Item | Value |
---|---|
geneid | 9966 |
ensemblid | ENSG00000181634.8 |
hgncid | 11931 |
symbol | TNFSF15 |
name | TNF superfamily member 15 |
refseq_nuc | NM_005118.4 |
refseq_prot | NP_005109.2 |
ensembl_nuc | ENST00000374045.5 |
ensembl_prot | ENSP00000363157.3 |
mane_status | MANE Select |
chr | chr9 |
start | 114784652 |
end | 114806039 |
strand | - |
ver | v1.2 |
region | chr9:114784652-114806039 |
region5000 | chr9:114779652-114811039 |
regionname0 | TNFSF15_chr9_114784652_114806039 |
regionname5000 | TNFSF15_chr9_114779652_114811039 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 251 | 397 | 86 | 78 | 173 | 14 | 44 | 134 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | MAEDL others(246): Show |
chr9 | 114779652 | 114811039 |
a0002 | 0/0 | 251 | 12 | 3 | 0 | 9 | 0 | 0 | 4 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | MAEDL others(246): Show |
chr9 | 114779652 | 114811039 |
a0003 | 0/0 | 251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | MAEDL others(246): Show |
chr9 | 114779652 | 114811039 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 753 | 273 | 79 | 57 | 90 | 11 | 35 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | ATGGC others(748): Show |
chr9 | 114779652 | 114811039 | ||
a0001c0002 | 1/0 | 753 | 124 | 7 | 21 | 83 | 3 | 9 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | ATGGC others(748): Show |
chr9 | 114779652 | 114811039 | ||
a0002c0003 | 0/0 | 753 | 12 | 3 | 0 | 9 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | ATGGC others(748): Show |
chr9 | 114779652 | 114811039 | ||
a0003c0004 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | ATGGC others(748): Show |
chr9 | 114779652 | 114811039 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6584 | 106 | 11 | 21 | 58 | 5 | 10 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0003 | 0/0 | 6587 | 30 | 0 | 0 | 16 | 1 | 13 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6582): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0004 | 0/0 | 6582 | 26 | 8 | 10 | 1 | 3 | 4 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6577): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0006 | 0/0 | 6584 | 21 | 16 | 3 | 0 | 0 | 2 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0007 | 0/0 | 6583 | 12 | 12 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0008 | 0/0 | 6584 | 12 | 3 | 8 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0009 | 0/0 | 6583 | 10 | 2 | 1 | 6 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0011 | 0/0 | 6583 | 8 | 7 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0012 | 0/0 | 6588 | 7 | 1 | 0 | 5 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6583): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0013 | 0/0 | 6587 | 5 | 0 | 5 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6582): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0014 | 0/0 | 6583 | 4 | 1 | 2 | 0 | 1 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0017 | 0/0 | 6587 | 3 | 0 | 3 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6582): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0018 | 0/0 | 6584 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0019 | 0/0 | 6583 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0022 | 0/0 | 6584 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0023 | 0/0 | 6584 | 2 | 0 | 0 | 0 | 1 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0024 | 0/0 | 6584 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0025 | 0/0 | 6582 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6577): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0026 | 0/0 | 6583 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0029 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0030 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0031 | 0/0 | 6584 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0032 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0033 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0034 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0035 | 0/0 | 6583 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0038 | 0/0 | 6583 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0040 | 0/0 | 6583 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0041 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0043 | 0/0 | 6582 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6577): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0044 | 0/0 | 6583 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0001c0001t0045 | 0/0 | 6583 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0001c0002t0002 | 1/0 | 6583 | 83 | 2 | 17 | 54 | 3 | 6 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0001c0002t0005 | 0/0 | 6582 | 25 | 2 | 3 | 18 | 0 | 2 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6577): Show |
chr9 | 114779652 | 114811039 |
a0001c0002t0010 | 0/0 | 6584 | 10 | 3 | 0 | 6 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6579): Show |
chr9 | 114779652 | 114811039 |
a0001c0002t0021 | 0/0 | 6583 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0001c0002t0028 | 0/0 | 6583 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0001c0002t0036 | 0/0 | 6582 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6577): Show |
chr9 | 114779652 | 114811039 |
a0001c0002t0037 | 0/0 | 6582 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6577): Show |
chr9 | 114779652 | 114811039 |
a0001c0002t0039 | 0/0 | 6583 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6578): Show |
chr9 | 114779652 | 114811039 |
a0002c0003t0015 | 0/0 | 6581 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6576): Show |
chr9 | 114779652 | 114811039 |
a0002c0003t0016 | 0/0 | 6580 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6575): Show |
chr9 | 114779652 | 114811039 |
a0002c0003t0020 | 0/0 | 6581 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6576): Show |
chr9 | 114779652 | 114811039 |
a0002c0003t0027 | 0/0 | 6582 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6577): Show |
chr9 | 114779652 | 114811039 |
