||
| chr18:31517197 | T | C | 1 | a0001c0003t0003g0264 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.46-1042T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517197 | |||||||
| chr18:31517406 | A | G | 2 | a0001c0003t0003g0105 a0002c0002t0002g0103 |
2 | HG04184.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.46-833A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517406 | |||||||
| chr18:31517506 | A | G | 47 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0004g0025 others(44): Show |
53 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.46-733A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517506 | |||||||
| chr18:31517578 | A | G | 46 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0004g0025 others(43): Show |
52 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.46-661A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517578 | |||||||
| chr18:31517635 | T | G | 27 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(24): Show |
36 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.46-604T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517635 | |||||||
| chr18:31517749 | G | A | 32 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(29): Show |
42 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.46-490G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517749 | |||||||
| chr18:31517772 | G | A | 1 | a0002c0002t0002g0129 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.46-467G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517772 | |||||||
| chr18:31517872 | A | C | 14 | a0001c0003t0003g0184 a0001c0005t0001g0006 a0001c0005t0001g0144 others(11): Show |
18 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.46-367A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517872 | |||||||
| chr18:31518169 | T | C | 2 | a0001c0010t0007g0276 a0001c0010t0007g0284 |
2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.46-70T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31518169 | |||||||
| chr18:31518348 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.81+74C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518348 | |||||||
| chr18:31518360 | G | A | 131 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0046 others(128): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.81+86G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518360 | |||||||
| chr18:31518382 | C | T | 81 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0046 others(78): Show |
99 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.81+108C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518382 | |||||||
| chr18:31518510 | C | T | 4 | a0002c0002t0002g0068 a0002c0002t0002g0279 a0002c0002t0002g0282 others(1): Show |
4 | HG00280.hp1 HG00738.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+236C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518510 | |||||||
| chr18:31518511 | A | G | 82 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0046 others(79): Show |
99 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.81+237A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518511 | |||||||
| chr18:31518539 | C | A | 2 | a0001c0006t0006g0250 a0006c0013t0012g0029 |
3 | HG03209.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.81+265C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518539 | |||||||
| chr18:31518549 | T | C | 1 | a0001c0003t0004g0249 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.81+275T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518549 | |||||||
| chr18:31518672 | G | A | 223 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0019 others(220): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.81+398G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518672 | |||||||
| chr18:31518714 | T | G | 1 | a0006c0013t0021g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.81+440T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518714 | |||||||
| chr18:31518725 | T | TA | 78 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0046 others(75): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.81+462dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr18 | 31518725 | ||||||
| chr18:31518793 | G | A | 9 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0015g0160 others(6): Show |
9 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+519G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518793 | |||||||
| chr18:31518862 | G | A | 1 | a0002c0002t0002g0060 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.81+588G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518862 | |||||||
| chr18:31518895 | A | G | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.81+621A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518895 | |||||||
| chr18:31519121 | T | C | 1 | a0002c0002t0002g0270 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.82-682T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31519121 | |||||||
| chr18:31519324 | A | C | 1 | a0001c0003t0004g0150 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.82-479A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31519324 | |||||||
| chr18:31519634 | C | G | 1 | a0001c0006t0005g0259 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.82-169C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31519634 | |||||||
| chr18:31520134 | C | T | 2 | a0006c0013t0012g0029 a0006c0013t0021g0262 |
3 | HG02922.hp1 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.216+197C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 3/14 | chr18 | 31520134 | |||||||
| chr18:31520457 | C | T | 5 | a0001c0010t0007g0059 a0001c0010t0007g0276 a0001c0010t0007g0281 others(2): Show |
5 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.217-346C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 3/14 | chr18 | 31520457 | |||||||
| chr18:31520470 | C | T | 1 | a0002c0002t0002g0099 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.217-333C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 3/14 | chr18 | 31520470 | |||||||
| chr18:31520714 | G | C | 1 | a0002c0002t0002g0122 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.217-89G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 3/14 | chr18 | 31520714 | |||||||
| chr18:31520738 | C | G | 29 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(26): Show |
38 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.217-65C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 3/14 | chr18 | 31520738 | |||||||
| chr18:31520798 | G | T | 1 | a0006c0013t0012g0029 | 2 | HG03209.hp1 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.217-5G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 3/14 | chr18 | 31520798 | |||||||
| chr18:31521252 | CT | C | 7 | a0001c0001t0001g0061 a0001c0001t0001g0243 a0001c0003t0004g0165 others(4): Show |
7 | HG01168.hp1 HG01168.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.523+24delT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 31521252 | ||||||
| chr18:31521267 | T | A | 46 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0004g0025 others(43): Show |
52 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.523+24T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521267 | |||||||
| chr18:31521444 | G | C | 2 | a0001c0003t0003g0116 a0001c0003t0003g0141 |
2 | NA18967.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.523+201G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521444 | |||||||
| chr18:31521495 | A | G | 79 | a0001c0001t0001g0052 a0001c0001t0001g0113 a0001c0001t0001g0114 others(76): Show |
94 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.523+252A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521495 | |||||||
| chr18:31521512 | A | G | 5 | a0001c0006t0020g0181 a0005c0012t0006g0132 a0005c0012t0013g0251 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.523+269A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521512 | |||||||
| chr18:31521649 | T | G | 160 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(157): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.523+406T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521649 | |||||||
| chr18:31521663 | A | G | 1 | a0006c0013t0021g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.523+420A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521663 | |||||||
