Item | Value |
---|---|
geneid | 3566 |
ensemblid | ENSG00000077238.14 |
hgncid | 6015 |
symbol | IL4R |
name | interleukin 4 receptor |
refseq_nuc | NM_000418.4 |
refseq_prot | NP_000409.1 |
ensembl_nuc | ENST00000395762.7 |
ensembl_prot | ENSP00000379111.2 |
mane_status | MANE Select |
chr | chr16 |
start | 27313974 |
end | 27364778 |
strand | + |
ver | v1.2 |
region | chr16:27313974-27364778 |
region5000 | chr16:27308974-27369778 |
regionname0 | IL4R_chr16_27313974_27364778 |
regionname5000 | IL4R_chr16_27308974_27369778 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 825 | 100 | 13 | 11 | 60 | 6 | 10 | 44 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0002 | 1/1 | 825 | 85 | 9 | 25 | 31 | 6 | 12 | 22 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0003 | 0/0 | 825 | 28 | 9 | 5 | 13 | 0 | 1 | 10 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0004 | 0/0 | 825 | 18 | 0 | 3 | 9 | 0 | 6 | 6 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0005 | 0/0 | 825 | 14 | 2 | 9 | 3 | 0 | 0 | 3 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0006 | 0/0 | 825 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0007 | 0/0 | 825 | 8 | 0 | 0 | 8 | 0 | 0 | 8 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0008 | 0/0 | 825 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0009 | 0/0 | 825 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0010 | 0/0 | 825 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0011 | 0/0 | 825 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0012 | 0/0 | 825 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0013 | 0/0 | 825 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0014 | 0/0 | 825 | 4 | 1 | 0 | 0 | 0 | 3 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0015 | 0/0 | 825 | 3 | 0 | 1 | 0 | 2 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0016 | 0/0 | 825 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0017 | 0/0 | 825 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0018 | 0/0 | 825 | 3 | 1 | 0 | 1 | 0 | 1 | 1 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0019 | 0/0 | 825 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0020 | 0/0 | 825 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0021 | 0/0 | 825 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0022 | 0/0 | 825 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0023 | 0/0 | 825 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0024 | 0/0 | 825 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0025 | 0/0 | 825 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0026 | 0/0 | 825 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0027 | 0/0 | 825 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0028 | 0/0 | 825 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0029 | 0/0 | 825 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0030 | 0/0 | 825 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0031 | 0/0 | 825 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0032 | 0/0 | 825 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0033 | 0/0 | 825 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
a0034 | 0/0 | 825 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | MGWLC others(820): Show |
chr16 | 27308974 | 27369778 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2475 | 93 | 11 | 8 | 60 | 4 | 10 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0001c0008 | 0/0 | 2475 | 7 | 2 | 3 | 0 | 2 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0002c0002 | 1/0 | 2475 | 81 | 8 | 23 | 31 | 6 | 12 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0002c0013 | 0/1 | 2475 | 4 | 1 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0003c0003 | 0/0 | 2475 | 28 | 9 | 5 | 13 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0004c0004 | 0/0 | 2475 | 18 | 0 | 3 | 9 | 0 | 6 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0005c0005 | 0/0 | 2475 | 12 | 0 | 9 | 3 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0005c0022 | 0/0 | 2475 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0006c0006 | 0/0 | 2475 | 10 | 10 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0006c0031 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0007c0007 | 0/0 | 2475 | 8 | 0 | 0 | 8 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0008c0009 | 0/0 | 2475 | 6 | 6 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0008c0047 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0009c0017 | 0/0 | 2475 | 3 | 3 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0009c0035 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0009c0037 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0009c0044 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0009c0046 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0010c0012 | 0/0 | 2475 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0010c0024 | 0/0 | 2475 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0010c0034 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0011c0010 | 0/0 | 2475 | 5 | 5 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0012c0016 | 0/0 | 2475 | 3 | 2 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0012c0042 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0013c0011 | 0/0 | 2475 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0014c0019 | 0/0 | 2475 | 3 | 0 | 0 | 0 | 0 | 3 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0014c0041 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0015c0014 | 0/0 | 2475 | 3 | 0 | 1 | 0 | 2 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0016c0018 | 0/0 | 2475 | 3 | 2 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0017c0020 | 0/0 | 2475 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0017c0032 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0018c0015 | 0/0 | 2475 | 3 | 1 | 0 | 1 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0019c0023 | 0/0 | 2475 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0020c0021 | 0/0 | 2475 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0021c0045 | 0/0 | 2475 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0022c0027 | 0/0 | 2475 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0023c0043 | 0/0 | 2475 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0024c0038 | 0/0 | 2475 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0025c0048 | 0/0 | 2475 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0026c0029 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0027c0036 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0028c0028 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0029c0039 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0030c0030 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0031c0025 | 0/0 | 2475 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0032c0040 | 0/0 | 2475 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0033c0033 | 0/0 | 2475 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 | ||
a0034c0026 | 0/0 | 2475 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ATGGG others(2470): Show |
chr16 | 27308974 | 27369778 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3624 | 18 | 0 | 3 | 12 | 2 | 1 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0001c0001t0002 | 0/0 | 3624 | 74 | 11 | 5 | 47 | 2 | 9 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0001c0001t0021 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0001c0008t0001 | 0/0 | 3624 | 4 | 0 | 3 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0001c0008t0002 | 0/0 | 3624 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0001c0008t0018 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0001c0008t0025 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0002c0002t0001 | 0/0 | 3624 | 56 | 5 | 18 | 21 | 1 | 11 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0002c0002t0002 | 1/0 | 3624 | 25 | 3 | 5 | 10 | 5 | 1 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0002c0013t0001 | 0/0 | 3624 | 3 | 1 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0002c0013t0019 | 0/1 | 3624 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0003c0003t0001 | 0/0 | 3624 | 22 | 6 | 2 | 13 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0003c0003t0002 | 0/0 | 3624 | 6 | 3 | 3 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0004c0004t0001 | 0/0 | 3624 | 5 | 0 | 1 | 0 | 0 | 4 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0004c0004t0003 | 0/0 | 3624 | 13 | 0 | 2 | 9 | 0 | 2 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0005c0005t0001 | 0/0 | 3624 | 7 | 0 | 4 | 3 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0005c0005t0002 | 0/0 | 3624 | 5 | 0 | 5 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0005c0022t0001 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0006c0006t0006 | 0/0 | 3624 | 6 | 6 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0006c0006t0008 | 0/0 | 3624 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0006c0031t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0007c0007t0001 | 0/0 | 3624 | 4 | 0 | 0 | 4 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0007c0007t0002 | 0/0 | 3624 | 2 | 0 | 0 | 2 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0007c0007t0015 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0007c0007t0022 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0008c0009t0007 | 0/0 | 3624 | 5 | 5 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0008c0009t0016 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0008c0047t0007 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0009c0017t0012 | 0/0 | 3624 | 3 | 3 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0009c0035t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0009c0037t0001 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0009c0044t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0009c0046t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0010c0012t0004 | 0/0 | 3624 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0010c0024t0004 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0010c0024t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0010c0034t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0011c0010t0004 | 0/0 | 3624 | 5 | 5 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0012c0016t0006 | 0/0 | 3624 | 3 | 2 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0012c0042t0007 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0013c0011t0009 | 0/0 | 3624 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0014c0019t0011 | 0/0 | 3624 | 3 | 0 | 0 | 0 | 0 | 3 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0014c0041t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0015c0014t0002 | 0/0 | 3624 | 3 | 0 | 1 | 0 | 2 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0016c0018t0005 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0016c0018t0023 | 0/0 | 3597 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3592): Show |
chr16 | 27308974 | 27369778 |
a0017c0020t0010 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0017c0032t0010 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0018c0015t0001 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0018c0015t0003 | 0/0 | 3624 | 2 | 0 | 0 | 1 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0019c0023t0013 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0020c0021t0002 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0021c0045t0024 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0022c0027t0003 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0023c0043t0017 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0024c0038t0002 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0025c0048t0002 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0026c0029t0014 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0027c0036t0014 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0028c0028t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0029c0039t0004 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0030c0030t0020 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0031c0025t0001 | 0/0 | 3624 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0032c0040t0002 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0033c0033t0004 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
a0034c0026t0002 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | ACTTC others(3619): Show |
chr16 | 27308974 | 27369778 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0002 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0021g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0008t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0008t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0008t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0008t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0008t0018g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0008t0025g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0001 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0013t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0013t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0013t0019g0224 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0022t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0006t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0006t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0006t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0006t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0006t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0006t0008g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0006t0008g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0031t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0007c0007t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0007c0007t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0007c0007t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0007c0007t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0007c0007t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0007c0007t0015g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0007c0007t0022g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0008c0009t0007g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0008c0009t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0008c0009t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0008c0009t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0008c0009t0016g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0008c0047t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0009c0017t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0009c0017t0012g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0009c0017t0012g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0009c0035t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0009c0037t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0009c0044t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0009c0046t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0010c0012t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0010c0012t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0010c0012t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0010c0024t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0010c0024t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0010c0034t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0011c0010t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0011c0010t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0011c0010t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0011c0010t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0011c0010t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0012c0016t0006g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0012c0016t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0012c0042t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0013c0011t0009g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0013c0011t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0013c0011t0009g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0014c0019t0011g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0014c0019t0011g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0014c0019t0011g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0014c0041t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0015c0014t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0015c0014t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0015c0014t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0016c0018t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0016c0018t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0016c0018t0023g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0017c0020t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0017c0020t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0017c0032t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0018c0015t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0018c0015t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0018c0015t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0019c0023t0013g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0019c0023t0013g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0020c0021t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0021c0045t0024g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0022c0027t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0023c0043t0017g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0024c0038t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0025c0048t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0026c0029t0014g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0027c0036t0014g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0028c0028t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0029c0039t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0030c0030t0020g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0031c0025t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0032c0040t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0033c0033t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0034c0026t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0140 | EUR | GBR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0101 | EUR | GBR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | GBR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0161 | EUR | GBR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0239 | EUR | FIN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00408 | hp1 | a0004 | c0004 | t0003 | g0120 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00597 | hp2 | a0003 | c0003 | t0001 | g0145 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0158 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00639 | hp2 | a0003 | c0003 | t0001 | g0128 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0218 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00642 | hp2 | a0001 | c0008 | t0001 | g0270 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00735 | hp2 | a0021 | c0045 | t0024 | g0169 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00738 | hp1 | a0015 | c0014 | t0002 | g0018 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00741 | hp2 | a0016 | c0018 | t0023 | g0173 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0216 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01069 | hp2 | a0005 | c0005 | t0001 | g0011 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01070 | hp1 | a0022 | c0027 | t0003 | g0204 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0213 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01074 | hp2 | a0003 | c0003 | t0002 | g0060 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01081 | hp1 | a0005 | c0005 | t0002 | g0257 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0149 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01099 | hp1 | a0005 | c0005 | t0002 | g0258 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0212 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01106 | hp2 | a0001 | c0008 | t0001 | g0028 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0241 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01109 | hp2 | a0012 | c0016 | t0006 | g0029 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01167 | hp1 | a0003 | c0003 | t0002 | g0059 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01168 | hp1 | a0002 | c0013 | t0001 | g0025 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01168 | hp2 | a0001 | c0008 | t0001 | g0028 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01169 | hp1 | a0003 | c0003 | t0002 | g0058 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01169 | hp2 | a0002 | c0013 | t0001 | g0189 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01243 | hp1 | a0005 | c0005 | t0002 | g0192 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01243 | hp2 | a0023 | c0043 | t0017 | g0045 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01258 | hp1 | a0005 | c0005 | t0001 | g0011 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0142 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01358 | hp1 | a0003 | c0003 | t0001 | g0205 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0182 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01361 | hp2 | a0005 | c0005 | t0001 | g0010 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01433 | hp1 | a0005 | c0005 | t0002 | g0269 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01496 | hp2 | a0004 | c0004 | t0001 | g0230 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0222 | EUR | IBS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01515 | hp2 | a0015 | c0014 | t0002 | g0151 | EUR | IBS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0017 | EUR | IBS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01516 | hp2 | a0001 | c0008 | t0001 | g0260 | EUR | IBS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0017 | EUR | IBS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0214 | EUR | IBS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01884 | hp1 | a0003 | c0003 | t0002 | g0248 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0233 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01891 | hp2 | a0001 | c0008 | t0018 | g0259 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0187 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0206 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0254 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01952 | hp1 | a0004 | c0004 | t0003 | g0201 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01952 | hp2 | a0024 | c0038 | t0002 | g0139 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02004 | hp2 | a0005 | c0005 | t0001 | g0144 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02055 | hp1 | a0017 | c0020 | t0010 | g0238 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02055 | hp2 | a0008 | c0009 | t0007 | g0084 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02056 | hp1 | a0004 | c0004 | t0003 | g0200 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02056 | hp2 | a0025 | c0048 | t0002 | g0125 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02071 | hp1 | a0003 | c0003 | t0001 | g0153 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02135 | hp1 | a0003 | c0003 | t0001 | g0136 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02145 | hp1 | a0019 | c0023 | t0013 | g0030 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02145 | hp2 | a0027 | c0036 | t0014 | g0051 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02148 | hp1 | a0004 | c0004 | t0003 | g0019 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0220 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CDX | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02258 | hp1 | a0009 | c0046 | t0005 | g0037 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02280 | hp1 | a0003 | c0003 | t0001 | g0162 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02300 | hp1 | a0005 | c0005 | t0002 | g0262 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02451 | hp1 | a0017 | c0032 | t0010 | g0043 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02451 | hp2 | a0002 | c0002 | t0002 | g0127 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02572 | hp1 | a0011 | c0010 | t0004 | g0179 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02572 | hp2 | a0009 | c0017 | t0012 | g0176 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02615 | hp1 | a0009 | c0017 | t0012 | g0274 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02622 | hp1 | a0008 | c0047 | t0007 | g0039 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02622 | hp2 | a0003 | c0003 | t0001 | g0250 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02630 | hp1 | a0006 | c0006 | t0006 | g0231 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02647 | hp1 | a0003 | c0003 | t0002 | g0126 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02647 | hp2 | a0013 | c0011 | t0009 | g0020 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0237 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02717 | hp1 | a0020 | c0021 | t0002 | g0016 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02717 | hp2 | a0012 | c0042 | t0007 | g0277 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02723 | hp1 | a0010 | c0024 | t0005 | g0171 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02723 | hp2 | a0003 | c0003 | t0001 | g0232 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02735 | hp2 | a0004 | c0004 | t0003 | g0019 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02738 | hp1 | a0014 | c0019 | t0011 | g0268 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02809 | hp1 | a0013 | c0011 | t0009 | g0020 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02809 | hp2 | a0029 | c0039 | t0004 | g0273 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02818 | hp1 | a0016 | c0018 | t0005 | g0174 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02818 | hp2 | a0006 | c0006 | t0006 | g0234 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02886 | hp1 | a0003 | c0003 | t0001 | g0044 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02886 | hp2 | a0020 | c0021 | t0002 | g0016 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02895 | hp1 | a0005 | c0022 | t0001 | g0021 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02895 | hp2 | a0012 | c0016 | t0006 | g0280 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0207 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02896 | hp2 | a0013 | c0011 | t0009 | g0178 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0226 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02897 | hp2 | a0005 | c0022 | t0001 | g0021 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02922 | hp1 | a0010 | c0024 | t0004 | g0279 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02922 | hp2 | a0010 | c0012 | t0004 | g0012 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02965 | hp1 | a0009 | c0017 | t0012 | g0175 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02965 | hp2 | a0010 | c0012 | t0004 | g0012 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02976 | hp1 | a0006 | c0006 | t0006 | g0209 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03041 | hp1 | a0010 | c0012 | t0004 | g0065 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03041 | hp2 | a0011 | c0010 | t0004 | g0047 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03098 | hp1 | a0009 | c0037 | t0001 | g0050 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03098 | hp2 | a0030 | c0030 | t0020 | g0235 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03130 | hp1 | a0016 | c0018 | t0005 | g0278 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03130 | hp2 | a0008 | c0009 | t0007 | g0008 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03139 | hp1 | a0006 | c0006 | t0008 | g0004 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03139 | hp2 | a0008 | c0009 | t0016 | g0249 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03195 | hp2 | a0019 | c0023 | t0013 | g0031 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03209 | hp1 | a0013 | c0011 | t0009 | g0048 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03225 | hp1 | a0006 | c0031 | t0005 | g0036 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03225 | hp2 | a0006 | c0006 | t0006 | g0004 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03239 | hp1 | a0014 | c0019 | t0011 | g0266 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03453 | hp1 | a0009 | c0035 | t0005 | g0038 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03453 | hp2 | a0002 | c0002 | t0002 | g0034 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03486 | hp1 | a0010 | c0034 | t0005 | g0177 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03486 | hp2 | a0003 | c0003 | t0001 | g0121 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0032 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03490 | hp2 | a0004 | c0004 | t0001 | g0009 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0185 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0183 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03492 | hp1 | a0004 | c0004 | t0001 | g0009 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0245 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03540 | hp1 | a0011 | c0010 | t0004 | g0035 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03540 | hp2 | a0008 | c0009 | t0007 | g0041 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03579 | hp1 | a0011 | c0010 | t0004 | g0033 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0276 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03669 | hp1 | a0004 | c0004 | t0001 | g0133 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03669 | hp2 | a0031 | c0025 | t0001 | g0022 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0227 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03710 | hp1 | a0004 | c0004 | t0003 | g0134 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03710 | hp2 | a0014 | c0019 | t0011 | g0265 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03834 | hp1 | a0004 | c0004 | t0001 | g0135 | SAS | BEB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0210 | SAS | BEB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03942 | hp1 | a0003 | c0003 | t0001 | g0180 | SAS | BEB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | BEB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | BEB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04184 | hp2 | a0018 | c0015 | t0003 | g0251 | SAS | BEB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0184 | SAS | STU | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0240 | SAS | STU | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | STU | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0267 | SAS | STU | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0191 | SAS | STU | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18522 | hp1 | a0010 | c0012 | t0004 | g0049 | AFR | YRI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18522 | hp2 | a0017 | c0020 | t0010 | g0042 | AFR | YRI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CHB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18747 | hp2 | a0004 | c0004 | t0003 | g0194 | EAS | CHB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18906 | hp1 | a0012 | c0016 | t0006 | g0029 | AFR | YRI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0272 | AFR | YRI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18945 | hp1 | a0007 | c0007 | t0002 | g0091 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18954 | hp1 | a0003 | c0003 | t0001 | g0155 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18954 | hp2 | a0007 | c0007 | t0002 | g0188 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18957 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18957 | hp2 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18967 | hp1 | a0003 | c0003 | t0001 | g0159 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18974 | hp2 | a0003 | c0003 | t0001 | g0143 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18975 | hp1 | a0004 | c0004 | t0003 | g0070 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18979 | hp1 | a0003 | c0003 | t0001 | g0152 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18983 | hp1 | a0005 | c0005 | t0001 | g0057 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18983 | hp2 | a0005 | c0005 | t0001 | g0104 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18986 | hp1 | a0007 | c0007 | t0001 | g0023 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18988 | hp2 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18990 | hp1 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18998 | hp1 | a0001 | c0001 | t0021 | g0098 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18998 | hp2 | a0007 | c0007 | t0022 | g0006 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19002 | hp2 | a0032 | c0040 | t0002 | g0015 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19003 | hp2 | a0007 | c0007 | t0001 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19005 | hp2 | a0004 | c0004 | t0003 | g0196 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19009 | hp1 | a0003 | c0003 | t0001 | g0243 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19011 | hp1 | a0018 | c0015 | t0003 | g0114 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19011 | hp2 | a0003 | c0003 | t0001 | g0157 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19012 | hp1 | a0007 | c0007 | t0001 | g0023 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19012 | hp2 | a0004 | c0004 | t0003 | g0066 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19030 | hp1 | a0003 | c0003 | t0002 | g0247 | AFR | LWK | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19030 | hp2 | a0008 | c0009 | t0007 | g0040 | AFR | LWK | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19043 | hp1 | a0033 | c0033 | t0004 | g0117 | AFR | LWK | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19043 | hp2 | a0006 | c0006 | t0008 | g0004 | AFR | LWK | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19057 | hp1 | a0003 | c0003 | t0001 | g0154 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19060 | hp2 | a0005 | c0005 | t0001 | g0010 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19062 | hp2 | a0004 | c0004 | t0003 | g0069 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19068 | hp2 | a0004 | c0004 | t0003 | g0199 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19077 | hp1 | a0007 | c0007 | t0015 | g0225 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19081 | hp1 | a0034 | c0026 | t0002 | g0244 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19085 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19085 | hp2 | a0007 | c0007 | t0001 | g0215 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19086 | hp2 | a0004 | c0004 | t0003 | g0198 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19240 | hp1 | a0006 | c0006 | t0008 | g0026 | AFR | YRI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19240 | hp2 | a0018 | c0015 | t0001 | g0119 | AFR | YRI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA20129 | hp1 | a0009 | c0044 | t0005 | g0255 | AFR | ASW | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | ASW | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA20805 | hp1 | a0015 | c0014 | t0002 | g0150 | EUR | TSI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA20805 | hp2 | a0001 | c0008 | t0002 | g0264 | EUR | TSI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02109 | hp1 | a0026 | c0029 | t0014 | g0122 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0211 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02486 | hp1 | a0028 | c0028 | t0005 | g0123 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02486 | hp2 | a0003 | c0003 | t0001 | g0172 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02559 | hp1 | a0006 | c0006 | t0006 | g0253 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02559 | hp2 | a0008 | c0009 | t0007 | g0008 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03471 | hp1 | a0006 | c0006 | t0008 | g0026 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG06807 | hp1 | a0001 | c0008 | t0025 | g0168 | AFR | USA | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG06807 | hp2 | a0006 | c0006 | t0006 | g0004 | AFR | USA | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | USA | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA20300 | hp2 | a0011 | c0010 | t0004 | g0046 | AFR | USA | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA21309 | hp1 | a0002 | c0013 | t0001 | g0025 | AFR | LWK | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA21309 | hp2 | a0014 | c0041 | t0005 | g0228 | AFR | LWK | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
homoSapiens | chm13v2 | a0002 | c0013 | t0019 | g0224 | REF | REF | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0146 | REF | REF | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:27330196 | C | A | 1 | a0007 | 1 | NA19077.hp1 | splice_region_variant | LOW | c.-21C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/11 | chr16 | 27330196 | |||||||
chr16:27342126 | A | G | 1 | a0025 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.76A>G | p.Met26Val | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/11 | 274/3624 | 76/2478 | 26/825 | chr16 | 27342126 | |||
chr16:27344882 | A | G | 17 | a0001 a0005 a0009 others(14): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
missense_variant | MODERATE | c.223A>G | p.Ile75Val | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/11 | 421/3624 | 223/2478 | 75/825 | chr16 | 27344882 | |||
chr16:27344903 | G | A | 1 | a0007 | 8 | NA18945.hp1 NA18954.hp2 NA18986.hp1 others(5): Show |
missense_variant | MODERATE | c.244G>A | p.Ala82Thr | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/11 | 442/3624 | 244/2478 | 82/825 | chr16 | 27344903 | |||
chr16:27346548 | C | A | 1 | a0031 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.443C>A | p.Pro148His | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/11 | 641/3624 | 443/2478 | 148/825 | chr16 | 27346548 | |||
chr16:27346578 | C | T | 1 | a0033 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.473C>T | p.Thr158Ile | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/11 | 671/3624 | 473/2478 | 158/825 | chr16 | 27346578 | |||
chr16:27352580 | G | A | 1 | a0024 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.554G>A | p.Arg185His | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/11 | 752/3624 | 554/2478 | 185/825 | chr16 | 27352580 | |||
chr16:27352625 | G | A | 1 | a0034 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.599G>A | p.Arg200Gln | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/11 | 797/3624 | 599/2478 | 200/825 | chr16 | 27352625 | |||
chr16:27362433 | T | C | 1 | a0022 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.1081T>C | p.Cys361Arg | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1279/3624 | 1081/2478 | 361/825 | chr16 | 27362433 | |||
chr16:27362452 | C | A | 1 | a0028 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1100C>A | p.Ala367Asp | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1298/3624 | 1100/2478 | 367/825 | chr16 | 27362452 | |||
chr16:27362496 | G | A | 1 | a0029 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1144G>A | p.Gly382Arg | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1342/3624 | 1144/2478 | 382/825 | chr16 | 27362496 | |||
chr16:27362551 | A | C | 13 | a0003 a0005 a0006 others(10): Show |
85 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(82): Show |
missense_variant | MODERATE | c.1199A>C | p.Glu400Ala | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1397/3624 | 1199/2478 | 400/825 | chr16 | 27362551 | |||
chr16:27362643 | T | C | 2 | a0003 a0005 |
42 | HG00597.hp2 HG00639.hp2 HG01069.hp2 others(39): Show |
missense_variant | MODERATE | c.1291T>C | p.Cys431Arg | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1489/3624 | 1291/2478 | 431/825 | chr16 | 27362643 | |||
chr16:27362659 | C | T | 2 | a0013 a0014 |
8 | HG02647.hp2 HG02738.hp1 HG02809.hp1 others(5): Show |
missense_variant | MODERATE | c.1307C>T | p.Ser436Leu | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1505/3624 | 1307/2478 | 436/825 | chr16 | 27362659 | |||
chr16:27362826 | G | A | 1 | a0017 | 3 | HG02055.hp1 HG02451.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.1474G>A | p.Ala492Thr | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1672/3624 | 1474/2478 | 492/825 | chr16 | 27362826 | |||
chr16:27362827 | C | T | 1 | a0028 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1475C>T | p.Ala492Val | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1673/3624 | 1475/2478 | 492/825 | chr16 | 27362827 | |||
chr16:27362859 | T | C | 11 | a0003 a0005 a0006 others(8): Show |
77 | HG00597.hp2 HG00639.hp2 HG00735.hp2 others(74): Show |
missense_variant | MODERATE | c.1507T>C | p.Ser503Pro | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1705/3624 | 1507/2478 | 503/825 | chr16 | 27362859 | |||
chr16:27363079 | A | G | 25 | a0003 a0004 a0005 others(22): Show |
131 | HG00408.hp1 HG00597.hp2 HG00639.hp2 others(128): Show |
missense_variant | MODERATE | c.1727A>G | p.Gln576Arg | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1925/3624 | 1727/2478 | 576/825 | chr16 | 27363079 | |||
chr16:27363087 | G | A | 4 | a0016 a0017 a0026 others(1): Show |
8 | HG00741.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
missense_variant | MODERATE | c.1735G>A | p.Val579Ile | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1933/3624 | 1735/2478 | 579/825 | chr16 | 27363087 | |||
chr16:27363126 | G | T | 1 | a0026 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1774G>T | p.Val592Leu | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1972/3624 | 1774/2478 | 592/825 | chr16 | 27363126 | |||
chr16:27363375 | C | T | 1 | a0015 | 3 | HG00738.hp1 HG01515.hp2 NA20805.hp1 |
missense_variant | MODERATE | c.2023C>T | p.Pro675Ser | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 2221/3624 | 2023/2478 | 675/825 | chr16 | 27363375 | |||
chr16:27363601 | A | G | 1 | a0032 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.2249A>G | p.Asp750Gly | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 2447/3624 | 2249/2478 | 750/825 | chr16 | 27363601 | |||
chr16:27363606 | T | G | 13 | a0008 a0010 a0011 others(10): Show |
42 | HG00735.hp2 HG00741.hp2 HG01109.hp2 others(39): Show |
missense_variant | MODERATE | c.2254T>G | p.Ser752Ala | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 2452/3624 | 2254/2478 | 752/825 | chr16 | 27363606 | |||
chr16:27363708 | T | C | 2 | a0019 a0021 |
3 | HG00735.hp2 HG02145.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.2356T>C | p.Ser786Pro | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 2554/3624 | 2356/2478 | 786/825 | chr16 | 27363708 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:27342158 | C | T | 1 | a0002c0013 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.108C>T | p.Ser36Ser | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/11 | 306/3624 | 108/2478 | 36/825 | chr16 | 27342158 | |||
chr16:27342257 | C | T | 1 | a0008c0047 | 1 | HG02622.hp1 | splice_region_variant&synonymous_variant | LOW | c.207C>T | p.Ser69Ser | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/11 | 405/3624 | 207/2478 | 69/825 | chr16 | 27342257 | |||
chr16:27344896 | C | T | 1 | a0009c0046 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.237C>T | p.Asn79Asn | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/11 | 435/3624 | 237/2478 | 79/825 | chr16 | 27344896 | |||
chr16:27344950 | T | C | 5 | a0009c0035 a0009c0037 a0009c0046 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
synonymous_variant | LOW | c.291T>C | p.Asp97Asp | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/11 | 489/3624 | 291/2478 | 97/825 | chr16 | 27344950 | |||
chr16:27346606 | C | T | 5 | a0001c0008 a0010c0024 a0014c0019 others(2): Show |
15 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(12): Show |
synonymous_variant | LOW | c.501C>T | p.Asn167Asn | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/11 | 699/3624 | 501/2478 | 167/825 | chr16 | 27346606 | |||
chr16:27352623 | A | C | 2 | a0009c0037 a0027c0036 |
2 | HG02145.hp2 HG03098.hp1 |
synonymous_variant | LOW | c.597A>C | p.Ala199Ala | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/11 | 795/3624 | 597/2478 | 199/825 | chr16 | 27352623 | |||
chr16:27355905 | C | G | 3 | a0005c0022 a0016c0018 a0017c0032 |
6 | HG00741.hp2 HG02451.hp1 HG02818.hp1 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.768C>G | p.Thr256Thr | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/11 | 966/3624 | 768/2478 | 256/825 | chr16 | 27355905 | |||
chr16:27362594 | G | T | 22 | a0003c0003 a0005c0005 a0005c0022 others(19): Show |
85 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(82): Show |
synonymous_variant | LOW | c.1242G>T | p.Leu414Leu | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1440/3624 | 1242/2478 | 414/825 | chr16 | 27362594 | |||
chr16:27362645 | C | T | 11 | a0006c0031 a0009c0035 a0009c0044 others(8): Show |
13 | HG00735.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
synonymous_variant | LOW | c.1293C>T | p.Cys431Cys | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1491/3624 | 1293/2478 | 431/825 | chr16 | 27362645 | |||
chr16:27362651 | T | C | 29 | a0003c0003 a0005c0005 a0005c0022 others(26): Show |
94 | HG00597.hp2 HG00639.hp2 HG00735.hp2 others(91): Show |
synonymous_variant | LOW | c.1299T>C | p.Leu433Leu | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1497/3624 | 1299/2478 | 433/825 | chr16 | 27362651 | |||
chr16:27363095 | G | A | 1 | a0026c0029 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.1743G>A | p.Ala581Ala | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1941/3624 | 1743/2478 | 581/825 | chr16 | 27363095 | |||
chr16:27363704 | C | T | 1 | a0012c0016 | 3 | HG01109.hp2 HG02895.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.2352C>T | p.Gly784Gly | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 2550/3624 | 2352/2478 | 784/825 | chr16 | 27363704 | |||
chr16:27363749 | T | C | 3 | a0006c0006 a0026c0029 a0027c0036 |
12 | HG02109.hp1 HG02145.hp2 HG02559.hp1 others(9): Show |
synonymous_variant | LOW | c.2397T>C | p.Pro799Pro | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 2595/3624 | 2397/2478 | 799/825 | chr16 | 27363749 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:27313979 | C | T | 2 | a0001c0008t0025 a0021c0045t0024 |
2 | HG00735.hp2 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-193C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/11 | 26225 | chr16 | 27313979 | ||||||
chr16:27363836 | T | C | 12 | a0004c0004t0003 a0008c0009t0007 a0008c0009t0016 others(9): Show |
36 | HG00408.hp1 HG01070.hp1 HG01952.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*6T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 6 | chr16 | 27363836 | ||||||
chr16:27363838 | T | C | 12 | a0006c0006t0006 a0006c0006t0008 a0008c0009t0007 others(9): Show |
27 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*8T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 8 | chr16 | 27363838 | ||||||
chr16:27363879 | C | T | 1 | a0009c0017t0012 | 3 | HG02572.hp2 HG02615.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*49C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 49 | chr16 | 27363879 | ||||||
