Item | Value |
---|---|
geneid | 51752 |
ensemblid | ENSG00000164307.13 |
hgncid | 18173 |
symbol | ERAP1 |
name | endoplasmic reticulum aminopeptidase 1 |
refseq_nuc | NM_001040458.3 |
refseq_prot | NP_001035548.1 |
ensembl_nuc | ENST00000443439.7 |
ensembl_prot | ENSP00000406304.2 |
mane_status | MANE Select |
chr | chr5 |
start | 96774484 |
end | 96807945 |
strand | - |
ver | v1.2 |
region | chr5:96774484-96807945 |
region5000 | chr5:96769484-96812945 |
regionname0 | ERAP1_chr5_96774484_96807945 |
regionname5000 | ERAP1_chr5_96769484_96812945 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 941 | 112 | 27 | 13 | 60 | 5 | 6 | 44 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0002 | 0/0 | 941 | 76 | 7 | 5 | 48 | 4 | 12 | 38 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0003 | 0/0 | 941 | 46 | 6 | 15 | 19 | 2 | 4 | 15 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0004 | 0/0 | 941 | 44 | 2 | 3 | 37 | 1 | 1 | 31 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0005 | 0/0 | 941 | 33 | 14 | 4 | 8 | 1 | 6 | 8 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0006 | 0/0 | 941 | 20 | 2 | 9 | 0 | 4 | 5 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0007 | 0/0 | 941 | 16 | 0 | 8 | 7 | 0 | 1 | 7 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0008 | 0/0 | 941 | 15 | 4 | 10 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0009 | 0/0 | 941 | 15 | 8 | 4 | 0 | 0 | 3 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0010 | 0/0 | 941 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0011 | 0/0 | 941 | 8 | 0 | 3 | 2 | 0 | 3 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0012 | 0/0 | 941 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0013 | 0/0 | 941 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0014 | 0/0 | 941 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0015 | 0/0 | 941 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0016 | 0/0 | 941 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0017 | 0/0 | 662 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(657): Show |
chr5 | 96769484 | 96812945 |
a0018 | 0/0 | 941 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0019 | 0/0 | 941 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0020 | 0/0 | 941 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0021 | 0/0 | 941 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0022 | 0/0 | 941 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(936): Show |
chr5 | 96769484 | 96812945 |
a0023 | 0/1 | 622 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | MVFLP others(617): Show |
chr5 | 96769484 | 96812945 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2823 | 96 | 24 | 13 | 47 | 5 | 6 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0001c0010 | 0/0 | 2823 | 13 | 0 | 0 | 13 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0001c0015 | 0/0 | 2823 | 3 | 3 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0002c0002 | 0/0 | 2823 | 74 | 7 | 5 | 46 | 4 | 12 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0002c0020 | 0/0 | 2823 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0003c0003 | 0/0 | 2823 | 46 | 6 | 15 | 19 | 2 | 4 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0004c0004 | 0/0 | 2823 | 44 | 2 | 3 | 37 | 1 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0005c0005 | 0/0 | 2823 | 27 | 9 | 4 | 8 | 1 | 5 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0005c0013 | 0/0 | 2823 | 5 | 5 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0005c0032 | 0/0 | 2823 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0006c0006 | 0/0 | 2823 | 17 | 2 | 7 | 0 | 4 | 4 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0006c0034 | 0/0 | 2823 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0006c0035 | 0/0 | 2823 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0006c0036 | 0/0 | 2823 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0007c0007 | 0/0 | 2823 | 16 | 0 | 8 | 7 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0008c0008 | 0/0 | 2823 | 14 | 4 | 9 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0008c0025 | 0/0 | 2823 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0009c0009 | 0/0 | 2823 | 14 | 7 | 4 | 0 | 0 | 3 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0009c0028 | 0/0 | 2823 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0010c0012 | 0/0 | 2823 | 7 | 6 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0010c0018 | 0/0 | 2823 | 2 | 1 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0011c0011 | 0/0 | 2823 | 8 | 0 | 3 | 2 | 0 | 3 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0012c0014 | 0/0 | 2823 | 4 | 4 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0013c0016 | 0/0 | 2823 | 3 | 0 | 2 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0014c0017 | 0/0 | 2823 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0014c0022 | 0/0 | 2823 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0015c0023 | 0/0 | 2823 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0015c0033 | 0/0 | 2823 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0016c0019 | 0/0 | 2823 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0017c0021 | 0/0 | 2823 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0018c0030 | 0/0 | 2823 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0019c0027 | 0/0 | 2823 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0020c0029 | 0/0 | 2823 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0021c0026 | 0/0 | 2823 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0022c0031 | 0/0 | 2823 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2818): Show |
chr5 | 96769484 | 96812945 | ||
a0023c0024 | 0/1 | 2819 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ATGGT others(2814): Show |
chr5 | 96769484 | 96812945 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4833 | 22 | 1 | 3 | 18 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0001c0001t0002 | 1/0 | 4841 | 72 | 23 | 10 | 27 | 5 | 6 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4836): Show |
chr5 | 96769484 | 96812945 |
a0001c0001t0012 | 0/0 | 4845 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4840): Show |
chr5 | 96769484 | 96812945 |
a0001c0010t0001 | 0/0 | 4833 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0001c0010t0002 | 0/0 | 4841 | 12 | 0 | 0 | 12 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4836): Show |
chr5 | 96769484 | 96812945 |
a0001c0015t0010 | 0/0 | 4836 | 3 | 3 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4831): Show |
chr5 | 96769484 | 96812945 |
a0002c0002t0001 | 0/0 | 4833 | 57 | 6 | 0 | 45 | 2 | 4 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0002c0002t0003 | 0/0 | 4849 | 5 | 0 | 1 | 0 | 0 | 4 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4844): Show |
chr5 | 96769484 | 96812945 |
a0002c0002t0006 | 0/0 | 4838 | 2 | 0 | 1 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4833): Show |
chr5 | 96769484 | 96812945 |
a0002c0002t0008 | 0/0 | 4834 | 5 | 0 | 2 | 0 | 2 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4829): Show |
chr5 | 96769484 | 96812945 |
a0002c0002t0014 | 0/0 | 4833 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0002c0002t0017 | 0/0 | 4833 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0002c0002t0018 | 0/0 | 4833 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0002c0002t0020 | 0/0 | 4833 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0002c0002t0021 | 0/0 | 4833 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0002c0020t0002 | 0/0 | 4841 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4836): Show |
chr5 | 96769484 | 96812945 |
a0003c0003t0001 | 0/0 | 4833 | 6 | 5 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0003c0003t0003 | 0/0 | 4849 | 40 | 1 | 15 | 18 | 2 | 4 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4844): Show |
chr5 | 96769484 | 96812945 |
a0004c0004t0001 | 0/0 | 4833 | 41 | 2 | 2 | 36 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0004c0004t0002 | 0/0 | 4841 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4836): Show |
chr5 | 96769484 | 96812945 |
a0004c0004t0005 | 0/0 | 4833 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0004c0004t0019 | 0/0 | 4833 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0005c0005t0001 | 0/0 | 4833 | 18 | 6 | 1 | 8 | 0 | 3 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0005c0005t0005 | 0/0 | 4833 | 8 | 3 | 3 | 0 | 1 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0005c0005t0006 | 0/0 | 4838 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4833): Show |
chr5 | 96769484 | 96812945 |
a0005c0013t0001 | 0/0 | 4833 | 5 | 5 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0005c0032t0005 | 0/0 | 4833 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0006c0006t0004 | 0/0 | 4839 | 15 | 2 | 5 | 0 | 4 | 4 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4834): Show |
chr5 | 96769484 | 96812945 |
a0006c0006t0011 | 0/0 | 4839 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4834): Show |
chr5 | 96769484 | 96812945 |
a0006c0034t0008 | 0/0 | 4834 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4829): Show |
chr5 | 96769484 | 96812945 |
a0006c0035t0004 | 0/0 | 4839 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4834): Show |
chr5 | 96769484 | 96812945 |
a0006c0036t0004 | 0/0 | 4839 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4834): Show |
chr5 | 96769484 | 96812945 |
a0007c0007t0001 | 0/0 | 4833 | 8 | 0 | 8 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0007c0007t0002 | 0/0 | 4841 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4836): Show |
chr5 | 96769484 | 96812945 |
a0007c0007t0007 | 0/0 | 4841 | 7 | 0 | 0 | 7 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4836): Show |
chr5 | 96769484 | 96812945 |
a0008c0008t0002 | 0/0 | 4841 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4836): Show |
chr5 | 96769484 | 96812945 |
a0008c0008t0003 | 0/0 | 4849 | 13 | 4 | 8 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4844): Show |
chr5 | 96769484 | 96812945 |
a0008c0025t0003 | 0/0 | 4849 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4844): Show |
chr5 | 96769484 | 96812945 |
a0009c0009t0001 | 0/0 | 4833 | 6 | 5 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0009c0009t0002 | 0/0 | 4841 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4836): Show |
chr5 | 96769484 | 96812945 |
a0009c0009t0006 | 0/0 | 4838 | 5 | 1 | 1 | 0 | 0 | 3 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4833): Show |
chr5 | 96769484 | 96812945 |
a0009c0009t0009 | 0/0 | 4837 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4832): Show |
chr5 | 96769484 | 96812945 |
a0009c0009t0016 | 0/0 | 4841 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4836): Show |
chr5 | 96769484 | 96812945 |
a0009c0028t0009 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4832): Show |
chr5 | 96769484 | 96812945 |
a0010c0012t0001 | 0/0 | 4833 | 7 | 6 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0010c0018t0001 | 0/0 | 4833 | 2 | 1 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0011c0011t0001 | 0/0 | 4833 | 7 | 0 | 3 | 1 | 0 | 3 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0011c0011t0015 | 0/0 | 4833 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0012c0014t0001 | 0/0 | 4833 | 4 | 4 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0013c0016t0002 | 0/0 | 4841 | 3 | 0 | 2 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4836): Show |
chr5 | 96769484 | 96812945 |
a0014c0017t0001 | 0/0 | 4833 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0014c0022t0009 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4832): Show |
chr5 | 96769484 | 96812945 |
a0015c0023t0001 | 0/0 | 4833 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0015c0033t0001 | 0/0 | 4833 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0016c0019t0001 | 0/0 | 4833 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0016c0019t0002 | 0/0 | 4841 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4836): Show |
chr5 | 96769484 | 96812945 |
a0017c0021t0013 | 0/0 | 4853 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4848): Show |
chr5 | 96769484 | 96812945 |
a0018c0030t0002 | 0/0 | 4841 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4836): Show |
chr5 | 96769484 | 96812945 |
a0019c0027t0006 | 0/0 | 4838 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4833): Show |
chr5 | 96769484 | 96812945 |
a0020c0029t0022 | 0/0 | 4849 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4844): Show |
chr5 | 96769484 | 96812945 |
a0021c0026t0001 | 0/0 | 4833 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0022c0031t0001 | 0/0 | 4833 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4828): Show |
chr5 | 96769484 | 96812945 |
a0023c0024t0001 | 0/1 | 4829 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | ACTTT others(4824): Show |
chr5 | 96769484 | 96812945 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0009 | 1/0 | 5 | 0 | 0 | 1 | 2 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0001t0012g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0010t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0010t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0010t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0010t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0010t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0010t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0010t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0010t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0010t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0010t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0010t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0010t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0015t0010g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0015t0010g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0001c0015t0010g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0001 | 0/0 | 10 | 1 | 0 | 7 | 0 | 2 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0019 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0003g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0006g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0008g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0008g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0008g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0008g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0008g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0014g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0017g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0018g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0020g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0002t0021g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0020t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0002c0020t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0004 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0003c0003t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0004c0004t0019g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0001g0006 | 0/0 | 5 | 1 | 1 | 2 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0005g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0005g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0005t0006g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0013t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0013t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0013t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0005c0032t0005g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0006t0004g0021 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0006t0004g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0006t0004g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0006t0004g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0006t0004g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0006t0004g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0006t0004g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0006t0004g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0006t0004g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0006t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0006t0004g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0006t0011g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0034t0008g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0035t0004g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0006c0036t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0007g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0007g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0007c0007t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0008c0008t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0008c0008t0003g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0008c0008t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0008c0008t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0008c0008t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0008c0008t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0008c0008t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0008c0008t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0008c0008t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0008c0025t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0009c0009t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0009c0009t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0009c0009t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0009c0009t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0009c0009t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0009c0009t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0009c0009t0006g0016 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0009c0009t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0009c0009t0006g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0009c0009t0009g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0009c0009t0016g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0009c0028t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0010c0012t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0010c0012t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0010c0012t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0010c0012t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0010c0012t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0010c0012t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0010c0012t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0010c0018t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0010c0018t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0011c0011t0001g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0011c0011t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0011c0011t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0011c0011t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0011c0011t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0011c0011t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0011c0011t0015g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0012c0014t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0012c0014t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0012c0014t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0012c0014t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0013c0016t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0013c0016t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0013c0016t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0014c0017t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0014c0017t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0014c0022t0009g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0015c0023t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0015c0033t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0016c0019t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0016c0019t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0017c0021t0013g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0017c0021t0013g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0018c0030t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0019c0027t0006g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0020c0029t0022g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0021c0026t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0022c0031t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