| chr18:31521723 | G | A | 50 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0004g0025 others(47): Show |
56 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.524-360G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521723 | |||||||
| chr18:31521812 | C | T | 5 | a0001c0006t0020g0181 a0005c0012t0006g0132 a0005c0012t0013g0251 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.524-271C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521812 | |||||||
| chr18:31521840 | G | C | 114 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(111): Show |
139 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.524-243G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521840 | |||||||
| chr18:31521939 | T | G | 1 | a0002c0002t0002g0117 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.524-144T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521939 | |||||||
| chr18:31521955 | G | A | 1 | a0001c0003t0004g0165 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.524-128G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521955 | |||||||
| chr18:31522074 | T | A | 9 | a0001c0003t0008g0253 a0001c0003t0008g0256 a0001c0003t0008g0257 others(6): Show |
10 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.524-9T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31522074 | |||||||
| chr18:31522310 | CTTTTT | C | 30 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(27): Show |
39 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.690+62_690+66delTT others(3): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31522310 | |||||||
| chr18:31522610 | T | C | 2 | a0001c0006t0006g0178 a0001c0006t0006g0179 |
2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.690+361T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31522610 | |||||||
| chr18:31522950 | G | A | 2 | a0001c0003t0004g0152 a0001c0003t0004g0175 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.690+701G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31522950 | |||||||
| chr18:31523018 | G | A | 1 | a0001c0003t0003g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.690+769G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523018 | |||||||
| chr18:31523101 | A | G | 5 | a0001c0006t0020g0181 a0005c0012t0006g0132 a0005c0012t0013g0251 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.690+852A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523101 | |||||||
| chr18:31523124 | G | A | 45 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0004g0025 others(42): Show |
51 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.690+875G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523124 | |||||||
| chr18:31523127 | C | T | 2 | a0002c0002t0002g0040 a0002c0002t0002g0047 |
2 | HG03704.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.690+878C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523127 | |||||||
| chr18:31523172 | C | T | 77 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(74): Show |
94 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.690+923C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523172 | |||||||
| chr18:31523198 | G | A | 74 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(71): Show |
91 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.690+949G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523198 | |||||||
| chr18:31523293 | C | T | 1 | a0001c0006t0017g0162 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.690+1044C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523293 | |||||||
| chr18:31523331 | A | G | 78 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(75): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.690+1082A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523331 | |||||||
| chr18:31523420 | A | G | 3 | a0001c0001t0001g0198 a0001c0001t0001g0203 a0001c0001t0001g0224 |
3 | HG01099.hp1 HG01192.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.691-1028A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523420 | |||||||
| chr18:31523451 | G | A | 1 | a0001c0006t0016g0079 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.691-997G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523451 | |||||||
| chr18:31523689 | C | T | 13 | a0001c0003t0003g0184 a0001c0005t0001g0006 a0001c0005t0001g0144 others(10): Show |
16 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.691-759C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523689 | |||||||
| chr18:31523732 | T | C | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.691-716T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523732 | |||||||
| chr18:31523746 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.691-702C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523746 | |||||||
| chr18:31523778 | G | A | 1 | a0005c0021t0019g0163 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.691-670G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523778 | |||||||
| chr18:31523803 | T | C | 43 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0004g0025 others(40): Show |
48 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.691-645T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523803 | |||||||
| chr18:31523807 | G | A | 5 | a0001c0006t0020g0181 a0005c0012t0006g0132 a0005c0012t0013g0251 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-641G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523807 | |||||||
| chr18:31524092 | C | T | 71 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(68): Show |
85 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.691-356C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31524092 | |||||||
| chr18:31524172 | A | G | 28 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(25): Show |
37 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.691-276A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31524172 | |||||||
| chr18:31524241 | G | A | 78 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(75): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.691-207G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31524241 | |||||||
| chr18:31524245 | A | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0161 a0001c0001t0001g0164 others(1): Show |
4 | HG02818.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-203A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31524245 | |||||||
| chr18:31524258 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.691-190G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31524258 | |||||||
| chr18:31524301 | T | C | 71 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(68): Show |
85 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.691-147T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31524301 | |||||||
| chr18:31524365 | C | T | 6 | a0001c0003t0004g0208 a0002c0004t0002g0036 a0002c0004t0002g0037 others(3): Show |
8 | HG00673.hp2 HG03486.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-83C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31524365 | |||||||
| chr18:31524601 | C | A | 74 | a0001c0006t0006g0178 a0001c0006t0006g0179 a0002c0002t0002g0003 others(71): Show |
89 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.828+16C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 7/14 | chr18 | 31524601 | |||||||
| chr18:31524915 | G | A | 77 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(74): Show |
93 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1014+27G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31524915 | |||||||
| chr18:31524939 | G | A | 1 | a0001c0003t0004g0165 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1014+51G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31524939 | |||||||
| chr18:31524998 | G | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1014+110G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31524998 | |||||||
| chr18:31525010 | T | C | 1 | a0002c0002t0002g0282 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1014+122T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525010 | |||||||
| chr18:31525107 | G | T | 13 | a0001c0003t0003g0184 a0001c0005t0001g0006 a0001c0005t0001g0144 others(10): Show |