chr16:27363918 | C | G | 2 | a0013c0011t0009 a0014c0019t0011 |
7 | HG02647.hp2 HG02738.hp1 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*88C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 88 | chr16 | 27363918 | ||||||
chr16:27363954 | T | A | 1 | a0008c0009t0016 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*124T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 124 | chr16 | 27363954 | ||||||
chr16:27364102 | G | A | 2 | a0017c0020t0010 a0017c0032t0010 |
3 | HG02055.hp1 HG02451.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*272G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 272 | chr16 | 27364102 | ||||||
chr16:27364112 | C | A | 1 | a0006c0006t0008 | 4 | HG03139.hp1 HG03471.hp1 NA19043.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*282C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 282 | chr16 | 27364112 | ||||||
chr16:27364129 | G | C | 2 | a0001c0008t0018 a0023c0043t0017 |
2 | HG01243.hp2 HG01891.hp2 |
3_prime_UTR_variant | MODIFIER | c.*299G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 299 | chr16 | 27364129 | ||||||
chr16:27364199 | TGCCCACC others(20): Show |
T | 1 | a0016c0018t0023 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*377_*403delAGATCA others(21): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 377 | INFO_REALIGN_3_PRIME | chr16 | 27364199 | |||||
chr16:27364221 | G | A | 19 | a0001c0001t0001 a0001c0008t0001 a0001c0008t0025 others(16): Show |
136 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*391G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 391 | chr16 | 27364221 | ||||||
chr16:27364235 | G | A | 1 | a0030c0030t0020 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*405G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 405 | chr16 | 27364235 | ||||||
chr16:27364280 | G | A | 1 | a0019c0023t0013 | 2 | HG02145.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*450G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 450 | chr16 | 27364280 | ||||||
chr16:27364466 | A | G | 19 | a0001c0001t0001 a0001c0008t0001 a0001c0008t0025 others(16): Show |
145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*636A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 636 | chr16 | 27364466 | ||||||
chr16:27364561 | T | C | 1 | a0001c0001t0021 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*731T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 731 | chr16 | 27364561 | ||||||
chr16:27364568 | C | T | 20 | a0006c0006t0006 a0006c0006t0008 a0006c0031t0005 others(17): Show |
40 | HG00741.hp2 HG01109.hp2 HG02258.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*738C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 738 | chr16 | 27364568 | ||||||
chr16:27364745 | A | G | 1 | a0007c0007t0022 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*915A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 915 | chr16 | 27364745 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:27314101 | C | T | 3 | a0010c0024t0004g0279 a0012c0016t0006g0029 a0012c0016t0006g0280 |
4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-152+81C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314101 | |||||||
chr16:27314105 | C | T | 1 | a0016c0018t0005g0278 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-152+85C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314105 | |||||||
chr16:27314194 | C | T | 5 | a0001c0001t0002g0275 a0002c0002t0001g0276 a0009c0017t0012g0274 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-152+174C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314194 | |||||||
chr16:27314200 | C | T | 1 | a0001c0001t0002g0272 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-152+180C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314200 | |||||||
chr16:27314313 | G | A | 2 | a0019c0023t0013g0030 a0019c0023t0013g0031 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-152+293G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314313 | |||||||
chr16:27314339 | G | GC | 5 | a0002c0002t0001g0032 a0002c0002t0002g0034 a0006c0031t0005g0036 others(2): Show |
5 | HG03225.hp1 HG03453.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.-152+323dupC | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27314339 | ||||||
chr16:27314446 | T | C | 8 | a0008c0009t0007g0008 a0008c0009t0007g0040 a0008c0009t0007g0041 others(5): Show |
9 | HG02258.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-152+426T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314446 | |||||||
chr16:27314452 | A | G | 1 | a0002c0002t0002g0271 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-152+432A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314452 | |||||||
chr16:27314534 | G | C | 1 | a0004c0004t0001g0009 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-152+514G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314534 | |||||||
chr16:27314610 | C | G | 1 | a0001c0008t0001g0270 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-152+590C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314610 | |||||||
chr16:27314662 | G | C | 1 | a0003c0003t0001g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-152+642G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314662 | |||||||
chr16:27314885 | A | C | 15 | a0001c0001t0001g0263 a0001c0001t0002g0261 a0001c0001t0002g0267 others(12): Show |
16 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.-152+865A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314885 | |||||||
chr16:27314947 | G | T | 139 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0236 others(136): Show |
164 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(161): Show |
intron_variant | MODIFIER | c.-152+927G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314947 | |||||||
chr16:27314958 | G | C | 2 | a0001c0008t0025g0168 a0021c0045t0024g0169 |
2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-152+938G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314958 | |||||||
chr16:27315448 | G | A | 1 | a0002c0002t0002g0170 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-152+1428G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315448 | |||||||
chr16:27315479 | G | A | 1 | a0001c0008t0025g0168 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-152+1459G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315479 | |||||||
chr16:27315521 | T | G | 152 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0236 others(149): Show |
178 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(175): Show |
intron_variant | MODIFIER | c.-152+1501T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315521 | |||||||
chr16:27315542 | C | T | 4 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0166 others(1): Show |
4 | NA18940.hp2 NA18964.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.-152+1522C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315542 | |||||||
chr16:27315592 | G | C | 2 | a0001c0001t0002g0052 a0001c0001t0002g0053 |
2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-152+1572G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315592 | |||||||
chr16:27315612 | G | C | 1 | a0023c0043t0017g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-152+1592G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315612 | |||||||
chr16:27315743 | C | G | 1 | a0002c0002t0002g0254 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-152+1723C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315743 | |||||||
chr16:27315795 | A | G | 97 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0236 others(94): Show |
118 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.-152+1775A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315795 | |||||||
chr16:27315871 | A | G | 8 | a0008c0009t0007g0008 a0008c0009t0007g0040 a0008c0009t0007g0041 others(5): Show |
9 | HG02258.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-152+1851A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315871 | |||||||
chr16:27315880 | G | A | 2 | a0002c0002t0001g0181 a0002c0002t0001g0182 |
2 | HG00741.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-152+1860G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315880 | |||||||
chr16:27315893 | T | G | 150 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0236 others(147): Show |
176 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(173): Show |
intron_variant | MODIFIER | c.-152+1873T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315893 | |||||||
chr16:27315914 | G | C | 2 | a0002c0002t0001g0183 a0002c0002t0001g0184 |
2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-152+1894G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315914 | |||||||
chr16:27315938 | T | C | 2 | a0009c0035t0005g0038 a0009c0046t0005g0037 |
2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-152+1918T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315938 | |||||||
chr16:27315994 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-152+1974G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315994 | |||||||
chr16:27316096 | G | A | 2 | a0005c0005t0002g0257 a0005c0005t0002g0258 |
2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-152+2076G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316096 | |||||||
chr16:27316300 | G | A | 1 | a0010c0024t0005g0171 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-152+2280G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316300 | |||||||
chr16:27316424 | A | G | 1 | a0006c0006t0006g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-152+2404A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316424 | |||||||
chr16:27316624 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-152+2604A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316624 | |||||||
chr16:27316633 | C | A | 1 | a0003c0003t0001g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-152+2613C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316633 | |||||||
chr16:27316683 | C | T | 1 | a0002c0002t0001g0252 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-152+2663C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316683 | |||||||
chr16:27316851 | C | A | 4 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0055 others(1): Show |
4 | HG02258.hp2 HG02615.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-152+2831C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316851 | |||||||
chr16:27316906 | C | CTT | 141 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0001g0263 others(138): Show |
167 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(164): Show |
intron_variant | MODIFIER | c.-152+2899_-152+290 others(6): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27316906 | ||||||
chr16:27316967 | A | G | 1 | a0003c0003t0001g0162 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-152+2947A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316967 | |||||||
chr16:27317045 | AGGTGTGT others(9): Show |
A | 1 | a0001c0008t0018g0259 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-152+3027_-152+304 others(20): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27317045 | ||||||
chr16:27317222 | C | T | 39 | a0001c0001t0001g0263 a0001c0001t0002g0261 a0001c0001t0002g0267 others(36): Show |
42 | HG00735.hp2 HG01081.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.-152+3202C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317222 | |||||||
chr16:27317228 | C | T | 8 | a0008c0009t0007g0008 a0008c0009t0007g0040 a0008c0009t0007g0041 others(5): Show |
9 | HG02258.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-152+3208C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317228 | |||||||
chr16:27317502 | G | A | 4 | a0001c0001t0001g0056 a0005c0005t0001g0010 a0005c0005t0001g0011 others(1): Show |
6 | HG01069.hp2 HG01175.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-152+3482G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317502 | |||||||
chr16:27317551 | C | T | 3 | a0010c0024t0004g0279 a0012c0016t0006g0029 a0012c0016t0006g0280 |
4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-152+3531C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317551 | |||||||
chr16:27317552 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-152+3532G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317552 | |||||||
chr16:27317604 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-152+3584C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317604 | |||||||
chr16:27317625 | A | G | 1 | a0003c0003t0001g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-152+3605A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317625 | |||||||
chr16:27317642 | G | A | 2 | a0016c0018t0005g0174 a0016c0018t0023g0173 |
2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-152+3622G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317642 | |||||||
chr16:27317682 | G | C | 3 | a0003c0003t0002g0058 a0003c0003t0002g0059 a0003c0003t0002g0060 |
3 | HG01074.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-152+3662G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317682 | |||||||
chr16:27317732 | C | T | 1 | a0013c0011t0009g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-152+3712C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317732 | |||||||
chr16:27317757 | T | C | 5 | a0010c0024t0004g0279 a0012c0016t0006g0029 a0012c0016t0006g0280 others(2): Show |
6 | HG00741.hp2 HG01109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-152+3737T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317757 | |||||||
chr16:27317797 | G | A | 253 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(250): Show |
295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.-152+3777G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317797 | |||||||
chr16:27317812 | A | G | 3 | a0004c0004t0001g0133 a0004c0004t0001g0135 a0004c0004t0003g0134 |
3 | HG03669.hp1 HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-152+3792A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317812 | |||||||
chr16:27318247 | C | T | 1 | a0001c0001t0002g0132 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-152+4227C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27318247 | |||||||
chr16:27318307 | ATGTC | A | 3 | a0002c0002t0002g0034 a0011c0010t0004g0033 a0011c0010t0004g0035 |
3 | HG03453.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-152+4290_-152+429 others(8): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27318307 | ||||||
chr16:27318447 | G | GAA | 101 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0002g0190 others(98): Show |
123 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.-152+4428_-152+442 others(6): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27318447 | ||||||
chr16:27318555 | C | T | 4 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0055 others(1): Show |
4 | HG02258.hp2 HG02615.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-152+4535C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27318555 | |||||||
chr16:27318638 | C | T | 1 | a0001c0008t0018g0259 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-152+4618C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27318638 | |||||||
chr16:27318725 | C | T | 1 | a0023c0043t0017g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-152+4705C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27318725 | |||||||
chr16:27318863 | G | A | 1 | a0003c0003t0001g0136 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-152+4843G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27318863 | |||||||
chr16:27319488 | G | C | 3 | a0003c0003t0001g0172 a0003c0003t0001g0180 a0011c0010t0004g0179 |
3 | HG02486.hp2 HG02572.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-152+5468G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27319488 | |||||||
chr16:27319573 | C | T | 3 | a0010c0024t0004g0279 a0012c0016t0006g0029 a0012c0016t0006g0280 |
4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-152+5553C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27319573 | |||||||
chr16:27319613 | A | T | 4 | a0001c0001t0002g0275 a0002c0002t0001g0276 a0009c0017t0012g0274 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-152+5593A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27319613 | |||||||
chr16:27319616 | A | G | 5 | a0010c0024t0004g0279 a0012c0016t0006g0029 a0012c0016t0006g0280 others(2): Show |
6 | HG00741.hp2 HG01109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-152+5596A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27319616 | |||||||
chr16:27319709 | G | A | 86 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0002g0190 others(83): Show |
107 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.-152+5689G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27319709 | |||||||
chr16:27319846 | C | T | 3 | a0001c0001t0002g0129 a0001c0001t0002g0130 a0001c0001t0002g0131 |
3 | HG02040.hp2 NA19081.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-152+5826C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27319846 | |||||||
chr16:27319926 | A | G | 2 | a0002c0002t0001g0276 a0012c0042t0007g0277 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-152+5906A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27319926 | |||||||
chr16:27320175 | G | A | 2 | a0002c0002t0001g0183 a0002c0002t0001g0184 |
2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-152+6155G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320175 | |||||||
chr16:27320393 | C | T | 2 | a0009c0037t0001g0050 a0027c0036t0014g0051 |
2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-152+6373C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320393 | |||||||
chr16:27320476 | C | G | 1 | a0002c0002t0001g0246 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-152+6456C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320476 | |||||||
chr16:27320573 | A | G | 152 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0001g0263 others(149): Show |
178 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(175): Show |
intron_variant | MODIFIER | c.-152+6553A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320573 | |||||||
chr16:27320593 | T | G | 2 | a0013c0011t0009g0020 a0013c0011t0009g0178 |
3 | HG02647.hp2 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-152+6573T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320593 | |||||||
chr16:27320653 | C | G | 152 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0001g0263 others(149): Show |
178 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(175): Show |
intron_variant | MODIFIER | c.-152+6633C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320653 | |||||||
chr16:27320676 | C | T | 1 | a0006c0006t0006g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-152+6656C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320676 | |||||||
chr16:27320852 | T | C | 1 | a0002c0002t0001g0187 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-152+6832T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320852 | |||||||
chr16:27320948 | C | CT | 115 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0002g0129 others(112): Show |
138 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.-152+6941dupT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27320948 | ||||||
chr16:27321005 | G | A | 1 | a0009c0037t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-152+6985G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321005 | |||||||
chr16:27321013 | A | G | 152 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0001g0263 others(149): Show |
178 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(175): Show |
intron_variant | MODIFIER | c.-152+6993A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321013 | |||||||
chr16:27321175 | C | A | 1 | a0010c0024t0004g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-152+7155C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321175 | |||||||
chr16:27321186 | C | T | 3 | a0002c0002t0001g0027 a0002c0002t0001g0185 a0002c0002t0001g0245 |
4 | HG03017.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-152+7166C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321186 | |||||||
chr16:27321190 | C | T | 2 | a0002c0002t0002g0127 a0003c0003t0002g0126 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-152+7170C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321190 | |||||||
chr16:27321290 | T | G | 2 | a0019c0023t0013g0030 a0019c0023t0013g0031 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-152+7270T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321290 | |||||||
chr16:27321337 | T | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | NA18950.hp1 NA19003.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-152+7317T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321337 | |||||||
chr16:27321820 | A | C | 1 | a0025c0048t0002g0125 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-152+7800A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321820 | |||||||
chr16:27322060 | A | C | 24 | a0001c0001t0001g0263 a0001c0001t0002g0261 a0001c0001t0002g0267 others(21): Show |
26 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.-151-8006A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322060 | |||||||
chr16:27322086 | T | C | 6 | a0001c0001t0002g0275 a0002c0002t0001g0276 a0009c0017t0012g0274 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-151-7980T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322086 | |||||||
chr16:27322103 | G | GT | 127 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0001g0263 others(124): Show |
151 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(148): Show |
intron_variant | MODIFIER | c.-151-7950dupT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27322103 | ||||||
chr16:27322103 | G | GTT | 19 | a0001c0001t0002g0275 a0002c0002t0001g0242 a0002c0002t0001g0276 others(16): Show |
20 | HG00438.hp2 HG00741.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.-151-7951_-151-795 others(6): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27322103 | ||||||
chr16:27322212 | T | G | 2 | a0008c0009t0007g0040 a0008c0047t0007g0039 |
2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-151-7854T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322212 | |||||||
chr16:27322333 | C | T | 3 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0002c0002t0001g0241 |
3 | HG00280.hp2 HG01109.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-151-7733C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322333 | |||||||
chr16:27322334 | G | A | 2 | a0019c0023t0013g0030 a0019c0023t0013g0031 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-151-7732G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322334 | |||||||
chr16:27322343 | A | C | 1 | a0017c0020t0010g0238 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-151-7723A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322343 | |||||||
chr16:27322618 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-151-7448G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322618 | |||||||
chr16:27322702 | A | G | 1 | a0016c0018t0005g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-151-7364A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322702 | |||||||
chr16:27322750 | A | C | 3 | a0010c0012t0004g0049 a0013c0011t0009g0048 a0023c0043t0017g0045 |
3 | HG01243.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-151-7316A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322750 | |||||||
chr16:27322852 | A | C | 4 | a0009c0017t0012g0175 a0009c0017t0012g0176 a0011c0010t0004g0046 others(1): Show |
4 | HG02572.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-151-7214A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322852 | |||||||
chr16:27322927 | C | T | 1 | a0020c0021t0002g0016 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-151-7139C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322927 | |||||||