a0023c0024t0001g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0003 | t0003 | g0004 | EUR | GBR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00099 | hp2 | a0004 | c0004 | t0001 | g0041 | EUR | GBR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0159 | EUR | GBR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0019 | EUR | GBR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | FIN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00280 | hp2 | a0006 | c0006 | t0004 | g0021 | EUR | FIN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0097 | EUR | FIN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0237 | EUR | FIN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0244 | EAS | CHS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | CHS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00544 | hp1 | a0004 | c0004 | t0001 | g0274 | EAS | CHS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00558 | hp1 | a0004 | c0004 | t0001 | g0276 | EAS | CHS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00558 | hp2 | a0015 | c0033 | t0001 | g0095 | EAS | CHS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | CHS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00597 | hp2 | a0004 | c0004 | t0001 | g0266 | EAS | CHS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00609 | hp1 | a0004 | c0004 | t0005 | g0270 | EAS | CHS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00609 | hp2 | a0003 | c0003 | t0003 | g0176 | EAS | CHS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | CHS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00639 | hp1 | a0003 | c0003 | t0003 | g0179 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00639 | hp2 | a0008 | c0008 | t0003 | g0005 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00733 | hp2 | a0002 | c0002 | t0003 | g0234 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00735 | hp1 | a0003 | c0003 | t0003 | g0202 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00738 | hp1 | a0011 | c0011 | t0001 | g0045 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00738 | hp2 | a0010 | c0012 | t0001 | g0293 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00741 | hp1 | a0018 | c0030 | t0002 | g0106 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG00741 | hp2 | a0003 | c0003 | t0003 | g0188 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01069 | hp1 | a0007 | c0007 | t0001 | g0116 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01069 | hp2 | a0003 | c0003 | t0003 | g0004 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01070 | hp1 | a0006 | c0006 | t0004 | g0044 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01070 | hp2 | a0003 | c0003 | t0003 | g0185 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01071 | hp1 | a0006 | c0006 | t0004 | g0044 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01071 | hp2 | a0007 | c0007 | t0001 | g0026 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01074 | hp1 | a0003 | c0003 | t0003 | g0004 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01081 | hp1 | a0006 | c0006 | t0004 | g0021 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01081 | hp2 | a0003 | c0003 | t0003 | g0030 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01099 | hp1 | a0003 | c0003 | t0003 | g0210 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01099 | hp2 | a0002 | c0002 | t0008 | g0214 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01106 | hp2 | a0006 | c0006 | t0004 | g0309 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01109 | hp1 | a0009 | c0009 | t0001 | g0170 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01109 | hp2 | a0009 | c0009 | t0009 | g0154 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01167 | hp1 | a0008 | c0008 | t0003 | g0005 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01168 | hp1 | a0008 | c0008 | t0003 | g0005 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01168 | hp2 | a0006 | c0006 | t0011 | g0043 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01169 | hp1 | a0006 | c0006 | t0011 | g0043 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01169 | hp2 | a0008 | c0008 | t0003 | g0005 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01175 | hp1 | a0006 | c0034 | t0008 | g0310 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01175 | hp2 | a0005 | c0005 | t0005 | g0064 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01192 | hp1 | a0003 | c0003 | t0003 | g0187 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01192 | hp2 | a0006 | c0006 | t0004 | g0305 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01243 | hp1 | a0008 | c0008 | t0002 | g0051 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01243 | hp2 | a0008 | c0025 | t0003 | g0052 | AMR | PUR | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01256 | hp1 | a0013 | c0016 | t0002 | g0126 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01257 | hp1 | a0008 | c0008 | t0003 | g0022 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01258 | hp2 | a0008 | c0008 | t0003 | g0022 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01261 | hp1 | a0008 | c0008 | t0003 | g0053 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01261 | hp2 | a0003 | c0003 | t0003 | g0030 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01346 | hp1 | a0004 | c0004 | t0001 | g0041 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01346 | hp2 | a0005 | c0005 | t0001 | g0006 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01358 | hp1 | a0003 | c0003 | t0003 | g0198 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01358 | hp2 | a0008 | c0008 | t0003 | g0005 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01361 | hp1 | a0019 | c0027 | t0006 | g0163 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01361 | hp2 | a0005 | c0005 | t0005 | g0074 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01433 | hp2 | a0002 | c0002 | t0006 | g0223 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01496 | hp1 | a0010 | c0018 | t0001 | g0294 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01496 | hp2 | a0009 | c0009 | t0016 | g0171 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01515 | hp1 | a0002 | c0002 | t0008 | g0235 | EUR | IBS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01515 | hp2 | a0006 | c0006 | t0004 | g0307 | EUR | IBS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01516 | hp1 | a0008 | c0008 | t0003 | g0054 | EUR | IBS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01516 | hp2 | a0006 | c0006 | t0004 | g0042 | EUR | IBS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01517 | hp1 | a0006 | c0006 | t0004 | g0042 | EUR | IBS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01517 | hp2 | a0002 | c0002 | t0008 | g0219 | EUR | IBS | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01884 | hp1 | a0010 | c0012 | t0001 | g0285 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01884 | hp2 | a0009 | c0009 | t0002 | g0167 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01891 | hp2 | a0010 | c0012 | t0001 | g0318 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01934 | hp1 | a0003 | c0003 | t0003 | g0177 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01934 | hp2 | a0006 | c0036 | t0004 | g0312 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01943 | hp1 | a0003 | c0003 | t0003 | g0017 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01975 | hp1 | a0011 | c0011 | t0001 | g0314 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01975 | hp2 | a0007 | c0007 | t0001 | g0158 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01978 | hp1 | a0002 | c0002 | t0008 | g0249 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01981 | hp1 | a0007 | c0007 | t0001 | g0117 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01981 | hp2 | a0011 | c0011 | t0001 | g0316 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01993 | hp1 | a0005 | c0005 | t0005 | g0023 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01993 | hp2 | a0004 | c0004 | t0002 | g0273 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02004 | hp1 | a0003 | c0003 | t0003 | g0178 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02004 | hp2 | a0007 | c0007 | t0001 | g0114 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02015 | hp1 | a0001 | c0010 | t0002 | g0122 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02015 | hp2 | a0011 | c0011 | t0015 | g0315 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02040 | hp1 | a0001 | c0010 | t0002 | g0118 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02055 | hp1 | a0002 | c0002 | t0020 | g0253 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02080 | hp2 | a0002 | c0020 | t0002 | g0248 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02083 | hp2 | a0003 | c0003 | t0003 | g0190 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02129 | hp2 | a0004 | c0004 | t0001 | g0281 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02135 | hp2 | a0004 | c0004 | t0001 | g0264 | EAS | KHV | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02148 | hp1 | a0007 | c0007 | t0001 | g0113 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02148 | hp2 | a0004 | c0004 | t0001 | g0280 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02155 | hp1 | a0001 | c0010 | t0001 | g0123 | EAS | CDX | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02155 | hp2 | a0003 | c0003 | t0003 | g0208 | EAS | CDX | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02257 | hp1 | a0006 | c0006 | t0004 | g0021 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02257 | hp2 | a0003 | c0003 | t0003 | g0192 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02258 | hp1 | a0008 | c0008 | t0003 | g0207 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02280 | hp1 | a0010 | c0012 | t0001 | g0296 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02293 | hp1 | a0003 | c0003 | t0003 | g0194 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02293 | hp2 | a0007 | c0007 | t0001 | g0026 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02300 | hp1 | a0002 | c0002 | t0014 | g0257 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02300 | hp2 | a0007 | c0007 | t0001 | g0084 | AMR | PEL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02451 | hp1 | a0005 | c0013 | t0001 | g0259 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02451 | hp2 | a0016 | c0019 | t0001 | g0189 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02572 | hp1 | a0005 | c0005 | t0005 | g0096 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02572 | hp2 | a0017 | c0021 | t0013 | g0060 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02602 | hp1 | a0011 | c0011 | t0001 | g0174 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02602 | hp2 | a0005 | c0005 | t0001 | g0105 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02615 | hp1 | a0012 | c0014 | t0001 | g0289 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02615 | hp2 | a0008 | c0008 | t0003 | g0206 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02622 | hp1 | a0004 | c0004 | t0001 | g0279 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02622 | hp2 | a0009 | c0009 | t0001 | g0029 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02630 | hp1 | a0009 | c0009 | t0001 | g0169 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02647 | hp1 | a0012 | c0014 | t0001 | g0287 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02647 | hp2 | a0008 | c0008 | t0003 | g0055 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02683 | hp1 | a0002 | c0002 | t0008 | g0258 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02683 | hp2 | a0003 | c0003 | t0003 | g0004 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02698 | hp2 | a0003 | c0003 | t0003 | g0201 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02735 | hp1 | a0006 | c0035 | t0004 | g0311 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02735 | hp2 | a0002 | c0002 | t0006 | g0218 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02738 | hp1 | a0003 | c0003 | t0003 | g0200 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02738 | hp2 | a0011 | c0011 | t0001 | g0175 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02809 | hp1 | a0005 | c0005 | t0001 | g0072 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02818 | hp1 | a0009 | c0009 | t0001 | g0029 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02818 | hp2 | a0010 | c0012 | t0001 | g0291 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02886 | hp1 | a0005 | c0005 | t0001 | g0006 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02886 | hp2 | a0004 | c0004 | t0001 | g0278 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0213 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02895 | hp2 | a0005 | c0005 | t0001 | g0152 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02896 | hp1 | a0003 | c0003 | t0001 | g0018 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02897 | hp2 | a0005 | c0005 | t0001 | g0112 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02922 | hp1 | a0014 | c0022 | t0009 | g0299 | AFR | ESN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02965 | hp2 | a0005 | c0013 | t0001 | g0020 | AFR | ESN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0254 | AFR | ESN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02970 | hp2 | a0009 | c0028 | t0009 | g0094 | AFR | ESN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02976 | hp2 | a0001 | c0015 | t0010 | g0261 | AFR | ESN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03098 | hp1 | a0017 | c0021 | t0013 | g0059 | AFR | MSL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03098 | hp2 | a0005 | c0005 | t0001 | g0076 | AFR | MSL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03130 | hp1 | a0008 | c0008 | t0003 | g0056 | AFR | ESN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03130 | hp2 | a0020 | c0029 | t0022 | g0061 | AFR | ESN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03195 | hp1 | a0003 | c0003 | t0001 | g0203 | AFR | ESN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ESN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03225 | hp1 | a0005 | c0005 | t0001 | g0068 | AFR | MSL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03225 | hp2 | a0005 | c0005 | t0005 | g0070 | AFR | MSL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03239 | hp1 | a0009 | c0009 | t0006 | g0162 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03239 | hp2 | a0005 | c0005 | t0006 | g0078 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03453 | hp1 | a0009 | c0009 | t0006 | g0161 | AFR | MSL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03453 | hp2 | a0015 | c0023 | t0001 | g0160 | AFR | MSL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03486 | hp1 | a0014 | c0017 | t0001 | g0298 | AFR | MSL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03486 | hp2 | a0009 | c0009 | t0001 | g0166 | AFR | MSL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03490 | hp1 | a0013 | c0016 | t0002 | g0133 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03490 | hp2 | a0002 | c0002 | t0003 | g0033 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03491 | hp1 | a0002 | c0002 | t0003 | g0221 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03492 | hp1 | a0002 | c0002 | t0003 | g0222 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03492 | hp2 | a0002 | c0002 | t0003 | g0033 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03516 | hp1 | a0012 | c0014 | t0001 | g0286 | AFR | ESN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03540 | hp1 | a0014 | c0017 | t0001 | g0290 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03540 | hp2 | a0016 | c0019 | t0002 | g0196 | AFR | GWD | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03579 | hp1 | a0005 | c0013 | t0001 | g0020 | AFR | MSL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03579 | hp2 | a0003 | c0003 | t0001 | g0018 | AFR | MSL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0238 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03669 | hp2 | a0006 | c0006 | t0004 | g0308 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03688 | hp1 | a0005 | c0005 | t0001 | g0006 | SAS | STU | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03688 | hp2 | a0002 | c0002 | t0018 | g0247 | SAS | STU | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03710 | hp2 | a0005 | c0005 | t0005 | g0062 | SAS | PJL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03831 | hp1 | a0009 | c0009 | t0006 | g0016 | SAS | BEB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03831 | hp2 | a0011 | c0011 | t0001 | g0173 | SAS | BEB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | BEB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03927 | hp2 | a0006 | c0006 | t0004 | g0306 | SAS | BEB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03942 | hp1 | a0003 | c0003 | t0003 | g0193 | SAS | BEB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03942 | hp2 | a0005 | c0032 | t0005 | g0067 | SAS | BEB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG04184 | hp1 | a0004 | c0004 | t0019 | g0272 | SAS | BEB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG04184 | hp2 | a0007 | c0007 | t0002 | g0083 | SAS | BEB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG04199 | hp1 | a0006 | c0006 | t0004 | g0304 | SAS | STU | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0034 | SAS | STU | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | STU | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG04204 | hp2 | a0006 | c0006 | t0004 | g0317 | SAS | STU | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG04228 | hp1 | a0002 | c0002 | t0017 | g0211 | SAS | STU | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | STU | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18522 | hp1 | a0003 | c0003 | t0001 | g0184 | AFR | YRI | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18522 | hp2 | a0005 | c0013 | t0001 | g0020 | AFR | YRI | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18612 | hp2 | a0003 | c0003 | t0003 | g0199 | EAS | CHB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18906 | hp1 | a0021 | c0026 | t0001 | g0216 | AFR | YRI | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | YRI | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18939 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18943 | hp1 | a0004 | c0004 | t0001 | g0039 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18945 | hp1 | a0001 | c0001 | t0012 | g0028 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18946 | hp1 | a0004 | c0004 | t0001 | g0037 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18946 | hp2 | a0003 | c0003 | t0003 | g0017 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18947 | hp1 | a0005 | c0005 | t0001 | g0066 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18947 | hp2 | a0001 | c0010 | t0002 | g0135 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18948 | hp1 | a0004 | c0004 | t0001 | g0040 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18949 | hp2 | a0007 | c0007 | t0007 | g0085 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18950 | hp1 | a0004 | c0004 | t0001 | g0038 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18953 | hp1 | a0004 | c0004 | t0001 | g0035 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18953 | hp2 | a0004 | c0004 | t0001 | g0035 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18954 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18957 | hp1 | a0001 | c0010 | t0002 | g0027 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18957 | hp2 | a0003 | c0003 | t0001 | g0183 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18960 | hp2 | a0003 | c0003 | t0003 | g0186 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18961 | hp1 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18961 | hp2 | a0004 | c0004 | t0001 | g0037 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18962 | hp2 | a0005 | c0005 | t0001 | g0075 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18963 | hp1 | a0003 | c0003 | t0003 | g0182 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18964 | hp1 | a0004 | c0004 | t0001 | g0040 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18967 | hp2 | a0004 | c0004 | t0001 | g0269 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18968 | hp1 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18972 | hp2 | a0001 | c0010 | t0002 | g0119 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18973 | hp1 | a0007 | c0007 | t0007 | g0092 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18974 | hp1 | a0011 | c0011 | t0001 | g0045 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18974 | hp2 | a0004 | c0004 | t0001 | g0275 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18975 | hp1 | a0004 | c0004 | t0001 | g0267 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18980 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18981 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18982 | hp1 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18984 | hp1 | a0005 | c0005 | t0001 | g0082 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18985 | hp1 | a0001 | c0010 | t0002 | g0065 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18985 | hp2 | a0005 | c0005 | t0001 | g0071 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18986 | hp1 | a0004 | c0004 | t0001 | g0036 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18988 | hp2 | a0003 | c0003 | t0003 | g0017 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18990 | hp2 | a0004 | c0004 | t0001 | g0038 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18991 | hp1 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18991 | hp2 | a0004 | c0004 | t0001 | g0271 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18993 | hp1 | a0004 | c0004 | t0001 | g0268 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18994 | hp2 | a0007 | c0007 | t0007 | g0091 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18995 | hp2 | a0003 | c0003 | t0003 | g0031 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18997 | hp2 | a0003 | c0003 | t0003 | g0181 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18999 | hp1 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19000 | hp1 | a0004 | c0004 | t0001 | g0265 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19001 | hp2 | a0007 | c0007 | t0007 | g0157 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19003 | hp2 | a0005 | c0005 | t0001 | g0063 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19004 | hp1 | a0001 | c0001 | t0012 | g0028 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19004 | hp2 | a0003 | c0003 | t0003 | g0205 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19005 | hp1 | a0003 | c0003 | t0003 | g0195 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19005 | hp2 | a0001 | c0010 | t0002 | g0124 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19006 | hp1 | a0002 | c0002 | t0021 | g0212 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19006 | hp2 | a0004 | c0004 | t0001 | g0204 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19010 | hp2 | a0005 | c0005 | t0001 | g0079 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19011 | hp1 | a0003 | c0003 | t0003 | g0031 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | LWK | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19030 | hp2 | a0001 | c0015 | t0010 | g0262 | AFR | LWK | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19059 | hp1 | a0003 | c0003 | t0003 | g0172 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19059 | hp2 | a0007 | c0007 | t0007 | g0090 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19060 | hp1 | a0004 | c0004 | t0001 | g0057 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19062 | hp1 | a0004 | c0004 | t0001 | g0284 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19063 | hp2 | a0001 | c0010 | t0002 | g0137 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19065 | hp1 | a0001 | c0010 | t0002 | g0151 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19065 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19067 | hp1 | a0007 | c0007 | t0007 | g0086 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19072 | hp1 | a0001 | c0010 | t0002 | g0027 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19074 | hp1 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19074 | hp2 | a0001 | c0010 | t0002 | g0120 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19075 | hp1 | a0007 | c0007 | t0007 | g0115 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19075 | hp2 | a0003 | c0003 | t0003 | g0191 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19076 | hp1 | a0001 | c0010 | t0002 | g0088 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19076 | hp2 | a0004 | c0004 | t0001 | g0277 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19080 | hp1 | a0002 | c0020 | t0002 | g0233 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19081 | hp1 | a0003 | c0003 | t0003 | g0197 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19081 | hp2 | a0004 | c0004 | t0001 | g0282 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19085 | hp2 | a0004 | c0004 | t0001 | g0036 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19087 | hp2 | a0004 | c0004 | t0001 | g0039 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19091 | hp1 | a0004 | c0004 | t0001 | g0283 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19240 | hp1 | a0010 | c0012 | t0001 | g0295 | AFR | YRI | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA19240 | hp2 | a0001 | c0015 | t0010 | g0263 | AFR | YRI | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA20129 | hp1 | a0012 | c0014 | t0001 | g0288 | AFR | ASW | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ASW | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA20752 | hp1 | a0005 | c0005 | t0005 | g0023 | EUR | TSI | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA20752 | hp2 | a0003 | c0003 | t0003 | g0180 | EUR | TSI | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0049 | EUR | TSI | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | TSI | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA20905 | hp1 | a0009 | c0009 | t0006 | g0016 | SAS | GIH | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA20905 | hp2 | a0005 | c0005 | t0001 | g0081 | SAS | GIH | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01123 | hp1 | a0013 | c0016 | t0002 | g0144 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG01123 | hp2 | a0009 | c0009 | t0006 | g0016 | AMR | CLM | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02109 | hp2 | a0006 | c0006 | t0004 | g0313 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02486 | hp1 | a0005 | c0005 | t0005 | g0077 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02559 | hp1 | a0010 | c0012 | t0001 | g0297 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG02559 | hp2 | a0003 | c0003 | t0001 | g0018 | AFR | ACB | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG03471 | hp2 | a0010 | c0018 | t0001 | g0292 | AFR | MSL | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0215 | AFR | USA | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | USA | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA20300 | hp1 | a0005 | c0013 | t0001 | g0260 | AFR | USA | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA20300 | hp2 | a0022 | c0031 | t0001 | g0131 | AFR | USA | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
NA21309 | hp2 | a0009 | c0009 | t0001 | g0168 | AFR | LWK | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
homoSapiens | chm13v2 | a0023 | c0024 | t0001 | g0050 | REF | REF | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0009 | REF | REF | ERAP1_chr5_96769484_96812945 | ERAP1 | chr5 | 96769484 | 96812945 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:96781844 | C | T | 1 | a0022 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.2296G>A | p.Asp766Asn | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 16/19 | 2399/4841 | 2296/2826 | 766/941 | chr5 | 96781844 | |||
chr5:96783128 | A | C | 1 | a0018 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.2208T>G | p.Cys736Trp | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/19 | 2311/4841 | 2208/2826 | 736/941 | chr5 | 96783128 | |||
chr5:96783148 | G | C | 17 | a0002 a0003 a0004 others(14): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
missense_variant | MODERATE | c.2188C>G | p.Gln730Glu | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/19 | 2291/4841 | 2188/2826 | 730/941 | chr5 | 96783148 | |||
chr5:96783162 | C | T | 2 | a0003 a0021 |
47 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(44): Show |
missense_variant | MODERATE | c.2174G>A | p.Arg725Gln | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/19 | 2277/4841 | 2174/2826 | 725/941 | chr5 | 96783162 | |||
chr5:96784035 | G | C | 1 | a0017 | 2 | HG02572.hp2 HG03098.hp1 |
stop_gained | HIGH | c.1989C>G | p.Tyr663* | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/19 | 2092/4841 | 1989/2826 | 663/941 | chr5 | 96784035 | |||
chr5:96785792 | C | T | 1 | a0013 | 3 | HG01123.hp1 HG01256.hp1 HG03490.hp1 |
missense_variant | MODERATE | c.1939G>A | p.Val647Ile | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/19 | 2042/4841 | 1939/2826 | 647/941 | chr5 | 96785792 | |||
chr5:96785968 | A | C | 1 | a0012 | 4 | HG02615.hp1 HG02647.hp1 HG03516.hp1 others(1): Show |
missense_variant | MODERATE | c.1763T>G | p.Val588Gly | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/19 | 1866/4841 | 1763/2826 | 588/941 | chr5 | 96785968 | |||
chr5:96786505 | T | C | 2 | a0017 a0020 |
3 | HG02572.hp2 HG03098.hp1 HG03130.hp2 |
missense_variant | MODERATE | c.1724A>G | p.Asp575Gly | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 12/19 | 1827/4841 | 1724/2826 | 575/941 | chr5 | 96786505 | |||
chr5:96786506 | C | T | 2 | a0003 a0016 |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
missense_variant | MODERATE | c.1723G>A | p.Asp575Asn | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 12/19 | 1826/4841 | 1723/2826 | 575/941 | chr5 | 96786506 | |||
chr5:96788627 | T | C | 16 | a0002 a0003 a0004 others(13): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
missense_variant | MODERATE | c.1583A>G | p.Lys528Arg | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/19 | 1686/4841 | 1583/2826 | 528/941 | chr5 | 96788627 | |||
chr5:96788670 | C | T | 1 | a0019 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.1540G>A | p.Gly514Arg | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/19 | 1643/4841 | 1540/2826 | 514/941 | chr5 | 96788670 | |||
chr5:96793832 | T | C | 2 | a0003 a0016 |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
missense_variant | MODERATE | c.1045A>G | p.Met349Val | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 6/19 | 1148/4841 | 1045/2826 | 349/941 | chr5 | 96793832 | |||
chr5:96793840 | C | T | 5 | a0009 a0010 a0012 others(2): Show |
32 | HG00738.hp2 HG01109.hp1 HG01109.hp2 others(29): Show |
missense_variant | MODERATE | c.1037G>A | p.Gly346Asp | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 6/19 | 1140/4841 | 1037/2826 | 346/941 | chr5 | 96793840 | |||
chr5:96795133 | T | C | 3 | a0002 a0015 a0021 |
79 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(76): Show |
missense_variant | MODERATE | c.828A>G | p.Ile276Met | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/19 | 931/4841 | 828/2826 | 276/941 | chr5 | 96795133 | |||
chr5:96803547 | C | G | 11 | a0002 a0003 a0004 others(8): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
missense_variant | MODERATE | c.380G>C | p.Arg127Pro | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/19 | 483/4841 | 380/2826 | 127/941 | chr5 | 96803547 | |||
chr5:96803761 | C | T | 3 | a0004 a0012 a0014 |
51 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(48): Show |
missense_variant | MODERATE | c.166G>A | p.Glu56Lys | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/19 | 269/4841 | 166/2826 | 56/941 | chr5 | 96803761 | |||
chr5:96803892 | G | A | 2 | a0006 a0011 |
28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
missense_variant | MODERATE | c.35C>T | p.Thr12Ile | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/19 | 138/4841 | 35/2826 | 12/941 | chr5 | 96803892 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:96776435 | G | A | 2 | a0009c0028 a0014c0022 |
2 | HG02922.hp1 HG02970.hp2 |
synonymous_variant | LOW | c.2787C>T | p.Ile929Ile | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 2890/4841 | 2787/2826 | 929/941 | chr5 | 96776435 | |||
chr5:96781104 | G | A | 3 | a0006c0006 a0006c0035 a0006c0036 |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
synonymous_variant | LOW | c.2542C>T | p.Leu848Leu | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 17/19 | 2645/4841 | 2542/2826 | 848/941 | chr5 | 96781104 | |||
chr5:96781773 | A | G | 1 | a0005c0032 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.2367T>C | p.Tyr789Tyr | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 16/19 | 2470/4841 | 2367/2826 | 789/941 | chr5 | 96781773 | |||
chr5:96781851 | C | T | 4 | a0008c0008 a0008c0025 a0017c0021 others(1): Show |
18 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(15): Show |
synonymous_variant | LOW | c.2289G>A | p.Leu763Leu | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 16/19 | 2392/4841 | 2289/2826 | 763/941 | chr5 | 96781851 | |||
chr5:96785793 | G | A | 1 | a0010c0018 | 2 | HG01496.hp1 HG03471.hp2 |
synonymous_variant | LOW | c.1938C>T | p.Leu646Leu | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/19 | 2041/4841 | 1938/2826 | 646/941 | chr5 | 96785793 | |||
chr5:96785820 | C | T | 21 | a0002c0002 a0002c0020 a0003c0003 others(18): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
synonymous_variant | LOW | c.1911G>A | p.Ala637Ala | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/19 | 2014/4841 | 1911/2826 | 637/941 | chr5 | 96785820 | |||
chr5:96788593 | C | G | 1 | a0001c0010 | 13 | HG02015.hp1 HG02040.hp1 HG02155.hp1 others(10): Show |
synonymous_variant | LOW | c.1617G>C | p.Gly539Gly | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/19 | 1720/4841 | 1617/2826 | 539/941 | chr5 | 96788593 | |||
chr5:96790599 | G | A | 1 | a0008c0025 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.1365C>T | p.Asp455Asp | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 9/19 | 1468/4841 | 1365/2826 | 455/941 | chr5 | 96790599 | |||
chr5:96790605 | A | G | 22 | a0002c0002 a0002c0020 a0003c0003 others(19): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
synonymous_variant | LOW | c.1359T>C | p.Ser453Ser | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 9/19 | 1462/4841 | 1359/2826 | 453/941 | chr5 | 96790605 | |||
chr5:96792130 | G | A | 6 | a0006c0006 a0006c0034 a0006c0035 others(3): Show |
44 | HG00280.hp2 HG00738.hp1 HG01069.hp1 others(41): Show |
synonymous_variant | LOW | c.1251C>T | p.His417His | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 8/19 | 1354/4841 | 1251/2826 | 417/941 | chr5 | 96792130 | |||
chr5:96792163 | G | A | 1 | a0002c0020 | 2 | HG02080.hp2 NA19080.hp1 |
synonymous_variant | LOW | c.1218C>T | p.Asp406Asp | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 8/19 | 1321/4841 | 1218/2826 | 406/941 | chr5 | 96792163 | |||
chr5:96793809 | A | G | 24 | a0002c0002 a0002c0020 a0003c0003 others(21): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
synonymous_variant | LOW | c.1068T>C | p.Ala356Ala | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 6/19 | 1171/4841 | 1068/2826 | 356/941 | chr5 | 96793809 | |||
chr5:96803570 | G | A | 1 | a0006c0035 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.357C>T | p.Pro119Pro | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/19 | 460/4841 | 357/2826 | 119/941 | chr5 | 96803570 | |||
chr5:96803723 | A | G | 3 | a0001c0015 a0005c0013 a0015c0023 |
9 | HG02451.hp1 HG02965.hp2 HG02976.hp2 others(6): Show |
synonymous_variant | LOW | c.204T>C | p.His68His | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/19 | 307/4841 | 204/2826 | 68/941 | chr5 | 96803723 | |||
chr5:96803756 | G | A | 1 | a0006c0036 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.171C>T | p.Tyr57Tyr | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/19 | 274/4841 | 171/2826 | 57/941 | chr5 | 96803756 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:96774507 | A | T | 6 | a0002c0002t0003 a0003c0003t0003 a0008c0008t0003 others(3): Show |
62 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1889T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1889 | chr5 | 96774507 | ||||||
chr5:96774610 | C | T | 1 | a0006c0006t0011 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1786G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1786 | chr5 | 96774610 | ||||||
chr5:96774696 | A | AT | 2 | a0002c0002t0008 a0006c0034t0008 |
6 | HG01099.hp2 HG01175.hp1 HG01515.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1699dupA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1699 | chr5 | 96774696 | ||||||
chr5:96774718 | A | T | 1 | a0005c0013t0001 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1678T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1678 | chr5 | 96774718 | ||||||
chr5:96774787 | A | G | 1 | a0002c0002t0018 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1609T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1609 | chr5 | 96774787 | ||||||
chr5:96774878 | T | G | 4 | a0006c0006t0004 a0006c0006t0011 a0006c0035t0004 others(1): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1518A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1518 | chr5 | 96774878 | ||||||
chr5:96774892 | G | A | 4 | a0006c0006t0004 a0006c0006t0011 a0006c0035t0004 others(1): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1504C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1504 | chr5 | 96774892 | ||||||
chr5:96774900 | A | AT | 4 | a0002c0002t0006 a0005c0005t0006 a0009c0009t0006 others(1): Show |
9 | HG01123.hp2 HG01361.hp1 HG01433.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1495dupA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1495 | chr5 | 96774900 | ||||||
chr5:96774918 | C | T | 4 | a0006c0006t0004 a0006c0006t0011 a0006c0035t0004 others(1): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1478G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1478 | chr5 | 96774918 | ||||||
chr5:96774920 | AATC | A | 4 | a0006c0006t0004 a0006c0006t0011 a0006c0035t0004 others(1): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1473_*1475delGAT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1473 | chr5 | 96774920 | ||||||
chr5:96774956 | C | CCTT | 4 | a0006c0006t0004 a0006c0006t0011 a0006c0035t0004 others(1): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1437_*1439dupAAG | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1439 | chr5 | 96774956 | ||||||
chr5:96775046 | G | GAATC | 4 | a0006c0006t0004 a0006c0006t0011 a0006c0035t0004 others(1): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1346_*1349dupGATT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1349 | chr5 | 96775046 | ||||||
chr5:96775172 | A | ATGTT | 5 | a0001c0001t0012 a0009c0009t0009 a0009c0028t0009 others(2): Show |
7 | HG01109.hp2 HG02572.hp2 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1220_*1223dupAACA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1223 | chr5 | 96775172 | ||||||
chr5:96775264 | AAAAG | A | 49 | a0001c0001t0001 a0001c0010t0001 a0001c0015t0010 others(46): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*1128_*1131delCTTT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1128 | chr5 | 96775264 | ||||||
chr5:96775325 | G | T | 1 | a0009c0009t0016 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1071C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1071 | chr5 | 96775325 | ||||||
chr5:96775333 | A | G | 1 | a0002c0002t0017 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1063T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1063 | chr5 | 96775333 | ||||||
chr5:96775339 | T | TATCA | 4 | a0006c0006t0004 a0006c0006t0011 a0006c0035t0004 others(1): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1053_*1056dupTGAT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1056 | chr5 | 96775339 | ||||||
chr5:96775388 | CTAGT | C | 4 | a0006c0006t0004 a0006c0006t0011 a0006c0035t0004 others(1): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1004_*1007delACTA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 1004 | chr5 | 96775388 | ||||||
chr5:96775524 | A | G | 6 | a0002c0002t0003 a0003c0003t0003 a0008c0008t0003 others(3): Show |
62 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*872T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 872 | chr5 | 96775524 | ||||||
chr5:96775532 | ACACT | A | 45 | a0001c0001t0001 a0001c0010t0001 a0001c0015t0010 others(42): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*860_*863delAGTG | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 860 | chr5 | 96775532 | ||||||
chr5:96775535 | C | G | 4 | a0002c0002t0006 a0005c0005t0006 a0009c0009t0006 others(1): Show |
9 | HG01123.hp2 HG01361.hp1 HG01433.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*861G>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 861 | chr5 | 96775535 | ||||||
chr5:96775536 | T | A | 4 | a0002c0002t0006 a0005c0005t0006 a0009c0009t0006 others(1): Show |
9 | HG01123.hp2 HG01361.hp1 HG01433.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*860A>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 860 | chr5 | 96775536 | ||||||
chr5:96775565 | T | C | 1 | a0007c0007t0007 | 7 | NA18949.hp2 NA18973.hp1 NA18994.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*831A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 831 | chr5 | 96775565 | ||||||
chr5:96775568 | A | AAAG | 1 | a0001c0015t0010 | 3 | HG02976.hp2 NA19030.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*825_*827dupCTT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 827 | chr5 | 96775568 | ||||||
chr5:96775598 | A | T | 4 | a0006c0006t0004 a0006c0006t0011 a0006c0035t0004 others(1): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*798T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 798 | chr5 | 96775598 | ||||||
chr5:96775667 | G | A | 6 | a0002c0002t0003 a0003c0003t0003 a0008c0008t0003 others(3): Show |
62 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*729C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 729 | chr5 | 96775667 | ||||||
chr5:96775716 | G | A | 1 | a0004c0004t0019 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 680 | chr5 | 96775716 | ||||||
chr5:96775743 | G | A | 1 | a0001c0015t0010 | 3 | HG02976.hp2 NA19030.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*653C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 653 | chr5 | 96775743 | ||||||
chr5:96775808 | T | C | 1 | a0002c0002t0020 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*588A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 588 | chr5 | 96775808 | ||||||
chr5:96776022 | G | A | 4 | a0006c0006t0004 a0006c0006t0011 a0006c0035t0004 others(1): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*374C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 374 | chr5 | 96776022 | ||||||
chr5:96776046 | A | C | 1 | a0011c0011t0015 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*350T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 350 | chr5 | 96776046 | ||||||
chr5:96776075 | A | G | 4 | a0006c0006t0004 a0006c0006t0011 a0006c0035t0004 others(1): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*321T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 321 | chr5 | 96776075 | ||||||
chr5:96776097 | C | CTG | 4 | a0006c0006t0004 a0006c0006t0011 a0006c0035t0004 others(1): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*298_*299insCA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 298 | chr5 | 96776097 | ||||||
chr5:96776101 | T | G | 4 | a0006c0006t0004 a0006c0006t0011 a0006c0035t0004 others(1): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*295A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 295 | chr5 | 96776101 | ||||||
chr5:96776144 | T | C | 1 | a0002c0002t0021 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*252A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 252 | chr5 | 96776144 | ||||||
chr5:96776223 | T | TAGCCCAT others(9): Show |
6 | a0002c0002t0003 a0003c0003t0003 a0008c0008t0003 others(3): Show |
62 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*157_*172dupTTTTCA others(10): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 172 | chr5 | 96776223 | ||||||
chr5:96776250 | A | G | 1 | a0002c0002t0014 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 146 | chr5 | 96776250 | ||||||
chr5:96776301 | C | T | 4 | a0006c0006t0004 a0006c0006t0011 a0006c0035t0004 others(1): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*95G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 95 | chr5 | 96776301 | ||||||
chr5:96776379 | T | G | 7 | a0002c0002t0003 a0003c0003t0003 a0004c0004t0005 others(4): Show |
69 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*17A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 19/19 | 17 | chr5 | 96776379 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:96776560 | G | A | 1 | a0002c0002t0008g0258 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2671-9C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96776560 | |||||||
chr5:96776580 | A | T | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2671-29T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96776580 | |||||||
chr5:96776591 | C | T | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2671-40G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96776591 | |||||||
chr5:96776759 | CTTTTG | C | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2671-213_2671-209d others(7): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96776759 | |||||||
chr5:96776848 | ATTCTG | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0073 others(84): Show |
113 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.2671-302_2671-298d others(7): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96776848 | |||||||
chr5:96776892 | A | C | 2 | a0004c0004t0001g0036 a0004c0004t0001g0281 |