16 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1014+219G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525107 | |||||||
| chr18:31525154 | T | C | 36 | a0001c0003t0004g0025 a0001c0003t0004g0026 a0001c0003t0004g0030 others(33): Show |
41 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1014+266T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525154 | |||||||
| chr18:31525213 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1014+325T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525213 | |||||||
| chr18:31525289 | G | A | 2 | a0001c0006t0006g0169 a0001c0006t0017g0162 |
2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1014+401G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525289 | |||||||
| chr18:31525536 | G | A | 11 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0015g0160 others(8): Show |
12 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1014+648G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525536 | |||||||
| chr18:31525612 | G | A | 1 | a0001c0011t0003g0225 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1014+724G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525612 | |||||||
| chr18:31525918 | G | A | 78 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(75): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1014+1030G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525918 | |||||||
| chr18:31525933 | G | A | 1 | a0001c0003t0003g0274 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1014+1045G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525933 | |||||||
| chr18:31525999 | C | T | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1014+1111C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525999 | |||||||
| chr18:31526091 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0048 |
3 | HG00735.hp1 HG02129.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1014+1203C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526091 | |||||||
| chr18:31526157 | A | G | 2 | a0007c0015t0011g0260 a0007c0015t0011g0263 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1014+1269A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526157 | |||||||
| chr18:31526293 | C | T | 5 | a0001c0010t0007g0059 a0001c0010t0007g0276 a0001c0010t0007g0281 others(2): Show |
5 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1014+1405C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526293 | |||||||
| chr18:31526379 | C | T | 82 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(79): Show |
97 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1014+1491C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526379 | |||||||
| chr18:31526603 | G | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0161 a0001c0001t0001g0164 others(1): Show |
4 | HG02818.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1014+1715G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526603 | |||||||
| chr18:31526649 | G | A | 1 | a0007c0015t0011g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1014+1761G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526649 | |||||||
| chr18:31526649 | G | T | 77 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(74): Show |
93 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1014+1761G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526649 | |||||||
| chr18:31526677 | A | G | 1 | a0005c0021t0019g0163 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1014+1789A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526677 | |||||||
| chr18:31526724 | T | G | 1 | a0001c0003t0003g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1014+1836T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526724 | |||||||
| chr18:31526762 | G | A | 1 | a0001c0005t0001g0211 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1014+1874G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526762 | |||||||
| chr18:31526858 | G | A | 77 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(74): Show |
93 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1014+1970G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526858 | |||||||
| chr18:31526935 | T | A | 78 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(75): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1014+2047T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526935 | |||||||
| chr18:31527491 | G | A | 51 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(48): Show |
61 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1014+2603G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527491 | |||||||
| chr18:31527583 | C | T | 9 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0015g0160 others(6): Show |
9 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1014+2695C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527583 | |||||||
| chr18:31527628 | C | T | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1014+2740C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527628 | |||||||
| chr18:31527651 | A | T | 77 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(74): Show |
93 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1014+2763A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527651 | |||||||
| chr18:31527693 | T | C | 2 | a0007c0015t0011g0260 a0007c0015t0011g0263 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1014+2805T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527693 | |||||||
| chr18:31527749 | A | G | 2 | a0001c0005t0001g0170 a0001c0005t0001g0283 |
2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1014+2861A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527749 | |||||||
| chr18:31527767 | T | G | 163 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(160): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1014+2879T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527767 | |||||||
| chr18:31527840 | G | A | 5 | a0001c0006t0020g0181 a0005c0012t0006g0132 a0005c0012t0013g0251 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+2952G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527840 | |||||||
| chr18:31527854 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0194 |
2 | NA18977.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1014+2966C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527854 | |||||||
| chr18:31527887 | G | A | 4 | a0005c0012t0006g0132 a0005c0012t0013g0251 a0005c0012t0013g0254 others(1): Show |
4 | HG02257.hp1 HG02976.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014+2999G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527887 | |||||||
| chr18:31527928 | G | A | 1 | a0001c0005t0001g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1014+3040G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527928 | |||||||
| chr18:31527975 | T | C | 1 | a0001c0003t0004g0158 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1015-3012T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527975 | |||||||
| chr18:31528119 | A | T | 9 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0015g0160 others(6): Show |
9 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1015-2868A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528119 | |||||||
| chr18:31528124 | G | A | 78 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(75): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1015-2863G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528124 | |||||||
| chr18:31528157 | A | G | 1 | a0010c0026t0005g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1015-2830A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528157 | |||||||
| chr18:31528195 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1015-2792G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528195 | |||||||
| chr18:31528418 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1015-2569C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528418 | |||||||
| chr18:31528437 | C | T | 1 | a0005c0012t0013g0251 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1015-2550C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528437 | |||||||
| chr18:31528438 | A | G | 165 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(162): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1015-2549A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528438 | |||||||
