Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64167 |
| ensemblid | ENSG00000164308.17 |
| hgncid | 29499 |
| symbol | ERAP2 |
| name | endoplasmic reticulum aminopeptidase 2 |
| refseq_nuc | NM_022350.5 |
| refseq_prot | NP_071745.1 |
| ensembl_nuc | ENST00000437043.8 |
| ensembl_prot | ENSP00000400376.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 96876500 |
| end | 96919703 |
| strand | + |
| ver | v1.2 |
| region | chr5:96876500-96919703 |
| region5000 | chr5:96871500-96924703 |
| regionname0 | ERAP2_chr5_96876500_96919703 |
| regionname5000 | ERAP2_chr5_96871500_96924703 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 960 | 193 | 56 | 39 | 69 | 9 | 19 | 54 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0002 | 1/0 | 960 | 128 | 27 | 25 | 59 | 2 | 14 | 47 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0003 | 0/0 | 960 | 30 | 0 | 2 | 26 | 0 | 2 | 24 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0004 | 0/0 | 960 | 15 | 0 | 1 | 14 | 0 | 0 | 12 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0005 | 0/0 | 960 | 13 | 0 | 6 | 0 | 3 | 4 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0006 | 0/0 | 960 | 4 | 0 | 0 | 1 | 0 | 3 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0007 | 0/0 | 960 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0008 | 0/0 | 960 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0009 | 0/0 | 784 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(779): Show |
chr5 | 96871500 | 96924703 |
| a0010 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0011 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0012 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0013 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0014 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0015 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0016 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFPSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0017 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| a0018 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | MFHSS others(955): Show |
chr5 | 96871500 | 96924703 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2880 | 155 | 34 | 30 | 69 | 6 | 16 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0001c0004 | 0/0 | 2880 | 26 | 21 | 3 | 0 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0001c0007 | 0/0 | 2880 | 10 | 0 | 6 | 0 | 3 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0001c0018 | 0/0 | 2880 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0001c0021 | 0/1 | 2880 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0002c0002 | 1/0 | 2880 | 127 | 27 | 25 | 59 | 2 | 13 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0002c0020 | 0/0 | 2880 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0003c0003 | 0/0 | 2880 | 30 | 0 | 2 | 26 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0004c0005 | 0/0 | 2880 | 15 | 0 | 1 | 14 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0005c0006 | 0/0 | 2880 | 13 | 0 | 6 | 0 | 3 | 4 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0006c0008 | 0/0 | 2880 | 4 | 0 | 0 | 1 | 0 | 3 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0007c0011 | 0/0 | 2880 | 2 | 1 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0008c0009 | 0/0 | 2880 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0009c0010 | 0/0 | 2354 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2349): Show |
chr5 | 96871500 | 96924703 | ||
| a0010c0012 | 0/0 | 2880 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0011c0019 | 0/0 | 2880 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0012c0014 | 0/0 | 2880 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0013c0016 | 0/0 | 2880 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0014c0022 | 0/0 | 2880 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0015c0017 | 0/0 | 2880 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0016c0023 | 0/0 | 2880 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0017c0015 | 0/0 | 2880 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 | ||
| a0018c0013 | 0/0 | 2880 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | ATGTT others(2875): Show |
chr5 | 96871500 | 96924703 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5131 | 155 | 34 | 30 | 69 | 6 | 16 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0001c0004t0001 | 0/0 | 5131 | 21 | 18 | 1 | 0 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0001c0004t0002 | 0/0 | 5131 | 5 | 3 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0001c0007t0001 | 0/0 | 5131 | 10 | 0 | 6 | 0 | 3 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0001c0018t0001 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0001c0021t0001 | 0/1 | 5131 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0002c0002t0001 | 1/0 | 5131 | 127 | 27 | 25 | 59 | 2 | 13 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0002c0020t0001 | 0/0 | 5131 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0003c0003t0001 | 0/0 | 5131 | 30 | 0 | 2 | 26 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0004c0005t0001 | 0/0 | 5131 | 15 | 0 | 1 | 14 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0005c0006t0001 | 0/0 | 5131 | 13 | 0 | 6 | 0 | 3 | 4 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0006c0008t0001 | 0/0 | 5131 | 4 | 0 | 0 | 1 | 0 | 3 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0007c0011t0001 | 0/0 | 5131 | 2 | 1 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0008c0009t0001 | 0/0 | 5131 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0009c0010t0003 | 0/0 | 2504 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(2499): Show |
chr5 | 96871500 | 96924703 |
| a0010c0012t0001 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0011c0019t0001 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0012c0014t0001 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0013c0016t0001 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0014c0022t0001 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0015c0017t0001 | 0/0 | 5131 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0016c0023t0001 | 0/0 | 5131 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0017c0015t0001 | 0/0 | 5131 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| a0018c0013t0001 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | AGTCA others(5126): Show |
chr5 | 96871500 | 96924703 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 1 | 0 | 7 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0002g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0004t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0007t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0007t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0007t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0007t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0007t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0007t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0007t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0007t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0018t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0001c0021t0001g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0002 | 0/0 | 8 | 0 | 0 | 5 | 0 | 3 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0026 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0031 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0002c0020t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0004c0005t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0004c0005t0001g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0004c0005t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0004c0005t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0004c0005t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0004c0005t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0004c0005t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0004c0005t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0004c0005t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0004c0005t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0004c0005t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0004c0005t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0005c0006t0001g0012 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0005c0006t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0005c0006t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0005c0006t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0005c0006t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0005c0006t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0005c0006t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0005c0006t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0005c0006t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0005c0006t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0006c0008t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0006c0008t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0006c0008t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0006c0008t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0007c0011t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0007c0011t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0008c0009t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0009c0010t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0010c0012t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0011c0019t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0012c0014t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0013c0016t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0014c0022t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0015c0017t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0016c0023t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0017c0015t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| a0018c0013t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0059 | EUR | GBR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | FIN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0023 | EUR | FIN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0262 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00597 | hp1 | a0004 | c0005 | t0001 | g0285 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0047 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00642 | hp1 | a0005 | c0006 | t0001 | g0194 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00735 | hp1 | a0005 | c0006 | t0001 | g0295 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0092 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01074 | hp1 | a0007 | c0011 | t0001 | g0148 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01109 | hp1 | a0001 | c0004 | t0002 | g0033 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01167 | hp1 | a0001 | c0007 | t0001 | g0238 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0302 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01168 | hp1 | a0001 | c0007 | t0001 | g0016 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01168 | hp2 | a0005 | c0006 | t0001 | g0297 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01243 | hp1 | a0001 | c0004 | t0001 | g0139 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01256 | hp1 | a0001 | c0007 | t0001 | g0248 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01257 | hp1 | a0003 | c0003 | t0001 | g0044 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01258 | hp2 | a0003 | c0003 | t0001 | g0044 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01261 | hp2 | a0001 | c0007 | t0001 | g0016 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01358 | hp2 | a0001 | c0007 | t0001 | g0237 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01361 | hp1 | a0005 | c0006 | t0001 | g0241 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0101 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01496 | hp1 | a0001 | c0004 | t0002 | g0136 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01516 | hp1 | a0005 | c0006 | t0001 | g0012 | EUR | IBS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01516 | hp2 | a0001 | c0007 | t0001 | g0247 | EUR | IBS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01517 | hp1 | a0005 | c0006 | t0001 | g0012 | EUR | IBS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | IBS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01884 | hp2 | a0001 | c0004 | t0002 | g0033 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01934 | hp1 | a0005 | c0006 | t0001 | g0012 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0052 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0303 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02004 | hp2 | a0001 | c0007 | t0001 | g0243 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02040 | hp1 | a0006 | c0008 | t0001 | g0165 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02055 | hp1 | a0010 | c0012 | t0001 | g0072 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0131 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02148 | hp1 | a0004 | c0005 | t0001 | g0050 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0218 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02451 | hp1 | a0001 | c0004 | t0001 | g0268 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0132 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02572 | hp1 | a0008 | c0009 | t0001 | g0032 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0251 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0068 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0085 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02615 | hp2 | a0012 | c0014 | t0001 | g0142 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02622 | hp1 | a0001 | c0004 | t0002 | g0135 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0030 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0133 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0111 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02698 | hp2 | a0006 | c0008 | t0001 | g0216 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02738 | hp1 | a0001 | c0004 | t0001 | g0206 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0120 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0030 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0146 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0127 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0222 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0037 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02965 | hp2 | a0013 | c0016 | t0001 | g0006 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0128 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0219 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03017 | hp2 | a0002 | c0020 | t0001 | g0265 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0081 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03098 | hp1 | a0008 | c0009 | t0001 | g0032 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0037 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0119 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0144 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03239 | hp2 | a0005 | c0006 | t0001 | g0242 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03486 | hp1 | a0001 | c0004 | t0002 | g0137 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0122 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0273 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0145 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0221 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0115 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0256 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0025 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03710 | hp2 | a0005 | c0006 | t0001 | g0245 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03831 | hp1 | a0001 | c0004 | t0001 | g0205 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03831 | hp2 | a0001 | c0007 | t0001 | g0246 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0094 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03927 | hp1 | a0006 | c0008 | t0001 | g0155 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03927 | hp2 | a0005 | c0006 | t0001 | g0012 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0071 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG04204 | hp1 | a0005 | c0006 | t0001 | g0298 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0104 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG04228 | hp2 | a0006 | c0008 | t0001 | g0166 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | YRI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0269 | AFR | YRI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18747 | hp2 | a0004 | c0005 | t0001 | g0287 | EAS | CHB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0134 | AFR | YRI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18942 | hp2 | a0004 | c0005 | t0001 | g0051 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18948 | hp1 | a0004 | c0005 | t0001 | g0050 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18950 | hp1 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18959 | hp1 | a0015 | c0017 | t0001 | g0301 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18961 | hp2 | a0004 | c0005 | t0001 | g0292 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18962 | hp1 | a0003 | c0003 | t0001 | g0258 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18964 | hp2 | a0003 | c0003 | t0001 | g0255 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18968 | hp1 | a0003 | c0003 | t0001 | g0047 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18973 | hp2 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18978 | hp2 | a0004 | c0005 | t0001 | g0051 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18981 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18982 | hp1 | a0004 | c0005 | t0001 | g0028 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18983 | hp2 | a0009 | c0010 | t0003 | g0039 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18984 | hp2 | a0003 | c0003 | t0001 | g0252 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18985 | hp2 | a0003 | c0003 | t0001 | g0264 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18986 | hp1 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18987 | hp1 | a0004 | c0005 | t0001 | g0288 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18990 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18991 | hp1 | a0003 | c0003 | t0001 | g0257 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18991 | hp2 | a0004 | c0005 | t0001 | g0274 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18992 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18994 | hp2 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19001 | hp1 | a0003 | c0003 | t0001 | g0254 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19002 | hp1 | a0016 | c0023 | t0001 | g0286 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0261 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19003 | hp1 | a0003 | c0003 | t0001 | g0253 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19005 | hp2 | a0017 | c0015 | t0001 | g0289 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19006 | hp2 | a0004 | c0005 | t0001 | g0290 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19010 | hp2 | a0003 | c0003 | t0001 | g0250 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0130 | AFR | LWK | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0124 | AFR | LWK | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | LWK | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0121 | AFR | LWK | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19057 | hp1 | a0003 | c0003 | t0001 | g0260 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19058 | hp1 | a0004 | c0005 | t0001 | g0190 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19060 | hp1 | a0004 | c0005 | t0001 | g0291 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19064 | hp1 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19068 | hp2 | a0009 | c0010 | t0003 | g0039 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19074 | hp1 | a0003 | c0003 | t0001 | g0228 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19077 | hp1 | a0003 | c0003 | t0001 | g0259 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19083 | hp2 | a0004 | c0005 | t0001 | g0293 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19087 | hp2 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0249 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19090 | hp1 | a0003 | c0003 | t0001 | g0263 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0204 | AFR | YRI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA19240 | hp2 | a0018 | c0013 | t0001 | g0272 | AFR | YRI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA20752 | hp1 | a0001 | c0007 | t0001 | g0016 | EUR | TSI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA20752 | hp2 | a0005 | c0006 | t0001 | g0296 | EUR | TSI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA20805 | hp1 | a0001 | c0007 | t0001 | g0266 | EUR | TSI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01123 | hp1 | a0005 | c0006 | t0001 | g0299 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0109 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02109 | hp1 | a0011 | c0019 | t0001 | g0197 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03471 | hp1 | a0001 | c0018 | t0001 | g0143 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG03471 | hp2 | a0014 | c0022 | t0001 | g0188 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG06807 | hp1 | a0007 | c0011 | t0001 | g0150 | AFR | USA | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0126 | AFR | USA | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA18955 | hp2 | a0004 | c0005 | t0001 | g0028 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0267 | AFR | USA | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | LWK | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0294 | AFR | LWK | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| homoSapiens | chm13v2 | a0001 | c0021 | t0001 | g0229 | REF | REF | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0031 | REF | REF | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96879693 | A | C | 1 | a0016 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.8A>C | p.His3Pro | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/19 | 158/5131 | 8/2883 | 3/960 | chr5 | 96879693 | |||