a0003c0004t0042 | 0/0 | 6582 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | AGAGG others(6577): Show |
chr9 | 114779652 | 114811039 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 36 | 0 | 6 | 30 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0003 | 0/0 | 25 | 9 | 6 | 4 | 2 | 4 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0004 | 0/0 | 17 | 0 | 0 | 17 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0017 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0022 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0033 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0003g0005 | 0/0 | 13 | 0 | 0 | 6 | 0 | 7 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0003g0029 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0003g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0004g0006 | 0/0 | 12 | 0 | 6 | 1 | 2 | 3 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0004g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0004g0035 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0004g0053 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0006g0009 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0006g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0006g0025 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0006g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0007g0008 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0007g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0008g0010 | 0/0 | 7 | 0 | 6 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0008g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0008g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0008g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0009g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0009g0034 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0009g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0009g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0011g0012 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0011g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0011g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0012g0013 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0012g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0012g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0013g0019 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0013g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0014g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0014g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0014g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0017g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0018g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0018g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0019g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0019g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0022g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0022g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0023g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0023g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0024g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0024g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0025g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0026g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0029g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0030g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0031g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0032g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0033g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0034g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0035g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0038g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0040g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0041g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0043g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0044g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0001t0045g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0001 | 0/0 | 42 | 2 | 8 | 26 | 2 | 4 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0014 | 1/0 | 5 | 0 | 4 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0016 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0005g0007 | 0/0 | 11 | 1 | 1 | 9 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0005g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0005g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0005g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0010g0015 | 0/0 | 5 | 3 | 0 | 2 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0010g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0010g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0010g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0010g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0010g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0021g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0028g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0036g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0037g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0001c0002t0039g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0002c0003t0015g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0002c0003t0015g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0002c0003t0015g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0002c0003t0016g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0002c0003t0016g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0002c0003t0016g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0002c0003t0020g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0002c0003t0027g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0002c0003t0027g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