| chr18:31528498 | G | A | 13 | a0001c0003t0003g0184 a0001c0005t0001g0006 a0001c0005t0001g0144 others(10): Show |
16 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1015-2489G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528498 | |||||||
| chr18:31528542 | A | T | 171 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(168): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1015-2445A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528542 | |||||||
| chr18:31528554 | C | T | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1015-2433C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528554 | |||||||
| chr18:31528613 | A | G | 78 | a0001c0003t0004g0165 a0001c0006t0006g0027 a0001c0006t0006g0169 others(75): Show |
94 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1015-2374A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528613 | |||||||
| chr18:31528626 | CCTGAACC others(214): Show |
C | 1 | a0001c0001t0001g0233 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1015-2358_1015-213 others(4): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr18 | 31528626 | ||||||
| chr18:31528709 | C | CA | 20 | a0001c0001t0009g0247 a0001c0003t0003g0141 a0001c0003t0003g0192 others(17): Show |
23 | HG00140.hp2 HG00544.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1015-2259dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr18 | 31528709 | ||||||
| chr18:31528709 | CA | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0005t0001g0212 others(6): Show |
9 | HG01168.hp2 HG01169.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1015-2259delA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr18 | 31528709 | ||||||
| chr18:31528743 | T | C | 86 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(83): Show |
101 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1015-2244T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528743 | |||||||
| chr18:31528774 | A | G | 1 | a0002c0002t0002g0285 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1015-2213A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528774 | |||||||
| chr18:31528963 | C | G | 3 | a0001c0003t0004g0026 a0001c0003t0004g0147 a0001c0003t0004g0149 |
4 | HG02165.hp2 NA19000.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-2024C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528963 | |||||||
| chr18:31529000 | A | G | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1015-1987A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31529000 | |||||||
| chr18:31529073 | A | G | 170 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(167): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1015-1914A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31529073 | |||||||
| chr18:31529172 | A | C | 12 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0015g0160 others(9): Show |
13 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1015-1815A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31529172 | |||||||
| chr18:31529336 | A | T | 2 | a0001c0006t0006g0169 a0001c0006t0017g0162 |
2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1015-1651A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31529336 | |||||||
| chr18:31529483 | A | G | 5 | a0001c0006t0020g0181 a0005c0012t0006g0132 a0005c0012t0013g0251 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015-1504A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31529483 | |||||||
| chr18:31529679 | C | A | 86 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(83): Show |
101 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1015-1308C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31529679 | |||||||
| chr18:31530155 | G | A | 1 | a0001c0025t0001g0261 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1015-832G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530155 | |||||||
| chr18:31530350 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1015-637A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530350 | |||||||
| chr18:31530363 | A | T | 17 | a0002c0004t0002g0012 a0002c0004t0002g0016 a0002c0004t0002g0023 others(14): Show |
22 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.1015-624A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530363 | |||||||
| chr18:31530517 | A | G | 13 | a0001c0003t0003g0184 a0001c0005t0001g0006 a0001c0005t0001g0144 others(10): Show |
16 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1015-470A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530517 | |||||||
| chr18:31530545 | G | A | 3 | a0001c0006t0006g0250 a0006c0013t0012g0029 a0006c0013t0021g0262 |
4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1015-442G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530545 | |||||||
| chr18:31530619 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1015-368A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530619 | |||||||
| chr18:31530721 | A | T | 1 | a0001c0001t0001g0048 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1015-266A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530721 | |||||||
| chr18:31530807 | C | A | 13 | a0001c0003t0003g0184 a0001c0005t0001g0006 a0001c0005t0001g0144 others(10): Show |
16 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1015-180C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530807 | |||||||
| chr18:31530915 | CATGTAT | C | 3 | a0001c0006t0006g0250 a0006c0013t0012g0029 a0006c0013t0021g0262 |
4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1015-58_1015-53del others(6): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr18 | 31530915 | ||||||
| chr18:31531401 | G | A | 34 | a0001c0003t0004g0025 a0001c0003t0004g0026 a0001c0003t0004g0030 others(31): Show |
39 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1280+149G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31531401 | |||||||
| chr18:31531486 | A | G | 90 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0015g0160 others(87): Show |
108 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1280+234A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31531486 | |||||||
| chr18:31531539 | C | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0090 |
2 | HG00642.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.1280+287C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31531539 | |||||||
| chr18:31531694 | G | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1280+442G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31531694 | |||||||
| chr18:31531702 | C | T | 12 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0015g0160 others(9): Show |
13 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1280+450C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31531702 | |||||||
| chr18:31531916 | G | A | 3 | a0002c0004t0002g0023 a0002c0004t0002g0070 a0002c0004t0002g0278 |
4 | HG02083.hp2 HG02129.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1280+664G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31531916 | |||||||
| chr18:31531918 | C | T | 5 | a0001c0006t0020g0181 a0005c0012t0006g0132 a0005c0012t0013g0251 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280+666C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31531918 | |||||||
| chr18:31532143 | T | C | 1 | a0001c0003t0003g0268 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1280+891T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532143 | |||||||
| chr18:31532178 | G | A | 3 | a0001c0003t0003g0192 a0001c0003t0003g0214 a0001c0003t0015g0160 |
3 | HG02630.hp2 HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1280+926G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532178 | |||||||
| chr18:31532215 | G | A | 3 | a0001c0006t0006g0250 a0006c0013t0012g0029 a0006c0013t0021g0262 |
4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1280+963G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532215 | |||||||
| chr18:31532250 | G | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1280+998G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532250 | |||||||
| chr18:31532315 | A | G | 12 | a0001c0005t0001g0006 a0001c0005t0001g0144 a0001c0005t0001g0145 others(9): Show |
15 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1280+1063A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532315 | |||||||