chr16:27322968 | A | C | 2 | a0010c0012t0004g0049 a0013c0011t0009g0048 |
2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-151-7098A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322968 | |||||||
chr16:27323084 | C | T | 3 | a0003c0003t0001g0172 a0003c0003t0001g0180 a0011c0010t0004g0179 |
3 | HG02486.hp2 HG02572.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-151-6982C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323084 | |||||||
chr16:27323209 | C | T | 1 | a0002c0002t0001g0237 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-151-6857C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323209 | |||||||
chr16:27323249 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0236 |
4 | HG00673.hp1 NA18956.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.-151-6817A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323249 | |||||||
chr16:27323309 | C | A | 1 | a0023c0043t0017g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-151-6757C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323309 | |||||||
chr16:27323386 | C | T | 1 | a0030c0030t0020g0235 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-151-6680C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323386 | |||||||
chr16:27323414 | AAG | A | 8 | a0008c0009t0007g0008 a0008c0009t0007g0040 a0008c0009t0007g0041 others(5): Show |
9 | HG02258.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-151-6649_-151-664 others(6): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27323414 | ||||||
chr16:27323457 | C | T | 2 | a0003c0003t0001g0159 a0003c0003t0001g0160 |
2 | NA18957.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.-151-6609C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323457 | |||||||
chr16:27323642 | G | C | 2 | a0002c0002t0001g0022 a0031c0025t0001g0022 |
2 | HG00735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-151-6424G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323642 | |||||||
chr16:27323681 | G | C | 20 | a0001c0001t0001g0263 a0001c0001t0002g0261 a0001c0001t0002g0267 others(17): Show |
22 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-151-6385G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323681 | |||||||
chr16:27323690 | C | T | 11 | a0002c0002t0002g0233 a0003c0003t0001g0232 a0004c0004t0001g0230 others(8): Show |
14 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-151-6376C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323690 | |||||||
chr16:27323801 | A | G | 1 | a0008c0009t0007g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-151-6265A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323801 | |||||||
chr16:27323847 | C | T | 1 | a0002c0002t0001g0229 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-151-6219C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323847 | |||||||
chr16:27323951 | G | A | 2 | a0010c0012t0004g0012 a0010c0012t0004g0065 |
3 | HG02922.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-151-6115G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323951 | |||||||
chr16:27324277 | T | TG | 109 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0002g0190 others(106): Show |
132 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.-151-5787dupG | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27324277 | ||||||
chr16:27324316 | C | T | 1 | a0002c0002t0002g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-151-5750C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27324316 | |||||||
chr16:27324357 | G | A | 1 | a0010c0024t0004g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-151-5709G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27324357 | |||||||
chr16:27324801 | G | A | 4 | a0009c0017t0012g0175 a0009c0017t0012g0176 a0009c0037t0001g0050 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-151-5265G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27324801 | |||||||
chr16:27324841 | G | A | 3 | a0010c0024t0004g0279 a0012c0016t0006g0029 a0012c0016t0006g0280 |
4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-151-5225G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27324841 | |||||||
chr16:27325106 | G | A | 116 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0002g0190 others(113): Show |
138 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.-151-4960G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325106 | |||||||
chr16:27325116 | C | T | 133 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0002g0190 others(130): Show |
157 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.-151-4950C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325116 | |||||||
chr16:27325232 | G | A | 1 | a0023c0043t0017g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-151-4834G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325232 | |||||||
chr16:27325241 | T | C | 5 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0004c0004t0003g0066 others(2): Show |
5 | NA18949.hp1 NA18975.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.-151-4825T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325241 | |||||||
chr16:27325284 | A | G | 2 | a0010c0012t0004g0049 a0013c0011t0009g0048 |
2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-151-4782A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325284 | |||||||
chr16:27325312 | C | T | 1 | a0001c0001t0002g0132 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-151-4754C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325312 | |||||||
chr16:27325328 | T | C | 1 | a0014c0041t0005g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-151-4738T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325328 | |||||||
chr16:27325407 | G | A | 3 | a0010c0012t0004g0049 a0013c0011t0009g0048 a0023c0043t0017g0045 |
3 | HG01243.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-151-4659G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325407 | |||||||
chr16:27325417 | C | CA | 7 | a0010c0012t0004g0049 a0010c0024t0004g0279 a0012c0016t0006g0029 others(4): Show |
8 | HG01109.hp2 HG01243.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-151-4642dupA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27325417 | ||||||
chr16:27325573 | CA | C | 14 | a0002c0002t0001g0226 a0002c0002t0001g0227 a0003c0003t0001g0044 others(11): Show |
15 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.-151-4480delA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27325573 | ||||||
chr16:27325715 | A | G | 1 | a0003c0003t0001g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-151-4351A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325715 | |||||||
chr16:27326274 | T | C | 2 | a0016c0018t0005g0174 a0016c0018t0023g0173 |
2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-151-3792T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326274 | |||||||
chr16:27326329 | A | G | 2 | a0010c0012t0004g0049 a0013c0011t0009g0048 |
2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-151-3737A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326329 | |||||||
chr16:27326401 | G | A | 20 | a0001c0001t0002g0071 a0002c0002t0001g0005 a0002c0002t0001g0193 others(17): Show |
22 | HG00438.hp2 HG01070.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.-151-3665G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326401 | |||||||
chr16:27326527 | A | G | 1 | a0014c0041t0005g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-151-3539A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326527 | |||||||
chr16:27326594 | A | G | 1 | a0003c0003t0001g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-151-3472A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326594 | |||||||
chr16:27326615 | G | A | 18 | a0001c0001t0002g0275 a0002c0002t0001g0276 a0003c0003t0001g0044 others(15): Show |
19 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-151-3451G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326615 | |||||||
chr16:27326647 | G | T | 2 | a0011c0010t0004g0046 a0011c0010t0004g0047 |
2 | HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-151-3419G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326647 | |||||||
chr16:27326648 | A | C | 1 | a0001c0001t0002g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-151-3418A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326648 | |||||||
chr16:27326648 | A | T | 2 | a0011c0010t0004g0046 a0011c0010t0004g0047 |
2 | HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-151-3418A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326648 | |||||||
chr16:27326649 | G | A | 2 | a0011c0010t0004g0046 a0011c0010t0004g0047 |
2 | HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-151-3417G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326649 | |||||||
chr16:27326650 | A | G | 2 | a0011c0010t0004g0046 a0011c0010t0004g0047 |
2 | HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-151-3416A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326650 | |||||||
chr16:27326728 | C | A | 8 | a0002c0002t0002g0127 a0003c0003t0002g0126 a0008c0009t0007g0008 others(5): Show |
9 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-151-3338C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326728 | |||||||
chr16:27326759 | G | A | 2 | a0016c0018t0005g0174 a0016c0018t0023g0173 |
2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-151-3307G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326759 | |||||||
chr16:27326811 | T | C | 2 | a0016c0018t0005g0174 a0016c0018t0023g0173 |
2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-151-3255T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326811 | |||||||
chr16:27327106 | G | A | 2 | a0019c0023t0013g0030 a0019c0023t0013g0031 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-151-2960G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327106 | |||||||
chr16:27327125 | C | T | 3 | a0003c0003t0001g0044 a0016c0018t0005g0174 a0016c0018t0023g0173 |
3 | HG00741.hp2 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-151-2941C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327125 | |||||||
chr16:27327309 | C | T | 8 | a0002c0002t0002g0127 a0003c0003t0002g0126 a0008c0009t0007g0008 others(5): Show |
9 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-151-2757C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327309 | |||||||
chr16:27327316 | T | C | 1 | a0023c0043t0017g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-151-2750T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327316 | |||||||
chr16:27327343 | G | A | 2 | a0002c0002t0001g0207 a0002c0002t0001g0226 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-151-2723G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327343 | |||||||
chr16:27327429 | A | T | 1 | a0001c0001t0002g0124 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-151-2637A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327429 | |||||||
chr16:27327444 | A | C | 6 | a0008c0009t0007g0008 a0008c0009t0007g0040 a0008c0009t0007g0041 others(3): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-151-2622A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327444 | |||||||
chr16:27327508 | G | A | 1 | a0002c0002t0002g0072 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-151-2558G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327508 | |||||||
chr16:27327636 | T | G | 2 | a0002c0002t0002g0137 a0002c0002t0002g0138 |
2 | NA19005.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-151-2430T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327636 | |||||||
chr16:27327703 | T | C | 97 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(94): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.-151-2363T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327703 | |||||||
chr16:27327706 | T | C | 99 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(96): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.-151-2360T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327706 | |||||||
chr16:27327794 | G | A | 3 | a0002c0002t0002g0034 a0011c0010t0004g0033 a0011c0010t0004g0035 |
3 | HG03453.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-151-2272G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327794 | |||||||
chr16:27327799 | G | A | 2 | a0016c0018t0005g0174 a0016c0018t0023g0173 |
2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-151-2267G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327799 | |||||||
chr16:27327824 | T | C | 92 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(89): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.-151-2242T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327824 | |||||||
chr16:27327936 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0073 |
3 | HG00621.hp1 HG00673.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-151-2130G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327936 | |||||||
chr16:27327968 | A | G | 1 | a0018c0015t0001g0119 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-151-2098A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327968 | |||||||
chr16:27327986 | C | G | 2 | a0016c0018t0005g0174 a0016c0018t0023g0173 |
2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-151-2080C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327986 | |||||||
chr16:27328136 | C | T | 4 | a0003c0003t0001g0044 a0011c0010t0004g0035 a0016c0018t0005g0174 others(1): Show |
4 | HG00741.hp2 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-151-1930C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328136 | |||||||
chr16:27328137 | G | A | 1 | a0001c0001t0002g0074 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-151-1929G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328137 | |||||||
chr16:27328190 | A | G | 8 | a0002c0002t0002g0127 a0003c0003t0002g0126 a0008c0009t0007g0008 others(5): Show |
9 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-151-1876A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328190 | |||||||
chr16:27328194 | A | G | 1 | a0010c0024t0005g0171 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-151-1872A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328194 | |||||||
chr16:27328205 | C | CAAAAAAA others(2): Show |
17 | a0001c0001t0002g0003 a0001c0001t0002g0014 a0001c0001t0002g0052 others(14): Show |
21 | HG00408.hp2 HG00558.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.-151-1851_-151-184 others(13): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27328205 | ||||||
chr16:27328205 | C | CAAAAAAA others(3): Show |
58 | a0001c0001t0001g0056 a0001c0001t0001g0061 a0001c0001t0001g0062 others(55): Show |
68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.-151-1852_-151-184 others(14): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27328205 | ||||||
chr16:27328205 | C | CAAAAAAA others(4): Show |
14 | a0001c0001t0001g0013 a0001c0001t0001g0083 a0001c0001t0001g0163 others(11): Show |
16 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.-151-1853_-151-184 others(15): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27328205 | ||||||
chr16:27328205 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0073 a0001c0001t0002g0075 |
2 | HG01346.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-151-1854_-151-184 others(16): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27328205 | ||||||
chr16:27328205 | C | CAAAAAAA others(6): Show |
2 | a0016c0018t0005g0174 a0016c0018t0023g0173 |
2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-151-1855_-151-184 others(17): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27328205 | ||||||
chr16:27328205 | C | CAAAAAAA others(8): Show |
3 | a0003c0003t0001g0044 a0009c0037t0001g0050 a0027c0036t0014g0051 |
3 | HG02145.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-151-1857_-151-184 others(19): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27328205 | ||||||
chr16:27328205 | CAA | C | 9 | a0001c0001t0002g0275 a0002c0002t0001g0276 a0009c0017t0012g0175 others(6): Show |
9 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-151-1844_-151-184 others(6): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27328205 | ||||||
chr16:27328224 | G | A | 20 | a0001c0001t0002g0003 a0001c0001t0002g0014 a0001c0001t0002g0052 others(17): Show |
24 | HG00408.hp2 HG00558.hp2 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-151-1842G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328224 | |||||||
chr16:27328253 | T | C | 2 | a0016c0018t0005g0174 a0016c0018t0023g0173 |
2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-151-1813T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328253 | |||||||
chr16:27328347 | G | A | 1 | a0002c0002t0001g0187 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-151-1719G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328347 | |||||||
chr16:27328348 | A | G | 1 | a0001c0001t0002g0093 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-151-1718A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328348 | |||||||
chr16:27328412 | C | T | 1 | a0003c0003t0001g0160 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-151-1654C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328412 | |||||||
chr16:27328441 | T | G | 151 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(148): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-151-1625T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328441 | |||||||
chr16:27328652 | G | C | 2 | a0007c0007t0001g0023 a0007c0007t0002g0188 |
3 | NA18954.hp2 NA18986.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-151-1414G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328652 | |||||||
chr16:27328943 | A | G | 2 | a0001c0001t0002g0014 a0001c0001t0002g0092 |
3 | HG02280.hp2 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-151-1123A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328943 | |||||||
chr16:27328982 | C | T | 1 | a0002c0002t0001g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-151-1084C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328982 | |||||||
chr16:27329043 | G | A | 2 | a0002c0002t0002g0072 a0002c0002t0002g0077 |
2 | HG00609.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.-151-1023G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329043 | |||||||
chr16:27329054 | C | T | 3 | a0010c0012t0004g0012 a0010c0012t0004g0049 a0010c0012t0004g0065 |
4 | HG02922.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-151-1012C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329054 | |||||||
chr16:27329349 | T | G | 2 | a0009c0037t0001g0050 a0027c0036t0014g0051 |
2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-151-717T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329349 | |||||||
chr16:27329414 | T | C | 105 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(102): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.-151-652T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329414 | |||||||
chr16:27329633 | C | G | 1 | a0010c0034t0005g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-151-433C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329633 | |||||||
chr16:27329676 | C | CA | 90 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0062 others(87): Show |
106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.-151-373dupA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27329676 | ||||||
chr16:27329676 | C | CAA | 9 | a0001c0001t0001g0061 a0001c0001t0002g0014 a0001c0001t0002g0052 others(6): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-151-374_-151-373d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27329676 | ||||||
chr16:27329676 | CA | C | 32 | a0001c0001t0001g0263 a0001c0001t0002g0261 a0001c0001t0002g0267 others(29): Show |
35 | HG00639.hp1 HG01081.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.-151-373delA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27329676 | ||||||
chr16:27329738 | A | G | 96 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(93): Show |
112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.-151-328A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329738 | |||||||
chr16:27329833 | C | A | 1 | a0003c0003t0001g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-151-233C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329833 | |||||||
chr16:27329836 | T | C | 1 | a0010c0034t0005g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-151-230T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329836 | |||||||
chr16:27329869 | TG | T | 3 | a0001c0001t0002g0064 a0001c0001t0002g0095 a0024c0038t0002g0139 |
3 | HG01952.hp2 HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-151-196delG | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329869 | |||||||
chr16:27329899 | T | A | 1 | a0006c0006t0006g0209 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-151-167T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329899 | |||||||
chr16:27330021 | T | C | 6 | a0001c0001t0002g0275 a0009c0017t0012g0175 a0009c0017t0012g0176 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-151-45T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27330021 | |||||||
chr16:27330027 | C | A | 1 | a0006c0006t0006g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-151-39C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27330027 | |||||||
chr16:27330214 | C | T | 3 | a0016c0018t0005g0174 a0016c0018t0023g0173 a0020c0021t0002g0016 |
4 | HG00741.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+16C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27330214 | |||||||
chr16:27330232 | T | C | 111 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(108): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.-19+34T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27330232 | |||||||
chr16:27330280 | G | C | 1 | a0003c0003t0001g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-19+82G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27330280 | |||||||
chr16:27330386 | C | CA | 129 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(126): Show |
148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-19+202dupA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27330386 | ||||||
chr16:27330449 | G | A | 1 | a0010c0034t0005g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-19+251G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27330449 | |||||||
chr16:27330457 | C | T | 2 | a0002c0002t0001g0183 a0002c0002t0001g0184 |
2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-19+259C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27330457 | |||||||
chr16:27330497 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-19+299C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27330497 | |||||||
chr16:27330657 | T | C | 3 | a0010c0024t0004g0279 a0012c0016t0006g0029 a0012c0016t0006g0280 |
4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+459T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27330657 | |||||||
chr16:27331055 | CA | C | 19 | a0001c0001t0001g0263 a0001c0001t0002g0261 a0001c0001t0002g0267 others(16): Show |
21 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-19+858delA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331055 | |||||||
chr16:27331058 | A | G | 19 | a0001c0001t0001g0263 a0001c0001t0002g0261 a0001c0001t0002g0267 others(16): Show |
21 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-19+860A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331058 | |||||||
chr16:27331060 | T | C | 19 | a0001c0001t0001g0263 a0001c0001t0002g0261 a0001c0001t0002g0267 others(16): Show |
21 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-19+862T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331060 | |||||||
chr16:27331087 | C | T | 1 | a0010c0024t0005g0171 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-19+889C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331087 | |||||||