a0003c0004t0042g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | GBR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0053 | EUR | GBR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | GBR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00323 | hp2 | a0001 | c0001 | t0023 | g0109 | EUR | FIN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00544 | hp2 | a0001 | c0002 | t0005 | g0020 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00558 | hp1 | a0002 | c0003 | t0015 | g0089 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0101 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00642 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00673 | hp1 | a0001 | c0002 | t0028 | g0110 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00733 | hp1 | a0001 | c0002 | t0037 | g0119 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00733 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00735 | hp1 | a0001 | c0001 | t0043 | g0145 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0083 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00738 | hp2 | a0001 | c0001 | t0008 | g0141 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0053 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG00741 | hp2 | a0001 | c0001 | t0009 | g0137 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01099 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01109 | hp1 | a0001 | c0001 | t0011 | g0012 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0023 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01167 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0025 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01192 | hp2 | a0001 | c0001 | t0035 | g0132 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01243 | hp1 | a0001 | c0001 | t0014 | g0086 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01243 | hp2 | a0001 | c0001 | t0044 | g0063 | AMR | PUR | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01255 | hp2 | a0001 | c0001 | t0013 | g0019 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0078 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01256 | hp2 | a0001 | c0001 | t0017 | g0026 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01257 | hp2 | a0001 | c0001 | t0013 | g0019 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01258 | hp2 | a0001 | c0001 | t0017 | g0026 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01358 | hp1 | a0001 | c0002 | t0005 | g0007 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01433 | hp2 | a0001 | c0001 | t0013 | g0019 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0143 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01496 | hp2 | a0001 | c0001 | t0014 | g0036 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01516 | hp2 | a0001 | c0001 | t0014 | g0081 | EUR | IBS | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01884 | hp1 | a0001 | c0001 | t0011 | g0012 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01891 | hp1 | a0001 | c0001 | t0026 | g0042 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01928 | hp1 | a0001 | c0002 | t0005 | g0082 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01934 | hp1 | a0001 | c0001 | t0006 | g0025 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01934 | hp2 | a0001 | c0001 | t0017 | g0026 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01952 | hp2 | a0001 | c0001 | t0013 | g0019 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01978 | hp2 | a0001 | c0001 | t0008 | g0098 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01981 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0113 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02027 | hp2 | a0002 | c0003 | t0027 | g0091 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02055 | hp2 | a0001 | c0002 | t0005 | g0058 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02071 | hp2 | a0001 | c0001 | t0012 | g0013 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02074 | hp1 | a0002 | c0003 | t0016 | g0151 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02074 | hp2 | a0002 | c0003 | t0015 | g0147 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02135 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02148 | hp1 | a0001 | c0001 | t0008 | g0010 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02148 | hp2 | a0001 | c0002 | t0005 | g0129 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | CDX | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02155 | hp2 | a0002 | c0003 | t0015 | g0052 | EAS | CDX | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | CDX | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0099 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02257 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02280 | hp1 | a0001 | c0001 | t0018 | g0057 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02293 | hp2 | a0001 | c0001 | t0013 | g0117 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02451 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02451 | hp2 | a0001 | c0001 | t0011 | g0038 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02572 | hp1 | a0001 | c0001 | t0014 | g0036 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02602 | hp2 | a0001 | c0001 | t0031 | g0139 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02615 | hp1 | a0002 | c0003 | t0020 | g0028 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02615 | hp2 | a0001 | c0001 | t0011 | g0012 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02622 | hp1 | a0001 | c0001 | t0018 | g0039 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02647 | hp1 | a0001 | c0001 | t0011 | g0120 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0056 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02717 | hp1 | a0001 | c0001 | t0032 | g0069 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0059 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02723 | hp2 | a0001 | c0001 | t0012 | g0097 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02738 | hp1 | a0001 | c0001 | t0038 | g0142 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02738 | hp2 | a0001 | c0001 | t0008 | g0010 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02809 | hp1 | a0001 | c0001 | t0024 | g0072 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02818 | hp1 | a0001 | c0001 | t0019 | g0037 