| chr18:31532477 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1280+1225T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532477 | |||||||
| chr18:31532500 | C | T | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1280+1248C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532500 | |||||||
| chr18:31532610 | T | C | 10 | a0001c0003t0003g0184 a0001c0003t0003g0192 a0001c0003t0003g0214 others(7): Show |
10 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1280+1358T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532610 | |||||||
| chr18:31532697 | G | A | 1 | a0001c0005t0001g0185 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1280+1445G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532697 | |||||||
| chr18:31532767 | T | A | 5 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280+1515T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532767 | |||||||
| chr18:31532778 | T | C | 4 | a0005c0012t0006g0132 a0005c0012t0013g0251 a0005c0012t0013g0254 others(1): Show |
4 | HG02257.hp1 HG02976.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1280+1526T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532778 | |||||||
| chr18:31532850 | A | G | 5 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280+1598A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532850 | |||||||
| chr18:31532903 | G | A | 12 | a0001c0003t0003g0184 a0001c0003t0003g0192 a0001c0003t0003g0214 others(9): Show |
13 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1280+1651G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532903 | |||||||
| chr18:31532904 | CTGTTT | C | 3 | a0001c0003t0004g0190 a0001c0003t0004g0209 a0001c0003t0004g0249 |
3 | HG01884.hp1 HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1280+1658_1280+166 others(9): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31532904 | ||||||
| chr18:31532907 | T | TTTTG | 21 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0240 others(18): Show |
22 | HG00609.hp1 HG02015.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.1280+1683_1280+168 others(8): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31532907 | ||||||
| chr18:31532907 | T | TTTTGTTT others(1): Show |
4 | a0001c0006t0005g0039 a0001c0006t0005g0252 a0001c0006t0005g0255 others(1): Show |
5 | HG02055.hp1 HG02886.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280+1679_1280+168 others(12): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31532907 | ||||||
| chr18:31532907 | TTTTG | T | 12 | a0001c0003t0003g0184 a0001c0003t0003g0192 a0001c0003t0003g0214 others(9): Show |
12 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1280+1683_1280+168 others(8): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31532907 | ||||||
| chr18:31532907 | TTTTGTTT others(1): Show |
T | 97 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0003t0003g0274 others(94): Show |
118 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1280+1679_1280+168 others(12): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31532907 | ||||||
| chr18:31532907 | TTTTGTTT others(5): Show |
T | 1 | a0006c0013t0012g0029 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1280+1675_1280+168 others(16): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31532907 | ||||||
| chr18:31532907 | TTTTGTTT others(9): Show |
T | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1280+1671_1280+168 others(20): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31532907 | ||||||
| chr18:31533045 | A | T | 1 | a0005c0012t0013g0251 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1280+1793A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31533045 | |||||||
| chr18:31533311 | A | C | 1 | a0002c0002t0002g0228 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1281-1959A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31533311 | |||||||
| chr18:31533314 | A | T | 1 | a0001c0001t0001g0014 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1281-1956A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31533314 | |||||||
| chr18:31533512 | A | C | 1 | a0002c0002t0002g0094 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1281-1758A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31533512 | |||||||
| chr18:31533698 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0194 |
2 | NA18977.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1281-1572T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31533698 | |||||||
| chr18:31533991 | C | CT | 36 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(33): Show |
45 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1281-1262dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31533991 | ||||||
| chr18:31533991 | C | CTT | 26 | a0001c0003t0003g0141 a0001c0003t0004g0025 a0001c0003t0004g0026 others(23): Show |
31 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1281-1263_1281-126 others(6): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31533991 | ||||||
| chr18:31533991 | C | CTTT | 6 | a0001c0003t0004g0095 a0001c0003t0004g0115 a0001c0003t0004g0150 others(3): Show |
6 | HG02074.hp1 HG04184.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.1281-1264_1281-126 others(7): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31533991 | ||||||
| chr18:31533991 | CT | C | 98 | a0001c0001t0001g0050 a0001c0001t0001g0197 a0001c0001t0001g0204 others(95): Show |
118 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1281-1262delT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31533991 | ||||||
| chr18:31534186 | A | C | 115 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0003t0003g0184 others(112): Show |
138 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1281-1084A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534186 | |||||||
| chr18:31534194 | G | A | 1 | a0005c0012t0006g0132 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1281-1076G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534194 | |||||||
| chr18:31534236 | A | C | 1 | a0002c0002t0002g0148 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1281-1034A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534236 | |||||||
| chr18:31534248 | G | A | 95 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(92): Show |
117 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1281-1022G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534248 | |||||||
| chr18:31534441 | A | C | 1 | a0001c0001t0001g0242 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1281-829A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534441 | |||||||
| chr18:31534479 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1281-791G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534479 | |||||||
| chr18:31534508 | A | AT | 18 | a0001c0001t0001g0064 a0001c0001t0001g0087 a0001c0001t0001g0198 others(15): Show |
19 | HG00741.hp1 HG02015.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1281-742dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31534508 | ||||||
| chr18:31534508 | A | ATT | 77 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(74): Show |
94 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1281-743_1281-742d others(4): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31534508 | ||||||
| chr18:31534508 | A | ATTTTT | 83 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0006t0006g0027 others(80): Show |
103 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1281-746_1281-742d others(7): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31534508 | ||||||
| chr18:31534508 | A | ATTTTTT | 11 | a0001c0006t0006g0178 a0002c0002t0002g0055 a0002c0002t0002g0060 others(8): Show |
12 | HG00621.hp2 HG02056.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.1281-747_1281-742d others(8): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31534508 | ||||||
| chr18:31534508 | AT | A | 7 | a0001c0001t0001g0042 a0001c0001t0001g0062 a0001c0001t0001g0090 others(4): Show |
7 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1281-742delT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31534508 | ||||||
| chr18:31534508 | ATT | A | 5 | a0001c0006t0005g0039 a0001c0006t0005g0252 a0001c0006t0005g0255 others(2): Show |