3 | HG02129.hp2 NA18986.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2671-341T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96776892 | |||||||
chr5:96776922 | C | CT | 24 | a0002c0020t0002g0233 a0002c0020t0002g0248 a0007c0007t0002g0083 others(21): Show |
25 | HG01109.hp1 HG01109.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.2671-372dupA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96776922 | |||||||
chr5:96776959 | G | A | 7 | a0002c0002t0006g0218 a0002c0002t0006g0223 a0005c0005t0006g0078 others(4): Show |
9 | HG01123.hp2 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.2671-408C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96776959 | |||||||
chr5:96776988 | GTATGT | G | 15 | a0005c0005t0001g0105 a0006c0006t0004g0021 a0006c0006t0004g0042 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2671-442_2671-438d others(7): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96776988 | |||||||
chr5:96777159 | C | T | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2671-608G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96777159 | |||||||
chr5:96777193 | G | C | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2671-642C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96777193 | |||||||
chr5:96777250 | A | G | 248 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0058 others(245): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.2671-699T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96777250 | |||||||
chr5:96777265 | C | T | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2671-714G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96777265 | |||||||
chr5:96777317 | G | A | 1 | a0001c0010t0002g0124 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2671-766C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96777317 | |||||||
chr5:96777327 | A | G | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2671-776T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96777327 | |||||||
chr5:96777338 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0073 others(57): Show |
85 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2671-787T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96777338 | |||||||
chr5:96777368 | T | A | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2671-817A>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96777368 | |||||||
chr5:96777541 | G | A | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2671-990C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96777541 | |||||||
chr5:96777605 | CTACTT | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0073 others(82): Show |
111 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.2671-1059_2671-105 others(9): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96777605 | |||||||
chr5:96777693 | C | T | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2671-1142G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96777693 | |||||||
chr5:96778134 | T | C | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2671-1583A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96778134 | |||||||
chr5:96778141 | T | G | 3 | a0017c0021t0013g0059 a0017c0021t0013g0060 a0020c0029t0022g0061 |
3 | HG02572.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2671-1590A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96778141 | |||||||
chr5:96778267 | A | G | 3 | a0001c0015t0010g0261 a0001c0015t0010g0262 a0001c0015t0010g0263 |
3 | HG02976.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2671-1716T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96778267 | |||||||
chr5:96778367 | T | C | 2 | a0013c0016t0002g0126 a0013c0016t0002g0133 |
2 | HG01256.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.2671-1816A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96778367 | |||||||
chr5:96778368 | C | T | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2671-1817G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96778368 | |||||||
chr5:96778446 | A | G | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2671-1895T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96778446 | |||||||
chr5:96778636 | A | G | 2 | a0004c0004t0001g0278 a0004c0004t0001g0279 |
2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2670+1787T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96778636 | |||||||
chr5:96778642 | A | C | 102 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0002c0002t0001g0001 others(99): Show |
129 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.2670+1781T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96778642 | |||||||
chr5:96778789 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0073 others(71): Show |
104 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.2670+1634A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96778789 | |||||||
chr5:96778813 | C | T | 3 | a0010c0012t0001g0285 a0010c0012t0001g0318 a0010c0018t0001g0294 |
3 | HG01496.hp1 HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.2670+1610G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96778813 | |||||||
chr5:96778846 | G | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0073 others(140): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.2670+1577C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96778846 | |||||||
chr5:96778859 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2670+1564A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96778859 | |||||||
chr5:96778915 | G | A | 3 | a0001c0015t0010g0261 a0001c0015t0010g0262 a0001c0015t0010g0263 |
3 | HG02976.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2670+1508C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96778915 | |||||||
chr5:96778991 | A | G | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2670+1432T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96778991 | |||||||
chr5:96779039 | A | C | 3 | a0017c0021t0013g0059 a0017c0021t0013g0060 a0020c0029t0022g0061 |
3 | HG02572.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2670+1384T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779039 | |||||||
chr5:96779106 | G | A | 1 | a0006c0006t0004g0308 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2670+1317C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779106 | |||||||
chr5:96779194 | G | A | 8 | a0001c0010t0001g0123 a0011c0011t0001g0045 a0011c0011t0001g0173 others(5): Show |
9 | HG00738.hp1 HG01975.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.2670+1229C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779194 | |||||||
chr5:96779208 | T | C | 2 | a0002c0002t0003g0033 a0003c0003t0003g0193 |
3 | HG03490.hp2 HG03492.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2670+1215A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779208 | |||||||
chr5:96779249 | C | G | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2670+1174G>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779249 | |||||||
chr5:96779335 | A | G | 4 | a0012c0014t0001g0286 a0012c0014t0001g0287 a0012c0014t0001g0289 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2670+1088T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779335 | |||||||
chr5:96779366 | T | G | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2670+1057A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779366 | |||||||
chr5:96779381 | G | C | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2670+1042C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779381 | |||||||
chr5:96779407 | G | A | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2670+1016C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779407 | |||||||
chr5:96779429 | T | C | 4 | a0009c0009t0001g0029 a0009c0009t0001g0166 a0009c0009t0001g0170 others(1): Show |
5 | HG01109.hp1 HG01496.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2670+994A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779429 | |||||||
chr5:96779433 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0139 |
2 | NA18973.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.2670+990T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779433 | |||||||
chr5:96779442 | A | T | 7 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(4): Show |
11 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2670+981T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779442 | |||||||
chr5:96779489 | G | A | 101 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0002c0002t0001g0001 others(98): Show |
128 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.2670+934C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779489 | |||||||
chr5:96779509 | T | C | 3 | a0017c0021t0013g0059 a0017c0021t0013g0060 a0020c0029t0022g0061 |
3 | HG02572.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2670+914A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779509 | |||||||
chr5:96779587 | T | TA | 7 | a0002c0002t0006g0218 a0002c0002t0006g0223 a0005c0005t0006g0078 others(4): Show |
9 | HG01123.hp2 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.2670+835dupT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779587 | |||||||
chr5:96779672 | A | C | 1 | a0009c0009t0001g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2670+751T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779672 | |||||||
chr5:96779815 | T | A | 1 | a0002c0002t0001g0231 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2670+608A>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779815 | |||||||
chr5:96779915 | T | A | 1 | a0001c0001t0002g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2670+508A>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96779915 | |||||||
chr5:96780014 | T | G | 1 | a0006c0006t0004g0306 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2670+409A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96780014 | |||||||
chr5:96780017 | C | T | 247 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0073 others(244): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.2670+406G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96780017 | |||||||
chr5:96780076 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2670+347G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96780076 | |||||||
chr5:96780094 | G | A | 1 | a0002c0002t0001g0238 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2670+329C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96780094 | |||||||
chr5:96780221 | C | T | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2670+202G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96780221 | |||||||
chr5:96780327 | AACTC | A | 77 | a0001c0001t0001g0164 a0002c0002t0001g0001 a0002c0002t0001g0010 others(74): Show |
98 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.2670+92_2670+95del others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96780327 | |||||||
chr5:96780405 | T | G | 3 | a0003c0003t0003g0200 a0003c0003t0003g0201 a0003c0003t0003g0202 |
3 | HG00735.hp1 HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2670+18A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96780405 | |||||||
chr5:96780408 | A | AT | 98 | a0001c0001t0001g0138 a0002c0002t0001g0226 a0002c0002t0001g0244 others(95): Show |
120 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.2670+14dupA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96780408 | |||||||
chr5:96780408 | AT | A | 37 | a0003c0003t0001g0018 a0003c0003t0001g0184 a0003c0003t0001g0203 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.2670+14delA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 18/18 | chr5 | 96780408 | |||||||
chr5:96780529 | G | A | 5 | a0012c0014t0001g0286 a0012c0014t0001g0287 a0012c0014t0001g0288 others(2): Show |
5 | HG02615.hp1 HG02647.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2589-25C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 17/18 | chr5 | 96780529 | |||||||
chr5:96780569 | G | T | 3 | a0001c0010t0001g0123 a0001c0010t0002g0088 a0001c0010t0002g0118 |
3 | HG02040.hp1 HG02155.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.2589-65C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 17/18 | chr5 | 96780569 | |||||||
chr5:96780582 | A | G | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2589-78T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 17/18 | chr5 | 96780582 | |||||||
chr5:96780956 | A | G | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2588+102T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 17/18 | chr5 | 96780956 | |||||||
chr5:96781036 | C | A | 6 | a0012c0014t0001g0286 a0012c0014t0001g0287 a0012c0014t0001g0288 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2588+22G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 17/18 | chr5 | 96781036 | |||||||
chr5:96781236 | G | A | 109 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(106): Show |
137 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.2448-38C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 16/18 | chr5 | 96781236 | |||||||
chr5:96781593 | T | C | 1 | a0002c0002t0001g0236 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2447+100A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 16/18 | chr5 | 96781593 | |||||||
chr5:96781596 | G | A | 234 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(231): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.2447+97C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 16/18 | chr5 | 96781596 | |||||||
chr5:96781684 | C | T | 1 | a0002c0002t0020g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2447+9G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 16/18 | chr5 | 96781684 | |||||||
chr5:96781875 | G | A | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2286-21C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96781875 | |||||||
chr5:96781884 | C | T | 1 | a0006c0006t0004g0042 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2286-30G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96781884 | |||||||
chr5:96781920 | G | GACTA | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2286-70_2286-67dup others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96781920 | |||||||
chr5:96781976 | T | C | 2 | a0001c0001t0002g0129 a0001c0001t0002g0142 |
2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2286-122A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96781976 | |||||||
chr5:96782007 | AATTTT | A | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2286-158_2286-154d others(7): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782007 | |||||||
chr5:96782008 | A | AT | 9 | a0001c0001t0002g0011 a0001c0001t0002g0015 a0001c0001t0002g0087 others(6): Show |
9 | HG02071.hp1 HG02071.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.2286-155dupA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782008 | |||||||
chr5:96782008 | AT | A | 69 | a0001c0001t0001g0058 a0001c0015t0010g0261 a0001c0015t0010g0263 others(66): Show |
89 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.2286-155delA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782008 | |||||||
chr5:96782008 | ATT | A | 67 | a0002c0002t0006g0218 a0002c0002t0006g0223 a0002c0020t0002g0233 others(64): Show |
77 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(74): Show |
intron_variant | MODIFIER | c.2286-156_2286-155d others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782008 | |||||||
chr5:96782008 | ATTT | A | 54 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(51): Show |
70 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.2286-157_2286-155d others(5): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782008 | |||||||
chr5:96782013 | T | C | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2286-159A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782013 | |||||||
chr5:96782031 | G | T | 17 | a0002c0020t0002g0233 a0002c0020t0002g0248 a0007c0007t0001g0026 others(14): Show |
18 | HG01069.hp1 HG01071.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.2286-177C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782031 | |||||||
chr5:96782034 | G | C | 3 | a0017c0021t0013g0059 a0017c0021t0013g0060 a0020c0029t0022g0061 |
3 | HG02572.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2286-180C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782034 | |||||||
chr5:96782066 | C | G | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2286-212G>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782066 | |||||||
chr5:96782093 | T | C | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2286-239A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782093 | |||||||
chr5:96782096 | G | A | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2286-242C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782096 | |||||||
chr5:96782098 | C | G | 2 | a0001c0001t0002g0097 a0001c0001t0002g0100 |
2 | HG00323.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2286-244G>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782098 | |||||||
chr5:96782135 | C | T | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2286-281G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782135 | |||||||
chr5:96782159 | C | G | 2 | a0008c0008t0003g0005 a0008c0008t0003g0053 |
6 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2286-305G>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782159 | |||||||
chr5:96782160 | G | A | 3 | a0010c0012t0001g0285 a0010c0012t0001g0318 a0010c0018t0001g0294 |
3 | HG01496.hp1 HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.2286-306C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782160 | |||||||
chr5:96782299 | G | A | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2286-445C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782299 | |||||||
chr5:96782300 | C | T | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2286-446G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782300 | |||||||
chr5:96782301 | G | A | 1 | a0014c0017t0001g0298 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2286-447C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782301 | |||||||
chr5:96782361 | T | G | 168 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(165): Show |
211 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.2286-507A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782361 | |||||||
chr5:96782393 | T | A | 1 | a0001c0001t0002g0153 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2286-539A>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782393 | |||||||
chr5:96782444 | T | C | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2286-590A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782444 | |||||||
chr5:96782516 | C | T | 1 | a0003c0003t0003g0172 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2285+535G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782516 | |||||||
chr5:96782642 | C | T | 1 | a0013c0016t0002g0133 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2285+409G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782642 | |||||||
chr5:96782671 | G | C | 2 | a0001c0001t0001g0164 a0001c0001t0002g0165 |
2 | NA18970.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2285+380C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782671 | |||||||
chr5:96782746 | A | C | 7 | a0011c0011t0001g0045 a0011c0011t0001g0173 a0011c0011t0001g0174 others(4): Show |
8 | HG00738.hp1 HG01975.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.2285+305T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782746 | |||||||
chr5:96782783 | A | C | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2285+268T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782783 | |||||||
chr5:96782891 | C | G | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2285+160G>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 15/18 | chr5 | 96782891 | |||||||
chr5:96783324 | G | A | 2 | a0001c0001t0002g0149 a0001c0001t0002g0150 |
2 | HG00642.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2101-89C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783324 | |||||||
chr5:96783340 | T | A | 12 | a0008c0008t0002g0051 a0008c0008t0003g0005 a0008c0008t0003g0022 others(9): Show |
17 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.2101-105A>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783340 | |||||||
chr5:96783351 | T | C | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2101-116A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783351 | |||||||
chr5:96783419 | CTT | C | 35 | a0002c0002t0001g0226 a0002c0002t0001g0244 a0004c0004t0001g0003 others(32): Show |
48 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.2101-186_2101-185d others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783419 | |||||||
chr5:96783501 | AAG | A | 3 | a0010c0012t0001g0291 a0010c0012t0001g0293 a0010c0018t0001g0292 |
3 | HG00738.hp2 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2101-268_2101-267d others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783501 | |||||||
chr5:96783569 | A | G | 219 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(216): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.2101-334T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783569 | |||||||
chr5:96783624 | C | A | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2100+300G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783624 | |||||||
chr5:96783635 | G | T | 38 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(35): Show |
49 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.2100+289C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783635 | |||||||
chr5:96783818 | T | TAC | 5 | a0001c0001t0002g0011 a0001c0001t0002g0134 a0001c0001t0002g0141 others(2): Show |
9 | HG02135.hp1 HG03490.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.2100+104_2100+105d others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783818 | |||||||
chr5:96783818 | TAC | T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0138 a0001c0001t0002g0007 others(19): Show |
30 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.2100+104_2100+105d others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783818 | |||||||
chr5:96783818 | TACAC | T | 3 | a0001c0001t0002g0013 a0001c0001t0002g0101 a0001c0010t0002g0122 |
5 | HG02015.hp1 HG02145.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2100+102_2100+105d others(6): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783818 | |||||||