| chr5:96879773 | C | T | 1 | a0014 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.88C>T | p.Pro30Ser | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/19 | 238/5131 | 88/2883 | 30/960 | chr5 | 96879773 | |||
| chr5:96880043 | G | C | 1 | a0010 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.358G>C | p.Ala120Pro | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/19 | 508/5131 | 358/2883 | 120/960 | chr5 | 96880043 | |||
| chr5:96883830 | G | A | 1 | a0018 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.614G>A | p.Arg205His | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/19 | 764/5131 | 614/2883 | 205/960 | chr5 | 96883830 | |||
| chr5:96883857 | C | T | 1 | a0003 | 30 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(27): Show |
missense_variant | MODERATE | c.641C>T | p.Pro214Leu | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/19 | 791/5131 | 641/2883 | 214/960 | chr5 | 96883857 | |||
| chr5:96886656 | T | C | 1 | a0012 | 1 | HG02615.hp2 | missense_variant&splice_region_variant | MODERATE | c.716T>C | p.Val239Ala | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/19 | 866/5131 | 716/2883 | 239/960 | chr5 | 96886656 | |||
| chr5:96889200 | T | G | 3 | a0004 a0016 a0017 |
17 | HG00597.hp1 HG02148.hp1 NA18747.hp2 others(14): Show |
missense_variant | MODERATE | c.865T>G | p.Ser289Ala | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/19 | 1015/5131 | 865/2883 | 289/960 | chr5 | 96889200 | |||
| chr5:96892368 | C | T | 1 | a0007 | 2 | HG01074.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.1040C>T | p.Thr347Met | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/19 | 1190/5131 | 1040/2883 | 347/960 | chr5 | 96892368 | |||
| chr5:96892446 | C | A | 1 | a0013 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.1118C>A | p.Ala373Glu | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/19 | 1268/5131 | 1118/2883 | 373/960 | chr5 | 96892446 | |||
| chr5:96895296 | G | T | 9 | a0001 a0006 a0007 others(6): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
missense_variant | MODERATE | c.1176G>T | p.Lys392Asn | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/19 | 1326/5131 | 1176/2883 | 392/960 | chr5 | 96895296 | |||
| chr5:96895339 | A | G | 1 | a0015 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1219A>G | p.Thr407Ala | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/19 | 1369/5131 | 1219/2883 | 407/960 | chr5 | 96895339 | |||
| chr5:96901626 | C | T | 1 | a0011 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1693C>T | p.Arg565Cys | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/19 | 1843/5131 | 1693/2883 | 565/960 | chr5 | 96901626 | |||
| chr5:96903530 | G | T | 2 | a0008 a0010 |
3 | HG02055.hp1 HG02572.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.1982G>T | p.Gly661Val | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/19 | 2132/5131 | 1982/2883 | 661/960 | chr5 | 96903530 | |||
| chr5:96903554 | T | A | 1 | a0005 | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
missense_variant | MODERATE | c.2006T>A | p.Leu669Gln | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/19 | 2156/5131 | 2006/2883 | 669/960 | chr5 | 96903554 | |||
| chr5:96909661 | C | T | 1 | a0006 | 4 | HG02040.hp1 HG02698.hp2 HG03927.hp1 others(1): Show |
missense_variant | MODERATE | c.2251C>T | p.Arg751Cys | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/19 | 2401/5131 | 2251/2883 | 751/960 | chr5 | 96909661 | |||
| chr5:96912223 | TGCCTTCA others(9786): Show |
T | 1 | a0009 | 2 | NA18983.hp2 NA19068.hp2 |
exon_loss_variant | HIGH | c.2355-413_*4411del | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/19 | chr5 | 96912223 | |||||||
| chr5:96912792 | T | C | 1 | a0002 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.2510T>C | p.Leu837Ser | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/19 | 2660/5131 | 2510/2883 | 837/960 | chr5 | 96912792 | |||
| chr5:96917577 | T | C | 1 | a0018 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.2855T>C | p.Leu952Pro | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 3005/5131 | 2855/2883 | 952/960 | chr5 | 96917577 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96879976 | C | T | 2 | a0001c0007 a0002c0020 |
11 | HG01167.hp1 HG01168.hp1 HG01256.hp1 others(8): Show |
synonymous_variant | LOW | c.291C>T | p.Ile97Ile | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/19 | 441/5131 | 291/2883 | 97/960 | chr5 | 96879976 | |||
| chr5:96896438 | T | A | 12 | a0001c0001 a0001c0004 a0001c0007 others(9): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
synonymous_variant | LOW | c.1305T>A | p.Pro435Pro | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 8/19 | 1455/5131 | 1305/2883 | 435/960 | chr5 | 96896438 | |||
| chr5:96901622 | G | A | 12 | a0001c0001 a0001c0004 a0001c0007 others(9): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
synonymous_variant | LOW | c.1689G>A | p.Gln563Gln | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/19 | 1839/5131 | 1689/2883 | 563/960 | chr5 | 96901622 | |||
| chr5:96909015 | T | C | 1 | a0005c0006 | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
synonymous_variant | LOW | c.2067T>C | p.His689His | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 14/19 | 2217/5131 | 2067/2883 | 689/960 | chr5 | 96909015 | |||
| chr5:96909030 | C | T | 1 | a0001c0018 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.2082C>T | p.Pro694Pro | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 14/19 | 2232/5131 | 2082/2883 | 694/960 | chr5 | 96909030 | |||
| chr5:96909639 | C | T | 11 | a0001c0001 a0001c0007 a0001c0018 others(8): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
synonymous_variant | LOW | c.2229C>T | p.Gly743Gly | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/19 | 2379/5131 | 2229/2883 | 743/960 | chr5 | 96909639 | |||
| chr5:96909735 | C | T | 12 | a0001c0001 a0001c0004 a0001c0007 others(9): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
synonymous_variant | LOW | c.2325C>T | p.Ser775Ser | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/19 | 2475/5131 | 2325/2883 | 775/960 | chr5 | 96909735 | |||
| chr5:96913411 | C | T | 11 | a0001c0001 a0001c0004 a0001c0007 others(8): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
synonymous_variant | LOW | c.2611C>T | p.Leu871Leu | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/19 | 2761/5131 | 2611/2883 | 871/960 | chr5 | 96913411 | |||
| chr5:96915724 | C | T | 1 | a0001c0001 | 2 | NA18985.hp1 NA19063.hp1 |
synonymous_variant | LOW | c.2694C>T | p.Ile898Ile | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/19 | 2844/5131 | 2694/2883 | 898/960 | chr5 | 96915724 | |||
| chr5:96917527 | G | A | 1 | a0004c0005 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.2805G>A | p.Leu935Leu | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 2955/5131 | 2805/2883 | 935/960 | chr5 | 96917527 | |||
| chr5:96917572 | G | A | 1 | a0001c0001 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.2850G>A | p.Pro950Pro | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 3000/5131 | 2850/2883 | 950/960 | chr5 | 96917572 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96879641 | C | T | 1 | a0001c0004t0002 | 5 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-45C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/19 | chr5 | 96879641 | |||||||
| chr5:96917679 | G | A | 1 | a0002c0002t0001 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*74G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 74 | chr5 | 96917679 | ||||||
| chr5:96917681 | C | T | 1 | a0001c0004t0001 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*76C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 76 | chr5 | 96917681 | ||||||
| chr5:96917744 | A | G | 3 | a0002c0002t0001 a0003c0003t0001 a0005c0006t0001 |
51 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*139A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 139 | chr5 | 96917744 | ||||||
| chr5:96917859 | T | C | 1 | a0001c0001t0001 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 254 | chr5 | 96917859 | ||||||
| chr5:96917905 | C | CA | 8 | a0001c0001t0001 a0001c0004t0001 a0001c0004t0002 others(5): Show |
58 | HG00544.hp1 HG00597.hp1 HG01109.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*323dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 324 | INFO_REALIGN_3_PRIME | chr5 | 96917905 | |||||
| chr5:96917905 | C | CAA | 6 | a0001c0004t0001 a0002c0002t0001 a0003c0003t0001 others(3): Show |
18 | HG00642.hp1 HG01123.hp1 HG01168.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*322_*323dupAA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 324 | INFO_REALIGN_3_PRIME | chr5 | 96917905 | |||||
| chr5:96917905 | C | CAAA | 3 | a0002c0002t0001 a0003c0003t0001 a0005c0006t0001 |
31 | HG00558.hp2 HG00609.hp1 HG00735.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*321_*323dupAAA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 324 | INFO_REALIGN_3_PRIME | chr5 | 96917905 | |||||
| chr5:96917905 | C | CAAAA | 2 | a0002c0002t0001 a0003c0003t0001 |
7 | HG01243.hp2 HG02647.hp1 HG03130.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*320_*323dupAAAA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 324 | INFO_REALIGN_3_PRIME | chr5 | 96917905 | |||||
| chr5:96917905 | CAAAAAAA others(5): Show |
C | 1 | a0002c0002t0001 | 2 | NA18949.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*312_*323delAAAAAA others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 312 | INFO_REALIGN_3_PRIME | chr5 | 96917905 | |||||
| chr5:96917922 | A | G | 1 | a0001c0001t0001 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*317A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 317 | chr5 | 96917922 | ||||||
| chr5:96917923 | A | G | 1 | a0001c0001t0001 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*318A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 318 | chr5 | 96917923 | ||||||
| chr5:96918486 | T | C | 1 | a0001c0004t0001 | 7 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*881T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 881 | chr5 | 96918486 | ||||||
| chr5:96918505 | A | G | 12 | a0001c0004t0001 a0001c0004t0002 a0002c0002t0001 others(9): Show |
217 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*900A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 900 | chr5 | 96918505 | ||||||
| chr5:96918597 | A | G | 3 | a0002c0002t0001 a0003c0003t0001 a0005c0006t0001 |
51 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*992A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 992 | chr5 | 96918597 | ||||||
| chr5:96918650 | T | A | 12 | a0001c0004t0001 a0001c0004t0002 a0002c0002t0001 others(9): Show |
217 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1045T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1045 | chr5 | 96918650 | ||||||
| chr5:96918795 | C | T | 1 | a0002c0002t0001 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1190C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1190 | chr5 | 96918795 | ||||||
| chr5:96918881 | AC | A | 3 | a0001c0004t0001 a0002c0002t0001 a0015c0017t0001 |
7 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1282delC | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1282 | INFO_REALIGN_3_PRIME | chr5 | 96918881 | |||||
| chr5:96918945 | T | A | 2 | a0001c0004t0001 a0001c0004t0002 |
17 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1340T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1340 | chr5 | 96918945 | ||||||
| chr5:96919025 | C | T | 1 | a0002c0002t0001 | 5 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1420C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1420 | chr5 | 96919025 | ||||||
| chr5:96919113 | G | A | 12 | a0001c0004t0001 a0001c0004t0002 a0002c0002t0001 others(9): Show |
217 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1508G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1508 | chr5 | 96919113 | ||||||
| chr5:96919175 | A | C | 1 | a0008c0009t0001 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1570A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1570 | chr5 | 96919175 | ||||||
| chr5:96919290 | T | A | 1 | a0005c0006t0001 | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1685T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1685 | chr5 | 96919290 | ||||||
| chr5:96919313 | T | C | 3 | a0002c0002t0001 a0003c0003t0001 a0005c0006t0001 |
51 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1708T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1708 | chr5 | 96919313 | ||||||
| chr5:96919548 | T | C | 1 | a0001c0004t0001 | 2 | HG02738.hp1 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1943T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1943 | chr5 | 96919548 | ||||||
| chr5:96919627 | A | G | 1 | a0001c0001t0001 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2022A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 2022 | chr5 | 96919627 | ||||||
| chr5:96919649 | T | C | 1 | a0002c0002t0001 | 4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2044T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 2044 | chr5 | 96919649 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96876861 | C | T | 4 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(1): Show |
5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-123+334C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96876861 | |||||||
| chr5:96876933 | A | G | 7 | a0001c0001t0001g0300 a0005c0006t0001g0012 a0005c0006t0001g0295 others(4): Show |
10 | HG00735.hp1 HG01123.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-123+406A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96876933 | |||||||
| chr5:96876999 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-123+472G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96876999 | |||||||
| chr5:96877006 | G | A | 2 | a0002c0002t0001g0054 a0002c0002t0001g0055 |
2 | HG00423.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.-123+479G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877006 | |||||||
| chr5:96877013 | C | T | 1 | a0002c0002t0001g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-123+486C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877013 | |||||||
| chr5:96877037 | C | T | 23 | a0001c0001t0001g0011 a0001c0001t0001g0275 a0001c0001t0001g0276 others(20): Show |
28 | HG00597.hp1 HG00597.hp2 HG02148.hp1 others(25): Show |
intron_variant | MODIFIER | c.-123+510C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877037 | |||||||
| chr5:96877077 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
215 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.-123+550C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877077 | |||||||
| chr5:96877136 | G | A | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0140 others(10): Show |
17 | HG00738.hp1 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-123+609G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877136 | |||||||
| chr5:96877191 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
214 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.-123+664T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877191 | |||||||
| chr5:96877241 | C | G | 9 | a0001c0001t0001g0049 a0001c0001t0001g0270 a0001c0001t0001g0271 others(6): Show |
10 | HG02451.hp1 HG02559.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-123+714C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877241 | |||||||
| chr5:96877355 | G | T | 1 | a0001c0004t0001g0273 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-123+828G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877355 | |||||||
| chr5:96877423 | C | CA | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
215 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.-123+896_-123+897i others(3): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877423 | |||||||
| chr5:96877426 | G | T | 6 | a0001c0004t0001g0133 a0001c0004t0001g0134 a0001c0004t0002g0033 others(3): Show |
7 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-123+899G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877426 | |||||||
| chr5:96877467 | C | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
215 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.-123+940C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877467 | |||||||
| chr5:96877536 | C | T | 1 | a0001c0004t0001g0273 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-123+1009C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877536 | |||||||
| chr5:96877629 | A | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
215 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.-123+1102A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877629 | |||||||
| chr5:96877682 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-123+1155T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877682 | |||||||
| chr5:96877683 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-123+1156C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877683 | |||||||
| chr5:96877731 | A | AT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
215 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.-123+1212dupT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 96877731 | ||||||
| chr5:96877766 | A | G | 11 | a0001c0001t0001g0300 a0002c0002t0001g0052 a0002c0002t0001g0302 others(8): Show |
15 | HG00735.hp1 HG00738.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.-123+1239A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877766 | |||||||
| chr5:96877812 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-123+1285T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877812 | |||||||
| chr5:96877857 | C | CTTTA | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
215 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.-123+1331_-123+133 others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 96877857 | ||||||
| chr5:96877903 | G | T | 46 | a0001c0001t0001g0147 a0001c0001t0001g0230 a0001c0001t0001g0231 others(43): Show |
55 | HG00280.hp2 HG00558.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-123+1376G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877903 | |||||||
| chr5:96878111 | G | A | 1 | a0002c0002t0001g0057 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-122-1453G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878111 | |||||||
| chr5:96878222 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
215 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.-122-1342G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878222 | |||||||
| chr5:96878228 | T | TA | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
215 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.-122-1329dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 96878228 | ||||||
| chr5:96878311 | C | T | 5 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-122-1253C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878311 | |||||||