6 | HG02055.hp1 HG02886.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1281-743_1281-742d others(4): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31534508 | ||||||
| chr18:31534533 | T | C | 115 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0003t0003g0184 others(112): Show |
138 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1281-737T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534533 | |||||||
| chr18:31534580 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1281-690G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534580 | |||||||
| chr18:31534589 | C | T | 96 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0006t0006g0027 others(93): Show |
117 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1281-681C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534589 | |||||||
| chr18:31534657 | C | T | 5 | a0001c0010t0007g0059 a0001c0010t0007g0276 a0001c0010t0007g0281 others(2): Show |
5 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281-613C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534657 | |||||||
| chr18:31534658 | G | A | 94 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(91): Show |
115 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1281-612G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534658 | |||||||
| chr18:31534691 | G | A | 3 | a0001c0006t0006g0250 a0006c0013t0012g0029 a0006c0013t0021g0262 |
4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281-579G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534691 | |||||||
| chr18:31534800 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1281-470G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534800 | |||||||
| chr18:31535198 | A | C | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1281-72A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31535198 | |||||||
| chr18:31535701 | G | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1423+289G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 10/14 | chr18 | 31535701 | |||||||
| chr18:31535739 | T | G | 1 | a0001c0001t0001g0242 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1423+327T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 10/14 | chr18 | 31535739 | |||||||
| chr18:31535740 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1423+328C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 10/14 | chr18 | 31535740 | |||||||
| chr18:31535774 | A | C | 1 | a0003c0007t0002g0230 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1423+362A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 10/14 | chr18 | 31535774 | |||||||
| chr18:31535781 | C | A | 1 | a0002c0002t0002g0103 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1423+369C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 10/14 | chr18 | 31535781 | |||||||
| chr18:31535947 | T | A | 189 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0003t0003g0002 others(186): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1424-255T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 10/14 | chr18 | 31535947 | |||||||
| chr18:31536499 | T | C | 47 | a0001c0003t0003g0214 a0001c0003t0004g0025 a0001c0003t0004g0026 others(44): Show |
54 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.1651+70T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31536499 | |||||||
| chr18:31536717 | G | A | 1 | a0001c0006t0006g0027 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1651+288G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31536717 | |||||||
| chr18:31536837 | T | C | 6 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0002c0004t0002g0012 others(3): Show |
7 | HG00609.hp2 HG02155.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.1651+408T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31536837 | |||||||
| chr18:31536936 | CAG | C | 2 | a0006c0013t0012g0029 a0006c0013t0021g0262 |
3 | HG02922.hp1 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1651+508_1651+509d others(4): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31536936 | |||||||
| chr18:31537150 | GT | G | 93 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0002c0002t0002g0003 others(90): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1651+731delT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr18 | 31537150 | ||||||
| chr18:31537152 | T | G | 1 | a0003c0007t0002g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1651+723T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537152 | |||||||
| chr18:31537186 | C | G | 2 | a0006c0013t0012g0029 a0006c0013t0021g0262 |
3 | HG02922.hp1 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1651+757C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537186 | |||||||
| chr18:31537219 | T | A | 2 | a0001c0005t0001g0166 a0001c0005t0001g0168 |
2 | HG02622.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1651+790T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537219 | |||||||
| chr18:31537236 | A | G | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1651+807A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537236 | |||||||
| chr18:31537418 | G | A | 91 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0002c0002t0002g0003 others(88): Show |
111 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1651+989G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537418 | |||||||
| chr18:31537447 | G | A | 46 | a0001c0003t0004g0025 a0001c0003t0004g0026 a0001c0003t0004g0030 others(43): Show |
53 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.1651+1018G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537447 | |||||||
| chr18:31537480 | G | A | 1 | a0002c0027t0002g0085 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1651+1051G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537480 | |||||||
| chr18:31537492 | A | G | 91 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0002c0002t0002g0003 others(88): Show |
111 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1651+1063A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537492 | |||||||
| chr18:31537537 | T | C | 91 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0002c0002t0002g0003 others(88): Show |
111 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1651+1108T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537537 | |||||||
| chr18:31537546 | A | G | 182 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0003t0003g0002 others(179): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1651+1117A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537546 | |||||||
| chr18:31537558 | G | T | 4 | a0002c0002t0002g0068 a0002c0002t0002g0279 a0002c0002t0002g0282 others(1): Show |
4 | HG00280.hp1 HG00738.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651+1129G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537558 | |||||||
| chr18:31537597 | T | C | 138 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0003t0004g0025 others(135): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1652-1154T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537597 | |||||||
| chr18:31537794 | G | A | 1 | a0001c0003t0003g0280 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1652-957G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537794 | |||||||
| chr18:31537836 | C | G | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1652-915C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537836 | |||||||
| chr18:31537898 | G | A | 91 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0002c0002t0002g0003 others(88): Show |
111 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1652-853G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537898 | |||||||
| chr18:31537923 | G | A | 2 | a0005c0012t0006g0132 a0005c0021t0019g0163 |
2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1652-828G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537923 | |||||||
| chr18:31537989 | A | T | 1 | a0001c0005t0001g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1652-762A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537989 | |||||||
| chr18:31537993 | C | T | 1 | a0001c0005t0001g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1652-758C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537993 | |||||||