chr5:96783818 | TACACAC | T | 6 | a0001c0001t0002g0080 a0001c0001t0002g0109 a0001c0001t0002g0143 others(3): Show |
6 | HG02572.hp2 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2100+100_2100+105d others(8): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783818 | |||||||
chr5:96783818 | TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0058 a0001c0001t0002g0104 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2100+96_2100+105de others(11): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783818 | |||||||
chr5:96783818 | TACACACA others(5): Show |
T | 5 | a0003c0003t0003g0030 a0003c0003t0003g0177 a0003c0003t0003g0185 others(2): Show |
6 | HG00741.hp2 HG01070.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.2100+94_2100+105de others(13): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783818 | |||||||
chr5:96783818 | TACACACA others(7): Show |
T | 48 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(45): Show |
63 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.2100+92_2100+105de others(15): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783818 | |||||||
chr5:96783818 | TACACACA others(9): Show |
T | 10 | a0008c0008t0002g0051 a0008c0008t0003g0005 a0008c0008t0003g0022 others(7): Show |
15 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.2100+90_2100+105de others(17): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783818 | |||||||
chr5:96783836 | CACACACA others(13): Show |
C | 1 | a0011c0011t0015g0315 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2100+68_2100+87del others(20): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783836 | |||||||
chr5:96783838 | CACACACA others(11): Show |
C | 3 | a0004c0004t0001g0281 a0009c0028t0009g0094 a0014c0022t0009g0299 |
3 | HG02129.hp2 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2100+68_2100+85del others(18): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783838 | |||||||
chr5:96783840 | CACACACA others(9): Show |
C | 83 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(80): Show |
107 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.2100+68_2100+83del others(16): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783840 | |||||||
chr5:96783842 | CACACACA others(7): Show |
C | 69 | a0002c0002t0001g0226 a0002c0002t0001g0229 a0002c0002t0001g0244 others(66): Show |
83 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.2100+68_2100+81del others(14): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783842 | |||||||
chr5:96783844 | CACACACA others(5): Show |
C | 6 | a0002c0002t0006g0218 a0002c0002t0006g0223 a0005c0005t0001g0006 others(3): Show |
8 | HG01123.hp2 HG01361.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.2100+68_2100+79del others(12): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783844 | |||||||
chr5:96783846 | CACACACA others(3): Show |
C | 8 | a0009c0009t0001g0029 a0009c0009t0001g0166 a0009c0009t0001g0169 others(5): Show |
9 | HG01109.hp1 HG01109.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.2100+68_2100+77del others(10): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783846 | |||||||
chr5:96783875 | A | ACT | 234 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(231): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.2100+47_2100+48dup others(2): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 14/18 | chr5 | 96783875 | |||||||
chr5:96784297 | C | T | 1 | a0006c0006t0004g0306 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1944-217G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96784297 | |||||||
chr5:96784324 | G | A | 1 | a0004c0004t0001g0265 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1944-244C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96784324 | |||||||
chr5:96784350 | G | C | 234 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(231): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.1944-270C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96784350 | |||||||
chr5:96784392 | C | T | 1 | a0002c0002t0020g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1944-312G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96784392 | |||||||
chr5:96784393 | G | A | 1 | a0010c0012t0001g0296 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1944-313C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96784393 | |||||||
chr5:96784410 | C | T | 1 | a0003c0003t0003g0195 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1944-330G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96784410 | |||||||
chr5:96784466 | G | A | 219 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(216): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.1944-386C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96784466 | |||||||
chr5:96784494 | TAAAC | T | 219 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(216): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.1944-418_1944-415d others(6): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96784494 | |||||||
chr5:96784555 | C | T | 219 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(216): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.1944-475G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96784555 | |||||||
chr5:96784596 | G | A | 2 | a0001c0001t0002g0129 a0001c0001t0002g0142 |
2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1944-516C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96784596 | |||||||
chr5:96784608 | C | CAT | 219 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(216): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.1944-529_1944-528i others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96784608 | |||||||
chr5:96784751 | C | T | 234 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(231): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.1944-671G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96784751 | |||||||
chr5:96784826 | G | A | 3 | a0017c0021t0013g0059 a0017c0021t0013g0060 a0020c0029t0022g0061 |
3 | HG02572.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1944-746C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96784826 | |||||||
chr5:96784929 | G | A | 2 | a0009c0028t0009g0094 a0014c0022t0009g0299 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1944-849C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96784929 | |||||||
chr5:96785081 | A | G | 1 | a0007c0007t0007g0085 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1943+707T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785081 | |||||||
chr5:96785134 | C | T | 4 | a0004c0004t0001g0037 a0004c0004t0001g0268 a0004c0004t0001g0275 others(1): Show |
5 | NA18946.hp1 NA18961.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1943+654G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785134 | |||||||
chr5:96785200 | G | GA | 76 | a0002c0020t0002g0233 a0002c0020t0002g0248 a0003c0003t0001g0018 others(73): Show |
94 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1943+587dupT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785200 | |||||||
chr5:96785206 | A | G | 2 | a0001c0001t0002g0025 a0018c0030t0002g0106 |
3 | HG00741.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1943+582T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785206 | |||||||
chr5:96785229 | T | A | 191 | a0001c0001t0001g0058 a0001c0001t0002g0080 a0001c0001t0002g0104 others(188): Show |
236 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.1943+559A>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785229 | |||||||
chr5:96785338 | T | C | 4 | a0009c0009t0006g0016 a0009c0009t0006g0161 a0009c0009t0006g0162 others(1): Show |
6 | HG01123.hp2 HG01361.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1943+450A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785338 | |||||||
chr5:96785365 | C | T | 58 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(55): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1943+423G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785365 | |||||||
chr5:96785386 | C | G | 3 | a0010c0012t0001g0285 a0010c0012t0001g0318 a0010c0018t0001g0294 |
3 | HG01496.hp1 HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1943+402G>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785386 | |||||||
chr5:96785443 | G | A | 38 | a0005c0005t0001g0006 a0005c0005t0001g0063 a0005c0005t0001g0066 others(35): Show |
43 | HG00738.hp2 HG01175.hp2 HG01346.hp2 others(40): Show |
intron_variant | MODIFIER | c.1943+345C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785443 | |||||||
chr5:96785448 | A | C | 55 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(52): Show |
71 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1943+340T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785448 | |||||||
chr5:96785479 | C | T | 39 | a0002c0020t0002g0233 a0002c0020t0002g0248 a0006c0006t0004g0021 others(36): Show |
46 | HG00280.hp2 HG00738.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1943+309G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785479 | |||||||
chr5:96785480 | G | A | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1943+308C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785480 | |||||||
chr5:96785539 | C | T | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1943+249G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785539 | |||||||
chr5:96785651 | G | T | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1943+137C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785651 | |||||||
chr5:96785666 | T | TA | 216 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(213): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.1943+121dupT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785666 | |||||||
chr5:96785680 | T | A | 1 | a0005c0005t0005g0070 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1943+108A>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785680 | |||||||
chr5:96785702 | A | G | 61 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(58): Show |
79 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1943+86T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785702 | |||||||
chr5:96785733 | GAAC | G | 31 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(28): Show |
44 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1943+52_1943+54del others(3): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785733 | |||||||
chr5:96785745 | C | G | 4 | a0004c0004t0001g0037 a0004c0004t0001g0268 a0004c0004t0001g0275 others(1): Show |
5 | NA18946.hp1 NA18961.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1943+43G>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785745 | |||||||
chr5:96785764 | G | A | 2 | a0008c0008t0003g0206 a0008c0008t0003g0207 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1943+24C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 13/18 | chr5 | 96785764 | |||||||
chr5:96786011 | C | T | 193 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(190): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1760-40G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 12/18 | chr5 | 96786011 | |||||||
chr5:96786072 | C | A | 3 | a0010c0012t0001g0285 a0010c0012t0001g0318 a0010c0018t0001g0294 |
3 | HG01496.hp1 HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1760-101G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 12/18 | chr5 | 96786072 | |||||||
chr5:96786223 | T | C | 1 | a0001c0001t0002g0132 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1759+247A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 12/18 | chr5 | 96786223 | |||||||
chr5:96786290 | A | G | 193 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(190): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1759+180T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 12/18 | chr5 | 96786290 | |||||||
chr5:96786556 | T | G | 193 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(190): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
splice_region_variant&intron_variant | LOW | c.1680-7A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96786556 | |||||||
chr5:96786577 | A | C | 193 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(190): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1680-28T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96786577 | |||||||
chr5:96786724 | G | C | 4 | a0004c0004t0001g0037 a0004c0004t0001g0268 a0004c0004t0001g0275 others(1): Show |
5 | NA18946.hp1 NA18961.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1680-175C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96786724 | |||||||
chr5:96786740 | C | G | 3 | a0011c0011t0001g0173 a0011c0011t0001g0174 a0011c0011t0001g0175 |
3 | HG02602.hp1 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1680-191G>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96786740 | |||||||
chr5:96786754 | C | T | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1680-205G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96786754 | |||||||
chr5:96786760 | T | G | 4 | a0001c0001t0002g0127 a0001c0001t0002g0130 a0001c0001t0002g0148 others(1): Show |
4 | HG00140.hp1 HG00735.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1680-211A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96786760 | |||||||
chr5:96786825 | C | T | 17 | a0002c0020t0002g0233 a0002c0020t0002g0248 a0007c0007t0001g0026 others(14): Show |
18 | HG01069.hp1 HG01071.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.1680-276G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96786825 | |||||||
chr5:96787111 | A | C | 143 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(140): Show |
179 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.1680-562T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787111 | |||||||
chr5:96787296 | G | A | 4 | a0008c0008t0002g0051 a0008c0008t0003g0055 a0008c0008t0003g0056 others(1): Show |
4 | HG01243.hp1 HG01243.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1680-747C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787296 | |||||||
chr5:96787335 | G | A | 4 | a0009c0009t0006g0016 a0009c0009t0006g0161 a0009c0009t0006g0162 others(1): Show |
6 | HG01123.hp2 HG01361.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1680-786C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787335 | |||||||
chr5:96787351 | C | T | 5 | a0012c0014t0001g0286 a0012c0014t0001g0287 a0012c0014t0001g0288 others(2): Show |
5 | HG02615.hp1 HG02647.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1680-802G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787351 | |||||||
chr5:96787352 | A | G | 208 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(205): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1680-803T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787352 | |||||||
chr5:96787385 | C | T | 193 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(190): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1680-836G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787385 | |||||||
chr5:96787387 | T | C | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1680-838A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787387 | |||||||
chr5:96787422 | T | C | 193 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(190): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1680-873A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787422 | |||||||
chr5:96787456 | G | C | 29 | a0009c0009t0001g0029 a0009c0009t0001g0166 a0009c0009t0001g0168 others(26): Show |
32 | HG00738.hp2 HG01109.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1680-907C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787456 | |||||||
chr5:96787457 | T | C | 208 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(205): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1680-908A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787457 | |||||||
chr5:96787507 | C | T | 193 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(190): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1680-958G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787507 | |||||||
chr5:96787561 | C | A | 193 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(190): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1679+970G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787561 | |||||||
chr5:96787633 | T | C | 193 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(190): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1679+898A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787633 | |||||||
chr5:96787663 | G | A | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1679+868C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787663 | |||||||
chr5:96787715 | G | T | 1 | a0008c0008t0003g0053 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1679+816C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787715 | |||||||
chr5:96787726 | A | G | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1679+805T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787726 | |||||||
chr5:96787768 | G | T | 2 | a0002c0002t0001g0227 a0002c0002t0001g0251 |
2 | NA19000.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1679+763C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787768 | |||||||
chr5:96787781 | ATATTATA others(38): Show |
A | 1 | a0003c0003t0003g0194 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1679+705_1679+749d others(47): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787781 | |||||||
chr5:96787784 | T | TA | 156 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(153): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1679+746_1679+747i others(3): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787784 | |||||||
chr5:96787784 | T | TATA | 36 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(33): Show |
47 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.1679+746_1679+747i others(5): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787784 | |||||||
chr5:96787787 | T | C | 36 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(33): Show |
47 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.1679+744A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787787 | |||||||
chr5:96787789 | T | C | 171 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(168): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1679+742A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787789 | |||||||
chr5:96787802 | G | T | 4 | a0004c0004t0001g0037 a0004c0004t0001g0268 a0004c0004t0001g0275 others(1): Show |
5 | NA18946.hp1 NA18961.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1679+729C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787802 | |||||||
chr5:96787803 | T | C | 4 | a0004c0004t0001g0037 a0004c0004t0001g0268 a0004c0004t0001g0275 others(1): Show |
5 | NA18946.hp1 NA18961.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1679+728A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787803 | |||||||
chr5:96787806 | A | G | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1679+725T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787806 | |||||||
chr5:96787817 | C | CAT | 191 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(188): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1679+712_1679+713d others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787817 | |||||||
chr5:96787833 | TAC | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0073 others(37): Show |
62 | HG00423.hp2 HG00621.hp1 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.1679+696_1679+697d others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787833 | |||||||
chr5:96787865 | CAT | C | 6 | a0006c0006t0004g0306 a0006c0006t0004g0307 a0006c0006t0004g0308 others(3): Show |
6 | HG01175.hp1 HG01515.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1679+664_1679+665d others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787865 | |||||||
chr5:96787875 | T | G | 4 | a0001c0015t0010g0261 a0001c0015t0010g0262 a0001c0015t0010g0263 others(1): Show |
4 | HG01496.hp1 HG02976.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1679+656A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787875 | |||||||
chr5:96787875 | TAG | T | 9 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(6): Show |
14 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1679+654_1679+655d others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787875 | |||||||
chr5:96787877 | G | T | 97 | a0002c0002t0001g0001 a0002c0020t0002g0233 a0002c0020t0002g0248 others(94): Show |
118 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.1679+654C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787877 | |||||||
chr5:96787879 | G | T | 4 | a0007c0007t0001g0114 a0012c0014t0001g0286 a0012c0014t0001g0288 others(1): Show |
4 | HG02004.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1679+652C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787879 | |||||||
chr5:96787963 | G | T | 191 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(188): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1679+568C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96787963 | |||||||
chr5:96788039 | C | A | 31 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(28): Show |
44 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1679+492G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96788039 | |||||||
chr5:96788112 | G | T | 59 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(56): Show |
77 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1679+419C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96788112 | |||||||
chr5:96788159 | C | T | 1 | a0005c0005t0005g0074 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1679+372G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96788159 | |||||||
chr5:96788296 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1679+235C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96788296 | |||||||
chr5:96788418 | C | A | 2 | a0017c0021t0013g0059 a0017c0021t0013g0060 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1679+113G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 11/18 | chr5 | 96788418 | |||||||
chr5:96788744 | G | C | 208 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(205): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1525-59C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96788744 | |||||||