| chr5:96878404 | G | GTAA | 265 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(262): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.-122-1151_-122-114 others(7): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 96878404 | ||||||
| chr5:96878432 | T | C | 8 | a0001c0001t0001g0049 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
9 | HG02451.hp1 HG02559.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-122-1132T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878432 | |||||||
| chr5:96878478 | A | G | 4 | a0001c0001t0001g0129 a0001c0004t0001g0130 a0001c0004t0001g0131 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-1086A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878478 | |||||||
| chr5:96878513 | C | T | 18 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0207 others(15): Show |
19 | HG01192.hp1 HG01358.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.-122-1051C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878513 | |||||||
| chr5:96878536 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
157 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.-122-1028G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878536 | |||||||
| chr5:96878621 | T | C | 3 | a0001c0004t0001g0139 a0002c0002t0001g0034 a0002c0002t0001g0138 |
4 | HG01243.hp1 HG01243.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-122-943T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878621 | |||||||
| chr5:96878803 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
215 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.-122-761C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878803 | |||||||
| chr5:96878877 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
215 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.-122-687A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878877 | |||||||
| chr5:96878955 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
237 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.-122-609G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878955 | |||||||
| chr5:96879084 | C | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0056 a0001c0001t0001g0118 others(3): Show |
8 | HG00280.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-122-480C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96879084 | |||||||
| chr5:96879107 | T | C | 6 | a0001c0004t0001g0133 a0001c0004t0001g0134 a0001c0004t0002g0033 others(3): Show |
7 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-122-457T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96879107 | |||||||
| chr5:96879227 | C | T | 1 | a0002c0002t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-122-337C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96879227 | |||||||
| chr5:96879382 | A | G | 2 | a0001c0004t0001g0205 a0001c0004t0001g0206 |
2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-122-182A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96879382 | |||||||
| chr5:96880372 | T | C | 6 | a0001c0004t0001g0133 a0001c0004t0001g0134 a0001c0004t0002g0033 others(3): Show |
7 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.575+112T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96880372 | |||||||
| chr5:96880469 | A | G | 45 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(42): Show |
54 | HG00280.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.575+209A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96880469 | |||||||
| chr5:96880513 | T | C | 15 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0147 others(12): Show |
16 | HG01175.hp1 HG01192.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.575+253T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96880513 | |||||||
| chr5:96880609 | A | T | 2 | a0001c0004t0001g0030 a0001c0004t0001g0120 |
3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.575+349A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96880609 | |||||||
| chr5:96880683 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
215 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.575+423A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96880683 | |||||||
| chr5:96880695 | GA | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
128 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.575+438delA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 96880695 | ||||||
| chr5:96880705 | A | T | 1 | a0002c0002t0001g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.575+445A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96880705 | |||||||
| chr5:96880920 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.575+660T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96880920 | |||||||
| chr5:96881043 | A | C | 4 | a0001c0004t0002g0033 a0001c0004t0002g0135 a0001c0004t0002g0136 others(1): Show |
5 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.575+783A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881043 | |||||||
| chr5:96881080 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
194 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.575+820G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881080 | |||||||
| chr5:96881189 | GCT | G | 28 | a0001c0001t0001g0011 a0001c0001t0001g0129 a0001c0001t0001g0275 others(25): Show |
34 | HG00597.hp1 HG00597.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.575+932_575+933del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 96881189 | ||||||
| chr5:96881200 | T | C | 1 | a0003c0003t0001g0228 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.575+940T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881200 | |||||||
| chr5:96881337 | C | T | 1 | a0001c0007t0001g0266 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.575+1077C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881337 | |||||||
| chr5:96881445 | C | T | 2 | a0002c0002t0001g0116 a0002c0002t0001g0117 |
2 | NA18994.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.575+1185C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881445 | |||||||
| chr5:96881591 | T | G | 1 | a0002c0002t0001g0059 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.575+1331T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881591 | |||||||
| chr5:96881642 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0191 others(3): Show |
13 | HG02258.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.575+1382A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881642 | |||||||
| chr5:96881686 | A | G | 24 | a0001c0001t0001g0011 a0001c0001t0001g0275 a0001c0001t0001g0276 others(21): Show |
30 | HG00597.hp1 HG00597.hp2 HG02148.hp1 others(27): Show |
intron_variant | MODIFIER | c.575+1426A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881686 | |||||||
| chr5:96881988 | G | GA | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
275 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.575+1730dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 96881988 | ||||||
| chr5:96882068 | C | G | 1 | a0004c0005t0001g0293 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.576-1724C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882068 | |||||||
| chr5:96882087 | G | A | 1 | a0007c0011t0001g0148 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.576-1705G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882087 | |||||||
| chr5:96882346 | G | T | 2 | a0004c0005t0001g0291 a0004c0005t0001g0292 |
2 | NA18961.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.576-1446G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882346 | |||||||
| chr5:96882389 | G | T | 1 | a0002c0002t0001g0115 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.576-1403G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882389 | |||||||
| chr5:96882429 | A | G | 14 | a0001c0004t0001g0037 a0001c0004t0001g0130 a0001c0004t0001g0131 others(11): Show |
16 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.576-1363A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882429 | |||||||
| chr5:96882464 | C | T | 4 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(1): Show |
5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.576-1328C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882464 | |||||||
| chr5:96882660 | C | T | 1 | a0002c0002t0001g0189 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.576-1132C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882660 | |||||||
| chr5:96882787 | TC | T | 11 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(8): Show |
15 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.576-1002delC | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 96882787 | ||||||
| chr5:96882844 | C | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0195 a0001c0001t0001g0223 others(2): Show |
6 | HG01975.hp2 HG01981.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.576-948C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882844 | |||||||
| chr5:96882894 | C | T | 59 | a0001c0004t0001g0030 a0001c0004t0001g0120 a0002c0002t0001g0034 others(56): Show |
75 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.576-898C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882894 | |||||||
| chr5:96882913 | A | T | 1 | a0002c0002t0001g0121 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.576-879A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882913 | |||||||
| chr5:96882962 | G | C | 2 | a0002c0002t0001g0034 a0002c0002t0001g0138 |
3 | HG01243.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.576-830G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882962 | |||||||
| chr5:96883034 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.576-758A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96883034 | |||||||
| chr5:96883173 | G | T | 36 | a0001c0004t0001g0030 a0001c0004t0001g0120 a0002c0002t0001g0034 others(33): Show |
45 | HG00597.hp1 HG00642.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.576-619G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96883173 | |||||||
| chr5:96883464 | A | G | 1 | a0002c0002t0001g0114 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.576-328A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96883464 | |||||||
| chr5:96883469 | T | G | 11 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(8): Show |
15 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.576-323T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96883469 | |||||||
| chr5:96883569 | G | A | 1 | a0002c0002t0001g0064 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.576-223G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96883569 | |||||||
| chr5:96883691 | C | A | 2 | a0003c0003t0001g0249 a0003c0003t0001g0250 |
2 | NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.576-101C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96883691 | |||||||
| chr5:96884034 | T | TTATC | 57 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0027 others(54): Show |
73 | HG00558.hp2 HG00609.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.714+149_714+152dup others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884034 | ||||||
| chr5:96884034 | TTATC | T | 90 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(87): Show |
123 | HG00423.hp1 HG00558.hp1 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.714+149_714+152del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884034 | ||||||
| chr5:96884034 | TTATCTAT others(1): Show |
T | 29 | a0001c0001t0001g0042 a0001c0001t0001g0056 a0001c0001t0001g0060 others(26): Show |
33 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.714+145_714+152del others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884034 | ||||||
| chr5:96884034 | TTATCTAT others(5): Show |
T | 38 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0040 others(35): Show |
45 | HG00280.hp1 HG00597.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.714+141_714+152del others(12): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884034 | ||||||
| chr5:96884034 | TTATCTAT others(13): Show |
T | 1 | a0001c0001t0001g0010 | 4 | HG00140.hp1 HG00735.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+133_714+152del others(20): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884034 | ||||||
| chr5:96884075 | T | A | 3 | a0001c0004t0001g0030 a0001c0004t0001g0120 a0002c0002t0001g0294 |
4 | HG02622.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+145T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96884075 | |||||||
| chr5:96884079 | T | A | 3 | a0001c0004t0001g0030 a0001c0004t0001g0120 a0002c0002t0001g0294 |
4 | HG02622.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+149T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96884079 | |||||||
| chr5:96884146 | CT | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.714+225delT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884146 | ||||||
| chr5:96884383 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
275 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.714+453C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96884383 | |||||||
| chr5:96884555 | T | TTTTGTTT others(1): Show |
151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.714+637_714+644dup others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884555 | ||||||
| chr5:96884555 | T | TTTTGTTT others(5): Show |
4 | a0001c0001t0001g0270 a0001c0004t0001g0205 a0001c0004t0001g0206 others(1): Show |
4 | HG02738.hp1 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+633_714+644dup others(12): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884555 | ||||||
| chr5:96884566 | T | C | 1 | a0002c0002t0001g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.714+636T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96884566 | |||||||
| chr5:96884667 | C | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0185 |
2 | NA18939.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.714+737C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96884667 | |||||||
| chr5:96884764 | T | A | 4 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(1): Show |
5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+834T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96884764 | |||||||
| chr5:96884825 | T | C | 1 | a0004c0005t0001g0190 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.714+895T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96884825 | |||||||
| chr5:96884962 | T | TG | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.714+1033dupG | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884962 | ||||||
| chr5:96885133 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.714+1203C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885133 | |||||||
| chr5:96885307 | C | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.715-1348C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885307 | |||||||
| chr5:96885371 | G | A | 7 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0295 others(4): Show |
10 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.715-1284G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885371 | |||||||
| chr5:96885637 | C | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.715-1018C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885637 | |||||||
| chr5:96885721 | AGGAGTTG others(9): Show |
A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0199 a0011c0019t0001g0197 |
4 | HG01106.hp2 HG01257.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-933_715-918del others(16): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885721 | |||||||
| chr5:96885722 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.715-933G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885722 | |||||||
| chr5:96885738 | T | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0199 a0011c0019t0001g0197 |
4 | HG01106.hp2 HG01257.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-917T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885738 | |||||||
| chr5:96885763 | G | T | 4 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0283 others(1): Show |
4 | NA18946.hp2 NA18961.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-892G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885763 | |||||||
| chr5:96885832 | G | A | 4 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-823G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885832 | |||||||
| chr5:96885861 | C | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.715-794C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885861 | |||||||
| chr5:96886049 | A | G | 1 | a0002c0002t0001g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.715-606A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886049 | |||||||
| chr5:96886109 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.715-546T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886109 | |||||||
| chr5:96886180 | C | T | 1 | a0001c0004t0001g0273 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.715-475C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886180 | |||||||
| chr5:96886185 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.715-470A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886185 | |||||||
| chr5:96886281 | G | A | 2 | a0001c0004t0001g0030 a0001c0004t0001g0120 |
3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.715-374G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886281 | |||||||
| chr5:96886316 | A | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.715-339A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886316 | |||||||
| chr5:96886316 | A | G | 23 | a0003c0003t0001g0017 a0003c0003t0001g0044 a0003c0003t0001g0045 others(20): Show |
30 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.715-339A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886316 | |||||||
| chr5:96886479 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.715-176A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886479 | |||||||
| chr5:96886481 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.715-174C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886481 | |||||||
| chr5:96886808 | G | A | 4 | a0001c0004t0001g0267 a0001c0004t0001g0268 a0001c0004t0001g0269 others(1): Show |
4 | HG02451.hp1 HG03540.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+19G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96886808 | |||||||
| chr5:96886815 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0060 |
2 | HG00323.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.849+26G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96886815 | |||||||
| chr5:96886849 | TTTG | T | 11 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(8): Show |
15 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.849+63_849+65delGT others(1): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96886849 | ||||||
| chr5:96886920 | T | G | 4 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(1): Show |
5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+131T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96886920 | |||||||
| chr5:96886923 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.849+134G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96886923 | |||||||
| chr5:96887060 | G | A | 1 | a0003c0003t0001g0046 | 2 | NA18973.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.849+271G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887060 | |||||||
| chr5:96887072 | A | AGT | 14 | a0001c0004t0001g0037 a0001c0004t0001g0130 a0001c0004t0001g0131 others(11): Show |
16 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.849+284_849+285dup others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887072 | ||||||
| chr5:96887073 | G | GTA | 49 | a0001c0001t0001g0077 a0002c0002t0001g0002 a0002c0002t0001g0007 others(46): Show |
72 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.849+311_849+312dup others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887073 | ||||||
| chr5:96887073 | G | GTATA | 16 | a0001c0001t0001g0027 a0002c0002t0001g0018 a0002c0002t0001g0026 others(13): Show |
19 | HG01192.hp1 HG02083.hp2 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.849+309_849+312dup others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887073 | ||||||
| chr5:96887073 | G | GTATATA | 7 | a0002c0002t0001g0023 a0002c0002t0001g0059 a0002c0002t0001g0082 others(4): Show |
8 | HG00140.hp2 HG00323.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.849+307_849+312dup others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887073 | ||||||
| chr5:96887073 | G | GTATATAT others(1): Show |
3 | a0002c0002t0001g0083 a0002c0002t0001g0112 a0002c0002t0001g0113 |
3 | NA18972.hp1 NA18977.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.849+305_849+312dup others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887073 | ||||||