| chr18:31538110 | T | TA | 41 | a0001c0003t0004g0025 a0001c0003t0004g0026 a0001c0003t0004g0030 others(38): Show |
47 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.1652-633dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr18 | 31538110 | ||||||
| chr18:31538298 | C | T | 1 | a0001c0003t0004g0165 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1652-453C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31538298 | |||||||
| chr18:31538316 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1652-435G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31538316 | |||||||
| chr18:31538343 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1652-408G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31538343 | |||||||
| chr18:31538393 | G | GT | 38 | a0001c0003t0004g0025 a0001c0003t0004g0026 a0001c0003t0004g0030 others(35): Show |
43 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.1652-349dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr18 | 31538393 | ||||||
| chr18:31538397 | T | A | 1 | a0002c0002t0002g0093 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1652-354T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31538397 | |||||||
| chr18:31538402 | T | A | 1 | a0002c0002t0002g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1652-349T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31538402 | |||||||
| chr18:31538585 | G | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1652-166G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31538585 | |||||||
| chr18:31538714 | G | A | 2 | a0001c0006t0006g0169 a0001c0006t0017g0162 |
2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1652-37G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31538714 | |||||||
| chr18:31539040 | G | A | 1 | a0001c0003t0003g0125 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1879+62G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539040 | |||||||
| chr18:31539082 | C | T | 2 | a0007c0015t0011g0260 a0007c0015t0011g0263 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1879+104C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539082 | |||||||
| chr18:31539155 | C | T | 1 | a0001c0010t0007g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1879+177C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539155 | |||||||
| chr18:31539295 | T | C | 86 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(83): Show |
102 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1879+317T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539295 | |||||||
| chr18:31539322 | A | C | 2 | a0007c0015t0011g0260 a0007c0015t0011g0263 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1879+344A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539322 | |||||||
| chr18:31539394 | T | C | 181 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(178): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1879+416T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539394 | |||||||
| chr18:31539527 | C | T | 27 | a0001c0003t0003g0002 a0001c0003t0003g0076 a0001c0003t0003g0078 others(24): Show |
35 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1879+549C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539527 | |||||||
| chr18:31539579 | C | T | 1 | a0004c0009t0003g0091 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1879+601C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539579 | |||||||
| chr18:31539601 | C | A | 1 | a0001c0006t0016g0079 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1879+623C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539601 | |||||||
| chr18:31539750 | C | A | 1 | a0001c0001t0001g0221 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1879+772C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539750 | |||||||
| chr18:31539825 | A | G | 1 | a0001c0006t0006g0027 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1879+847A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539825 | |||||||
| chr18:31540020 | T | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1879+1042T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540020 | |||||||
| chr18:31540236 | A | G | 2 | a0002c0002t0002g0205 a0002c0002t0002g0218 |
2 | NA18959.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1880-957A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540236 | |||||||
| chr18:31540446 | C | T | 89 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0017 others(86): Show |
109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1880-747C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540446 | |||||||
| chr18:31540474 | C | G | 89 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0017 others(86): Show |
109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1880-719C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540474 | |||||||
| chr18:31540567 | G | A | 89 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0017 others(86): Show |
109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1880-626G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540567 | |||||||
| chr18:31540576 | G | A | 2 | a0007c0015t0011g0260 a0007c0015t0011g0263 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1880-617G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540576 | |||||||
| chr18:31540612 | G | A | 6 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(3): Show |
7 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1880-581G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540612 | |||||||
| chr18:31540812 | C | T | 2 | a0005c0012t0013g0251 a0005c0012t0013g0254 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1880-381C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540812 | |||||||
| chr18:31540840 | A | AT | 33 | a0001c0003t0004g0025 a0001c0003t0004g0026 a0001c0003t0004g0030 others(30): Show |
38 | HG00140.hp2 HG00609.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.1880-344dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 31540840 | ||||||
| chr18:31540845 | T | G | 1 | a0001c0008t0002g0080 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1880-348T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540845 | |||||||
| chr18:31540912 | T | C | 76 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(73): Show |
90 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.1880-281T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540912 | |||||||
| chr18:31541525 | C | T | 89 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0017 others(86): Show |
109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2001+211C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541525 | |||||||
| chr18:31541558 | G | C | 89 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0017 others(86): Show |
109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2001+244G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541558 | |||||||
| chr18:31541622 | C | T | 14 | a0001c0005t0001g0006 a0001c0005t0001g0144 a0001c0005t0001g0145 others(11): Show |
17 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2001+308C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541622 | |||||||
| chr18:31541649 | T | G | 2 | a0007c0015t0011g0260 a0007c0015t0011g0263 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2001+335T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541649 | |||||||
| chr18:31541800 | C | A | 89 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0017 others(86): Show |
109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2001+486C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541800 | |||||||
| chr18:31541866 | C | A | 6 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(3): Show |
7 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2001+552C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541866 | |||||||
| chr18:31541933 | T | A | 84 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(81): Show |
100 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2002-587T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541933 | |||||||
| chr18:31541977 | TG | T | 14 | a0001c0005t0001g0006 a0001c0005t0001g0144 a0001c0005t0001g0145 others(11): Show |
17 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2002-542delG | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541977 | |||||||