chr5:96788750 | A | G | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1525-65T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96788750 | |||||||
chr5:96788790 | C | T | 4 | a0005c0005t0001g0068 a0005c0005t0001g0076 a0005c0005t0001g0112 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-105G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96788790 | |||||||
chr5:96788801 | A | G | 2 | a0017c0021t0013g0059 a0017c0021t0013g0060 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1525-116T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96788801 | |||||||
chr5:96788962 | T | C | 2 | a0002c0002t0001g0232 a0002c0002t0001g0245 |
2 | HG00597.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1525-277A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96788962 | |||||||
chr5:96789104 | G | A | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1525-419C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789104 | |||||||
chr5:96789212 | C | A | 1 | a0005c0005t0001g0071 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1525-527G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789212 | |||||||
chr5:96789213 | G | A | 4 | a0011c0011t0001g0045 a0011c0011t0001g0314 a0011c0011t0001g0316 others(1): Show |
5 | HG00738.hp1 HG01975.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-528C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789213 | |||||||
chr5:96789215 | G | A | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1525-530C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789215 | |||||||
chr5:96789227 | C | A | 2 | a0002c0002t0006g0218 a0002c0002t0006g0223 |
2 | HG01433.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1525-542G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789227 | |||||||
chr5:96789236 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1525-551A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789236 | |||||||
chr5:96789256 | T | G | 208 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(205): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1525-571A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789256 | |||||||
chr5:96789344 | G | A | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1525-659C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789344 | |||||||
chr5:96789356 | G | A | 15 | a0007c0007t0001g0026 a0007c0007t0001g0084 a0007c0007t0001g0113 others(12): Show |
16 | HG01069.hp1 HG01071.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.1525-671C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789356 | |||||||
chr5:96789368 | T | G | 2 | a0001c0001t0002g0025 a0018c0030t0002g0106 |
3 | HG00741.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1525-683A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789368 | |||||||
chr5:96789443 | C | T | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1525-758G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789443 | |||||||
chr5:96789456 | C | T | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1525-771G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789456 | |||||||
chr5:96789459 | C | T | 1 | a0003c0003t0001g0183 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1525-774G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789459 | |||||||
chr5:96789486 | C | CA | 148 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(145): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1525-802dupT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789486 | |||||||
chr5:96789486 | C | CAA | 8 | a0007c0007t0007g0115 a0011c0011t0001g0045 a0011c0011t0001g0173 others(5): Show |
9 | HG00738.hp1 HG01975.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1525-803_1525-802d others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789486 | |||||||
chr5:96789556 | G | A | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524+740C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789556 | |||||||
chr5:96789590 | T | G | 15 | a0007c0007t0001g0026 a0007c0007t0001g0084 a0007c0007t0001g0113 others(12): Show |
16 | HG01069.hp1 HG01071.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.1524+706A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789590 | |||||||
chr5:96789611 | A | T | 208 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(205): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1524+685T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789611 | |||||||
chr5:96789627 | C | T | 5 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 others(2): Show |
5 | HG00323.hp1 HG01074.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+669G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789627 | |||||||
chr5:96789762 | G | A | 208 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(205): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1524+534C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789762 | |||||||
chr5:96789830 | T | A | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524+466A>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789830 | |||||||
chr5:96789891 | G | A | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524+405C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96789891 | |||||||
chr5:96790082 | G | T | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1524+214C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96790082 | |||||||
chr5:96790178 | A | T | 2 | a0017c0021t0013g0059 a0017c0021t0013g0060 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1524+118T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96790178 | |||||||
chr5:96790207 | C | T | 192 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(189): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1524+89G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 10/18 | chr5 | 96790207 | |||||||
chr5:96790483 | A | G | 1 | a0006c0036t0004g0312 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1452+29T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 9/18 | chr5 | 96790483 | |||||||
chr5:96790485 | T | C | 1 | a0006c0036t0004g0312 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1452+27A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 9/18 | chr5 | 96790485 | |||||||
chr5:96790486 | G | A | 1 | a0006c0036t0004g0312 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1452+26C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 9/18 | chr5 | 96790486 | |||||||
chr5:96790488 | A | G | 1 | a0006c0036t0004g0312 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1452+24T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 9/18 | chr5 | 96790488 | |||||||
chr5:96790489 | G | A | 1 | a0006c0036t0004g0312 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1452+23C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 9/18 | chr5 | 96790489 | |||||||
chr5:96790490 | A | C | 1 | a0006c0036t0004g0312 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1452+22T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 9/18 | chr5 | 96790490 | |||||||
chr5:96790494 | A | G | 194 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(191): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.1452+18T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 9/18 | chr5 | 96790494 | |||||||
chr5:96790707 | A | T | 6 | a0001c0015t0010g0261 a0001c0015t0010g0262 a0001c0015t0010g0263 others(3): Show |
8 | HG02451.hp1 HG02965.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1321-64T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 8/18 | chr5 | 96790707 | |||||||
chr5:96790741 | G | A | 1 | a0007c0007t0001g0158 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1321-98C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 8/18 | chr5 | 96790741 | |||||||
chr5:96791168 | A | T | 1 | a0002c0002t0001g0217 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1321-525T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 8/18 | chr5 | 96791168 | |||||||
chr5:96791235 | G | A | 35 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(32): Show |
46 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1321-592C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 8/18 | chr5 | 96791235 | |||||||
chr5:96791440 | G | GCCT | 3 | a0011c0011t0001g0173 a0011c0011t0001g0174 a0011c0011t0001g0175 |
3 | HG02602.hp1 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1320+618_1320+620d others(5): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 8/18 | chr5 | 96791440 | |||||||
chr5:96791560 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0002g0087 |
2 | NA18997.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1320+501A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 8/18 | chr5 | 96791560 | |||||||
chr5:96791751 | A | G | 110 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(107): Show |
138 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1320+310T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 8/18 | chr5 | 96791751 | |||||||
chr5:96791781 | A | G | 1 | a0020c0029t0022g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1320+280T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 8/18 | chr5 | 96791781 | |||||||
chr5:96791941 | G | A | 13 | a0001c0001t0002g0102 a0009c0009t0001g0029 a0009c0009t0001g0166 others(10): Show |
16 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1320+120C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 8/18 | chr5 | 96791941 | |||||||
chr5:96792202 | T | C | 205 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(202): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1189-10A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 7/18 | chr5 | 96792202 | |||||||
chr5:96792258 | G | A | 1 | a0005c0032t0005g0067 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1189-66C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 7/18 | chr5 | 96792258 | |||||||
chr5:96792319 | T | C | 4 | a0001c0001t0002g0024 a0001c0001t0002g0093 a0001c0001t0002g0110 others(1): Show |
5 | HG00642.hp1 HG01106.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-127A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 7/18 | chr5 | 96792319 | |||||||
chr5:96792508 | T | C | 2 | a0008c0008t0003g0056 a0008c0025t0003g0052 |
2 | HG01243.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1189-316A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 7/18 | chr5 | 96792508 | |||||||
chr5:96792596 | C | A | 37 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(34): Show |
44 | HG00280.hp2 HG00738.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1189-404G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 7/18 | chr5 | 96792596 | |||||||
chr5:96792605 | G | C | 1 | a0002c0002t0001g0229 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1189-413C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 7/18 | chr5 | 96792605 | |||||||
chr5:96792675 | T | C | 1 | a0001c0001t0002g0107 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1189-483A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 7/18 | chr5 | 96792675 | |||||||
chr5:96792697 | G | T | 204 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(201): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1189-505C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 7/18 | chr5 | 96792697 | |||||||
chr5:96792730 | A | AT | 61 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(58): Show |
79 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1189-539dupA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 7/18 | chr5 | 96792730 | |||||||
chr5:96792800 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1188+600G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 7/18 | chr5 | 96792800 | |||||||
chr5:96793002 | GTTACC | G | 2 | a0003c0003t0001g0018 a0003c0003t0001g0203 |
4 | HG02559.hp2 HG02896.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1188+393_1188+397d others(7): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 7/18 | chr5 | 96793002 | |||||||
chr5:96793078 | T | C | 15 | a0007c0007t0001g0026 a0007c0007t0001g0084 a0007c0007t0001g0113 others(12): Show |
16 | HG01069.hp1 HG01071.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.1188+322A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 7/18 | chr5 | 96793078 | |||||||
chr5:96793155 | GA | G | 3 | a0005c0013t0001g0020 a0005c0013t0001g0259 a0005c0013t0001g0260 |
5 | HG02451.hp1 HG02965.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1188+244delT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 7/18 | chr5 | 96793155 | |||||||
chr5:96793259 | C | T | 15 | a0007c0007t0001g0026 a0007c0007t0001g0084 a0007c0007t0001g0113 others(12): Show |
16 | HG01069.hp1 HG01071.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.1188+141G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 7/18 | chr5 | 96793259 | |||||||
chr5:96793688 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0002g0142 |
2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1074+115G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 6/18 | chr5 | 96793688 | |||||||
chr5:96793972 | A | G | 1 | a0010c0018t0001g0294 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.920-15T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96793972 | |||||||
chr5:96794099 | G | A | 31 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(28): Show |
44 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.920-142C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794099 | |||||||
chr5:96794134 | G | A | 1 | a0003c0003t0003g0186 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.920-177C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794134 | |||||||
chr5:96794171 | C | CCT | 9 | a0007c0007t0001g0026 a0007c0007t0001g0084 a0007c0007t0001g0114 others(6): Show |
10 | HG01071.hp2 HG01975.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-215_920-214ins others(2): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794171 | |||||||
chr5:96794171 | C | CCTT | 4 | a0007c0007t0001g0113 a0007c0007t0001g0117 a0007c0007t0007g0085 others(1): Show |
4 | HG01981.hp1 HG02148.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-215_920-214ins others(3): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794171 | |||||||
chr5:96794171 | C | CT | 108 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0058 others(105): Show |
150 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.920-215dupA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794171 | |||||||
chr5:96794171 | C | CTT | 31 | a0001c0001t0002g0087 a0001c0001t0002g0146 a0001c0001t0002g0165 others(28): Show |
33 | HG00423.hp1 HG00423.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.920-216_920-215dup others(2): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794171 | |||||||
chr5:96794171 | C | CTTT | 20 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(17): Show |
26 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.920-217_920-215dup others(3): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794171 | |||||||
chr5:96794171 | C | T | 1 | a0001c0001t0002g0156 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.920-214G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794171 | |||||||
chr5:96794171 | CTTT | C | 23 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0203 others(20): Show |
31 | HG00099.hp1 HG00609.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.920-217_920-215del others(3): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794171 | |||||||
chr5:96794171 | CTTTT | C | 12 | a0003c0003t0001g0184 a0003c0003t0003g0017 a0003c0003t0003g0031 others(9): Show |
15 | HG00639.hp1 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.920-218_920-215del others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794171 | |||||||
chr5:96794171 | CTTTTTTT | C | 29 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(26): Show |
42 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.920-221_920-215del others(7): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794171 | |||||||
chr5:96794171 | CTTTTTTT others(2): Show |
C | 10 | a0008c0008t0002g0051 a0008c0008t0003g0005 a0008c0008t0003g0022 others(7): Show |
15 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.920-223_920-215del others(9): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794171 | |||||||
chr5:96794171 | CTTTTTTT others(4): Show |
C | 2 | a0017c0021t0013g0059 a0017c0021t0013g0060 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.920-225_920-215del others(11): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794171 | |||||||
chr5:96794248 | G | A | 1 | a0022c0031t0001g0131 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.920-291C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794248 | |||||||
chr5:96794311 | T | C | 215 | a0001c0001t0001g0058 a0001c0015t0010g0261 a0001c0015t0010g0262 others(212): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.920-354A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794311 | |||||||
chr5:96794312 | G | C | 204 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(201): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.920-355C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794312 | |||||||
chr5:96794320 | C | T | 1 | a0005c0005t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.920-363G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794320 | |||||||
chr5:96794335 | T | C | 10 | a0008c0008t0002g0051 a0008c0008t0003g0005 a0008c0008t0003g0022 others(7): Show |
15 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.920-378A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794335 | |||||||
chr5:96794336 | G | A | 2 | a0016c0019t0001g0189 a0016c0019t0002g0196 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.920-379C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794336 | |||||||
chr5:96794362 | TG | T | 36 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(33): Show |
43 | HG00280.hp2 HG00738.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.920-406delC | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794362 | |||||||
chr5:96794363 | G | T | 1 | a0006c0036t0004g0312 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.920-406C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794363 | |||||||
chr5:96794365 | A | T | 2 | a0017c0021t0013g0059 a0017c0021t0013g0060 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.920-408T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794365 | |||||||
chr5:96794401 | G | A | 1 | a0021c0026t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.920-444C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794401 | |||||||
chr5:96794486 | C | T | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.920-529G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794486 | |||||||
chr5:96794499 | C | T | 4 | a0009c0009t0006g0016 a0009c0009t0006g0161 a0009c0009t0006g0162 others(1): Show |
6 | HG01123.hp2 HG01361.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-542G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794499 | |||||||
chr5:96794529 | G | A | 1 | a0015c0023t0001g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.919+513C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794529 | |||||||
chr5:96794567 | C | T | 1 | a0006c0036t0004g0312 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.919+475G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794567 | |||||||
chr5:96794780 | T | C | 3 | a0017c0021t0013g0059 a0017c0021t0013g0060 a0020c0029t0022g0061 |
3 | HG02572.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.919+262A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794780 | |||||||
chr5:96794907 | G | A | 6 | a0001c0015t0010g0261 a0001c0015t0010g0262 a0001c0015t0010g0263 others(3): Show |
8 | HG02451.hp1 HG02965.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+135C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 5/18 | chr5 | 96794907 | |||||||
chr5:96795257 | G | A | 1 | a0010c0012t0001g0297 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.799-95C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96795257 | |||||||
chr5:96795290 | G | A | 1 | a0004c0004t0001g0038 | 2 | NA18950.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.799-128C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96795290 | |||||||
chr5:96795334 | C | A | 97 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(94): Show |
120 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.799-172G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96795334 | |||||||
chr5:96795494 | C | T | 61 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(58): Show |
79 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.799-332G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96795494 | |||||||
chr5:96795778 | T | C | 1 | a0001c0001t0002g0132 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.799-616A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96795778 | |||||||
chr5:96795780 | G | T | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.799-618C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96795780 | |||||||
chr5:96795896 | G | C | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.799-734C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96795896 | |||||||
chr5:96795978 | G | T | 1 | a0001c0001t0002g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.799-816C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96795978 | |||||||
chr5:96796030 | G | A | 215 | a0001c0001t0001g0058 a0001c0015t0010g0261 a0001c0015t0010g0262 others(212): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.799-868C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96796030 | |||||||
chr5:96796038 | C | T | 2 | a0016c0019t0001g0189 a0016c0019t0002g0196 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.799-876G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96796038 | |||||||
chr5:96796090 | C | T | 31 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(28): Show |
44 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.799-928G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96796090 | |||||||
chr5:96796171 | A | G | 1 | a0004c0004t0001g0271 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.798+1004T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96796171 | |||||||
chr5:96796299 | G | A | 1 | a0002c0002t0001g0237 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.798+876C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96796299 | |||||||