| chr5:96887073 | GTATA | G | 6 | a0001c0001t0001g0184 a0001c0007t0001g0243 a0005c0006t0001g0241 others(3): Show |
6 | HG01361.hp1 HG02004.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+309_849+312del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887073 | ||||||
| chr5:96887075 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.849+286A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887075 | |||||||
| chr5:96887077 | A | G | 1 | a0001c0004t0001g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.849+288A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887077 | |||||||
| chr5:96887079 | A | G | 6 | a0001c0001t0001g0184 a0001c0007t0001g0243 a0005c0006t0001g0241 others(3): Show |
6 | HG01361.hp1 HG02004.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+290A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887079 | |||||||
| chr5:96887094 | T | C | 28 | a0001c0001t0001g0011 a0001c0001t0001g0043 a0001c0001t0001g0053 others(25): Show |
32 | HG00597.hp2 HG01175.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.849+305T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887094 | |||||||
| chr5:96887094 | TATATATA others(1): Show |
T | 6 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0295 others(3): Show |
9 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.849+307_849+314del others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887094 | ||||||
| chr5:96887094 | TATATATA others(3): Show |
T | 1 | a0005c0006t0001g0298 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.849+307_849+316del others(10): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887094 | ||||||
| chr5:96887096 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.849+307T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887096 | |||||||
| chr5:96887096 | TATATACA others(3): Show |
T | 1 | a0002c0002t0001g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.849+309_849+318del others(10): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887096 | ||||||
| chr5:96887098 | TATAC | T | 2 | a0002c0002t0001g0034 a0002c0002t0001g0138 |
3 | HG01243.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.849+311_849+314del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887098 | ||||||
| chr5:96887098 | TATACAC | T | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 |
3 | HG02559.hp2 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.849+311_849+316del others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887098 | ||||||
| chr5:96887098 | TATACACA others(3): Show |
T | 1 | a0004c0005t0001g0274 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.849+311_849+320del others(10): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887098 | ||||||
| chr5:96887100 | T | C | 1 | a0002c0002t0001g0119 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.849+311T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887100 | |||||||
| chr5:96887100 | TAC | T | 7 | a0001c0004t0001g0030 a0001c0004t0001g0120 a0002c0002t0001g0086 others(4): Show |
9 | HG00558.hp2 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.849+337_849+338del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887100 | ||||||
| chr5:96887100 | TACAC | T | 4 | a0004c0005t0001g0050 a0004c0005t0001g0290 a0010c0012t0001g0072 others(1): Show |
5 | HG02055.hp1 HG02148.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+335_849+338del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887100 | ||||||
| chr5:96887100 | TACACAC | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.849+333_849+338del others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887100 | ||||||
| chr5:96887100 | TACACACA others(1): Show |
T | 3 | a0002c0002t0001g0052 a0002c0002t0001g0303 a0015c0017t0001g0301 |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+331_849+338del others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887100 | ||||||
| chr5:96887102 | C | T | 24 | a0001c0004t0001g0030 a0001c0004t0001g0205 a0001c0004t0001g0206 others(21): Show |
27 | HG01943.hp2 HG02056.hp2 HG02738.hp1 others(24): Show |
intron_variant | MODIFIER | c.849+313C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887102 | |||||||
| chr5:96887104 | C | T | 50 | a0001c0001t0001g0184 a0001c0004t0001g0030 a0001c0004t0001g0037 others(47): Show |
57 | HG00558.hp2 HG01109.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.849+315C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887104 | |||||||
| chr5:96887106 | C | T | 55 | a0001c0001t0001g0184 a0001c0004t0001g0030 a0001c0004t0001g0037 others(52): Show |
63 | HG00558.hp2 HG01109.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.849+317C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887106 | |||||||
| chr5:96887108 | C | T | 35 | a0002c0002t0001g0119 a0002c0002t0001g0302 a0003c0003t0001g0017 others(32): Show |
44 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.849+319C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887108 | |||||||
| chr5:96887110 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.849+321C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887110 | |||||||
| chr5:96887300 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.849+511C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887300 | |||||||
| chr5:96887303 | C | CT | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.849+529dupT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887303 | ||||||
| chr5:96887341 | G | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.849+552G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887341 | |||||||
| chr5:96887370 | G | A | 1 | a0002c0002t0001g0083 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.849+581G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887370 | |||||||
| chr5:96887396 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.849+607A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887396 | |||||||
| chr5:96887468 | T | G | 14 | a0004c0005t0001g0028 a0004c0005t0001g0050 a0004c0005t0001g0051 others(11): Show |
17 | HG00597.hp1 HG02148.hp1 NA18747.hp2 others(14): Show |
intron_variant | MODIFIER | c.849+679T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887468 | |||||||
| chr5:96887495 | T | C | 2 | a0002c0002t0001g0021 a0002c0002t0001g0100 |
3 | NA18960.hp2 NA18988.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.849+706T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887495 | |||||||
| chr5:96887588 | C | G | 2 | a0002c0002t0001g0034 a0002c0002t0001g0138 |
3 | HG01243.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.849+799C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887588 | |||||||
| chr5:96887596 | G | A | 1 | a0002c0002t0001g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.849+807G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887596 | |||||||
| chr5:96887598 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.849+809C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887598 | |||||||
| chr5:96887607 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0140 |
3 | HG00738.hp1 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.849+818A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887607 | |||||||
| chr5:96887724 | G | A | 3 | a0001c0004t0001g0030 a0001c0004t0001g0120 a0002c0002t0001g0294 |
4 | HG02622.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+935G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887724 | |||||||
| chr5:96887725 | C | T | 1 | a0001c0004t0001g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.849+936C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887725 | |||||||
| chr5:96887776 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.849+987A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887776 | |||||||
| chr5:96887810 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.849+1021A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887810 | |||||||
| chr5:96887848 | G | A | 24 | a0001c0001t0001g0011 a0001c0001t0001g0043 a0001c0001t0001g0053 others(21): Show |
28 | HG00597.hp2 HG01192.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.849+1059G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887848 | |||||||
| chr5:96888056 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.850-1129C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888056 | |||||||
| chr5:96888129 | G | GA | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.850-1045dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96888129 | ||||||
| chr5:96888163 | AAAAAG | A | 5 | a0002c0002t0001g0121 a0002c0002t0001g0219 a0002c0002t0001g0220 others(2): Show |
5 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-1017_850-1013d others(7): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96888163 | ||||||
| chr5:96888164 | A | AAG | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.850-1020_850-1019i others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96888164 | ||||||
| chr5:96888165 | A | G | 11 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(8): Show |
15 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.850-1020A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888165 | |||||||
| chr5:96888176 | T | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
228 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.850-1009T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888176 | |||||||
| chr5:96888210 | T | TA | 7 | a0002c0002t0001g0034 a0002c0002t0001g0121 a0002c0002t0001g0138 others(4): Show |
8 | HG01243.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-974dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96888210 | ||||||
| chr5:96888241 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.850-944T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888241 | |||||||
| chr5:96888417 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.850-768A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888417 | |||||||
| chr5:96888462 | T | C | 1 | a0002c0002t0001g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.850-723T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888462 | |||||||
| chr5:96888472 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.850-713A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888472 | |||||||
| chr5:96888613 | A | G | 1 | a0001c0004t0001g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.850-572A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888613 | |||||||
| chr5:96888626 | C | T | 10 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0007t0001g0016 others(7): Show |
12 | HG00323.hp1 HG01167.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-559C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888626 | |||||||
| chr5:96888767 | T | C | 7 | a0002c0002t0001g0034 a0002c0002t0001g0121 a0002c0002t0001g0138 others(4): Show |
8 | HG01243.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-418T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888767 | |||||||
| chr5:96888801 | T | C | 1 | a0002c0002t0001g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.850-384T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888801 | |||||||
| chr5:96888816 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.850-369G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888816 | |||||||
| chr5:96888866 | T | C | 7 | a0002c0002t0001g0034 a0002c0002t0001g0121 a0002c0002t0001g0138 others(4): Show |
8 | HG01243.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-319T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888866 | |||||||
| chr5:96888875 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.850-310C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888875 | |||||||
| chr5:96888902 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.850-283T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888902 | |||||||
| chr5:96888950 | A | T | 2 | a0001c0004t0001g0205 a0001c0004t0001g0206 |
2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.850-235A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888950 | |||||||
| chr5:96889005 | A | G | 7 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0295 others(4): Show |
10 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-180A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96889005 | |||||||
| chr5:96889122 | T | C | 1 | a0012c0014t0001g0142 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.850-63T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96889122 | |||||||
| chr5:96889375 | CTCTT | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0196 |
3 | HG01884.hp1 HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.970+74_970+77delTT others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96889375 | ||||||
| chr5:96889398 | G | C | 1 | a0003c0003t0001g0260 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.970+93G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889398 | |||||||
| chr5:96889423 | G | A | 1 | a0002c0002t0001g0007 | 4 | NA18970.hp2 NA18975.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.970+118G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889423 | |||||||
| chr5:96889548 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.970+243G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889548 | |||||||
| chr5:96889613 | G | A | 2 | a0002c0002t0001g0073 a0002c0002t0001g0109 |
2 | HG01123.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.970+308G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889613 | |||||||
| chr5:96889818 | A | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.970+513A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889818 | |||||||
| chr5:96889831 | T | TAC | 8 | a0002c0002t0001g0021 a0002c0002t0001g0068 a0002c0002t0001g0074 others(5): Show |
9 | HG01361.hp2 HG01934.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.970+557_970+558dup others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96889831 | ||||||
| chr5:96889831 | T | TACAC | 5 | a0002c0002t0001g0123 a0002c0002t0001g0219 a0002c0002t0001g0220 others(2): Show |
5 | HG01496.hp2 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.970+555_970+558dup others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96889831 | ||||||
| chr5:96889831 | TAC | T | 58 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0129 others(55): Show |
73 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.970+557_970+558del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96889831 | ||||||
| chr5:96889831 | TACAC | T | 17 | a0001c0001t0001g0213 a0001c0004t0001g0030 a0001c0004t0001g0120 others(14): Show |
22 | HG00423.hp1 HG00642.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.970+555_970+558del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96889831 | ||||||
| chr5:96889831 | TACACAC | T | 17 | a0001c0001t0001g0036 a0001c0001t0001g0141 a0001c0001t0001g0168 others(14): Show |
18 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.970+553_970+558del others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96889831 | ||||||
| chr5:96889831 | TACACACA others(1): Show |
T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.970+551_970+558del others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96889831 | ||||||
| chr5:96889835 | C | T | 1 | a0002c0002t0001g0104 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.970+530C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889835 | |||||||
| chr5:96889862 | A | G | 1 | a0002c0002t0001g0084 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.970+557A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889862 | |||||||
| chr5:96889893 | T | C | 7 | a0002c0002t0001g0034 a0002c0002t0001g0121 a0002c0002t0001g0138 others(4): Show |
8 | HG01243.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.970+588T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889893 | |||||||
| chr5:96890070 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.970+765T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890070 | |||||||
| chr5:96890152 | C | A | 1 | a0001c0001t0001g0207 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.970+847C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890152 | |||||||
| chr5:96890155 | T | A | 2 | a0003c0003t0001g0254 a0003c0003t0001g0255 |
2 | NA18964.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.970+850T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890155 | |||||||
| chr5:96890423 | C | T | 1 | a0001c0004t0001g0134 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.970+1118C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890423 | |||||||
| chr5:96890434 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(48): Show |
82 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.970+1129C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890434 | |||||||
| chr5:96890492 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
275 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.970+1187A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890492 | |||||||
| chr5:96890508 | G | A | 1 | a0001c0004t0001g0139 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.970+1203G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890508 | |||||||
| chr5:96890610 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.970+1305G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890610 | |||||||
| chr5:96890664 | T | C | 1 | a0001c0007t0001g0266 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.970+1359T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890664 | |||||||
| chr5:96890703 | A | C | 7 | a0002c0002t0001g0034 a0002c0002t0001g0121 a0002c0002t0001g0138 others(4): Show |
8 | HG01243.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.970+1398A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890703 | |||||||
| chr5:96890749 | C | A | 1 | a0002c0002t0001g0119 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.970+1444C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890749 | |||||||
| chr5:96890826 | T | TTA | 11 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(8): Show |
15 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.971-1469_971-1468d others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96890826 | ||||||
| chr5:96890831 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.971-1468T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890831 | |||||||
| chr5:96890991 | G | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.971-1308G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890991 | |||||||
| chr5:96891000 | C | T | 1 | a0002c0002t0001g0054 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.971-1299C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891000 | |||||||
| chr5:96891025 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.971-1274G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891025 | |||||||
| chr5:96891026 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.971-1273A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891026 | |||||||
| chr5:96891074 | T | C | 1 | a0002c0002t0001g0022 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.971-1225T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891074 | |||||||
| chr5:96891159 | A | G | 7 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0295 others(4): Show |
10 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.971-1140A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891159 | |||||||
| chr5:96891221 | C | T | 1 | a0001c0004t0001g0273 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.971-1078C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891221 | |||||||
| chr5:96891322 | C | T | 1 | a0001c0004t0001g0273 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.971-977C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891322 | |||||||
| chr5:96891367 | ATG | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.971-928_971-927del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891367 | ||||||
| chr5:96891369 | G | GTA | 4 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-929_971-928ins others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891369 | ||||||
| chr5:96891371 | G | A | 26 | a0001c0004t0001g0037 a0001c0004t0001g0130 a0001c0004t0001g0131 others(23): Show |
29 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.971-928G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891371 | |||||||
| chr5:96891371 | G | GTA | 33 | a0001c0004t0001g0030 a0001c0004t0001g0120 a0002c0002t0001g0015 others(30): Show |
43 | HG00558.hp2 HG00609.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.971-914_971-913dup others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891371 | ||||||