chr16:27331227 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-19+1029G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331227 | |||||||
chr16:27331275 | T | A | 110 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(107): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.-19+1077T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331275 | |||||||
chr16:27331294 | T | C | 1 | a0002c0002t0001g0276 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+1096T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331294 | |||||||
chr16:27331371 | A | G | 6 | a0001c0001t0002g0275 a0009c0017t0012g0175 a0009c0017t0012g0176 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+1173A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331371 | |||||||
chr16:27331411 | G | A | 3 | a0010c0024t0004g0279 a0012c0016t0006g0029 a0012c0016t0006g0280 |
4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+1213G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331411 | |||||||
chr16:27331422 | AAAT | A | 12 | a0001c0001t0002g0015 a0001c0001t0002g0082 a0001c0001t0002g0112 others(9): Show |
12 | HG02155.hp2 NA18747.hp1 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19+1229_-19+1231d others(5): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27331422 | ||||||
chr16:27331441 | A | G | 1 | a0002c0002t0001g0208 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-19+1243A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331441 | |||||||
chr16:27331558 | C | T | 32 | a0001c0001t0002g0003 a0001c0001t0002g0014 a0001c0001t0002g0052 others(29): Show |
38 | HG00408.hp2 HG00558.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.-19+1360C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331558 | |||||||
chr16:27331692 | A | G | 1 | a0021c0045t0024g0169 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-19+1494A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331692 | |||||||
chr16:27331717 | C | G | 1 | a0001c0008t0018g0259 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-19+1519C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331717 | |||||||
chr16:27332097 | C | T | 1 | a0002c0002t0002g0072 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-19+1899C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332097 | |||||||
chr16:27332158 | A | G | 77 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(74): Show |
89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.-19+1960A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332158 | |||||||
chr16:27332194 | T | C | 107 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(104): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.-19+1996T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332194 | |||||||
chr16:27332214 | A | G | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | NA18949.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.-19+2016A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332214 | |||||||
chr16:27332256 | A | G | 1 | a0009c0037t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-19+2058A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332256 | |||||||
chr16:27332304 | C | A | 1 | a0009c0017t0012g0274 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-19+2106C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332304 | |||||||
chr16:27332393 | A | G | 12 | a0001c0001t0002g0015 a0001c0001t0002g0082 a0001c0001t0002g0112 others(9): Show |
12 | HG02155.hp2 NA18747.hp1 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19+2195A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332393 | |||||||
chr16:27332427 | G | A | 1 | a0010c0034t0005g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-19+2229G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332427 | |||||||
chr16:27332577 | G | A | 1 | a0002c0002t0002g0254 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-19+2379G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332577 | |||||||
chr16:27332642 | T | C | 75 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(72): Show |
87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.-19+2444T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332642 | |||||||
chr16:27332680 | A | G | 1 | a0004c0004t0001g0135 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-19+2482A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332680 | |||||||
chr16:27332685 | C | T | 8 | a0003c0003t0001g0152 a0003c0003t0001g0153 a0003c0003t0001g0154 others(5): Show |
8 | HG02071.hp1 NA18954.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+2487C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332685 | |||||||
chr16:27332780 | T | C | 2 | a0009c0037t0001g0050 a0027c0036t0014g0051 |
2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-19+2582T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332780 | |||||||
chr16:27332794 | T | C | 32 | a0001c0001t0002g0003 a0001c0001t0002g0014 a0001c0001t0002g0052 others(29): Show |
38 | HG00408.hp2 HG00558.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.-19+2596T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332794 | |||||||
chr16:27332838 | C | T | 1 | a0001c0001t0002g0111 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-19+2640C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332838 | |||||||
chr16:27332878 | T | G | 58 | a0001c0001t0001g0263 a0001c0001t0002g0003 a0001c0001t0002g0014 others(55): Show |
67 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.-19+2680T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332878 | |||||||
chr16:27332956 | C | G | 1 | a0010c0024t0004g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-19+2758C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332956 | |||||||
chr16:27332956 | C | T | 2 | a0002c0002t0002g0127 a0003c0003t0002g0126 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-19+2758C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332956 | |||||||
chr16:27333100 | T | A | 3 | a0010c0024t0005g0171 a0019c0023t0013g0030 a0019c0023t0013g0031 |
3 | HG02145.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+2902T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333100 | |||||||
chr16:27333199 | C | CTT | 28 | a0001c0001t0002g0003 a0001c0001t0002g0014 a0001c0001t0002g0052 others(25): Show |
33 | HG00408.hp2 HG00558.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.-19+3013_-19+3014d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27333199 | ||||||
chr16:27333311 | G | A | 2 | a0009c0037t0001g0050 a0027c0036t0014g0051 |
2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-19+3113G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333311 | |||||||
chr16:27333373 | C | T | 2 | a0001c0008t0025g0168 a0021c0045t0024g0169 |
2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-19+3175C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333373 | |||||||
chr16:27333793 | A | G | 145 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(142): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.-19+3595A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333793 | |||||||
chr16:27333800 | T | C | 21 | a0001c0001t0002g0003 a0001c0001t0002g0014 a0001c0001t0002g0052 others(18): Show |
25 | HG00408.hp2 HG00558.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.-19+3602T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333800 | |||||||
chr16:27333888 | CT | C | 107 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(104): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.-19+3702delT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27333888 | ||||||
chr16:27333896 | T | C | 3 | a0010c0024t0004g0279 a0012c0016t0006g0029 a0012c0016t0006g0280 |
4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+3698T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333896 | |||||||
chr16:27333909 | G | C | 11 | a0001c0001t0002g0275 a0003c0003t0001g0044 a0009c0017t0012g0175 others(8): Show |
12 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-19+3711G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333909 | |||||||
chr16:27334031 | C | T | 64 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(61): Show |
75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.-19+3833C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27334031 | |||||||
chr16:27334034 | C | T | 1 | a0016c0018t0005g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-19+3836C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27334034 | |||||||
chr16:27334150 | G | C | 2 | a0009c0035t0005g0038 a0009c0046t0005g0037 |
2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-19+3952G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27334150 | |||||||
chr16:27334161 | C | T | 1 | a0006c0006t0006g0234 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-19+3963C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27334161 | |||||||
chr16:27334378 | A | G | 1 | a0001c0008t0018g0259 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-19+4180A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27334378 | |||||||
chr16:27334390 | C | T | 2 | a0002c0002t0002g0137 a0002c0002t0002g0138 |
2 | NA19005.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-19+4192C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27334390 | |||||||
chr16:27334418 | G | A | 3 | a0010c0012t0004g0012 a0010c0012t0004g0049 a0010c0012t0004g0065 |
4 | HG02922.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+4220G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27334418 | |||||||
chr16:27335033 | T | C | 160 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(157): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.-19+4835T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27335033 | |||||||
chr16:27335054 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-19+4856G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27335054 | |||||||
chr16:27335266 | G | A | 1 | a0001c0001t0002g0261 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-18-4920G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27335266 | |||||||
chr16:27335271 | T | C | 2 | a0001c0008t0025g0168 a0021c0045t0024g0169 |
2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-18-4915T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27335271 | |||||||
chr16:27335477 | C | G | 1 | a0018c0015t0001g0119 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-18-4709C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27335477 | |||||||
chr16:27335918 | G | A | 1 | a0005c0022t0001g0021 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-18-4268G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27335918 | |||||||
chr16:27336011 | A | G | 2 | a0013c0011t0009g0020 a0013c0011t0009g0178 |
3 | HG02647.hp2 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-18-4175A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336011 | |||||||
chr16:27336079 | G | A | 1 | a0004c0004t0001g0009 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-18-4107G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336079 | |||||||
chr16:27336152 | A | G | 1 | a0002c0002t0001g0223 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-18-4034A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336152 | |||||||
chr16:27336194 | G | A | 1 | a0003c0003t0001g0152 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-18-3992G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336194 | |||||||
chr16:27336207 | C | T | 3 | a0010c0024t0004g0279 a0012c0016t0006g0029 a0012c0016t0006g0280 |
4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-3979C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336207 | |||||||
chr16:27336298 | G | A | 5 | a0004c0004t0001g0230 a0013c0011t0009g0020 a0013c0011t0009g0048 others(2): Show |
6 | HG01243.hp2 HG01496.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-3888G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336298 | |||||||
chr16:27336324 | A | G | 4 | a0011c0010t0004g0046 a0011c0010t0004g0047 a0014c0041t0005g0228 others(1): Show |
4 | HG03041.hp2 NA19043.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-3862A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336324 | |||||||
chr16:27336659 | CAG | C | 3 | a0002c0002t0002g0206 a0002c0002t0002g0254 a0003c0003t0001g0205 |
3 | HG01358.hp1 HG01928.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-18-3524_-18-3523d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27336659 | ||||||
chr16:27336676 | C | CA | 6 | a0001c0001t0001g0061 a0001c0001t0002g0085 a0001c0001t0002g0086 others(3): Show |
6 | HG03239.hp2 HG04228.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-3490dupA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27336676 | ||||||
chr16:27336676 | CA | C | 41 | a0001c0001t0001g0263 a0001c0001t0002g0068 a0001c0001t0002g0071 others(38): Show |
44 | HG00642.hp2 HG01070.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.-18-3490delA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27336676 | ||||||
chr16:27336676 | CAA | C | 15 | a0001c0001t0002g0275 a0005c0005t0002g0258 a0009c0017t0012g0175 others(12): Show |
17 | HG00741.hp2 HG01099.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-18-3491_-18-3490d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27336676 | ||||||
chr16:27336694 | A | AAAGGAAA others(37): Show |
1 | a0009c0037t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-18-3490_-18-3447d others(46): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27336694 | ||||||
chr16:27336694 | A | AAGGAAAG others(36): Show |
1 | a0027c0036t0014g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18-3491_-18-3490i others(45): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27336694 | ||||||
chr16:27336712 | G | T | 1 | a0006c0031t0005g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-18-3474G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336712 | |||||||
chr16:27336719 | C | T | 4 | a0011c0010t0004g0046 a0011c0010t0004g0047 a0014c0041t0005g0228 others(1): Show |
4 | HG03041.hp2 NA19043.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-3467C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336719 | |||||||
chr16:27336843 | C | T | 1 | a0002c0002t0001g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-18-3343C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336843 | |||||||
chr16:27336844 | T | C | 44 | a0001c0001t0001g0263 a0001c0001t0002g0261 a0001c0001t0002g0267 others(41): Show |
49 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-18-3342T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336844 | |||||||
chr16:27336914 | A | G | 2 | a0009c0037t0001g0050 a0027c0036t0014g0051 |
2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-18-3272A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336914 | |||||||
chr16:27336954 | G | A | 4 | a0011c0010t0004g0046 a0011c0010t0004g0047 a0014c0041t0005g0228 others(1): Show |
4 | HG03041.hp2 NA19043.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-3232G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336954 | |||||||
chr16:27337001 | T | C | 44 | a0001c0001t0001g0263 a0001c0001t0002g0261 a0001c0001t0002g0267 others(41): Show |
49 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-18-3185T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337001 | |||||||
chr16:27337009 | G | A | 3 | a0010c0024t0004g0279 a0012c0016t0006g0029 a0012c0016t0006g0280 |
4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-3177G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337009 | |||||||
chr16:27337057 | A | G | 1 | a0014c0041t0005g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-3129A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337057 | |||||||
chr16:27337111 | G | A | 2 | a0009c0037t0001g0050 a0027c0036t0014g0051 |
2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-18-3075G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337111 | |||||||
chr16:27337124 | A | AAAG | 44 | a0001c0001t0001g0263 a0001c0001t0002g0261 a0001c0001t0002g0267 others(41): Show |
49 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-18-3055_-18-3053d others(5): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27337124 | ||||||
chr16:27337163 | G | C | 2 | a0001c0008t0025g0168 a0021c0045t0024g0169 |
2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-18-3023G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337163 | |||||||
chr16:27337199 | G | T | 1 | a0001c0001t0002g0111 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-18-2987G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337199 | |||||||
chr16:27337271 | C | T | 3 | a0010c0024t0004g0279 a0012c0016t0006g0029 a0012c0016t0006g0280 |
4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-2915C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337271 | |||||||
chr16:27337309 | G | A | 89 | a0001c0001t0002g0190 a0002c0002t0001g0001 a0002c0002t0001g0005 others(86): Show |
108 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-18-2877G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337309 | |||||||
chr16:27337328 | C | T | 1 | a0002c0002t0002g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18-2858C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337328 | |||||||
chr16:27337404 | A | G | 3 | a0003c0003t0001g0172 a0003c0003t0001g0180 a0011c0010t0004g0179 |
3 | HG02486.hp2 HG02572.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-18-2782A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337404 | |||||||
chr16:27337410 | A | G | 1 | a0005c0022t0001g0021 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-18-2776A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337410 | |||||||
chr16:27337489 | G | C | 1 | a0001c0001t0002g0111 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-18-2697G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337489 | |||||||
chr16:27337561 | C | CT | 4 | a0011c0010t0004g0046 a0011c0010t0004g0047 a0014c0041t0005g0228 others(1): Show |
4 | HG03041.hp2 NA19043.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-2618dupT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27337561 | ||||||
chr16:27337619 | G | A | 2 | a0003c0003t0002g0247 a0003c0003t0002g0248 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-2567G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337619 | |||||||
chr16:27337648 | C | T | 1 | a0001c0001t0002g0116 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-18-2538C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337648 | |||||||
chr16:27337766 | G | C | 1 | a0001c0001t0002g0074 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-18-2420G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337766 | |||||||
chr16:27337847 | C | T | 64 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(61): Show |
75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.-18-2339C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337847 | |||||||
chr16:27337853 | C | G | 1 | a0006c0031t0005g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-18-2333C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337853 | |||||||
chr16:27337922 | T | C | 1 | a0014c0041t0005g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-2264T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337922 | |||||||
chr16:27337925 | G | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | NA18949.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.-18-2261G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337925 | |||||||
chr16:27337945 | A | AT | 65 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(62): Show |
76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.-18-2234dupT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27337945 | ||||||
chr16:27337959 | C | CT | 7 | a0001c0001t0002g0167 a0002c0002t0001g0221 a0003c0003t0001g0157 others(4): Show |
7 | HG01433.hp1 HG02723.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18-2212dupT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27337959 | ||||||
chr16:27337959 | CT | C | 36 | a0001c0001t0001g0141 a0001c0001t0001g0263 a0001c0001t0002g0261 others(33): Show |
41 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.-18-2212delT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27337959 | ||||||
chr16:27338031 | G | A | 4 | a0001c0001t0001g0263 a0005c0005t0002g0257 a0005c0005t0002g0258 others(1): Show |
4 | HG01081.hp1 HG01099.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-2155G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338031 | |||||||
chr16:27338073 | C | T | 2 | a0009c0037t0001g0050 a0027c0036t0014g0051 |
2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-18-2113C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338073 | |||||||
chr16:27338075 | G | C | 2 | a0019c0023t0013g0030 a0019c0023t0013g0031 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-2111G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338075 | |||||||
chr16:27338082 | G | A | 4 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0256 others(1): Show |
4 | HG01891.hp1 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-2104G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338082 | |||||||
chr16:27338117 | T | C | 129 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(126): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.-18-2069T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338117 | |||||||
chr16:27338172 | G | T | 38 | a0001c0001t0001g0141 a0001c0001t0001g0263 a0001c0001t0002g0261 others(35): Show |
43 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.-18-2014G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338172 | |||||||
chr16:27338197 | C | T | 1 | a0021c0045t0024g0169 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-18-1989C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338197 | |||||||
chr16:27338236 | T | G | 1 | a0007c0007t0015g0225 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-18-1950T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338236 | |||||||
chr16:27338335 | A | T | 4 | a0013c0011t0009g0020 a0013c0011t0009g0048 a0013c0011t0009g0178 others(1): Show |
5 | HG01243.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-1851A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338335 | |||||||
chr16:27338526 | AT | A | 139 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(136): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-18-1653delT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27338526 | ||||||
chr16:27338597 | C | T | 3 | a0002c0002t0001g0202 a0004c0004t0003g0201 a0022c0027t0003g0204 |
3 | HG01070.hp1 HG01952.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-18-1589C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338597 | |||||||
chr16:27338650 | A | G | 1 | a0005c0022t0001g0021 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-18-1536A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338650 | |||||||
chr16:27338691 | C | T | 145 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(142): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.-18-1495C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338691 | |||||||
chr16:27338719 | C | A | 2 | a0002c0002t0002g0127 a0003c0003t0002g0126 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-18-1467C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338719 | |||||||
chr16:27338801 | G | T | 1 | a0005c0005t0001g0057 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-18-1385G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338801 | |||||||
chr16:27338893 | G | A | 1 | a0011c0010t0004g0179 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-18-1293G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338893 | |||||||
chr16:27339043 | C | T | 1 | a0003c0003t0001g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-18-1143C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339043 | |||||||