chr5:96796313 | T | C | 17 | a0009c0028t0009g0094 a0010c0012t0001g0285 a0010c0012t0001g0291 others(14): Show |
17 | HG00738.hp2 HG01496.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.798+862A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96796313 | |||||||
chr5:96796367 | A | G | 37 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(34): Show |
44 | HG00280.hp2 HG00738.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.798+808T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96796367 | |||||||
chr5:96796386 | T | C | 2 | a0009c0028t0009g0094 a0014c0022t0009g0299 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.798+789A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96796386 | |||||||
chr5:96796401 | C | T | 2 | a0001c0001t0002g0121 a0001c0001t0002g0146 |
2 | HG00423.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.798+774G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96796401 | |||||||
chr5:96796565 | G | A | 6 | a0001c0015t0010g0261 a0001c0015t0010g0262 a0001c0015t0010g0263 others(3): Show |
8 | HG02451.hp1 HG02965.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.798+610C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96796565 | |||||||
chr5:96796640 | T | C | 171 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(168): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.798+535A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96796640 | |||||||
chr5:96797081 | C | T | 1 | a0015c0023t0001g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.798+94G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96797081 | |||||||
chr5:96797092 | G | A | 41 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(38): Show |
59 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.798+83C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 4/18 | chr5 | 96797092 | |||||||
chr5:96797327 | CA | C | 31 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(28): Show |
44 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.664-19delT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96797327 | |||||||
chr5:96797331 | T | C | 31 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(28): Show |
44 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.664-22A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96797331 | |||||||
chr5:96797337 | A | C | 1 | a0001c0001t0002g0153 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.664-28T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96797337 | |||||||
chr5:96797724 | C | T | 208 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(205): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.664-415G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96797724 | |||||||
chr5:96797804 | T | C | 6 | a0012c0014t0001g0286 a0012c0014t0001g0287 a0012c0014t0001g0288 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.664-495A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96797804 | |||||||
chr5:96797815 | T | A | 6 | a0001c0015t0010g0261 a0001c0015t0010g0262 a0001c0015t0010g0263 others(3): Show |
8 | HG02451.hp1 HG02965.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.664-506A>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96797815 | |||||||
chr5:96797889 | C | G | 61 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(58): Show |
79 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.664-580G>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96797889 | |||||||
chr5:96797976 | G | A | 2 | a0016c0019t0001g0189 a0016c0019t0002g0196 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.664-667C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96797976 | |||||||
chr5:96798009 | A | C | 205 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(202): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.664-700T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798009 | |||||||
chr5:96798010 | G | A | 3 | a0002c0002t0001g0220 a0002c0002t0001g0250 a0002c0002t0001g0255 |
3 | NA18945.hp2 NA18993.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.664-701C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798010 | |||||||
chr5:96798091 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0136 |
2 | NA18992.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.664-782G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798091 | |||||||
chr5:96798092 | G | A | 15 | a0007c0007t0001g0026 a0007c0007t0001g0084 a0007c0007t0001g0113 others(12): Show |
16 | HG01069.hp1 HG01071.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.664-783C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798092 | |||||||
chr5:96798097 | G | A | 2 | a0002c0020t0002g0233 a0002c0020t0002g0248 |
2 | HG02080.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.664-788C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798097 | |||||||
chr5:96798112 | T | C | 1 | a0014c0017t0001g0290 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.664-803A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798112 | |||||||
chr5:96798217 | C | T | 208 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(205): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.664-908G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798217 | |||||||
chr5:96798249 | C | T | 5 | a0002c0002t0001g0217 a0002c0002t0001g0230 a0002c0002t0001g0241 others(2): Show |
5 | NA18949.hp1 NA18972.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.664-940G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798249 | |||||||
chr5:96798321 | T | A | 1 | a0009c0009t0001g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664-1012A>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798321 | |||||||
chr5:96798324 | C | CA | 53 | a0001c0001t0002g0099 a0001c0001t0002g0108 a0001c0015t0010g0262 others(50): Show |
58 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.664-1016dupT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798324 | |||||||
chr5:96798324 | C | CAAA | 66 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(63): Show |
89 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.664-1018_664-1016d others(5): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798324 | |||||||
chr5:96798324 | C | CAAAAAA | 31 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(28): Show |
41 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.664-1021_664-1016d others(8): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798324 | |||||||
chr5:96798324 | C | CAAAAAAA | 6 | a0003c0003t0003g0031 a0003c0003t0003g0180 a0003c0003t0003g0187 others(3): Show |
7 | HG00741.hp2 HG01192.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.664-1022_664-1016d others(9): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798324 | |||||||
chr5:96798367 | G | A | 1 | a0001c0001t0002g0134 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.664-1058C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798367 | |||||||
chr5:96798410 | A | G | 215 | a0001c0001t0002g0149 a0001c0015t0010g0261 a0001c0015t0010g0262 others(212): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.664-1101T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798410 | |||||||
chr5:96798472 | T | G | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.664-1163A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798472 | |||||||
chr5:96798514 | G | A | 10 | a0008c0008t0002g0051 a0008c0008t0003g0005 a0008c0008t0003g0022 others(7): Show |
15 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.664-1205C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798514 | |||||||
chr5:96798532 | G | A | 60 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(57): Show |
76 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.664-1223C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798532 | |||||||
chr5:96798580 | T | C | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.664-1271A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798580 | |||||||
chr5:96798581 | C | CT | 77 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0032 others(74): Show |
103 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.664-1273dupA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798581 | |||||||
chr5:96798581 | C | CTT | 91 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(88): Show |
114 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.664-1274_664-1273d others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798581 | |||||||
chr5:96798581 | C | CTTT | 16 | a0004c0004t0005g0270 a0006c0006t0004g0021 a0006c0006t0004g0042 others(13): Show |
21 | HG00280.hp2 HG00609.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.664-1275_664-1273d others(5): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798581 | |||||||
chr5:96798588 | T | TG | 20 | a0002c0002t0001g0019 a0002c0002t0001g0209 a0002c0002t0001g0220 others(17): Show |
23 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.664-1280_664-1279i others(3): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798588 | |||||||
chr5:96798603 | T | C | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.664-1294A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798603 | |||||||
chr5:96798605 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.664-1296C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798605 | |||||||
chr5:96798651 | G | C | 29 | a0009c0009t0001g0029 a0009c0009t0001g0166 a0009c0009t0001g0168 others(26): Show |
32 | HG00738.hp2 HG01109.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.664-1342C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798651 | |||||||
chr5:96798871 | C | CTTTT | 53 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(50): Show |
70 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.664-1566_664-1563d others(6): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798871 | |||||||
chr5:96798871 | C | CTTTTGT | 15 | a0007c0007t0001g0026 a0007c0007t0001g0084 a0007c0007t0001g0113 others(12): Show |
16 | HG01069.hp1 HG01071.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.664-1563_664-1562i others(8): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798871 | |||||||
chr5:96798871 | C | CTTTTT | 9 | a0002c0002t0001g0226 a0002c0002t0001g0227 a0002c0002t0001g0228 others(6): Show |
9 | HG02071.hp1 HG02572.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.664-1567_664-1563d others(7): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798871 | |||||||
chr5:96798871 | C | CTTTTTT | 30 | a0003c0003t0003g0191 a0003c0003t0003g0197 a0006c0006t0004g0021 others(27): Show |
36 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.664-1568_664-1563d others(8): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798871 | |||||||
chr5:96798871 | C | CTTTTTTT | 60 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(57): Show |
78 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.664-1569_664-1563d others(9): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798871 | |||||||
chr5:96798871 | C | CTTTTTTT others(1): Show |
9 | a0003c0003t0003g0176 a0003c0003t0003g0181 a0004c0004t0001g0276 others(6): Show |
10 | HG00558.hp1 HG00609.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.664-1570_664-1563d others(10): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798871 | |||||||
chr5:96798871 | C | CTTTTTTT others(2): Show |
28 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(25): Show |
41 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.664-1571_664-1563d others(11): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798871 | |||||||
chr5:96798871 | C | CTTTTTTT others(3): Show |
2 | a0004c0004t0001g0204 a0004c0004t0001g0269 |
2 | NA18967.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.664-1572_664-1563d others(12): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798871 | |||||||
chr5:96798960 | A | T | 1 | a0005c0005t0005g0064 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.664-1651T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96798960 | |||||||
chr5:96799025 | G | A | 22 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(19): Show |
28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.664-1716C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96799025 | |||||||
chr5:96799104 | T | G | 1 | a0005c0005t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.663+1758A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96799104 | |||||||
chr5:96799212 | GATTAA | G | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.663+1645_663+1649d others(7): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96799212 | |||||||
chr5:96799275 | C | T | 1 | a0001c0015t0010g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.663+1587G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96799275 | |||||||
chr5:96799329 | T | G | 60 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(57): Show |
78 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.663+1533A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96799329 | |||||||
chr5:96799453 | A | G | 60 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(57): Show |
78 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.663+1409T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96799453 | |||||||
chr5:96799617 | C | T | 60 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(57): Show |
78 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.663+1245G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96799617 | |||||||
chr5:96799763 | T | C | 1 | a0019c0027t0006g0163 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.663+1099A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96799763 | |||||||
chr5:96799889 | C | T | 1 | a0017c0021t0013g0059 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.663+973G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96799889 | |||||||
chr5:96799995 | T | C | 3 | a0008c0008t0003g0005 a0008c0008t0003g0053 a0008c0008t0003g0054 |
7 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.663+867A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96799995 | |||||||
chr5:96800020 | C | T | 97 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(94): Show |
120 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.663+842G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96800020 | |||||||
chr5:96800075 | C | T | 1 | a0009c0009t0006g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.663+787G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96800075 | |||||||
chr5:96800222 | A | T | 60 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(57): Show |
78 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.663+640T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96800222 | |||||||
chr5:96800342 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.663+520A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96800342 | |||||||
chr5:96800598 | T | G | 60 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(57): Show |
78 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.663+264A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96800598 | |||||||
chr5:96800637 | A | C | 10 | a0008c0008t0002g0051 a0008c0008t0003g0005 a0008c0008t0003g0022 others(7): Show |
15 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.663+225T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96800637 | |||||||
chr5:96800698 | C | A | 7 | a0011c0011t0001g0045 a0011c0011t0001g0173 a0011c0011t0001g0174 others(4): Show |
8 | HG00738.hp1 HG01975.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.663+164G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96800698 | |||||||
chr5:96800822 | T | C | 97 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(94): Show |
120 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.663+40A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96800822 | |||||||
chr5:96800850 | G | A | 1 | a0002c0002t0001g0238 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.663+12C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96800850 | |||||||
chr5:96800861 | C | T | 2 | a0005c0005t0001g0112 a0005c0005t0001g0152 |
2 | HG02895.hp2 HG02897.hp2 |
splice_donor_variant&intron_variant | HIGH | c.663+1G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 3/18 | chr5 | 96800861 | |||||||
chr5:96801293 | A | G | 1 | a0004c0004t0001g0283 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.525-293T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801293 | |||||||
chr5:96801368 | C | T | 1 | a0004c0004t0001g0264 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.525-368G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801368 | |||||||
chr5:96801437 | G | A | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.525-437C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801437 | |||||||
chr5:96801463 | G | GA | 151 | a0001c0001t0001g0058 a0001c0015t0010g0261 a0001c0015t0010g0262 others(148): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.525-464dupT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801463 | |||||||
chr5:96801501 | G | A | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.525-501C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801501 | |||||||
chr5:96801502 | G | A | 1 | a0009c0009t0001g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.525-502C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801502 | |||||||
chr5:96801544 | T | C | 1 | a0002c0002t0001g0213 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.525-544A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801544 | |||||||
chr5:96801603 | T | G | 1 | a0001c0001t0002g0146 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.525-603A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801603 | |||||||
chr5:96801725 | G | A | 3 | a0017c0021t0013g0059 a0017c0021t0013g0060 a0020c0029t0022g0061 |
3 | HG02572.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.525-725C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801725 | |||||||
chr5:96801729 | G | A | 1 | a0002c0002t0001g0239 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.525-729C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801729 | |||||||
chr5:96801742 | C | T | 3 | a0001c0010t0002g0119 a0001c0010t0002g0120 a0001c0010t0002g0135 |
3 | NA18947.hp2 NA18972.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.525-742G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801742 | |||||||
chr5:96801755 | G | A | 15 | a0007c0007t0001g0026 a0007c0007t0001g0084 a0007c0007t0001g0113 others(12): Show |
16 | HG01069.hp1 HG01071.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.525-755C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801755 | |||||||
chr5:96801793 | G | A | 204 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(201): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.525-793C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801793 | |||||||
chr5:96801801 | G | A | 1 | a0002c0002t0021g0212 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.525-801C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801801 | |||||||
chr5:96801851 | C | A | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.525-851G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801851 | |||||||
chr5:96801854 | C | CA | 69 | a0001c0001t0001g0073 a0001c0001t0001g0136 a0001c0001t0001g0138 others(66): Show |
77 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.525-855dupT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801854 | |||||||
chr5:96801854 | C | CAA | 17 | a0001c0001t0001g0058 a0001c0001t0002g0046 a0001c0001t0002g0080 others(14): Show |
17 | HG01106.hp2 HG01175.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.525-856_525-855dup others(2): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801854 | |||||||
chr5:96801854 | C | CAAA | 33 | a0002c0002t0001g0001 a0002c0002t0001g0019 a0002c0002t0001g0032 others(30): Show |
47 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.525-857_525-855dup others(3): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801854 | |||||||
chr5:96801854 | C | CAAAA | 21 | a0002c0002t0001g0010 a0002c0002t0001g0213 a0002c0002t0001g0215 others(18): Show |
25 | HG00423.hp1 HG00544.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.525-858_525-855dup others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801854 | |||||||
chr5:96801854 | C | CAAAAA | 7 | a0002c0002t0001g0251 a0002c0002t0001g0252 a0002c0002t0001g0254 others(4): Show |
7 | HG02055.hp1 HG02280.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.525-859_525-855dup others(5): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801854 | |||||||
chr5:96801854 | CA | C | 67 | a0001c0001t0002g0024 a0001c0001t0002g0093 a0001c0001t0002g0110 others(64): Show |
95 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.525-855delT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96801854 | |||||||
chr5:96802007 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.525-1007C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802007 | |||||||
chr5:96802065 | T | C | 1 | a0003c0003t0003g0198 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.525-1065A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802065 | |||||||
chr5:96802101 | A | G | 204 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(201): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.525-1101T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802101 | |||||||
chr5:96802137 | A | G | 204 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(201): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.525-1137T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802137 | |||||||
chr5:96802179 | A | G | 207 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(204): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.525-1179T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802179 | |||||||
chr5:96802237 | C | A | 3 | a0017c0021t0013g0059 a0017c0021t0013g0060 a0020c0029t0022g0061 |
3 | HG02572.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.524+1166G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802237 | |||||||
chr5:96802237 | C | T | 1 | a0003c0003t0003g0210 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.524+1166G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802237 | |||||||
chr5:96802238 | G | A | 49 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(46): Show |