| chr5:96891371 | GTA | G | 7 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0295 others(4): Show |
10 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.971-914_971-913del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891371 | ||||||
| chr5:96891385 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.971-914A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891385 | |||||||
| chr5:96891447 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.971-852A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891447 | |||||||
| chr5:96891450 | TAC | T | 2 | a0002c0002t0001g0121 a0004c0005t0001g0028 |
3 | NA18955.hp2 NA18982.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.971-837_971-836del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891450 | ||||||
| chr5:96891471 | G | T | 2 | a0001c0004t0001g0205 a0001c0004t0001g0206 |
2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.971-828G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891471 | |||||||
| chr5:96891471 | GTA | G | 16 | a0001c0001t0001g0040 a0001c0001t0001g0149 a0001c0001t0001g0195 others(13): Show |
18 | HG01069.hp2 HG01071.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.971-816_971-815del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891471 | ||||||
| chr5:96891471 | GTATA | G | 4 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | HG04184.hp2 NA18949.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-818_971-815del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891471 | ||||||
| chr5:96891483 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.971-816A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891483 | |||||||
| chr5:96891485 | G | A | 4 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(1): Show |
5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-814G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891485 | |||||||
| chr5:96891497 | G | GTA | 23 | a0003c0003t0001g0017 a0003c0003t0001g0044 a0003c0003t0001g0045 others(20): Show |
30 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.971-801_971-800ins others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891497 | ||||||
| chr5:96891499 | G | A | 23 | a0003c0003t0001g0017 a0003c0003t0001g0044 a0003c0003t0001g0045 others(20): Show |
30 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.971-800G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891499 | |||||||
| chr5:96891499 | GTA | G | 27 | a0001c0004t0001g0030 a0001c0004t0001g0120 a0002c0002t0001g0034 others(24): Show |
35 | HG00597.hp1 HG00642.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.971-784_971-783del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891499 | ||||||
| chr5:96891501 | A | G | 32 | a0001c0001t0001g0172 a0001c0001t0001g0198 a0001c0001t0001g0200 others(29): Show |
35 | HG00738.hp2 HG01109.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.971-798A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891501 | |||||||
| chr5:96891503 | A | G | 18 | a0002c0002t0001g0034 a0002c0002t0001g0052 a0002c0002t0001g0121 others(15): Show |
23 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.971-796A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891503 | |||||||
| chr5:96891504 | TATATATA others(9): Show |
T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
176 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.971-789_971-774del others(16): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891504 | ||||||
| chr5:96891505 | A | G | 4 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-794A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891505 | |||||||
| chr5:96891506 | TATATATA others(7): Show |
T | 23 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0201 others(20): Show |
25 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.971-787_971-774del others(14): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891506 | ||||||
| chr5:96891525 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.971-774A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891525 | |||||||
| chr5:96891528 | G | GTA | 21 | a0003c0003t0001g0017 a0003c0003t0001g0044 a0003c0003t0001g0045 others(18): Show |
28 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.971-764_971-763dup others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891528 | ||||||
| chr5:96891533 | T | TAC | 12 | a0004c0005t0001g0028 a0004c0005t0001g0050 a0004c0005t0001g0051 others(9): Show |
15 | HG00597.hp1 HG02148.hp1 NA18747.hp2 others(12): Show |
intron_variant | MODIFIER | c.971-765_971-764ins others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891533 | ||||||
| chr5:96891535 | T | C | 16 | a0002c0002t0001g0102 a0002c0002t0001g0108 a0004c0005t0001g0028 others(13): Show |
19 | HG00597.hp1 HG02056.hp2 HG02148.hp1 others(16): Show |
intron_variant | MODIFIER | c.971-764T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891535 | |||||||
| chr5:96891535 | TAC | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
176 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.971-736_971-735del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891535 | ||||||
| chr5:96891535 | TACAC | T | 41 | a0001c0001t0001g0029 a0001c0001t0001g0040 a0001c0001t0001g0041 others(38): Show |
46 | HG00280.hp1 HG00280.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.971-738_971-735del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891535 | ||||||
| chr5:96891537 | C | T | 14 | a0001c0001t0001g0129 a0001c0001t0001g0211 a0001c0004t0001g0205 others(11): Show |
15 | HG00738.hp2 HG01167.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.971-762C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891537 | |||||||
| chr5:96891539 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
172 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.971-760C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891539 | |||||||
| chr5:96891541 | C | T | 59 | a0001c0001t0001g0029 a0001c0001t0001g0040 a0001c0001t0001g0041 others(56): Show |
65 | HG00280.hp1 HG00280.hp2 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.971-758C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891541 | |||||||
| chr5:96891543 | C | T | 2 | a0001c0001t0001g0153 a0002c0002t0001g0119 |
2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.971-756C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891543 | |||||||
| chr5:96891545 | C | T | 1 | a0002c0002t0001g0121 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.971-754C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891545 | |||||||
| chr5:96891563 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
183 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.971-736C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891563 | |||||||
| chr5:96891565 | T | C | 1 | a0002c0002t0001g0102 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.971-734T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891565 | |||||||
| chr5:96891571 | G | GTA | 38 | a0001c0001t0001g0141 a0001c0001t0001g0164 a0001c0001t0001g0183 others(35): Show |
46 | HG00558.hp2 HG00609.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.971-727_971-726dup others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891571 | ||||||
| chr5:96891572 | TAC | T | 22 | a0001c0001t0001g0077 a0001c0001t0001g0281 a0001c0004t0001g0030 others(19): Show |
27 | HG00597.hp1 HG00597.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.971-706_971-705del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891572 | ||||||
| chr5:96891572 | TACAC | T | 2 | a0004c0005t0001g0051 a0016c0023t0001g0286 |
3 | NA18942.hp2 NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.971-708_971-705del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891572 | ||||||
| chr5:96891574 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.971-725C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891574 | |||||||
| chr5:96891576 | C | T | 5 | a0001c0001t0001g0281 a0001c0004t0001g0030 a0001c0004t0001g0120 others(2): Show |
6 | HG00597.hp2 HG02622.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.971-723C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891576 | |||||||
| chr5:96891687 | A | G | 2 | a0001c0004t0001g0205 a0001c0004t0001g0206 |
2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.971-612A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891687 | |||||||
| chr5:96891750 | TAGA | T | 4 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-544_971-542del others(3): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891750 | ||||||
| chr5:96891882 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.971-417A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891882 | |||||||
| chr5:96891916 | A | T | 4 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-383A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891916 | |||||||
| chr5:96891923 | A | G | 1 | a0010c0012t0001g0072 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.971-376A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891923 | |||||||
| chr5:96892021 | A | G | 1 | a0002c0002t0001g0085 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.971-278A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96892021 | |||||||
| chr5:96892028 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.971-271C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96892028 | |||||||
| chr5:96892271 | C | T | 15 | a0001c0004t0001g0037 a0001c0004t0001g0130 a0001c0004t0001g0131 others(12): Show |
17 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.971-28C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96892271 | |||||||
| chr5:96892536 | A | G | 19 | a0001c0004t0001g0037 a0001c0004t0001g0130 a0001c0004t0001g0131 others(16): Show |
21 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.1125+83A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96892536 | |||||||
| chr5:96892724 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1125+271G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96892724 | |||||||
| chr5:96892758 | G | C | 1 | a0010c0012t0001g0072 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1125+305G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96892758 | |||||||
| chr5:96892763 | C | T | 1 | a0002c0002t0001g0105 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1125+310C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96892763 | |||||||
| chr5:96892933 | T | A | 4 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(1): Show |
5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1125+480T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96892933 | |||||||
| chr5:96892996 | A | AGCTGTTC | 3 | a0001c0001t0001g0042 a0001c0001t0001g0199 a0011c0019t0001g0197 |
4 | HG01106.hp2 HG01257.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+544_1125+550d others(9): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 96892996 | ||||||
| chr5:96893031 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1125+578G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893031 | |||||||
| chr5:96893073 | T | C | 2 | a0002c0002t0001g0034 a0002c0002t0001g0138 |
3 | HG01243.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1125+620T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893073 | |||||||
| chr5:96893078 | A | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1125+625A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893078 | |||||||
| chr5:96893119 | C | T | 1 | a0002c0002t0001g0067 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1125+666C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893119 | |||||||
| chr5:96893150 | C | T | 3 | a0001c0004t0001g0030 a0001c0004t0001g0120 a0002c0002t0001g0294 |
4 | HG02622.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+697C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893150 | |||||||
| chr5:96893355 | C | T | 1 | a0002c0002t0001g0071 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1125+902C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893355 | |||||||
| chr5:96893374 | T | G | 1 | a0002c0002t0001g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1125+921T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893374 | |||||||
| chr5:96893488 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1125+1035C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893488 | |||||||
| chr5:96893521 | G | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
184 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.1125+1068G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893521 | |||||||
| chr5:96893568 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
168 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1125+1115G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893568 | |||||||
| chr5:96893693 | A | T | 1 | a0001c0004t0001g0269 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1125+1240A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893693 | |||||||
| chr5:96893720 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1125+1267C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893720 | |||||||
| chr5:96893723 | T | C | 1 | a0002c0002t0001g0119 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1125+1270T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893723 | |||||||
| chr5:96893838 | T | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
159 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.1125+1385T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893838 | |||||||
| chr5:96893841 | T | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0140 |
3 | HG00738.hp1 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1125+1388T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893841 | |||||||
| chr5:96894046 | G | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1126-1200G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894046 | |||||||
| chr5:96894404 | T | C | 43 | a0002c0002t0001g0034 a0002c0002t0001g0079 a0002c0002t0001g0112 others(40): Show |
53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1126-842T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894404 | |||||||
| chr5:96894418 | G | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1126-828G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894418 | |||||||
| chr5:96894474 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1126-772G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894474 | |||||||
| chr5:96894513 | CA | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1126-732delA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894513 | |||||||
| chr5:96894535 | A | G | 1 | a0001c0004t0002g0136 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1126-711A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894535 | |||||||
| chr5:96894679 | A | G | 1 | a0001c0004t0001g0273 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1126-567A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894679 | |||||||
| chr5:96894699 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1126-547G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894699 | |||||||
| chr5:96894830 | C | A | 1 | a0001c0001t0001g0169 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1126-416C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894830 | |||||||
| chr5:96894921 | A | G | 1 | a0002c0002t0001g0104 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1126-325A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894921 | |||||||
| chr5:96894990 | T | C | 2 | a0002c0002t0001g0089 a0002c0002t0001g0187 |
2 | HG00609.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1126-256T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894990 | |||||||
| chr5:96895000 | G | C | 1 | a0005c0006t0001g0245 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1126-246G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96895000 | |||||||
| chr5:96895140 | G | A | 14 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(11): Show |
18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1126-106G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96895140 | |||||||
| chr5:96895154 | T | TA | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
217 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1126-83dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 96895154 | ||||||
| chr5:96895179 | A | ATT | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1126-62_1126-61dup others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 96895179 | ||||||
| chr5:96895371 | A | G | 1 | a0002c0002t0001g0083 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1239+12A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895371 | |||||||
| chr5:96895391 | T | C | 1 | a0007c0011t0001g0148 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1239+32T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895391 | |||||||
| chr5:96895496 | C | T | 10 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0241 others(7): Show |
13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1239+137C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895496 | |||||||
| chr5:96895649 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1239+290T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895649 | |||||||
| chr5:96895668 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
272 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1239+309T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895668 | |||||||
| chr5:96895732 | G | A | 1 | a0002c0002t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1239+373G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895732 | |||||||
| chr5:96895800 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1239+441C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895800 | |||||||
| chr5:96895816 | G | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1239+457G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895816 | |||||||
| chr5:96895819 | T | C | 43 | a0002c0002t0001g0034 a0002c0002t0001g0079 a0002c0002t0001g0112 others(40): Show |
53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1239+460T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895819 | |||||||
| chr5:96895830 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0214 |
2 | HG00741.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1239+471G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895830 | |||||||
| chr5:96895859 | G | T | 21 | a0001c0004t0001g0030 a0001c0004t0001g0037 a0001c0004t0001g0120 others(18): Show |
24 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1239+500G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895859 | |||||||
| chr5:96895874 | A | C | 14 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(11): Show |
18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1240-499A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895874 | |||||||
| chr5:96895938 | CTCT | C | 3 | a0001c0004t0001g0267 a0001c0004t0001g0268 a0001c0004t0001g0269 |
3 | HG02451.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1240-430_1240-428d others(5): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 96895938 | ||||||
| chr5:96896040 | TTGACAGG others(8): Show |
T | 1 | a0002c0002t0001g0082 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1240-329_1240-315d others(17): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 96896040 | ||||||
| chr5:96896308 | A | G | 1 | a0001c0004t0001g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1240-65A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96896308 | |||||||
| chr5:96896518 | G | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1371+14G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 8/18 | chr5 | 96896518 | |||||||
| chr5:96896519 | G | A | 4 | a0003c0003t0001g0228 a0003c0003t0001g0257 a0003c0003t0001g0258 others(1): Show |
4 | NA18962.hp1 NA18991.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1371+15G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 8/18 | chr5 | 96896519 | |||||||
| chr5:96896546 | G | GAAA | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1371+42_1371+43ins others(3): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 8/18 | chr5 | 96896546 | |||||||
| chr5:96896582 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1371+78C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 8/18 | chr5 | 96896582 | |||||||
| chr5:96896641 | CAT | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1372-90_1372-89del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 8/18 | chr5 | 96896641 | |||||||
| chr5:96896698 | T | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1372-34T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 8/18 | chr5 | 96896698 | |||||||
| chr5:96896864 | G | GTAAGTCA others(93): Show |