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0040 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02886 | hp2 | a0001 | c0001 | t0024 | g0084 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02895 | hp2 | a0001 | c0002 | t0010 | g0015 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02896 | hp1 | a0001 | c0001 | t0022 | g0085 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02897 | hp1 | a0001 | c0002 | t0010 | g0015 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02965 | hp2 | a0001 | c0001 | t0019 | g0037 | AFR | ESN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02970 | hp1 | a0001 | c0001 | t0019 | g0055 | AFR | ESN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03098 | hp1 | a0001 | c0001 | t0018 | g0039 | AFR | MSL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | MSL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03130 | hp1 | a0003 | c0004 | t0042 | g0054 | AFR | ESN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | ESN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03139 | hp1 | a0001 | c0001 | t0045 | g0073 | AFR | ESN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0133 | AFR | ESN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | ESN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | ESN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03209 | hp1 | a0002 | c0003 | t0020 | g0028 | AFR | MSL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03209 | hp2 | a0001 | c0001 | t0011 | g0012 | AFR | MSL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0023 | AFR | MSL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0040 | AFR | MSL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03453 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | MSL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03453 | hp2 | a0001 | c0001 | t0011 | g0038 | AFR | MSL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | MSL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0024 | AFR | MSL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0079 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03516 | hp1 | a0001 | c0001 | t0025 | g0051 | AFR | ESN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0024 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03540 | hp2 | a0001 | c0001 | t0040 | g0060 | AFR | GWD | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | MSL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03654 | hp2 | a0001 | c0002 | t0005 | g0044 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0148 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03688 | hp1 | a0001 | c0001 | t0009 | g0034 | SAS | STU | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | STU | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0094 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03710 | hp1 | a0001 | c0001 | t0023 | g0104 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03831 | hp1 | a0001 | c0002 | t0010 | g0105 | SAS | BEB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03942 | hp1 | a0001 | c0001 | t0012 | g0013 | SAS | BEB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG04115 | hp1 | a0001 | c0002 | t0005 | g0044 | SAS | STU | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0035 | SAS | STU | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG04184 | hp2 | a0001 | c0001 | t0006 | g0025 | SAS | BEB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | STU | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | STU | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG04204 | hp2 | a0001 | c0001 | t0006 | g0093 | SAS | STU | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | STU | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | STU | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | YRI | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18747 | hp2 | a0001 | c0002 | t0005 | g0020 | EAS | CHB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | YRI | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0024 | AFR | YRI | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18939 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18947 | hp1 | a0002 | c0003 | t0016 | g0125 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18950 | hp1 | a0001 | c0002 | t0039 | g0108 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18950 | hp2 | a0001 | c0002 | t0005 | g0077 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18954 | hp2 | a0001 | c0002 | t0010 | g0071 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18957 | hp1 | a0001 | c0002 | t0005 | g0047 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18964 | hp2 | a0001 | c0002 | t0010 | g0134 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18965 | hp1 | a0001 | c0001 | t0009 | g0064 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18968 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18970 | hp2 | a0001 | c0002 | t0005 | g0121 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18972 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18977 | hp1 | a0001 | c0001 | t0029 | g0065 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18982 | hp2 | a0001 | c0002 | t0005 | g0020 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18984 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18985 | hp1 | a0001 | c0002 | t0036 | g0116 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18986 | hp2 | a0001 | c0001 | t0034 | g0067 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18995 | hp2 | a0002 | c0003 | t0027 | g0090 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18997 | hp1 | a0001 | c0001 | t0033 | g0070 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18998 | hp1 | a0001 | c0002 | t0010 | g0107 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19000 | hp1 | a0001 | c0001 | t0012 | g0013 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19001 | hp1 | a0001 | c0001 | t0012 | g0013 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19005 | hp2 | a0002 | c0003 | t0016 | g0152 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19009 | hp1 | a0001 | c0002 | t0010 | g0015 