59 | HG00280.hp2 HG00738.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.524+1165C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802238 | |||||||
chr5:96802273 | T | G | 4 | a0001c0001t0002g0024 a0001c0001t0002g0093 a0001c0001t0002g0110 others(1): Show |
5 | HG00642.hp1 HG01106.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.524+1130A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802273 | |||||||
chr5:96802298 | T | C | 7 | a0011c0011t0001g0045 a0011c0011t0001g0173 a0011c0011t0001g0174 others(4): Show |
8 | HG00738.hp1 HG01975.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.524+1105A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802298 | |||||||
chr5:96802403 | G | T | 1 | a0002c0002t0001g0213 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.524+1000C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802403 | |||||||
chr5:96802409 | C | A | 4 | a0009c0009t0006g0016 a0009c0009t0006g0161 a0009c0009t0006g0162 others(1): Show |
6 | HG01123.hp2 HG01361.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.524+994G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802409 | |||||||
chr5:96802647 | A | G | 4 | a0001c0001t0002g0024 a0001c0001t0002g0093 a0001c0001t0002g0110 others(1): Show |
5 | HG00642.hp1 HG01106.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.524+756T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802647 | |||||||
chr5:96802688 | T | C | 1 | a0014c0017t0001g0298 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.524+715A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802688 | |||||||
chr5:96802733 | A | C | 3 | a0017c0021t0013g0059 a0017c0021t0013g0060 a0020c0029t0022g0061 |
3 | HG02572.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.524+670T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802733 | |||||||
chr5:96802768 | G | A | 60 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(57): Show |
78 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.524+635C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802768 | |||||||
chr5:96802924 | T | G | 1 | a0001c0001t0002g0148 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.524+479A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96802924 | |||||||
chr5:96803003 | A | G | 1 | a0009c0009t0001g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.524+400T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96803003 | |||||||
chr5:96803064 | T | C | 213 | a0001c0001t0001g0058 a0001c0015t0010g0261 a0001c0015t0010g0262 others(210): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.524+339A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96803064 | |||||||
chr5:96803109 | A | G | 202 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(199): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.524+294T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96803109 | |||||||
chr5:96803120 | G | A | 3 | a0011c0011t0001g0173 a0011c0011t0001g0174 a0011c0011t0001g0175 |
3 | HG02602.hp1 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.524+283C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96803120 | |||||||
chr5:96803133 | G | A | 4 | a0011c0011t0001g0045 a0011c0011t0001g0314 a0011c0011t0001g0316 others(1): Show |
5 | HG00738.hp1 HG01975.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.524+270C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96803133 | |||||||
chr5:96803158 | C | T | 205 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(202): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.524+245G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96803158 | |||||||
chr5:96803201 | G | C | 15 | a0007c0007t0001g0026 a0007c0007t0001g0084 a0007c0007t0001g0113 others(12): Show |
16 | HG01069.hp1 HG01071.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.524+202C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96803201 | |||||||
chr5:96803331 | C | T | 16 | a0010c0012t0001g0285 a0010c0012t0001g0291 a0010c0012t0001g0293 others(13): Show |
16 | HG00738.hp2 HG01496.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.524+72G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96803331 | |||||||
chr5:96803358 | G | A | 2 | a0001c0001t0002g0149 a0001c0001t0002g0150 |
2 | HG00642.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.524+45C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96803358 | |||||||
chr5:96803363 | C | T | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.524+40G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 2/18 | chr5 | 96803363 | |||||||
chr5:96804011 | AG | A | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-17-69delC | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804011 | |||||||
chr5:96804163 | A | C | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-17-220T>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804163 | |||||||
chr5:96804211 | G | C | 1 | a0010c0012t0001g0297 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-17-268C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804211 | |||||||
chr5:96804348 | A | T | 10 | a0008c0008t0002g0051 a0008c0008t0003g0005 a0008c0008t0003g0022 others(7): Show |
15 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-405T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804348 | |||||||
chr5:96804658 | G | A | 3 | a0011c0011t0001g0173 a0011c0011t0001g0174 a0011c0011t0001g0175 |
3 | HG02602.hp1 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-17-715C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804658 | |||||||
chr5:96804664 | C | T | 175 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(172): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.-17-721G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804664 | |||||||
chr5:96804685 | C | T | 1 | a0001c0010t0002g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-17-742G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804685 | |||||||
chr5:96804731 | A | G | 3 | a0011c0011t0001g0173 a0011c0011t0001g0174 a0011c0011t0001g0175 |
3 | HG02602.hp1 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-17-788T>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804731 | |||||||
chr5:96804743 | T | C | 175 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(172): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.-17-800A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804743 | |||||||
chr5:96804812 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-17-869C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804812 | |||||||
chr5:96804838 | T | G | 31 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(28): Show |
44 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.-17-895A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804838 | |||||||
chr5:96804839 | G | A | 31 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(28): Show |
44 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.-17-896C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804839 | |||||||
chr5:96804850 | G | A | 1 | a0005c0005t0001g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-17-907C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804850 | |||||||
chr5:96804926 | A | T | 47 | a0004c0004t0001g0003 a0004c0004t0001g0035 a0004c0004t0001g0036 others(44): Show |
60 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-17-983T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804926 | |||||||
chr5:96804938 | T | C | 1 | a0001c0010t0002g0151 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-17-995A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804938 | |||||||
chr5:96804944 | T | TA | 96 | a0001c0001t0002g0111 a0001c0001t0002g0153 a0002c0002t0001g0001 others(93): Show |
118 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-17-1002dupT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804944 | |||||||
chr5:96804944 | TA | T | 56 | a0003c0003t0003g0172 a0004c0004t0001g0003 a0004c0004t0001g0035 others(53): Show |
74 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-17-1002delT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96804944 | |||||||
chr5:96805012 | T | TAAGTTTT others(312): Show |
3 | a0004c0004t0001g0040 a0004c0004t0001g0280 a0004c0004t0001g0284 |
4 | HG02148.hp2 NA18948.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-1070_-17-1069i others(321): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805012 | |||||||
chr5:96805012 | T | TAAGTTTT others(311): Show |
2 | a0004c0004t0001g0278 a0004c0004t0001g0279 |
2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-17-1070_-17-1069i others(320): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805012 | |||||||
chr5:96805012 | T | TAAGTTTT others(312): Show |
16 | a0004c0004t0001g0003 a0004c0004t0001g0036 a0004c0004t0001g0037 others(13): Show |
27 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.-17-1070_-17-1069i others(321): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805012 | |||||||
chr5:96805012 | T | TAAGTTTT others(313): Show |
10 | a0004c0004t0001g0035 a0004c0004t0001g0057 a0004c0004t0001g0204 others(7): Show |
11 | HG00597.hp2 HG02129.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-1070_-17-1069i others(322): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805012 | |||||||
chr5:96805037 | C | T | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-17-1094G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805037 | |||||||
chr5:96805103 | ACTC | A | 22 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(19): Show |
28 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-17-1163_-17-1161d others(5): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805103 | |||||||
chr5:96805138 | T | C | 1 | a0001c0001t0002g0049 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-17-1195A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805138 | |||||||
chr5:96805210 | C | G | 1 | a0003c0003t0003g0177 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-17-1267G>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805210 | |||||||
chr5:96805346 | G | GT | 41 | a0002c0002t0003g0221 a0002c0002t0003g0222 a0002c0002t0006g0223 others(38): Show |
52 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.-17-1404dupA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805346 | |||||||
chr5:96805346 | G | GTT | 29 | a0003c0003t0003g0176 a0004c0004t0001g0003 a0004c0004t0001g0035 others(26): Show |
42 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-17-1405_-17-1404d others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805346 | |||||||
chr5:96805356 | T | A | 1 | a0006c0006t0004g0313 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-17-1413A>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805356 | |||||||
chr5:96805356 | T | TA | 14 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(11): Show |
19 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-1414_-17-1413i others(3): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805356 | |||||||
chr5:96805357 | T | A | 18 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(15): Show |
24 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.-17-1414A>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805357 | |||||||
chr5:96805357 | TA | T | 89 | a0001c0001t0001g0058 a0001c0001t0001g0073 a0001c0001t0001g0155 others(86): Show |
108 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.-17-1415delT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805357 | |||||||
chr5:96805358 | A | T | 104 | a0001c0010t0001g0123 a0001c0015t0010g0261 a0001c0015t0010g0262 others(101): Show |
130 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-17-1415T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805358 | |||||||
chr5:96805359 | A | T | 91 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(88): Show |
116 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-17-1416T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805359 | |||||||
chr5:96805360 | A | T | 21 | a0002c0002t0001g0213 a0002c0002t0001g0215 a0002c0002t0008g0214 others(18): Show |
21 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17-1417T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805360 | |||||||
chr5:96805361 | A | T | 1 | a0010c0012t0001g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-17-1418T>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805361 | |||||||
chr5:96805404 | GA | G | 37 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(34): Show |
48 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-17-1462delT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805404 | |||||||
chr5:96805598 | C | T | 2 | a0017c0021t0013g0059 a0017c0021t0013g0060 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-17-1655G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805598 | |||||||
chr5:96805607 | G | A | 4 | a0011c0011t0001g0045 a0011c0011t0001g0314 a0011c0011t0001g0316 others(1): Show |
5 | HG00738.hp1 HG01975.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-1664C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805607 | |||||||
chr5:96805704 | G | C | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-17-1761C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96805704 | |||||||
chr5:96806235 | G | C | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+1625C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806235 | |||||||
chr5:96806495 | T | C | 1 | a0002c0002t0014g0257 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-18+1365A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806495 | |||||||
chr5:96806623 | C | CT | 34 | a0001c0001t0001g0058 a0001c0001t0001g0073 a0001c0001t0002g0012 others(31): Show |
41 | HG00621.hp1 HG01175.hp2 HG01346.hp2 others(38): Show |
intron_variant | MODIFIER | c.-18+1236dupA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806623 | |||||||
chr5:96806623 | CT | C | 13 | a0001c0001t0001g0155 a0001c0001t0002g0156 a0001c0001t0002g0159 others(10): Show |
14 | HG00140.hp1 HG01109.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-18+1236delA | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806623 | |||||||
chr5:96806623 | CTTT | C | 80 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(77): Show |
104 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-18+1234_-18+1236d others(5): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806623 | |||||||
chr5:96806623 | CTTTTTT | C | 56 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(53): Show |
74 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-18+1231_-18+1236d others(8): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806623 | |||||||
chr5:96806623 | CTTTTTTT | C | 7 | a0002c0002t0008g0258 a0008c0008t0003g0022 a0011c0011t0001g0045 others(4): Show |
9 | HG00738.hp1 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+1230_-18+1236d others(9): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806623 | |||||||
chr5:96806623 | CTTTTTTT others(1): Show |
C | 26 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(23): Show |
35 | HG00280.hp2 HG00639.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.-18+1229_-18+1236d others(10): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806623 | |||||||
chr5:96806623 | CTTTTTTT others(4): Show |
C | 7 | a0001c0015t0010g0261 a0001c0015t0010g0262 a0001c0015t0010g0263 others(4): Show |
9 | HG02451.hp1 HG02965.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+1226_-18+1236d others(13): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806623 | |||||||
chr5:96806630 | T | C | 1 | a0010c0012t0001g0285 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-18+1230A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806630 | |||||||
chr5:96806631 | T | C | 80 | a0003c0003t0001g0018 a0003c0003t0001g0183 a0003c0003t0001g0184 others(77): Show |
104 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-18+1229A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806631 | |||||||
chr5:96806632 | T | C | 3 | a0003c0003t0003g0205 a0004c0004t0001g0283 a0004c0004t0001g0284 |
3 | NA19004.hp2 NA19062.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-18+1228A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806632 | |||||||
chr5:96806780 | T | G | 32 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(29): Show |
43 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.-18+1080A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806780 | |||||||
chr5:96806851 | G | GA | 38 | a0003c0003t0003g0172 a0006c0006t0004g0021 a0006c0006t0004g0042 others(35): Show |
44 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-18+1008dupT | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806851 | |||||||
chr5:96806851 | G | GAA | 78 | a0002c0002t0001g0209 a0003c0003t0001g0018 a0003c0003t0001g0183 others(75): Show |
107 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.-18+1007_-18+1008d others(4): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806851 | |||||||
chr5:96806851 | G | GAAA | 59 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(56): Show |
77 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-18+1006_-18+1008d others(5): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806851 | |||||||
chr5:96806873 | T | C | 7 | a0001c0015t0010g0261 a0001c0015t0010g0262 a0001c0015t0010g0263 others(4): Show |
9 | HG02451.hp1 HG02965.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+987A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806873 | |||||||
chr5:96806892 | C | T | 1 | a0005c0013t0001g0259 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-18+968G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806892 | |||||||
chr5:96806907 | C | T | 16 | a0010c0012t0001g0285 a0010c0012t0001g0291 a0010c0012t0001g0293 others(13): Show |
16 | HG00738.hp2 HG01496.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+953G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806907 | |||||||
chr5:96806961 | T | TTTTTG | 13 | a0001c0001t0001g0164 a0001c0001t0002g0165 a0009c0009t0001g0029 others(10): Show |
16 | HG01109.hp1 HG01123.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+894_-18+898dup others(5): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806961 | |||||||
chr5:96806961 | TTTTTG | T | 175 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(172): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.-18+894_-18+898del others(5): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806961 | |||||||
chr5:96806986 | G | T | 175 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(172): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.-18+874C>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806986 | |||||||
chr5:96806988 | T | C | 175 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(172): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.-18+872A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96806988 | |||||||
chr5:96807103 | G | C | 175 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(172): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.-18+757C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807103 | |||||||
chr5:96807121 | C | T | 1 | a0005c0005t0005g0062 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18+739G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807121 | |||||||
chr5:96807232 | G | A | 76 | a0002c0002t0001g0001 a0002c0002t0001g0010 a0002c0002t0001g0019 others(73): Show |
94 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-18+628C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807232 | |||||||
chr5:96807498 | G | A | 1 | a0004c0004t0001g0041 | 2 | HG00099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-18+362C>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807498 | |||||||
chr5:96807580 | G | C | 56 | a0001c0015t0010g0261 a0001c0015t0010g0262 a0001c0015t0010g0263 others(53): Show |
71 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.-18+280C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807580 | |||||||
chr5:96807668 | TCGCGCCC others(14): Show |
T | 4 | a0001c0001t0001g0058 a0017c0021t0013g0059 a0017c0021t0013g0060 others(1): Show |
4 | HG02572.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+171_-18+191del others(21): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807668 | |||||||
chr5:96807713 | C | CGCCCCGT others(14): Show |
1 | a0004c0004t0001g0057 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-18+126_-18+146dup others(21): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807713 | |||||||
chr5:96807720 | T | TCGCCTTC | 4 | a0011c0011t0001g0045 a0011c0011t0001g0314 a0011c0011t0001g0316 others(1): Show |
5 | HG00738.hp1 HG01975.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+139_-18+140ins others(7): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807720 | |||||||
chr5:96807722 | T | G | 15 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(12): Show |
20 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+138A>C | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807722 | |||||||
chr5:96807725 | C | CGCGCCCC others(7): Show |
4 | a0011c0011t0001g0045 a0011c0011t0001g0314 a0011c0011t0001g0316 others(1): Show |
5 | HG00738.hp1 HG01975.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+134_-18+135ins others(14): Show |
ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807725 | |||||||
chr5:96807725 | C | T | 26 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 others(23): Show |
36 | HG00280.hp2 HG00639.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.-18+135G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807725 | |||||||
chr5:96807734 | T | C | 19 | a0006c0006t0004g0021 a0006c0006t0004g0042 a0006c0006t0004g0044 others(16): Show |
25 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18+126A>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807734 | |||||||
chr5:96807776 | C | A | 1 | a0006c0006t0004g0317 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-18+84G>T | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807776 | |||||||
chr5:96807816 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-18+44G>A | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807816 | |||||||
chr5:96807821 | G | C | 1 | a0010c0012t0001g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-18+39C>G | ERAP1 | ENSG00000164307.13 | transcript | ENST00000443439.7 | protein_coding | 1/18 | chr5 | 96807821 |