133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1503+3_1503+102dup others(100): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96896864 | ||||||
| chr5:96896892 | T | C | 13 | a0002c0002t0001g0079 a0002c0002t0001g0112 a0004c0005t0001g0028 others(10): Show |
15 | HG00597.hp1 HG02083.hp2 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.1503+29T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96896892 | |||||||
| chr5:96896995 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1503+132A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96896995 | |||||||
| chr5:96896996 | T | C | 14 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(11): Show |
18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1503+133T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96896996 | |||||||
| chr5:96896996 | T | G | 4 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503+133T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96896996 | |||||||
| chr5:96897045 | G | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0154 |
2 | NA19009.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1503+182G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897045 | |||||||
| chr5:96897085 | C | G | 1 | a0001c0004t0001g0273 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1503+222C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897085 | |||||||
| chr5:96897102 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1503+239C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897102 | |||||||
| chr5:96897544 | C | CT | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1503+688dupT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96897544 | ||||||
| chr5:96897652 | A | G | 1 | a0003c0003t0001g0258 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1503+789A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897652 | |||||||
| chr5:96897746 | T | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1503+883T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897746 | |||||||
| chr5:96897759 | C | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
131 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1503+896C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897759 | |||||||
| chr5:96897904 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1503+1041G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897904 | |||||||
| chr5:96897919 | G | A | 4 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503+1056G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897919 | |||||||
| chr5:96897921 | G | A | 4 | a0001c0001t0001g0168 a0001c0001t0001g0176 a0001c0001t0001g0179 others(1): Show |
4 | NA18947.hp1 NA18972.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503+1058G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897921 | |||||||
| chr5:96898392 | T | TA | 22 | a0003c0003t0001g0017 a0003c0003t0001g0045 a0003c0003t0001g0046 others(19): Show |
28 | HG00558.hp2 HG00609.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1503+1530dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96898392 | ||||||
| chr5:96898488 | T | C | 4 | a0002c0002t0001g0009 a0002c0002t0001g0069 a0002c0002t0001g0124 others(1): Show |
7 | HG00741.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1503+1625T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898488 | |||||||
| chr5:96898508 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1504-1613G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898508 | |||||||
| chr5:96898510 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1504-1611G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898510 | |||||||
| chr5:96898532 | A | T | 43 | a0002c0002t0001g0034 a0002c0002t0001g0079 a0002c0002t0001g0112 others(40): Show |
53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1504-1589A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898532 | |||||||
| chr5:96898565 | T | C | 2 | a0007c0011t0001g0148 a0007c0011t0001g0150 |
2 | HG01074.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1504-1556T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898565 | |||||||
| chr5:96898572 | C | CA | 19 | a0002c0002t0001g0052 a0002c0002t0001g0065 a0002c0002t0001g0078 others(16): Show |
23 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1504-1529dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96898572 | ||||||
| chr5:96898572 | C | CAA | 38 | a0001c0001t0001g0164 a0001c0001t0001g0174 a0001c0001t0001g0192 others(35): Show |
48 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1504-1530_1504-152 others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96898572 | ||||||
| chr5:96898572 | C | CAAA | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1504-1531_1504-152 others(7): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96898572 | ||||||
| chr5:96898572 | C | CAAAA | 16 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0098 others(13): Show |
18 | HG00423.hp2 HG01074.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.1504-1532_1504-152 others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96898572 | ||||||
| chr5:96898572 | C | CAAAAA | 14 | a0001c0004t0001g0037 a0001c0004t0001g0130 a0001c0004t0001g0132 others(11): Show |
16 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1504-1533_1504-152 others(9): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96898572 | ||||||
| chr5:96898572 | C | CAAAAAA | 8 | a0001c0004t0001g0120 a0001c0004t0001g0131 a0001c0004t0001g0144 others(5): Show |
8 | HG02055.hp2 HG02738.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1504-1534_1504-152 others(10): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96898572 | ||||||
| chr5:96898602 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1504-1519T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898602 | |||||||
| chr5:96898611 | T | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
277 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.1504-1510T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898611 | |||||||
| chr5:96898648 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1504-1473G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898648 | |||||||
| chr5:96898671 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1504-1450C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898671 | |||||||
| chr5:96898829 | A | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1504-1292A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898829 | |||||||
| chr5:96898874 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1504-1247G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898874 | |||||||
| chr5:96898917 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1504-1204C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898917 | |||||||
| chr5:96898979 | A | C | 10 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0241 others(7): Show |
13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1504-1142A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898979 | |||||||
| chr5:96899022 | T | TAAAAAGA others(331): Show |
2 | a0003c0003t0001g0263 a0003c0003t0001g0264 |
2 | NA18985.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1504-1084_1504-108 others(342): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96899022 | ||||||
| chr5:96899168 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1504-953T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899168 | |||||||
| chr5:96899232 | T | TTCTGAC | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1504-886_1504-885i others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96899232 | ||||||
| chr5:96899289 | T | TCCCACCC others(6): Show |
1 | a0002c0002t0001g0082 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1504-829_1504-828i others(15): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96899289 | ||||||
| chr5:96899334 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.1504-787T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899334 | |||||||
| chr5:96899400 | T | A | 1 | a0004c0005t0001g0287 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1504-721T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899400 | |||||||
| chr5:96899415 | C | T | 1 | a0002c0002t0001g0091 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1504-706C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899415 | |||||||
| chr5:96899520 | T | C | 1 | a0004c0005t0001g0287 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1504-601T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899520 | |||||||
| chr5:96899568 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1504-553A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899568 | |||||||
| chr5:96899659 | G | A | 1 | a0002c0002t0001g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1504-462G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899659 | |||||||
| chr5:96899759 | T | C | 1 | a0002c0002t0001g0101 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1504-362T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899759 | |||||||
| chr5:96899789 | A | G | 1 | a0018c0013t0001g0272 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1504-332A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899789 | |||||||
| chr5:96899889 | T | G | 14 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(11): Show |
18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1504-232T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899889 | |||||||
| chr5:96900013 | A | G | 10 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0241 others(7): Show |
13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1504-108A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96900013 | |||||||
| chr5:96900192 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
splice_region_variant&intron_variant | LOW | c.1572+3A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900192 | |||||||
| chr5:96900378 | C | T | 1 | a0001c0004t0002g0136 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1572+189C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900378 | |||||||
| chr5:96900440 | G | A | 3 | a0002c0002t0001g0023 a0002c0002t0001g0059 a0002c0002t0001g0110 |
4 | HG00140.hp2 HG00323.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+251G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900440 | |||||||
| chr5:96900614 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1572+425G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900614 | |||||||
| chr5:96900708 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1572+519A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900708 | |||||||
| chr5:96900757 | A | C | 2 | a0008c0009t0001g0032 a0010c0012t0001g0072 |
3 | HG02055.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1572+568A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900757 | |||||||
| chr5:96900837 | C | T | 21 | a0001c0004t0001g0030 a0001c0004t0001g0037 a0001c0004t0001g0120 others(18): Show |
24 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1572+648C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900837 | |||||||
| chr5:96900916 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1573-590T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900916 | |||||||
| chr5:96901139 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1573-367C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901139 | |||||||
| chr5:96901152 | T | C | 23 | a0003c0003t0001g0017 a0003c0003t0001g0044 a0003c0003t0001g0045 others(20): Show |
30 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.1573-354T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901152 | |||||||
| chr5:96901188 | G | GTTTT | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
192 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1573-318_1573-317i others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901188 | |||||||
| chr5:96901189 | A | T | 12 | a0001c0001t0001g0029 a0001c0001t0001g0056 a0001c0001t0001g0061 others(9): Show |
13 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1573-317A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901189 | |||||||
| chr5:96901193 | T | A | 12 | a0001c0001t0001g0029 a0001c0001t0001g0056 a0001c0001t0001g0061 others(9): Show |
13 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1573-313T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901193 | |||||||
| chr5:96901194 | G | T | 12 | a0001c0001t0001g0029 a0001c0001t0001g0056 a0001c0001t0001g0061 others(9): Show |
13 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1573-312G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901194 | |||||||
| chr5:96901410 | C | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1573-96C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901410 | |||||||
| chr5:96901451 | C | A | 1 | a0004c0005t0001g0287 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1573-55C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901451 | |||||||
| chr5:96901709 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1748+28C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96901709 | |||||||
| chr5:96901845 | C | T | 1 | a0008c0009t0001g0032 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1748+164C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96901845 | |||||||
| chr5:96901892 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0140 a0001c0018t0001g0143 |
4 | HG00738.hp1 HG02818.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1748+211T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96901892 | |||||||
| chr5:96901920 | T | C | 21 | a0001c0004t0001g0030 a0001c0004t0001g0037 a0001c0004t0001g0120 others(18): Show |
24 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1748+239T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96901920 | |||||||
| chr5:96902007 | T | C | 14 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(11): Show |
18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1749-267T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96902007 | |||||||
| chr5:96902034 | A | G | 2 | a0007c0011t0001g0148 a0007c0011t0001g0150 |
2 | HG01074.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1749-240A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96902034 | |||||||
| chr5:96902039 | T | C | 1 | a0001c0004t0001g0139 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1749-235T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96902039 | |||||||
| chr5:96902052 | C | T | 1 | a0003c0003t0001g0262 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1749-222C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96902052 | |||||||
| chr5:96902066 | T | G | 1 | a0002c0002t0001g0112 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1749-208T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96902066 | |||||||
| chr5:96902175 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1749-99G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96902175 | |||||||
| chr5:96902398 | A | G | 2 | a0002c0002t0001g0034 a0002c0002t0001g0138 |
3 | HG01243.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1828+45A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902398 | |||||||
| chr5:96902403 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1828+50G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902403 | |||||||
| chr5:96902413 | A | G | 2 | a0001c0004t0001g0030 a0001c0004t0001g0120 |
3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1828+60A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902413 | |||||||
| chr5:96902552 | C | T | 1 | a0002c0002t0001g0076 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1828+199C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902552 | |||||||
| chr5:96902565 | TAG | T | 43 | a0002c0002t0001g0034 a0002c0002t0001g0079 a0002c0002t0001g0112 others(40): Show |
53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1828+216_1828+217d others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 96902565 | ||||||
| chr5:96902607 | T | A | 1 | a0002c0002t0001g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1828+254T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902607 | |||||||
| chr5:96902697 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1828+344A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902697 | |||||||
| chr5:96902847 | T | G | 10 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0241 others(7): Show |
13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1828+494T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902847 | |||||||
| chr5:96902874 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.1829-503C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902874 | |||||||
| chr5:96902910 | A | G | 10 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0241 others(7): Show |
13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1829-467A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902910 | |||||||
| chr5:96902990 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0199 a0011c0019t0001g0197 |
4 | HG01106.hp2 HG01257.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1829-387A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902990 | |||||||
| chr5:96903109 | C | A | 10 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0241 others(7): Show |
13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1829-268C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96903109 | |||||||
| chr5:96903235 | C | T | 43 | a0002c0002t0001g0034 a0002c0002t0001g0079 a0002c0002t0001g0112 others(40): Show |
53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1829-142C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96903235 | |||||||
| chr5:96903256 | C | T | 1 | a0002c0002t0001g0187 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1829-121C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96903256 | |||||||
| chr5:96903590 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2012+30A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96903590 | |||||||
| chr5:96903647 | G | A | 1 | a0002c0002t0001g0070 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2012+87G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96903647 | |||||||
| chr5:96903726 | G | GACCCAC | 23 | a0003c0003t0001g0017 a0003c0003t0001g0044 a0003c0003t0001g0045 others(20): Show |
30 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.2012+169_2012+174d others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96903726 | ||||||
| chr5:96903941 | G | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2012+381G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96903941 | |||||||
| chr5:96904009 | G | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2012+449G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904009 | |||||||
| chr5:96904010 | T | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2012+450T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904010 | |||||||
| chr5:96904043 | T | A | 1 | a0001c0001t0001g0170 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2012+483T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904043 | |||||||
| chr5:96904133 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2012+573G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904133 | |||||||
| chr5:96904223 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2012+663T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904223 | |||||||
| chr5:96904318 | T | G | 2 | a0001c0004t0001g0205 a0001c0004t0001g0206 |
2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2012+758T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904318 | |||||||
| chr5:96904370 | T | C | 1 | a0002c0002t0001g0123 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2012+810T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904370 | |||||||
| chr5:96904439 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0184 |
4 | NA18980.hp1 NA18987.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2012+879A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904439 | |||||||
| chr5:96904510 | C | A | 43 | a0002c0002t0001g0034 a0002c0002t0001g0079 a0002c0002t0001g0112 others(40): Show |
53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2012+950C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904510 | |||||||
| chr5:96904516 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2012+956T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904516 | |||||||
| chr5:96904520 | G | A | 43 | a0002c0002t0001g0034 a0002c0002t0001g0079 a0002c0002t0001g0112 others(40): Show |
53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2012+960G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904520 | |||||||