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19009 | hp2 | a0001 | c0002 | t0005 | g0020 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19010 | hp1 | a0001 | c0002 | t0010 | g0015 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19011 | hp1 | a0001 | c0001 | t0009 | g0018 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19012 | hp1 | a0001 | c0001 | t0012 | g0127 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19030 | hp1 | a0001 | c0001 | t0041 | g0061 | AFR | LWK | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0074 | AFR | LWK | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19043 | hp2 | a0001 | c0001 | t0022 | g0068 | AFR | LWK | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19054 | hp2 | a0001 | c0002 | t0021 | g0046 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19057 | hp2 | a0001 | c0002 | t0005 | g0128 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19058 | hp1 | a0001 | c0001 | t0009 | g0076 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19062 | hp1 | a0001 | c0002 | t0005 | g0047 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19065 | hp1 | a0001 | c0001 | t0012 | g0013 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19068 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19074 | hp2 | a0001 | c0001 | t0009 | g0018 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19075 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19075 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19076 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19077 | hp2 | a0001 | c0001 | t0030 | g0066 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19082 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19083 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19084 | hp2 | a0001 | c0001 | t0009 | g0018 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19085 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19086 | hp2 | a0001 | c0002 | t0010 | g0114 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19088 | hp1 | a0001 | c0001 | t0009 | g0018 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19088 | hp2 | a0001 | c0002 | t0021 | g0046 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19240 | hp1 | a0001 | c0002 | t0010 | g0015 | AFR | YRI | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA19240 | hp2 | a0001 | c0001 | t0025 | g0051 | AFR | YRI | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | ASW | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA20129 | hp2 | a0001 | c0001 | t0011 | g0012 | AFR | ASW | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0095 | EUR | TSI | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0096 | EUR | TSI | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | TSI | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | GIH | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0144 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG02486 | hp2 | a0002 | c0003 | t0020 | g0028 | AFR | ACB | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0062 | AFR | MSL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG06807 | hp1 | a0001 | c0002 | t0005 | g0007 | AFR | USA | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | USA | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18955 | hp1 | a0002 | c0003 | t0015 | g0052 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA21309 | hp1 | a0001 | c0001 | t0026 | g0042 | AFR | LWK | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
NA21309 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | LWK | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0138 | REF | REF | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0014 | REF | REF | TNFSF15_chr9_114779652_114811039 | TNFSF15 | chr9 | 114779652 | 114811039 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114790878 | A | T | 1 | a0002 | 12 | HG00558.hp1 HG02027.hp2 HG02074.hp1 others(9): Show |
missense_variant | MODERATE | c.330T>A | p.Phe110Leu | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 357/6583 | 330/756 | 110/251 | chr9 | 114790878 | |||
chr9:114805939 | C | T | 1 | a0003 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.74G>A | p.Arg25Lys | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/4 | 101/6583 | 74/756 | 25/251 | chr9 | 114805939 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114790605 | T | C | 3 | a0001c0001 a0002c0003 a0003c0004 |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
synonymous_variant | LOW | c.603A>G | p.Val201Val | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 630/6583 | 603/756 | 201/251 | chr9 | 114790605 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114784780 | G | A | 3 | a0002c0003t0015 a0002c0003t0016 a0002c0003t0027 |
9 | HG00558.hp1 HG02027.hp2 HG02074.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5672C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 5672 | chr9 | 114784780 | ||||||
chr9:114784916 | A | T | 1 | a0002c0003t0020 | 3 | HG02486.hp2 HG02615.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5536T>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 5536 | chr9 | 114784916 | ||||||
chr9:114784918 | CA | C | 4 | a0001c0001t0004 a0001c0001t0025 a0001c0001t0038 others(1): Show |
30 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*5533delT | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 5533 | chr9 | 114784918 | ||||||
chr9:114785083 | A | C | 1 | a0001c0001t0026 | 2 | HG01891.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5369T>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 5369 | chr9 | 114785083 | ||||||
chr9:114785091 | G | T | 1 | a0001c0001t0041 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5361C>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 5361 | chr9 | 114785091 | ||||||
chr9:114785257 | G | A | 1 | a0001c0002t0036 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5195C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 5195 | chr9 | 114785257 | ||||||
chr9:114785268 | T | C | 1 | a0001c0001t0034 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5184A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 5184 | chr9 | 114785268 | ||||||