chr16:27339293 | T | C | 1 | a0025c0048t0002g0125 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-18-893T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339293 | |||||||
chr16:27339366 | A | G | 130 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(127): Show |
152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.-18-820A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339366 | |||||||
chr16:27339422 | G | A | 1 | a0003c0003t0001g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18-764G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339422 | |||||||
chr16:27339672 | C | A | 1 | a0002c0002t0001g0195 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-18-514C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339672 | |||||||
chr16:27339707 | A | T | 2 | a0008c0009t0007g0040 a0008c0047t0007g0039 |
2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-18-479A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339707 | |||||||
chr16:27339771 | A | G | 1 | a0014c0041t0005g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-415A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339771 | |||||||
chr16:27339785 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-18-401G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339785 | |||||||
chr16:27339972 | G | A | 7 | a0008c0009t0007g0008 a0008c0009t0007g0040 a0008c0009t0007g0041 others(4): Show |
8 | HG02055.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-214G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339972 | |||||||
chr16:27340017 | A | G | 126 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(123): Show |
148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-18-169A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27340017 | |||||||
chr16:27340354 | G | A | 2 | a0002c0002t0002g0142 a0002c0002t0002g0158 |
2 | HG00639.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.70+81G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340354 | |||||||
chr16:27340392 | A | G | 1 | a0014c0041t0005g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70+119A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340392 | |||||||
chr16:27340477 | C | G | 2 | a0012c0016t0006g0029 a0012c0016t0006g0280 |
3 | HG01109.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.70+204C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340477 | |||||||
chr16:27340581 | G | A | 4 | a0003c0003t0001g0044 a0011c0010t0004g0046 a0011c0010t0004g0047 others(1): Show |
4 | HG02886.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+308G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340581 | |||||||
chr16:27340647 | A | G | 3 | a0010c0024t0005g0171 a0019c0023t0013g0030 a0019c0023t0013g0031 |
3 | HG02145.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+374A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340647 | |||||||
chr16:27340677 | G | A | 1 | a0014c0041t0005g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70+404G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340677 | |||||||
chr16:27340678 | C | T | 1 | a0002c0002t0002g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.70+405C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340678 | |||||||
chr16:27340792 | G | C | 1 | a0001c0001t0002g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.70+519G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340792 | |||||||
chr16:27340800 | T | C | 22 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0002g0003 others(19): Show |
28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.70+527T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340800 | |||||||
chr16:27340918 | G | A | 1 | a0002c0002t0001g0242 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.70+645G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340918 | |||||||
chr16:27340920 | C | T | 2 | a0001c0001t0002g0082 a0001c0001t0002g0115 |
2 | HG02155.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.70+647C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340920 | |||||||
chr16:27340927 | G | T | 2 | a0012c0016t0006g0029 a0012c0016t0006g0280 |
3 | HG01109.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.70+654G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340927 | |||||||
chr16:27341271 | G | A | 2 | a0012c0016t0006g0029 a0012c0016t0006g0280 |
3 | HG01109.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.71-850G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341271 | |||||||
chr16:27341389 | A | G | 1 | a0018c0015t0001g0119 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.71-732A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341389 | |||||||
chr16:27341392 | C | T | 27 | a0001c0001t0001g0141 a0001c0001t0001g0263 a0001c0001t0002g0261 others(24): Show |
30 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.71-729C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341392 | |||||||
chr16:27341498 | G | A | 27 | a0001c0001t0001g0141 a0001c0001t0001g0263 a0001c0001t0002g0261 others(24): Show |
30 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.71-623G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341498 | |||||||
chr16:27341565 | C | T | 5 | a0003c0003t0001g0044 a0011c0010t0004g0046 a0011c0010t0004g0047 others(2): Show |
5 | HG02886.hp1 HG03041.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-556C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341565 | |||||||
chr16:27341587 | A | T | 2 | a0002c0002t0001g0185 a0002c0002t0001g0245 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.71-534A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341587 | |||||||
chr16:27341604 | T | G | 1 | a0003c0003t0001g0143 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.71-517T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341604 | |||||||
chr16:27341614 | C | G | 9 | a0002c0002t0002g0127 a0003c0003t0002g0126 a0008c0009t0007g0008 others(6): Show |
10 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.71-507C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341614 | |||||||
chr16:27341617 | T | A | 9 | a0002c0002t0002g0127 a0003c0003t0002g0126 a0008c0009t0007g0008 others(6): Show |
10 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.71-504T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341617 | |||||||
chr16:27341644 | T | C | 5 | a0003c0003t0001g0044 a0011c0010t0004g0046 a0011c0010t0004g0047 others(2): Show |
5 | HG02886.hp1 HG03041.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-477T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341644 | |||||||
chr16:27341700 | G | A | 2 | a0002c0013t0001g0025 a0002c0013t0001g0189 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.71-421G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341700 | |||||||
chr16:27341797 | G | A | 4 | a0013c0011t0009g0020 a0013c0011t0009g0048 a0013c0011t0009g0178 others(1): Show |
5 | HG01243.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-324G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341797 | |||||||
chr16:27341867 | G | A | 4 | a0011c0010t0004g0046 a0011c0010t0004g0047 a0014c0041t0005g0228 others(1): Show |
4 | HG03041.hp2 NA19043.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-254G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341867 | |||||||
chr16:27341909 | G | A | 31 | a0001c0001t0001g0141 a0001c0001t0001g0263 a0001c0001t0002g0261 others(28): Show |
34 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.71-212G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341909 | |||||||
chr16:27342036 | C | T | 27 | a0001c0001t0001g0141 a0001c0001t0001g0263 a0001c0001t0002g0261 others(24): Show |
30 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.71-85C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27342036 | |||||||
chr16:27342076 | G | A | 2 | a0013c0011t0009g0020 a0013c0011t0009g0178 |
3 | HG02647.hp2 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.71-45G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27342076 | |||||||
chr16:27342268 | G | C | 2 | a0012c0016t0006g0029 a0012c0016t0006g0280 |
3 | HG01109.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.209+9G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342268 | |||||||
chr16:27342304 | A | G | 4 | a0013c0011t0009g0020 a0013c0011t0009g0048 a0013c0011t0009g0178 others(1): Show |
5 | HG01243.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.209+45A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342304 | |||||||
chr16:27342464 | G | A | 5 | a0001c0001t0002g0275 a0009c0017t0012g0175 a0009c0017t0012g0176 others(2): Show |
5 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+205G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342464 | |||||||
chr16:27342480 | G | A | 4 | a0013c0011t0009g0020 a0013c0011t0009g0048 a0013c0011t0009g0178 others(1): Show |
5 | HG01243.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.209+221G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342480 | |||||||
chr16:27342554 | T | G | 1 | a0001c0001t0002g0261 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.209+295T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342554 | |||||||
chr16:27342640 | T | A | 1 | a0010c0024t0005g0171 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.209+381T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342640 | |||||||
chr16:27342694 | G | C | 1 | a0004c0004t0003g0069 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.209+435G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342694 | |||||||
chr16:27342746 | C | A | 27 | a0001c0001t0001g0141 a0001c0001t0001g0263 a0001c0001t0002g0261 others(24): Show |
30 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.209+487C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342746 | |||||||
chr16:27342834 | G | A | 3 | a0017c0020t0010g0042 a0017c0020t0010g0238 a0017c0032t0010g0043 |
3 | HG02055.hp1 HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.209+575G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342834 | |||||||
chr16:27342855 | C | T | 1 | a0011c0010t0004g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.209+596C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342855 | |||||||
chr16:27342968 | T | A | 13 | a0002c0002t0002g0127 a0003c0003t0001g0044 a0003c0003t0002g0126 others(10): Show |
14 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.209+709T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342968 | |||||||
chr16:27342969 | G | A | 13 | a0002c0002t0002g0127 a0003c0003t0001g0044 a0003c0003t0002g0126 others(10): Show |
14 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.209+710G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342969 | |||||||
chr16:27343005 | C | A | 10 | a0002c0002t0001g0202 a0004c0004t0003g0066 a0004c0004t0003g0069 others(7): Show |
10 | HG00408.hp1 HG01070.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.209+746C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343005 | |||||||
chr16:27343040 | C | T | 40 | a0001c0001t0001g0141 a0001c0001t0001g0263 a0001c0001t0002g0261 others(37): Show |
44 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.209+781C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343040 | |||||||
chr16:27343170 | T | G | 3 | a0011c0010t0004g0046 a0011c0010t0004g0047 a0033c0033t0004g0117 |
3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.209+911T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343170 | |||||||
chr16:27343179 | G | C | 2 | a0019c0023t0013g0030 a0019c0023t0013g0031 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.209+920G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343179 | |||||||
chr16:27343210 | C | G | 145 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(142): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.209+951C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343210 | |||||||
chr16:27343408 | G | GTTTT | 26 | a0001c0001t0001g0141 a0001c0001t0001g0263 a0001c0001t0002g0261 others(23): Show |
29 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.209+1152_209+1155d others(6): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27343408 | ||||||
chr16:27343411 | T | TTTTG | 56 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(53): Show |
66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.209+1176_209+1179d others(6): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27343411 | ||||||
chr16:27343413 | TTG | T | 12 | a0002c0002t0002g0127 a0003c0003t0002g0126 a0008c0009t0007g0008 others(9): Show |
13 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.209+1156_209+1157d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27343413 | ||||||
chr16:27343415 | G | T | 2 | a0009c0037t0001g0050 a0029c0039t0004g0273 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.209+1156G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343415 | |||||||
chr16:27343450 | G | C | 1 | a0004c0004t0003g0201 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.209+1191G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343450 | |||||||
chr16:27343518 | C | G | 13 | a0002c0002t0002g0127 a0003c0003t0001g0044 a0003c0003t0002g0126 others(10): Show |
14 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.209+1259C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343518 | |||||||
chr16:27343626 | T | C | 40 | a0001c0001t0001g0141 a0001c0001t0001g0263 a0001c0001t0002g0261 others(37): Show |
44 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.210-1243T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343626 | |||||||
chr16:27343680 | A | G | 13 | a0002c0002t0002g0127 a0003c0003t0001g0044 a0003c0003t0002g0126 others(10): Show |
14 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.210-1189A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343680 | |||||||
chr16:27343683 | G | C | 139 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(136): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.210-1186G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343683 | |||||||
chr16:27343729 | C | T | 9 | a0002c0002t0002g0127 a0003c0003t0002g0126 a0008c0009t0007g0008 others(6): Show |
10 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.210-1140C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343729 | |||||||
chr16:27343867 | G | GA | 3 | a0011c0010t0004g0046 a0011c0010t0004g0047 a0033c0033t0004g0117 |
3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.210-1001dupA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27343867 | ||||||
chr16:27343964 | G | T | 27 | a0001c0001t0001g0141 a0001c0001t0001g0263 a0001c0001t0002g0261 others(24): Show |
30 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.210-905G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343964 | |||||||
chr16:27344028 | A | G | 40 | a0001c0001t0001g0141 a0001c0001t0001g0263 a0001c0001t0002g0261 others(37): Show |
44 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.210-841A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344028 | |||||||
chr16:27344041 | G | A | 88 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(85): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.210-828G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344041 | |||||||
chr16:27344109 | G | A | 13 | a0002c0002t0002g0127 a0003c0003t0001g0044 a0003c0003t0002g0126 others(10): Show |
14 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.210-760G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344109 | |||||||
chr16:27344174 | G | A | 1 | a0023c0043t0017g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.210-695G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344174 | |||||||
chr16:27344288 | G | A | 1 | a0002c0002t0002g0271 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.210-581G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344288 | |||||||
chr16:27344303 | A | AG | 5 | a0008c0009t0007g0040 a0008c0047t0007g0039 a0017c0020t0010g0042 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-564dupG | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27344303 | ||||||
chr16:27344337 | C | T | 4 | a0009c0035t0005g0038 a0009c0037t0001g0050 a0009c0046t0005g0037 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.210-532C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344337 | |||||||
chr16:27344364 | C | CA | 16 | a0001c0001t0001g0141 a0002c0002t0002g0127 a0002c0002t0002g0191 others(13): Show |
18 | HG01109.hp2 HG02451.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.210-487dupA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27344364 | ||||||
chr16:27344364 | CA | C | 16 | a0001c0001t0002g0124 a0001c0001t0002g0275 a0001c0001t0021g0098 others(13): Show |
17 | HG00099.hp1 HG01884.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.210-487delA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27344364 | ||||||
chr16:27344364 | CAA | C | 84 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(81): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.210-488_210-487del others(2): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27344364 | ||||||
chr16:27344364 | CAAA | C | 11 | a0001c0001t0002g0109 a0001c0001t0002g0132 a0001c0001t0002g0166 others(8): Show |
11 | HG00735.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.210-489_210-487del others(3): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27344364 | ||||||
chr16:27344528 | G | A | 2 | a0001c0008t0025g0168 a0021c0045t0024g0169 |
2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.210-341G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344528 | |||||||
chr16:27344567 | C | T | 5 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0166 others(2): Show |
5 | HG03486.hp1 NA18940.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-302C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344567 | |||||||
chr16:27345038 | C | T | 75 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(72): Show |
86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.361+18C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345038 | |||||||
chr16:27345077 | C | T | 105 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(102): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.361+57C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345077 | |||||||
chr16:27345091 | G | A | 24 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0002g0003 others(21): Show |
30 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.361+71G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345091 | |||||||
chr16:27345133 | C | T | 2 | a0002c0002t0001g0183 a0002c0002t0001g0184 |
2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.361+113C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345133 | |||||||
chr16:27345286 | A | G | 7 | a0009c0035t0005g0038 a0009c0037t0001g0050 a0009c0046t0005g0037 others(4): Show |
8 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+266A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345286 | |||||||
chr16:27345334 | G | T | 2 | a0001c0008t0025g0168 a0021c0045t0024g0169 |
2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.361+314G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345334 | |||||||
chr16:27345346 | T | G | 120 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(117): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.361+326T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345346 | |||||||
chr16:27345359 | G | A | 7 | a0009c0035t0005g0038 a0009c0037t0001g0050 a0009c0046t0005g0037 others(4): Show |
8 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+339G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345359 | |||||||
chr16:27345368 | G | C | 7 | a0009c0035t0005g0038 a0009c0037t0001g0050 a0009c0046t0005g0037 others(4): Show |
8 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+348G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345368 | |||||||
chr16:27345403 | G | A | 3 | a0012c0016t0006g0029 a0012c0016t0006g0280 a0020c0021t0002g0016 |
5 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.361+383G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345403 | |||||||
chr16:27345420 | C | T | 4 | a0010c0012t0004g0049 a0011c0010t0004g0046 a0011c0010t0004g0047 others(1): Show |
4 | HG03041.hp2 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.361+400C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345420 | |||||||
chr16:27345569 | A | G | 1 | a0003c0003t0002g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.361+549A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345569 | |||||||
chr16:27345571 | G | A | 9 | a0001c0001t0002g0275 a0005c0022t0001g0021 a0009c0017t0012g0175 others(6): Show |
10 | HG00741.hp2 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.361+551G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345571 | |||||||
chr16:27345603 | T | A | 1 | a0003c0003t0001g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.361+583T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345603 | |||||||
chr16:27345641 | G | A | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | NA18945.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.361+621G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345641 | |||||||
chr16:27345692 | C | T | 7 | a0003c0003t0002g0126 a0008c0009t0007g0008 a0008c0009t0007g0040 others(4): Show |
8 | HG02055.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+672C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345692 | |||||||
chr16:27345693 | G | A | 3 | a0012c0016t0006g0029 a0012c0016t0006g0280 a0020c0021t0002g0016 |
5 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.361+673G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345693 | |||||||
chr16:27345743 | A | G | 7 | a0009c0035t0005g0038 a0009c0037t0001g0050 a0009c0046t0005g0037 others(4): Show |
8 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+723A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345743 | |||||||
chr16:27345787 | A | G | 7 | a0009c0035t0005g0038 a0009c0037t0001g0050 a0009c0046t0005g0037 others(4): Show |
8 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-680A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345787 | |||||||
chr16:27345951 | G | A | 1 | a0002c0002t0002g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.362-516G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345951 | |||||||
chr16:27345958 | T | C | 7 | a0009c0035t0005g0038 a0009c0037t0001g0050 a0009c0046t0005g0037 others(4): Show |
8 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-509T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345958 | |||||||
chr16:27346085 | G | A | 1 | a0001c0001t0002g0124 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.362-382G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27346085 | |||||||
chr16:27346087 | G | A | 2 | a0002c0002t0001g0185 a0002c0002t0001g0245 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.362-380G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27346087 | |||||||
chr16:27346210 | G | A | 5 | a0008c0009t0007g0084 a0010c0012t0004g0049 a0011c0010t0004g0046 others(2): Show |
5 | HG02055.hp2 HG03041.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-257G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27346210 | |||||||
chr16:27346463 | G | A | 9 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(6): Show |
10 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.362-4G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27346463 | |||||||
chr16:27346639 | G | A | 1 | a0001c0008t0002g0264 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.513+21G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346639 | |||||||
chr16:27346719 | C | T | 5 | a0008c0009t0007g0084 a0010c0012t0004g0049 a0011c0010t0004g0046 others(2): Show |
5 | HG02055.hp2 HG03041.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+101C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346719 | |||||||