| chr5:96904584 | C | G | 1 | a0002c0002t0001g0085 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2012+1024C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904584 | |||||||
| chr5:96904682 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2012+1122A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904682 | |||||||
| chr5:96904934 | C | T | 1 | a0002c0002t0001g0121 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2012+1374C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904934 | |||||||
| chr5:96904984 | TTTTTTAA others(2): Show |
T | 10 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0241 others(7): Show |
13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2012+1432_2012+144 others(13): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96904984 | ||||||
| chr5:96905245 | G | C | 2 | a0008c0009t0001g0032 a0010c0012t0001g0072 |
3 | HG02055.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2012+1685G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96905245 | |||||||
| chr5:96905307 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2012+1747A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96905307 | |||||||
| chr5:96905358 | G | C | 1 | a0005c0006t0001g0295 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2012+1798G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96905358 | |||||||
| chr5:96905412 | A | C | 21 | a0001c0004t0001g0030 a0001c0004t0001g0037 a0001c0004t0001g0120 others(18): Show |
24 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.2012+1852A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96905412 | |||||||
| chr5:96905490 | T | C | 4 | a0002c0002t0001g0080 a0002c0002t0001g0082 a0002c0002t0001g0095 others(1): Show |
4 | HG02300.hp1 NA18949.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.2012+1930T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96905490 | |||||||
| chr5:96905944 | A | AT | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.2012+2399dupT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96905944 | ||||||
| chr5:96905944 | AT | A | 43 | a0002c0002t0001g0034 a0002c0002t0001g0079 a0002c0002t0001g0112 others(40): Show |
53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2012+2399delT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96905944 | ||||||
| chr5:96906185 | CTTTT | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2012+2632_2012+263 others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96906185 | ||||||
| chr5:96906236 | T | C | 1 | a0002c0002t0001g0119 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2012+2676T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906236 | |||||||
| chr5:96906240 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0191 others(3): Show |
13 | HG02258.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2012+2680T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906240 | |||||||
| chr5:96906370 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2013-2591G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906370 | |||||||
| chr5:96906417 | C | T | 1 | a0002c0002t0001g0057 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2013-2544C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906417 | |||||||
| chr5:96906566 | A | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2013-2395A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906566 | |||||||
| chr5:96906573 | A | T | 1 | a0002c0002t0001g0117 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2013-2388A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906573 | |||||||
| chr5:96906696 | T | C | 14 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(11): Show |
18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.2013-2265T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906696 | |||||||
| chr5:96906708 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2013-2253T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906708 | |||||||
| chr5:96906731 | C | T | 2 | a0002c0002t0001g0034 a0002c0002t0001g0138 |
3 | HG01243.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2013-2230C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906731 | |||||||
| chr5:96906738 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2013-2223G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906738 | |||||||
| chr5:96906758 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2013-2203G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906758 | |||||||
| chr5:96906790 | G | C | 1 | a0001c0001t0001g0029 | 2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2013-2171G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906790 | |||||||
| chr5:96907099 | A | G | 1 | a0001c0001t0001g0284 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2013-1862A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907099 | |||||||
| chr5:96907153 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.2013-1808T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907153 | |||||||
| chr5:96907162 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2013-1799G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907162 | |||||||
| chr5:96907163 | G | A | 1 | a0002c0002t0001g0070 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2013-1798G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907163 | |||||||
| chr5:96907277 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2013-1684C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907277 | |||||||
| chr5:96907573 | A | AT | 63 | a0001c0001t0001g0042 a0001c0001t0001g0199 a0002c0002t0001g0034 others(60): Show |
78 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.2013-1375dupT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96907573 | ||||||
| chr5:96907573 | A | ATT | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.2013-1376_2013-137 others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96907573 | ||||||
| chr5:96907604 | G | A | 1 | a0003c0003t0001g0044 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2013-1357G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907604 | |||||||
| chr5:96907652 | C | T | 10 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0241 others(7): Show |
13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2013-1309C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907652 | |||||||
| chr5:96907653 | G | A | 13 | a0002c0002t0001g0079 a0002c0002t0001g0112 a0004c0005t0001g0028 others(10): Show |
15 | HG00597.hp1 HG02083.hp2 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.2013-1308G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907653 | |||||||
| chr5:96907839 | T | C | 2 | a0005c0006t0001g0295 a0005c0006t0001g0296 |
2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2013-1122T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907839 | |||||||
| chr5:96907883 | CA | C | 52 | a0002c0002t0001g0015 a0002c0002t0001g0052 a0002c0002t0001g0079 others(49): Show |
65 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2013-1066delA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96907883 | ||||||
| chr5:96907883 | CAAA | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2013-1068_2013-106 others(7): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96907883 | ||||||
| chr5:96907892 | A | T | 2 | a0002c0002t0001g0034 a0002c0002t0001g0138 |
3 | HG01243.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2013-1069A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907892 | |||||||
| chr5:96907894 | A | AT | 4 | a0002c0002t0001g0020 a0002c0002t0001g0090 a0002c0002t0001g0094 others(1): Show |
5 | HG02027.hp2 HG03834.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.2013-1067_2013-106 others(5): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907894 | |||||||
| chr5:96907894 | A | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.2013-1067A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907894 | |||||||
| chr5:96908305 | C | T | 1 | a0018c0013t0001g0272 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2013-656C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96908305 | |||||||
| chr5:96908377 | G | C | 10 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0241 others(7): Show |
13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2013-584G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96908377 | |||||||
| chr5:96908385 | C | T | 1 | a0002c0002t0001g0071 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2013-576C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96908385 | |||||||
| chr5:96908845 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2013-116C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96908845 | |||||||
| chr5:96908881 | A | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.2013-80A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96908881 | |||||||
| chr5:96908934 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2013-27A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96908934 | |||||||
| chr5:96909814 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2354+50A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96909814 | |||||||
| chr5:96909913 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2354+149T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96909913 | |||||||
| chr5:96909914 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2354+150G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96909914 | |||||||
| chr5:96910080 | C | A | 2 | a0001c0004t0001g0205 a0001c0004t0001g0206 |
2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2354+316C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910080 | |||||||
| chr5:96910187 | C | T | 12 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0098 others(9): Show |
14 | HG00323.hp1 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.2354+423C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910187 | |||||||
| chr5:96910188 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2354+424C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910188 | |||||||
| chr5:96910199 | A | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2354+435A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910199 | |||||||
| chr5:96910206 | C | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2354+442C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910206 | |||||||
| chr5:96910264 | C | CA | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.2354+516dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96910264 | ||||||
| chr5:96910264 | C | CAA | 25 | a0001c0001t0001g0186 a0001c0001t0001g0202 a0001c0004t0001g0030 others(22): Show |
28 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.2354+515_2354+516d others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96910264 | ||||||
| chr5:96910396 | T | G | 4 | a0002c0002t0001g0024 a0002c0002t0001g0057 a0002c0002t0001g0093 others(1): Show |
5 | HG00544.hp1 NA18948.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.2354+632T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910396 | |||||||
| chr5:96910453 | G | GA | 57 | a0002c0002t0001g0034 a0002c0002t0001g0052 a0002c0002t0001g0079 others(54): Show |
71 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2354+700dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96910453 | ||||||
| chr5:96910634 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2354+870T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910634 | |||||||
| chr5:96910705 | G | T | 1 | a0001c0001t0001g0149 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2354+941G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910705 | |||||||
| chr5:96910897 | A | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2354+1133A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910897 | |||||||
| chr5:96911026 | T | C | 2 | a0002c0002t0001g0021 a0002c0002t0001g0100 |
3 | NA18960.hp2 NA18988.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2354+1262T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911026 | |||||||
| chr5:96911236 | G | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2355-1401G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911236 | |||||||
| chr5:96911248 | A | G | 2 | a0002c0002t0001g0064 a0002c0002t0001g0088 |
2 | NA18990.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2355-1389A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911248 | |||||||
| chr5:96911552 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2355-1085G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911552 | |||||||
| chr5:96911569 | A | T | 2 | a0007c0011t0001g0148 a0007c0011t0001g0150 |
2 | HG01074.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2355-1068A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911569 | |||||||
| chr5:96911586 | A | G | 43 | a0002c0002t0001g0034 a0002c0002t0001g0079 a0002c0002t0001g0112 others(40): Show |
53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2355-1051A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911586 | |||||||
| chr5:96911615 | G | C | 1 | a0001c0004t0002g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2355-1022G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911615 | |||||||
| chr5:96911723 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2355-914A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911723 | |||||||
| chr5:96911730 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2355-907G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911730 | |||||||
| chr5:96911740 | C | T | 43 | a0002c0002t0001g0034 a0002c0002t0001g0079 a0002c0002t0001g0112 others(40): Show |
53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2355-897C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911740 | |||||||
| chr5:96911765 | C | G | 1 | a0009c0010t0003g0039 | 2 | NA18983.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2355-872C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911765 | |||||||
| chr5:96911818 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2355-819G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911818 | |||||||
| chr5:96911858 | C | A | 1 | a0002c0002t0001g0187 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2355-779C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911858 | |||||||
| chr5:96911866 | C | CA | 9 | a0002c0002t0001g0019 a0002c0002t0001g0075 a0002c0002t0001g0078 others(6): Show |
10 | HG00544.hp2 HG00609.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.2355-756dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | ||||||
| chr5:96911866 | C | CAAAAAAA | 13 | a0001c0004t0001g0037 a0001c0004t0001g0130 a0001c0004t0001g0131 others(10): Show |
15 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.2355-762_2355-756d others(9): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | ||||||
| chr5:96911866 | C | CAAAAAAA others(1): Show |
6 | a0001c0004t0001g0030 a0001c0004t0001g0120 a0001c0004t0001g0267 others(3): Show |
7 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2355-763_2355-756d others(10): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | ||||||
| chr5:96911866 | C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0060 a0001c0001t0001g0162 a0001c0001t0001g0172 others(4): Show |
7 | HG00323.hp1 HG01167.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.2355-764_2355-756d others(11): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | ||||||
| chr5:96911866 | C | CAAAAAAA others(3): Show |
87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
126 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.2355-765_2355-756d others(12): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | ||||||
| chr5:96911866 | C | CAAAAAAA others(4): Show |
37 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0043 others(34): Show |
42 | HG00280.hp2 HG00597.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.2355-766_2355-756d others(13): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | ||||||
| chr5:96911866 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0147 a0001c0001t0001g0233 |
2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.2355-767_2355-756d others(14): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | ||||||
| chr5:96911866 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2355-768_2355-756d others(15): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | ||||||
| chr5:96911866 | CA | C | 25 | a0002c0002t0001g0034 a0002c0002t0001g0052 a0002c0002t0001g0066 others(22): Show |
30 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.2355-756delA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | ||||||
| chr5:96911882 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2355-755G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911882 | |||||||
| chr5:96911883 | AAAGAAAG others(298): Show |
A | 1 | a0009c0010t0003g0039 | 2 | NA18983.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2355-751_2355-447d others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911883 | ||||||
| chr5:96911915 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2355-722C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911915 | |||||||
| chr5:96911941 | G | A | 1 | a0002c0002t0001g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2355-696G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911941 | |||||||
| chr5:96911954 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2355-683C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911954 | |||||||
| chr5:96911965 | G | A | 1 | a0004c0005t0001g0285 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2355-672G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911965 | |||||||
| chr5:96911986 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0191 others(2): Show |
11 | HG02258.hp1 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2355-651G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911986 | |||||||
| chr5:96912046 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2355-591C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912046 | |||||||
| chr5:96912089 | C | A | 1 | a0001c0001t0001g0004 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2355-548C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912089 | |||||||
| chr5:96912106 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
274 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.2355-531T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912106 | |||||||
| chr5:96912123 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2355-514G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912123 | |||||||
| chr5:96912145 | C | T | 1 | a0004c0005t0001g0028 | 2 | NA18955.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.2355-492C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912145 | |||||||
| chr5:96912148 | G | A | 2 | a0001c0007t0001g0016 a0001c0007t0001g0243 |
2 | HG02004.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2355-489G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912148 | |||||||
| chr5:96912188 | C | CA | 23 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(20): Show |
25 | HG00280.hp1 HG00597.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.2355-433dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96912188 | ||||||
| chr5:96912194 | AAAAAAAA others(4): Show |
A | 1 | a0001c0007t0001g0246 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2355-438_2355-428d others(13): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96912194 | ||||||
| chr5:96912201 | A | G | 1 | a0009c0010t0003g0039 | 2 | NA18983.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2355-436A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912201 | |||||||
| chr5:96912204 | AG | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0063 others(2): Show |
5 | HG00558.hp1 HG02451.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2355-432delG | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912204 | |||||||
| chr5:96912205 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.2355-432G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912205 | |||||||
| chr5:96912265 | T | TA | 44 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(41): Show |
67 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2355-362dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96912265 | ||||||
| chr5:96912289 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.2355-348A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912289 | |||||||
| chr5:96912294 | G | A | 15 | a0001c0004t0001g0037 a0001c0004t0001g0130 a0001c0004t0001g0131 others(12): Show |
17 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.2355-343G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912294 | |||||||
| chr5:96912513 | G | T | 4 | a0006c0008t0001g0155 a0006c0008t0001g0165 a0006c0008t0001g0166 others(1): Show |