chr9:114785492 | T | C | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(34): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*4960A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 4960 | chr9 | 114785492 | ||||||
chr9:114785825 | C | T | 1 | a0002c0003t0016 | 3 | HG02074.hp1 NA18947.hp1 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4627G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 4627 | chr9 | 114785825 | ||||||
chr9:114786263 | G | A | 1 | a0001c0002t0037 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4189C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 4189 | chr9 | 114786263 | ||||||
chr9:114786708 | C | T | 1 | a0001c0001t0007 | 12 | HG01884.hp2 HG02257.hp2 HG02647.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3744G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 3744 | chr9 | 114786708 | ||||||
chr9:114786801 | A | ACTCG | 4 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0013 others(1): Show |
45 | HG00423.hp1 HG00438.hp1 HG01255.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*3647_*3650dupCGAG | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 3650 | chr9 | 114786801 | ||||||
chr9:114786911 | C | CA | 17 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(14): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*3540dupT | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 3540 | chr9 | 114786911 | ||||||
chr9:114786911 | CA | C | 5 | a0001c0002t0005 a0001c0002t0036 a0001c0002t0037 others(2): Show |
30 | HG00544.hp2 HG00733.hp1 HG01358.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3540delT | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 3540 | chr9 | 114786911 | ||||||
chr9:114786911 | CAA | C | 3 | a0002c0003t0015 a0002c0003t0016 a0002c0003t0020 |
10 | HG00558.hp1 HG02074.hp1 HG02074.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3539_*3540delTT | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 3539 | chr9 | 114786911 | ||||||
chr9:114786957 | T | G | 4 | a0002c0003t0015 a0002c0003t0016 a0002c0003t0020 others(1): Show |
12 | HG00558.hp1 HG02027.hp2 HG02074.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3495A>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 3495 | chr9 | 114786957 | ||||||
chr9:114787047 | G | A | 4 | a0001c0001t0004 a0001c0001t0025 a0001c0001t0038 others(1): Show |
30 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3405C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 3405 | chr9 | 114787047 | ||||||
chr9:114787155 | T | C | 1 | a0001c0001t0025 | 2 | HG03516.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3297A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 3297 | chr9 | 114787155 | ||||||
chr9:114787249 | A | G | 1 | a0001c0001t0033 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3203T>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 3203 | chr9 | 114787249 | ||||||
chr9:114787573 | T | C | 1 | a0001c0001t0035 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2879A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 2879 | chr9 | 114787573 | ||||||
chr9:114787759 | G | A | 1 | a0001c0001t0032 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2693C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 2693 | chr9 | 114787759 | ||||||
chr9:114787887 | A | G | 1 | a0003c0004t0042 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2565T>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 2565 | chr9 | 114787887 | ||||||
chr9:114788060 | T | C | 1 | a0001c0002t0039 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2392A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 2392 | chr9 | 114788060 | ||||||
chr9:114788393 | G | A | 1 | a0001c0002t0028 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2059C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 2059 | chr9 | 114788393 | ||||||
chr9:114788596 | C | G | 1 | a0003c0004t0042 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1856G>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1856 | chr9 | 114788596 | ||||||
chr9:114788680 | G | A | 1 | a0001c0001t0026 | 2 | HG01891.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1772C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1772 | chr9 | 114788680 | ||||||
chr9:114788713 | C | T | 2 | a0001c0001t0022 a0001c0001t0032 |
3 | HG02717.hp1 HG02896.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1739G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1739 | chr9 | 114788713 | ||||||
chr9:114788975 | C | T | 3 | a0001c0001t0011 a0001c0001t0019 a0001c0001t0044 |
12 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1477G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1477 | chr9 | 114788975 | ||||||
chr9:114789173 | C | T | 5 | a0001c0001t0024 a0002c0003t0015 a0002c0003t0016 others(2): Show |
14 | HG00558.hp1 HG02027.hp2 HG02074.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1279G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1279 | chr9 | 114789173 | ||||||
chr9:114789209 | C | T | 1 | a0001c0001t0023 | 2 | HG00323.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1243G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1243 | chr9 | 114789209 | ||||||
chr9:114789239 | C | G | 4 | a0002c0003t0015 a0002c0003t0016 a0002c0003t0020 others(1): Show |
12 | HG00558.hp1 HG02027.hp2 HG02074.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1213G>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1213 | chr9 | 114789239 | ||||||
chr9:114789317 | T | A | 1 | a0002c0003t0016 | 3 | HG02074.hp1 NA18947.hp1 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1135A>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1135 | chr9 | 114789317 | ||||||
chr9:114789318 | TA | T | 1 | a0002c0003t0016 | 3 | HG02074.hp1 NA18947.hp1 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1133delT | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1133 | chr9 | 114789318 | ||||||
chr9:114789323 | T | A | 13 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(10): Show |