chr16:27346724 | G | A | 3 | a0002c0002t0001g0237 a0002c0002t0002g0214 a0002c0002t0002g0222 |
3 | HG01515.hp1 HG01517.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.513+106G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346724 | |||||||
chr16:27346737 | A | T | 6 | a0002c0002t0002g0034 a0003c0003t0001g0172 a0003c0003t0001g0180 others(3): Show |
6 | HG02486.hp2 HG02572.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.513+119A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346737 | |||||||
chr16:27346777 | A | C | 264 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(261): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.513+159A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346777 | |||||||
chr16:27346809 | A | G | 1 | a0003c0003t0001g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.513+191A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346809 | |||||||
chr16:27346811 | C | T | 93 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(90): Show |
106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.513+193C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346811 | |||||||
chr16:27346849 | C | T | 1 | a0003c0003t0001g0232 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.513+231C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346849 | |||||||
chr16:27346869 | G | A | 16 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(13): Show |
17 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.513+251G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346869 | |||||||
chr16:27346882 | A | G | 154 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(151): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.513+264A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346882 | |||||||
chr16:27347030 | G | A | 9 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(6): Show |
10 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.513+412G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347030 | |||||||
chr16:27347111 | A | G | 1 | a0004c0004t0003g0120 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.513+493A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347111 | |||||||
chr16:27347251 | C | T | 1 | a0003c0003t0001g0148 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.513+633C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347251 | |||||||
chr16:27347276 | C | T | 1 | a0001c0001t0002g0071 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.513+658C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347276 | |||||||
chr16:27347323 | C | T | 3 | a0002c0002t0002g0127 a0009c0035t0005g0038 a0009c0046t0005g0037 |
3 | HG02258.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.513+705C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347323 | |||||||
chr16:27347442 | T | C | 143 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(140): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.513+824T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347442 | |||||||
chr16:27347537 | C | A | 2 | a0014c0041t0005g0228 a0028c0028t0005g0123 |
2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.513+919C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347537 | |||||||
chr16:27347554 | A | T | 1 | a0014c0041t0005g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.513+936A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347554 | |||||||
chr16:27347563 | G | A | 1 | a0014c0041t0005g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.513+945G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347563 | |||||||
chr16:27347567 | G | A | 61 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0002g0003 others(58): Show |
71 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.513+949G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347567 | |||||||
chr16:27347627 | A | G | 180 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(177): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.513+1009A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347627 | |||||||
chr16:27347700 | A | C | 122 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(119): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.513+1082A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347700 | |||||||
chr16:27347740 | A | T | 114 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(111): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.513+1122A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347740 | |||||||
chr16:27347745 | A | G | 3 | a0012c0016t0006g0029 a0012c0016t0006g0280 a0020c0021t0002g0016 |
5 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+1127A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347745 | |||||||
chr16:27347873 | G | T | 9 | a0001c0001t0002g0275 a0005c0022t0001g0021 a0009c0017t0012g0175 others(6): Show |
10 | HG00741.hp2 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.513+1255G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347873 | |||||||
chr16:27347902 | G | A | 1 | a0029c0039t0004g0273 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.513+1284G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347902 | |||||||
chr16:27347975 | G | A | 22 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(19): Show |
24 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.513+1357G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347975 | |||||||
chr16:27348194 | C | A | 2 | a0001c0008t0025g0168 a0021c0045t0024g0169 |
2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.513+1576C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348194 | |||||||
chr16:27348254 | G | A | 5 | a0008c0009t0007g0084 a0010c0012t0004g0049 a0011c0010t0004g0046 others(2): Show |
5 | HG02055.hp2 HG03041.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+1636G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348254 | |||||||
chr16:27348267 | G | C | 4 | a0003c0003t0001g0044 a0013c0011t0009g0020 a0013c0011t0009g0048 others(1): Show |
5 | HG02647.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+1649G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348267 | |||||||
chr16:27348311 | G | T | 1 | a0001c0001t0002g0090 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.513+1693G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348311 | |||||||
chr16:27348503 | C | G | 1 | a0023c0043t0017g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.513+1885C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348503 | |||||||
chr16:27348523 | G | A | 148 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(145): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.513+1905G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348523 | |||||||
chr16:27348671 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.513+2053G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348671 | |||||||
chr16:27348720 | G | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0161 |
2 | HG00140.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.513+2102G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348720 | |||||||
chr16:27348764 | T | C | 2 | a0010c0012t0004g0049 a0033c0033t0004g0117 |
2 | NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513+2146T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348764 | |||||||
chr16:27348772 | G | C | 1 | a0014c0041t0005g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.513+2154G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348772 | |||||||
chr16:27348773 | G | T | 1 | a0014c0041t0005g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.513+2155G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348773 | |||||||
chr16:27348901 | G | A | 3 | a0012c0016t0006g0029 a0012c0016t0006g0280 a0020c0021t0002g0016 |
5 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+2283G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348901 | |||||||
chr16:27348910 | GA | G | 19 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(16): Show |
22 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.513+2293delA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348910 | |||||||
chr16:27348952 | T | C | 1 | a0003c0003t0001g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.513+2334T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348952 | |||||||
chr16:27349136 | G | A | 1 | a0002c0002t0001g0183 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.513+2518G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349136 | |||||||
chr16:27349257 | C | T | 1 | a0001c0001t0002g0113 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.513+2639C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349257 | |||||||
chr16:27349279 | G | A | 1 | a0002c0002t0002g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.513+2661G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349279 | |||||||
chr16:27349306 | A | G | 163 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(160): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.513+2688A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349306 | |||||||
chr16:27349307 | T | C | 163 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(160): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.513+2689T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349307 | |||||||
chr16:27349535 | A | T | 4 | a0005c0022t0001g0021 a0016c0018t0005g0174 a0016c0018t0023g0173 others(1): Show |
5 | HG00741.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+2917A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349535 | |||||||
chr16:27349611 | T | A | 4 | a0005c0022t0001g0021 a0016c0018t0005g0174 a0016c0018t0023g0173 others(1): Show |
5 | HG00741.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-2929T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349611 | |||||||
chr16:27349731 | A | G | 16 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(13): Show |
17 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.514-2809A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349731 | |||||||
chr16:27349747 | T | TTTG | 3 | a0002c0002t0001g0195 a0010c0012t0004g0012 a0010c0012t0004g0065 |
4 | HG02922.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-2774_514-2772d others(5): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 27349747 | ||||||
chr16:27349846 | A | C | 110 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(107): Show |
126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.514-2694A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349846 | |||||||
chr16:27349906 | C | T | 3 | a0003c0003t0002g0248 a0009c0037t0001g0050 a0027c0036t0014g0051 |
3 | HG01884.hp1 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.514-2634C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349906 | |||||||
chr16:27349992 | C | A | 19 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(16): Show |
22 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.514-2548C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349992 | |||||||
chr16:27350016 | G | A | 2 | a0009c0035t0005g0038 a0009c0046t0005g0037 |
2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.514-2524G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27350016 | |||||||
chr16:27350041 | G | A | 37 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0002g0003 others(34): Show |
44 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.514-2499G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27350041 | |||||||
chr16:27350256 | A | G | 3 | a0002c0002t0002g0127 a0009c0035t0005g0038 a0009c0046t0005g0037 |
3 | HG02258.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.514-2284A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27350256 | |||||||
chr16:27350395 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.514-2145A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27350395 | |||||||
chr16:27350472 | C | T | 45 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0002g0003 others(42): Show |
52 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.514-2068C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27350472 | |||||||
chr16:27350674 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.514-1866G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27350674 | |||||||
chr16:27350838 | C | T | 1 | a0001c0001t0002g0089 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.514-1702C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27350838 | |||||||
chr16:27351128 | A | G | 5 | a0001c0001t0002g0275 a0009c0017t0012g0175 a0009c0017t0012g0176 others(2): Show |
5 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-1412A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351128 | |||||||
chr16:27351212 | G | C | 16 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(13): Show |
17 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.514-1328G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351212 | |||||||
chr16:27351496 | A | ATC | 41 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0002g0003 others(38): Show |
48 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.514-1030_514-1029d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 27351496 | ||||||
chr16:27351510 | CT | C | 100 | a0001c0001t0001g0100 a0001c0001t0001g0263 a0001c0001t0002g0275 others(97): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.514-1011delT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 27351510 | ||||||
chr16:27351510 | CTT | C | 27 | a0002c0002t0001g0006 a0002c0002t0001g0217 a0002c0002t0001g0227 others(24): Show |
30 | HG00741.hp2 HG01496.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.514-1012_514-1011d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 27351510 | ||||||
chr16:27351512 | T | C | 41 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0002g0003 others(38): Show |
48 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.514-1028T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351512 | |||||||
chr16:27351527 | TTTC | T | 20 | a0001c0001t0002g0002 a0001c0008t0001g0028 a0001c0008t0001g0260 others(17): Show |
23 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.514-1012_514-1010d others(5): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351527 | |||||||
chr16:27351528 | TTC | T | 89 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(86): Show |
101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.514-1011_514-1010d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351528 | |||||||
chr16:27351530 | C | T | 1 | a0019c0023t0013g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.514-1010C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351530 | |||||||
chr16:27351714 | C | T | 3 | a0012c0016t0006g0029 a0012c0016t0006g0280 a0020c0021t0002g0016 |
5 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-826C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351714 | |||||||
chr16:27351720 | G | A | 19 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(16): Show |
22 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.514-820G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351720 | |||||||
chr16:27351726 | G | A | 14 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(11): Show |
15 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.514-814G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351726 | |||||||
chr16:27351783 | G | A | 1 | a0007c0007t0001g0215 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.514-757G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351783 | |||||||
chr16:27351788 | T | G | 2 | a0009c0037t0001g0050 a0027c0036t0014g0051 |
2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.514-752T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351788 | |||||||
chr16:27351909 | T | C | 19 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(16): Show |
22 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.514-631T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351909 | |||||||
chr16:27351944 | T | C | 7 | a0008c0009t0007g0008 a0008c0009t0007g0040 a0008c0009t0007g0041 others(4): Show |
8 | HG02055.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-596T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351944 | |||||||
chr16:27352032 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.514-508C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27352032 | |||||||
chr16:27352182 | G | C | 4 | a0003c0003t0001g0044 a0013c0011t0009g0020 a0013c0011t0009g0048 others(1): Show |
5 | HG02647.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-358G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27352182 | |||||||
chr16:27352290 | G | A | 19 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(16): Show |
22 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.514-250G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27352290 | |||||||
chr16:27352365 | G | C | 245 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(242): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.514-175G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27352365 | |||||||
chr16:27352413 | C | T | 3 | a0002c0002t0002g0127 a0009c0035t0005g0038 a0009c0046t0005g0037 |
3 | HG02258.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.514-127C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27352413 | |||||||
chr16:27352837 | C | T | 104 | a0001c0001t0001g0007 a0001c0001t0001g0100 a0001c0001t0001g0236 others(101): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.670+141C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27352837 | |||||||
chr16:27352879 | A | C | 210 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(207): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.670+183A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27352879 | |||||||
chr16:27352912 | G | A | 229 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(226): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.670+216G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27352912 | |||||||
chr16:27352932 | C | T | 102 | a0001c0001t0001g0007 a0001c0001t0001g0100 a0001c0001t0001g0236 others(99): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.670+236C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27352932 | |||||||
chr16:27353024 | G | A | 229 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(226): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.670+328G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353024 | |||||||
chr16:27353034 | A | C | 1 | a0016c0018t0005g0278 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.670+338A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353034 | |||||||
chr16:27353124 | C | T | 2 | a0002c0002t0001g0207 a0002c0002t0001g0226 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.670+428C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353124 | |||||||
chr16:27353151 | T | A | 5 | a0001c0001t0002g0275 a0009c0017t0012g0175 a0009c0017t0012g0176 others(2): Show |
5 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+455T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353151 | |||||||
chr16:27353189 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.670+493G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353189 | |||||||
chr16:27353251 | A | G | 13 | a0008c0009t0007g0008 a0008c0009t0007g0040 a0008c0009t0007g0041 others(10): Show |
14 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.670+555A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353251 | |||||||
chr16:27353343 | G | GAAATA | 19 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(16): Show |
22 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.670+660_670+664dup others(5): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 27353343 | ||||||
chr16:27353485 | G | A | 93 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(90): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.670+789G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353485 | |||||||
chr16:27353597 | G | C | 245 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(242): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.670+901G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353597 | |||||||
chr16:27353756 | C | T | 2 | a0002c0002t0001g0032 a0002c0002t0002g0140 |
2 | HG00099.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.670+1060C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353756 | |||||||
chr16:27353797 | C | T | 19 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(16): Show |
22 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.670+1101C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353797 | |||||||
chr16:27353957 | A | G | 5 | a0001c0008t0025g0168 a0012c0016t0006g0029 a0012c0016t0006g0280 others(2): Show |
7 | HG00735.hp2 HG01109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+1261A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353957 | |||||||
chr16:27353989 | G | A | 5 | a0001c0008t0025g0168 a0012c0016t0006g0029 a0012c0016t0006g0280 others(2): Show |
7 | HG00735.hp2 HG01109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+1293G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353989 | |||||||
chr16:27353990 | T | A | 1 | a0010c0034t0005g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.670+1294T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353990 | |||||||
chr16:27354013 | T | G | 1 | a0023c0043t0017g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.670+1317T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354013 | |||||||
chr16:27354132 | C | G | 92 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0061 others(89): Show |
105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.670+1436C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354132 | |||||||
chr16:27354147 | A | G | 14 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(11): Show |
15 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.670+1451A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354147 | |||||||
chr16:27354293 | A | G | 102 | a0001c0001t0001g0007 a0001c0001t0001g0100 a0001c0001t0001g0236 others(99): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.671-1515A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354293 | |||||||
chr16:27354351 | G | A | 4 | a0003c0003t0001g0044 a0013c0011t0009g0020 a0013c0011t0009g0048 others(1): Show |
5 | HG02647.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.671-1457G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354351 | |||||||
chr16:27354359 | C | T | 4 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0055 others(1): Show |
4 | HG02258.hp2 HG02615.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1449C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354359 | |||||||
chr16:27354361 | G | A | 4 | a0003c0003t0001g0044 a0013c0011t0009g0020 a0013c0011t0009g0048 others(1): Show |
5 | HG02647.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.671-1447G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354361 | |||||||
chr16:27354398 | C | T | 1 | a0029c0039t0004g0273 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.671-1410C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354398 | |||||||
chr16:27354615 | G | A | 1 | a0003c0003t0001g0232 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.671-1193G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354615 | |||||||
chr16:27354706 | C | A | 1 | a0002c0002t0002g0233 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.671-1102C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354706 | |||||||
chr16:27354709 | A | G | 246 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(243): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.671-1099A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354709 | |||||||
chr16:27354719 | T | C | 1 | a0003c0003t0001g0157 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.671-1089T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354719 | |||||||