4 | HG02040.hp1 HG02698.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.2355-124G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912513 | |||||||
| chr5:96912550 | T | G | 14 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(11): Show |
18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.2355-87T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912550 | |||||||
| chr5:96912981 | T | TGTTTCAT others(17): Show |
1 | a0002c0002t0001g0112 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2516+183_2516+184i others(26): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96912981 | |||||||
| chr5:96912983 | G | C | 1 | a0002c0002t0001g0112 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2516+185G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96912983 | |||||||
| chr5:96912985 | T | A | 1 | a0002c0002t0001g0112 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2516+187T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96912985 | |||||||
| chr5:96913003 | G | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2516+205G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96913003 | |||||||
| chr5:96913091 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
284 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.2517-226T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96913091 | |||||||
| chr5:96913158 | T | C | 1 | a0002c0002t0001g0019 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2517-159T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96913158 | |||||||
| chr5:96913182 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2517-135A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96913182 | |||||||
| chr5:96913201 | A | G | 1 | a0002c0002t0001g0121 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2517-116A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96913201 | |||||||
| chr5:96913619 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2657+162G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96913619 | |||||||
| chr5:96913647 | T | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2657+190T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96913647 | |||||||
| chr5:96913674 | A | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2657+217A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96913674 | |||||||
| chr5:96913930 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.2657+473A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96913930 | |||||||
| chr5:96913930 | A | T | 2 | a0001c0004t0001g0205 a0001c0004t0001g0206 |
2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2657+473A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96913930 | |||||||
| chr5:96913944 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
275 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.2657+487T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96913944 | |||||||
| chr5:96914041 | A | G | 43 | a0002c0002t0001g0034 a0002c0002t0001g0079 a0002c0002t0001g0112 others(40): Show |
53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2657+584A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914041 | |||||||
| chr5:96914054 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2657+597T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914054 | |||||||
| chr5:96914129 | G | GTCTC | 18 | a0001c0001t0001g0236 a0001c0004t0001g0037 a0001c0004t0001g0130 others(15): Show |
20 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.2657+689_2657+692d others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914129 | ||||||
| chr5:96914146 | T | TCACACAC others(9): Show |
4 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2657+690_2657+691i others(18): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914146 | ||||||
| chr5:96914148 | T | A | 5 | a0001c0001t0001g0141 a0002c0002t0001g0219 a0002c0002t0001g0220 others(2): Show |
5 | HG02280.hp2 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2657+691T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914148 | |||||||
| chr5:96914148 | T | TCACA | 3 | a0001c0001t0001g0118 a0001c0001t0001g0129 a0001c0001t0001g0211 |
3 | HG02258.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2657+708_2657+711d others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCACACAC others(5): Show |
1 | a0004c0005t0001g0290 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2657+700_2657+711d others(14): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCACACAC others(7): Show |
2 | a0002c0002t0001g0015 a0002c0002t0001g0294 |
2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2657+698_2657+711d others(16): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCACACAC others(9): Show |
13 | a0002c0002t0001g0015 a0002c0002t0001g0079 a0002c0002t0001g0112 others(10): Show |
15 | HG00597.hp1 HG02055.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2657+696_2657+711d others(18): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCACACAC others(11): Show |
5 | a0002c0002t0001g0034 a0002c0002t0001g0138 a0002c0002t0001g0189 others(2): Show |
7 | HG01243.hp2 HG01255.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2657+694_2657+711d others(20): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCACACAC others(13): Show |
1 | a0003c0003t0001g0044 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2657+692_2657+711d others(22): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCACACAC others(17): Show |
2 | a0003c0003t0001g0017 a0003c0003t0001g0047 |
4 | NA18950.hp1 NA18968.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.2657+711_2657+712i others(26): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCTCA | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
173 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.2657+692_2657+693i others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCTCACA | 5 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0151 others(2): Show |
5 | HG02027.hp1 NA18612.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.2657+692_2657+693i others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCTCACAC others(3): Show |
4 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(1): Show |
5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.2657+692_2657+693i others(12): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCTCACAC others(9): Show |
10 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0241 others(7): Show |
11 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.2657+692_2657+693i others(18): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCTCACAC others(11): Show |
4 | a0003c0003t0001g0048 a0003c0003t0001g0260 a0004c0005t0001g0051 others(1): Show |
5 | NA18942.hp2 NA18978.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.2657+692_2657+693i others(20): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCTCACAC others(13): Show |
1 | a0003c0003t0001g0251 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2657+692_2657+693i others(22): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCTCACAC others(15): Show |
15 | a0003c0003t0001g0045 a0003c0003t0001g0047 a0003c0003t0001g0048 others(12): Show |
16 | HG00558.hp2 HG00609.hp1 HG03688.hp2 others(13): Show |
intron_variant | MODIFIER | c.2657+692_2657+693i others(24): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCTCACAC others(17): Show |
1 | a0003c0003t0001g0046 | 2 | NA18973.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2657+692_2657+693i others(26): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCTCACAC others(19): Show |
2 | a0003c0003t0001g0249 a0003c0003t0001g0250 |
2 | NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2657+692_2657+693i others(28): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCTCTCAC others(5): Show |
1 | a0003c0003t0001g0259 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2657+692_2657+693i others(14): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCTCTCAC others(9): Show |
1 | a0005c0006t0001g0012 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2657+692_2657+693i others(18): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914148 | T | TCTCTCAC others(15): Show |
1 | a0002c0002t0001g0121 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2657+692_2657+693i others(24): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | ||||||
| chr5:96914324 | T | A | 1 | a0002c0002t0001g0022 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2657+867T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914324 | |||||||
| chr5:96914343 | G | C | 11 | a0001c0004t0001g0037 a0001c0004t0001g0133 a0001c0004t0001g0134 others(8): Show |
13 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.2657+886G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914343 | |||||||
| chr5:96914560 | C | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2657+1103C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914560 | |||||||
| chr5:96914631 | A | ACCAT | 1 | a0002c0002t0001g0007 | 4 | NA18970.hp2 NA18975.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2658-1056_2658-105 others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914631 | ||||||
| chr5:96914753 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.2658-935G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914753 | |||||||
| chr5:96914875 | A | G | 1 | a0001c0004t0001g0273 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2658-813A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914875 | |||||||
| chr5:96914881 | A | G | 14 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(11): Show |
18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.2658-807A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914881 | |||||||
| chr5:96914945 | ATTAT | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.2658-736_2658-733d others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914945 | ||||||
| chr5:96915013 | T | A | 14 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(11): Show |
18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.2658-675T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915013 | |||||||
| chr5:96915076 | T | C | 4 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(1): Show |
5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.2658-612T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915076 | |||||||
| chr5:96915100 | C | T | 23 | a0003c0003t0001g0017 a0003c0003t0001g0044 a0003c0003t0001g0045 others(20): Show |
30 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.2658-588C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915100 | |||||||
| chr5:96915224 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2658-464G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915224 | |||||||
| chr5:96915235 | C | G | 2 | a0001c0004t0001g0205 a0001c0004t0001g0206 |
2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2658-453C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915235 | |||||||
| chr5:96915298 | C | T | 4 | a0002c0002t0001g0009 a0002c0002t0001g0069 a0002c0002t0001g0124 others(1): Show |
7 | HG00741.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2658-390C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915298 | |||||||
| chr5:96915299 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2658-389G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915299 | |||||||
| chr5:96915484 | ATT | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2658-201_2658-200d others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96915484 | ||||||
| chr5:96915539 | T | A | 2 | a0001c0004t0001g0030 a0001c0004t0001g0120 |
3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2658-149T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915539 | |||||||
| chr5:96915557 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0147 a0001c0001t0001g0215 |
3 | HG01175.hp1 HG01993.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2658-131T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915557 | |||||||
| chr5:96915572 | G | A | 1 | a0002c0002t0001g0059 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2658-116G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915572 | |||||||
| chr5:96915971 | C | A | 89 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(86): Show |
120 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2739+202C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96915971 | |||||||
| chr5:96915975 | C | T | 1 | a0004c0005t0001g0287 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2739+206C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96915975 | |||||||
| chr5:96915997 | T | C | 146 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(143): Show |
191 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.2739+228T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96915997 | |||||||
| chr5:96916009 | T | C | 43 | a0002c0002t0001g0034 a0002c0002t0001g0079 a0002c0002t0001g0112 others(40): Show |
53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2739+240T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916009 | |||||||
| chr5:96916153 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2739+384G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916153 | |||||||
| chr5:96916246 | AC | A | 144 | a0001c0004t0001g0205 a0001c0004t0001g0206 a0002c0002t0001g0002 others(141): Show |
188 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.2739+478delC | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916246 | |||||||
| chr5:96916247 | C | A | 21 | a0001c0004t0001g0030 a0001c0004t0001g0037 a0001c0004t0001g0120 others(18): Show |
24 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.2739+478C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916247 | |||||||
| chr5:96916247 | CA | C | 4 | a0002c0002t0001g0052 a0002c0002t0001g0302 a0002c0002t0001g0303 others(1): Show |
5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.2739+484delA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916247 | ||||||
| chr5:96916261 | A | C | 2 | a0001c0004t0001g0205 a0001c0004t0001g0206 |
2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2739+492A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916261 | |||||||
| chr5:96916374 | C | T | 22 | a0001c0001t0001g0167 a0001c0004t0001g0030 a0001c0004t0001g0037 others(19): Show |
25 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.2739+605C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916374 | |||||||
| chr5:96916375 | G | A | 89 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(86): Show |
120 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2739+606G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916375 | |||||||
| chr5:96916456 | C | CT | 29 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(26): Show |
29 | HG00621.hp2 HG01192.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.2739+710dupT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916456 | ||||||
| chr5:96916456 | CT | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0140 a0001c0001t0001g0161 others(5): Show |
11 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.2739+710delT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916456 | ||||||
| chr5:96916456 | CTT | C | 6 | a0001c0004t0001g0205 a0002c0002t0001g0112 a0002c0002t0001g0121 others(3): Show |
6 | HG02602.hp1 HG03831.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.2739+709_2739+710d others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916456 | ||||||
| chr5:96916456 | CTTT | C | 42 | a0002c0002t0001g0002 a0002c0002t0001g0034 a0002c0002t0001g0055 others(39): Show |
52 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.2739+708_2739+710d others(5): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916456 | ||||||
| chr5:96916456 | CTTTT | C | 79 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(76): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2739+707_2739+710d others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916456 | ||||||
| chr5:96916456 | CTTTTT | C | 21 | a0002c0002t0001g0015 a0002c0002t0001g0020 a0002c0002t0001g0052 others(18): Show |
27 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2739+706_2739+710d others(7): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916456 | ||||||
| chr5:96916519 | T | G | 1 | a0001c0001t0001g0029 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2739+750T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916519 | |||||||
| chr5:96916550 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2739+781G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916550 | |||||||
| chr5:96916588 | C | T | 9 | a0002c0002t0001g0019 a0002c0002t0001g0054 a0002c0002t0001g0055 others(6): Show |
9 | HG00423.hp1 HG00609.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.2739+819C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916588 | |||||||
| chr5:96916614 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2739+845C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916614 | |||||||
| chr5:96916690 | G | A | 1 | a0001c0004t0002g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2740-772G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916690 | |||||||
| chr5:96916702 | T | C | 10 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0241 others(7): Show |
13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2740-760T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916702 | |||||||
| chr5:96916725 | C | T | 4 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2740-737C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916725 | |||||||
| chr5:96916727 | C | T | 21 | a0001c0004t0001g0030 a0001c0004t0001g0037 a0001c0004t0001g0120 others(18): Show |
24 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.2740-735C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916727 | |||||||
| chr5:96916728 | G | A | 132 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(129): Show |
173 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.2740-734G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916728 | |||||||
| chr5:96916760 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2740-702C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916760 | |||||||
| chr5:96916765 | C | CT | 153 | a0001c0001t0001g0036 a0001c0001t0001g0058 a0001c0001t0001g0060 others(150): Show |
193 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.2740-683dupT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916765 | ||||||
| chr5:96916765 | C | CTT | 7 | a0002c0002t0001g0021 a0002c0002t0001g0052 a0002c0002t0001g0100 others(4): Show |
9 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.2740-684_2740-683d others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916765 | ||||||
| chr5:96916765 | C | CTTT | 10 | a0005c0006t0001g0012 a0005c0006t0001g0194 a0005c0006t0001g0241 others(7): Show |
13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2740-685_2740-683d others(5): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916765 | ||||||
| chr5:96916765 | CT | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(38): Show |
58 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.2740-683delT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916765 | ||||||
| chr5:96916779 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2740-683T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916779 | |||||||
| chr5:96916885 | T | C | 132 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(129): Show |
173 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.2740-577T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916885 | |||||||
| chr5:96917098 | C | T | 1 | a0002c0002t0001g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2740-364C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96917098 | |||||||
| chr5:96917099 | G | A | 88 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(85): Show |
119 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.2740-363G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96917099 | |||||||
| chr5:96917239 | TG | T | 89 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(86): Show |
120 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2740-220delG | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96917239 | ||||||
| chr5:96917294 | A | G | 89 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(86): Show |
120 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2740-168A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96917294 | |||||||
| chr5:96917400 | T | C | 89 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(86): Show |
120 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2740-62T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96917400 |