| chr18:31542023 | C | T | 2 | a0007c0015t0011g0260 a0007c0015t0011g0263 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2002-497C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31542023 | |||||||
| chr18:31542304 | T | C | 6 | a0001c0006t0005g0039 a0001c0006t0005g0252 a0001c0006t0005g0255 others(3): Show |
7 | HG02055.hp1 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002-216T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31542304 | |||||||
| chr18:31542325 | T | C | 2 | a0001c0005t0001g0211 a0001c0005t0001g0212 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2002-195T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31542325 | |||||||
| chr18:31542385 | A | G | 6 | a0001c0006t0005g0039 a0001c0006t0005g0252 a0001c0006t0005g0255 others(3): Show |
7 | HG02055.hp1 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002-135A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31542385 | |||||||
| chr18:31542959 | GT | G | 93 | a0001c0003t0003g0264 a0001c0003t0008g0253 a0001c0006t0006g0027 others(90): Show |
114 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2334+121delT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr18 | 31542959 | ||||||
| chr18:31542987 | A | G | 3 | a0001c0006t0020g0181 a0005c0012t0013g0251 a0005c0012t0013g0254 |
3 | HG01884.hp2 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2334+135A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31542987 | |||||||
| chr18:31543351 | G | T | 1 | a0002c0002t0002g0148 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2334+499G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543351 | |||||||
| chr18:31543368 | T | G | 14 | a0001c0005t0001g0006 a0001c0005t0001g0144 a0001c0005t0001g0145 others(11): Show |
17 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2334+516T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543368 | |||||||
| chr18:31543371 | G | A | 1 | a0001c0014t0001g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2334+519G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543371 | |||||||
| chr18:31543459 | G | T | 2 | a0005c0012t0006g0132 a0005c0021t0019g0163 |
2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2334+607G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543459 | |||||||
| chr18:31543462 | A | G | 1 | a0001c0006t0006g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2334+610A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543462 | |||||||
| chr18:31543500 | A | G | 2 | a0005c0012t0006g0132 a0005c0021t0019g0163 |
2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2334+648A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543500 | |||||||
| chr18:31543516 | G | A | 1 | a0002c0002t0002g0092 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2334+664G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543516 | |||||||
| chr18:31543615 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2334+763C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543615 | |||||||
| chr18:31543796 | G | A | 3 | a0001c0003t0008g0253 a0001c0003t0008g0256 a0001c0003t0008g0257 |
3 | HG02109.hp1 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2334+944G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543796 | |||||||
| chr18:31543861 | G | A | 38 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(35): Show |
47 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.2334+1009G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543861 | |||||||
| chr18:31543864 | T | TA | 96 | a0001c0001t0001g0013 a0001c0001t0001g0042 a0001c0001t0001g0127 others(93): Show |
114 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.2334+1032dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr18 | 31543864 | ||||||
| chr18:31543864 | T | TAA | 14 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0017g0162 others(11): Show |
17 | HG00140.hp1 HG00438.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2334+1031_2334+103 others(6): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr18 | 31543864 | ||||||
| chr18:31543892 | A | G | 5 | a0001c0010t0007g0059 a0001c0010t0007g0276 a0001c0010t0007g0281 others(2): Show |
5 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2334+1040A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543892 | |||||||
| chr18:31543973 | A | G | 1 | a0001c0003t0004g0187 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2334+1121A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543973 | |||||||
| chr18:31544104 | G | C | 95 | a0001c0008t0002g0063 a0001c0008t0002g0073 a0001c0008t0002g0080 others(92): Show |
115 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.2334+1252G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544104 | |||||||
| chr18:31544147 | A | T | 1 | a0002c0002t0002g0060 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2334+1295A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544147 | |||||||
| chr18:31544404 | G | A | 3 | a0005c0012t0006g0132 a0005c0021t0019g0163 a0009c0024t0018g0174 |
3 | HG01243.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2335-1317G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544404 | |||||||
| chr18:31544461 | C | T | 105 | a0001c0006t0006g0027 a0001c0006t0006g0169 a0001c0006t0006g0178 others(102): Show |
127 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2335-1260C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544461 | |||||||
| chr18:31544487 | A | G | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2335-1234A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544487 | |||||||
| chr18:31544748 | T | C | 71 | a0001c0003t0003g0002 a0001c0003t0003g0032 a0001c0003t0003g0076 others(68): Show |
85 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.2335-973T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544748 | |||||||
| chr18:31544769 | T | C | 1 | a0001c0003t0004g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2335-952T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544769 | |||||||
| chr18:31544859 | A | G | 2 | a0007c0015t0011g0260 a0007c0015t0011g0263 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2335-862A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544859 | |||||||
| chr18:31544901 | A | G | 8 | a0001c0006t0016g0079 a0001c0010t0007g0059 a0001c0010t0007g0276 others(5): Show |
9 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2335-820A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544901 | |||||||
| chr18:31544947 | C | T | 2 | a0001c0006t0006g0169 a0001c0006t0017g0162 |
2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2335-774C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544947 | |||||||
| chr18:31545014 | G | T | 2 | a0006c0013t0012g0029 a0006c0013t0021g0262 |
3 | HG02922.hp1 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2335-707G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31545014 | |||||||
| chr18:31545097 | C | T | 1 | a0001c0005t0001g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2335-624C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31545097 | |||||||
| chr18:31545178 | T | C | 2 | a0005c0012t0006g0132 a0005c0021t0019g0163 |
2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2335-543T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31545178 | |||||||
| chr18:31545274 | A | G | 2 | a0005c0012t0013g0251 a0005c0012t0013g0254 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2335-447A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31545274 | |||||||
| chr18:31545457 | T | C | 1 | a0002c0002t0002g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2335-264T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31545457 | |||||||
| chr18:31545515 | A | AT | 7 | a0001c0005t0001g0168 a0001c0006t0005g0039 a0001c0006t0005g0252 others(4): Show |
8 | HG02055.hp1 HG02055.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2335-200dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr18 | 31545515 | ||||||
| chr18:31545687 | GT | G | 4 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0014t0001g0213 others(1): Show |
4 | HG02809.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2335-30delT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr18 | 31545687 |