chr16:27354782 | G | A | 1 | a0010c0034t0005g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671-1026G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354782 | |||||||
chr16:27354805 | A | G | 20 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(17): Show |
23 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.671-1003A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354805 | |||||||
chr16:27354975 | T | C | 18 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(15): Show |
19 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.671-833T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354975 | |||||||
chr16:27355067 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.671-741C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355067 | |||||||
chr16:27355178 | A | G | 15 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(12): Show |
17 | HG00642.hp2 HG01106.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.671-630A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355178 | |||||||
chr16:27355241 | A | G | 70 | a0001c0001t0002g0275 a0001c0008t0001g0028 a0001c0008t0001g0260 others(67): Show |
75 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.671-567A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355241 | |||||||
chr16:27355413 | G | T | 1 | a0002c0002t0001g0213 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.671-395G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355413 | |||||||
chr16:27355548 | C | T | 10 | a0001c0001t0002g0275 a0005c0022t0001g0021 a0009c0017t0012g0175 others(7): Show |
11 | HG00741.hp2 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.671-260C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355548 | |||||||
chr16:27355654 | A | G | 1 | a0014c0041t0005g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.671-154A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355654 | |||||||
chr16:27355661 | T | C | 9 | a0001c0008t0001g0028 a0001c0008t0001g0260 a0001c0008t0001g0270 others(6): Show |
10 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.671-147T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355661 | |||||||
chr16:27355749 | G | A | 1 | a0005c0005t0002g0192 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.671-59G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355749 | |||||||
chr16:27355939 | C | T | 4 | a0004c0004t0003g0194 a0004c0004t0003g0199 a0004c0004t0003g0201 others(1): Show |
4 | HG01070.hp1 HG01952.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+32C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27355939 | |||||||
chr16:27355958 | G | A | 1 | a0010c0012t0004g0012 | 2 | HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.770+51G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27355958 | |||||||
chr16:27356013 | C | T | 226 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(223): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.770+106C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356013 | |||||||
chr16:27356037 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.770+130C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356037 | |||||||
chr16:27356084 | C | CT | 7 | a0002c0002t0002g0034 a0003c0003t0001g0156 a0003c0003t0001g0159 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+202dupT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 27356084 | ||||||
chr16:27356084 | CT | C | 196 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(193): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.770+202delT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 27356084 | ||||||
chr16:27356084 | CTT | C | 10 | a0001c0001t0002g0080 a0001c0001t0002g0085 a0001c0001t0002g0101 others(7): Show |
12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.770+201_770+202del others(2): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 27356084 | ||||||
chr16:27356084 | CTTTTTTT others(11): Show |
C | 5 | a0008c0009t0007g0084 a0010c0012t0004g0049 a0011c0010t0004g0046 others(2): Show |
5 | HG02055.hp2 HG03041.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+185_770+202del others(18): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 27356084 | ||||||
chr16:27356088 | T | C | 2 | a0008c0009t0007g0040 a0008c0047t0007g0039 |
2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.770+181T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356088 | |||||||
chr16:27356090 | T | TC | 8 | a0001c0001t0002g0275 a0005c0022t0001g0021 a0009c0017t0012g0175 others(5): Show |
9 | HG00741.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.770+183_770+184ins others(1): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356090 | |||||||
chr16:27356092 | T | C | 2 | a0001c0001t0002g0105 a0001c0001t0002g0115 |
2 | HG02155.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.770+185T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356092 | |||||||
chr16:27356093 | T | C | 181 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(178): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.770+186T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356093 | |||||||
chr16:27356094 | T | C | 8 | a0001c0001t0002g0080 a0001c0001t0002g0085 a0001c0001t0002g0101 others(5): Show |
8 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.770+187T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356094 | |||||||
chr16:27356184 | C | T | 3 | a0010c0024t0005g0171 a0023c0043t0017g0045 a0029c0039t0004g0273 |
3 | HG01243.hp2 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.770+277C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356184 | |||||||
chr16:27356206 | C | T | 2 | a0009c0035t0005g0038 a0009c0046t0005g0037 |
2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.770+299C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356206 | |||||||
chr16:27356412 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.770+505C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356412 | |||||||
chr16:27356412 | CG | C | 7 | a0005c0022t0001g0021 a0016c0018t0005g0174 a0016c0018t0005g0278 others(4): Show |
8 | HG00741.hp2 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.770+507delG | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 27356412 | ||||||
chr16:27356416 | A | C | 7 | a0005c0022t0001g0021 a0016c0018t0005g0174 a0016c0018t0005g0278 others(4): Show |
8 | HG00741.hp2 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.770+509A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356416 | |||||||
chr16:27356505 | C | G | 215 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(212): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.770+598C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356505 | |||||||
chr16:27356517 | C | G | 1 | a0001c0008t0001g0270 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.770+610C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356517 | |||||||
chr16:27356542 | G | C | 9 | a0008c0009t0007g0008 a0008c0009t0007g0040 a0008c0009t0007g0041 others(6): Show |
10 | HG02055.hp2 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.770+635G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356542 | |||||||
chr16:27356586 | C | T | 5 | a0008c0009t0007g0084 a0010c0012t0004g0049 a0011c0010t0004g0046 others(2): Show |
5 | HG02055.hp2 HG03041.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+679C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356586 | |||||||
chr16:27356651 | G | A | 215 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(212): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.770+744G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356651 | |||||||
chr16:27356678 | C | T | 241 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(238): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.770+771C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356678 | |||||||
chr16:27356777 | C | T | 2 | a0009c0035t0005g0038 a0009c0046t0005g0037 |
2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.770+870C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356777 | |||||||
chr16:27357108 | G | A | 1 | a0002c0002t0001g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.770+1201G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357108 | |||||||
chr16:27357175 | C | G | 3 | a0012c0016t0006g0029 a0012c0016t0006g0280 a0020c0021t0002g0016 |
5 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+1268C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357175 | |||||||
chr16:27357176 | G | A | 2 | a0001c0001t0002g0107 a0002c0002t0001g0229 |
2 | HG02523.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.770+1269G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357176 | |||||||
chr16:27357342 | C | T | 3 | a0013c0011t0009g0020 a0013c0011t0009g0048 a0013c0011t0009g0178 |
4 | HG02647.hp2 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+1435C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357342 | |||||||
chr16:27357355 | C | T | 1 | a0008c0009t0016g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.770+1448C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357355 | |||||||
chr16:27357424 | C | T | 2 | a0009c0035t0005g0038 a0009c0046t0005g0037 |
2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.771-1492C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357424 | |||||||
chr16:27357469 | A | T | 206 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(203): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.771-1447A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357469 | |||||||
chr16:27357488 | G | A | 1 | a0001c0001t0002g0103 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.771-1428G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357488 | |||||||
chr16:27357491 | T | C | 1 | a0010c0034t0005g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.771-1425T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357491 | |||||||
chr16:27357512 | G | A | 191 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(188): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.771-1404G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357512 | |||||||
chr16:27357527 | G | T | 1 | a0002c0002t0001g0212 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.771-1389G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357527 | |||||||
chr16:27357779 | TAG | T | 12 | a0001c0001t0002g0275 a0005c0022t0001g0021 a0009c0017t0012g0175 others(9): Show |
13 | HG00741.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.771-1133_771-1132d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 27357779 | ||||||
chr16:27357892 | G | GT | 16 | a0001c0001t0002g0124 a0001c0001t0002g0165 a0001c0008t0025g0168 others(13): Show |
16 | HG00735.hp2 HG01928.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.771-1009dupT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 27357892 | ||||||
chr16:27357898 | T | G | 1 | a0003c0003t0001g0180 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.771-1018T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357898 | |||||||
chr16:27357907 | T | C | 2 | a0002c0002t0002g0017 a0002c0002t0002g0149 |
3 | HG01081.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.771-1009T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357907 | |||||||
chr16:27357916 | T | G | 5 | a0009c0037t0001g0050 a0013c0011t0009g0020 a0013c0011t0009g0048 others(2): Show |
6 | HG02145.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.771-1000T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357916 | |||||||
chr16:27357928 | T | C | 1 | a0028c0028t0005g0123 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.771-988T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357928 | |||||||
chr16:27358174 | G | A | 5 | a0008c0009t0007g0008 a0008c0009t0007g0040 a0008c0009t0007g0041 others(2): Show |
6 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.771-742G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358174 | |||||||
chr16:27358181 | A | G | 210 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(207): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.771-735A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358181 | |||||||
chr16:27358240 | G | A | 2 | a0013c0011t0009g0020 a0013c0011t0009g0178 |
3 | HG02647.hp2 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.771-676G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358240 | |||||||
chr16:27358275 | C | T | 5 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0073 others(2): Show |
5 | HG01167.hp2 HG02300.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.771-641C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358275 | |||||||
chr16:27358288 | G | A | 20 | a0001c0001t0001g0100 a0002c0002t0001g0022 a0002c0002t0001g0024 others(17): Show |
22 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.771-628G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358288 | |||||||
chr16:27358462 | G | A | 1 | a0029c0039t0004g0273 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.771-454G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358462 | |||||||
chr16:27358616 | T | C | 1 | a0008c0009t0007g0008 | 2 | HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.771-300T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358616 | |||||||
chr16:27358701 | C | T | 1 | a0003c0003t0001g0152 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.771-215C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358701 | |||||||
chr16:27358738 | G | T | 1 | a0010c0034t0005g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.771-178G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358738 | |||||||
chr16:27359007 | G | A | 1 | a0003c0003t0001g0250 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.849+13G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359007 | |||||||
chr16:27359133 | A | G | 233 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(230): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.849+139A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359133 | |||||||
chr16:27359196 | A | T | 4 | a0012c0016t0006g0029 a0012c0016t0006g0280 a0020c0021t0002g0016 others(1): Show |
6 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+202A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359196 | |||||||
chr16:27359225 | T | G | 4 | a0012c0016t0006g0029 a0012c0016t0006g0280 a0020c0021t0002g0016 others(1): Show |
6 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+231T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359225 | |||||||
chr16:27359484 | T | G | 1 | a0009c0046t0005g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.849+490T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359484 | |||||||
chr16:27359611 | AGTG | A | 196 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(193): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.849+621_849+623del others(3): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 27359611 | ||||||
chr16:27359626 | G | C | 2 | a0019c0023t0013g0030 a0019c0023t0013g0031 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.849+632G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359626 | |||||||
chr16:27359665 | G | A | 2 | a0019c0023t0013g0030 a0019c0023t0013g0031 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.849+671G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359665 | |||||||
chr16:27359837 | C | T | 195 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(192): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.849+843C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359837 | |||||||
chr16:27359927 | C | T | 5 | a0009c0017t0012g0175 a0009c0017t0012g0176 a0009c0017t0012g0274 others(2): Show |
5 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-839C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359927 | |||||||
chr16:27359984 | G | A | 1 | a0002c0002t0001g0213 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.850-782G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359984 | |||||||
chr16:27360041 | G | A | 1 | a0018c0015t0001g0119 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.850-725G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360041 | |||||||
chr16:27360075 | C | T | 1 | a0011c0010t0004g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-691C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360075 | |||||||
chr16:27360076 | G | A | 105 | a0001c0001t0001g0007 a0001c0001t0001g0083 a0001c0001t0001g0100 others(102): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.850-690G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360076 | |||||||
chr16:27360099 | C | G | 1 | a0016c0018t0005g0278 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850-667C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360099 | |||||||
chr16:27360103 | T | C | 224 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(221): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.850-663T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360103 | |||||||
chr16:27360206 | G | T | 1 | a0002c0002t0002g0271 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.850-560G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360206 | |||||||
chr16:27360218 | C | T | 209 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(206): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.850-548C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360218 | |||||||
chr16:27360250 | G | A | 195 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(192): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.850-516G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360250 | |||||||
chr16:27360263 | T | C | 212 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(209): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.850-503T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360263 | |||||||
chr16:27360331 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0002g0131 |
2 | NA19081.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.850-435C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360331 | |||||||
chr16:27360348 | G | A | 5 | a0001c0008t0025g0168 a0013c0011t0009g0020 a0013c0011t0009g0048 others(2): Show |
6 | HG00735.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-418G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360348 | |||||||
chr16:27360383 | G | A | 1 | a0010c0034t0005g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.850-383G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360383 | |||||||
chr16:27360628 | A | G | 218 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0056 others(215): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.850-138A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360628 | |||||||
chr16:27360677 | G | A | 1 | a0003c0003t0001g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.850-89G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360677 | |||||||
chr16:27360995 | C | A | 7 | a0010c0012t0004g0049 a0010c0024t0004g0279 a0010c0024t0005g0171 others(4): Show |
7 | HG02723.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.899+180C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27360995 | |||||||
chr16:27361074 | G | T | 9 | a0010c0012t0004g0049 a0010c0024t0004g0279 a0011c0010t0004g0046 others(6): Show |
9 | HG00741.hp2 HG02818.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.899+259G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361074 | |||||||
chr16:27361173 | CTG | C | 46 | a0003c0003t0001g0121 a0003c0003t0001g0128 a0003c0003t0001g0136 others(43): Show |
50 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.899+361_899+362del others(2): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 27361173 | ||||||
chr16:27361202 | G | A | 7 | a0013c0011t0009g0020 a0013c0011t0009g0048 a0013c0011t0009g0178 others(4): Show |
8 | HG02647.hp2 HG02738.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.899+387G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361202 | |||||||
chr16:27361329 | T | G | 29 | a0004c0004t0001g0009 a0004c0004t0001g0133 a0004c0004t0001g0135 others(26): Show |
32 | HG00408.hp1 HG01070.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.899+514T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361329 | |||||||
chr16:27361371 | C | T | 5 | a0012c0016t0006g0029 a0012c0016t0006g0280 a0017c0020t0010g0042 others(2): Show |
6 | HG01109.hp2 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.899+556C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361371 | |||||||
chr16:27361426 | G | A | 2 | a0002c0002t0002g0214 a0002c0002t0002g0222 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.899+611G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361426 | |||||||
chr16:27361610 | CT | C | 63 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0163 others(60): Show |
71 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.900-620delT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 27361610 | ||||||
chr16:27361610 | CTT | C | 53 | a0001c0001t0001g0073 a0002c0002t0002g0254 a0003c0003t0001g0044 others(50): Show |
58 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.900-621_900-620del others(2): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 27361610 | ||||||
chr16:27361610 | CTTT | C | 46 | a0003c0003t0002g0059 a0004c0004t0001g0009 a0004c0004t0001g0133 others(43): Show |
53 | HG00408.hp1 HG01070.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.900-622_900-620del others(3): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 27361610 | ||||||
chr16:27361610 | CTTTT | C | 11 | a0006c0006t0006g0234 a0009c0017t0012g0176 a0009c0017t0012g0274 others(8): Show |
11 | HG00735.hp2 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.900-623_900-620del others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 27361610 | ||||||
chr16:27361636 | C | T | 3 | a0017c0020t0010g0042 a0017c0020t0010g0238 a0017c0032t0010g0043 |
3 | HG02055.hp1 HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.900-616C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361636 | |||||||
chr16:27361642 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.900-610G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361642 | |||||||
chr16:27361771 | AT | A | 7 | a0013c0011t0009g0020 a0013c0011t0009g0048 a0013c0011t0009g0178 others(4): Show |
8 | HG02647.hp2 HG02738.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.900-477delT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 27361771 | ||||||
chr16:27361810 | G | A | 41 | a0006c0006t0006g0004 a0006c0006t0006g0209 a0006c0006t0006g0231 others(38): Show |
47 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.900-442G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361810 | |||||||
chr16:27362009 | T | C | 1 | a0016c0018t0005g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.900-243T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27362009 | |||||||
chr16:27362146 | A | C | 23 | a0010c0012t0004g0012 a0010c0012t0004g0049 a0010c0012t0004g0065 others(20): Show |
24 | HG00735.hp2 HG00741.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.900-106A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27362146 | |||||||
chr16:27362149 | T | C | 1 | a0020c0021t0002g0016 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.900-103T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27362149 | |||||||
chr16:27362156 | C | T | 1 | a0002c0002t0002g0149 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.900-96C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27362156 | |||||||
chr16:27362237 | C | A | 91 | a0003c0003t0001g0044 a0003c0003t0001g0121 a0003c0003t0001g0128 others(88): Show |
100 | HG00597.hp2 HG00639.hp2 HG00735.hp2 others(97): Show |
intron_variant | MODIFIER | c.900-15C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27362237 |