149 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*1129A>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1129 | chr9 | 114789323 | ||||||
chr9:114789324 | T | A | 3 | a0001c0001t0043 a0001c0001t0045 a0003c0004t0042 |
3 | HG00735.hp1 HG03130.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1128A>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1128 | chr9 | 114789324 | ||||||
chr9:114789325 | T | A | 1 | a0001c0001t0019 | 3 | HG02818.hp1 HG02965.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1127A>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1127 | chr9 | 114789325 | ||||||
chr9:114789377 | C | T | 1 | a0001c0001t0030 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1075G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1075 | chr9 | 114789377 | ||||||
chr9:114789431 | C | T | 1 | a0001c0001t0029 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1021G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1021 | chr9 | 114789431 | ||||||
chr9:114789438 | C | T | 10 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0022 others(7): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1014G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 1014 | chr9 | 114789438 | ||||||
chr9:114789475 | C | T | 1 | a0001c0001t0018 | 3 | HG02280.hp1 HG02622.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*977G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 977 | chr9 | 114789475 | ||||||
chr9:114789503 | G | A | 2 | a0001c0001t0013 a0001c0001t0017 |
8 | HG01255.hp2 HG01256.hp2 HG01257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*949C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 949 | chr9 | 114789503 | ||||||
chr9:114789542 | G | A | 2 | a0002c0003t0015 a0002c0003t0027 |
6 | HG00558.hp1 HG02027.hp2 HG02074.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*910C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 910 | chr9 | 114789542 | ||||||
chr9:114789792 | G | C | 2 | a0002c0003t0015 a0002c0003t0027 |
6 | HG00558.hp1 HG02027.hp2 HG02074.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*660C>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 660 | chr9 | 114789792 | ||||||
chr9:114789911 | T | C | 7 | a0001c0001t0026 a0001c0001t0044 a0001c0001t0045 others(4): Show |
16 | HG00558.hp1 HG01243.hp2 HG01891.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*541A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 541 | chr9 | 114789911 | ||||||
chr9:114789961 | C | T | 2 | a0001c0002t0021 a0001c0002t0028 |
3 | HG00673.hp1 NA19054.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*491G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 491 | chr9 | 114789961 | ||||||
chr9:114790153 | C | T | 1 | a0001c0001t0017 | 3 | HG01256.hp2 HG01258.hp2 HG01934.hp2 |
3_prime_UTR_variant | MODIFIER | c.*299G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 299 | chr9 | 114790153 | ||||||
chr9:114790411 | C | T | 1 | a0002c0003t0016 | 3 | HG02074.hp1 NA18947.hp1 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*41G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 4/4 | 41 | chr9 | 114790411 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114790942 | G | T | 9 | a0002c0003t0015g0052 a0002c0003t0015g0089 a0002c0003t0015g0147 others(6): Show |
12 | HG00558.hp1 HG02027.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.302-36C>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114790942 | |||||||
chr9:114790969 | T | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.302-63A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114790969 | |||||||
chr9:114791130 | T | C | 1 | a0001c0002t0005g0121 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.302-224A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114791130 | |||||||
chr9:114791150 | A | G | 1 | a0001c0002t0010g0107 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.302-244T>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114791150 | |||||||
chr9:114791216 | C | T | 1 | a0001c0001t0034g0067 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.302-310G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114791216 | |||||||
chr9:114791603 | G | A | 3 | a0002c0003t0016g0125 a0002c0003t0016g0151 a0002c0003t0016g0152 |
3 | HG02074.hp1 NA18947.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.302-697C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114791603 | |||||||
chr9:114791789 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0027 others(13): Show |
73 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.301+618T>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114791789 | |||||||
chr9:114791821 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0009g0076 a0001c0001t0029g0065 others(1): Show |
39 | HG00423.hp2 HG00609.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.301+586G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114791821 | |||||||
chr9:114792007 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.301+400C>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792007 | |||||||
chr9:114792057 | C | T | 1 | a0001c0001t0006g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.301+350G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792057 | |||||||
chr9:114792061 | C | G | 1 | a0002c0003t0020g0028 | 3 | HG02486.hp2 HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.301+346G>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792061 | |||||||
chr9:114792168 | A | C | 1 | a0001c0001t0044g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.301+239T>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792168 | |||||||
chr9:114792209 | A | G | 6 | a0001c0001t0006g0009 a0001c0001t0006g0025 a0001c0001t0006g0093 others(3): Show |
16 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.301+198T>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792209 | |||||||
chr9:114792217 | ATG | A | 4 | a0002c0003t0015g0089 a0002c0003t0016g0125 a0002c0003t0016g0152 others(1): Show |
4 | HG00558.hp1 HG02027.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+188_301+189del others(2): Show |
TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792217 | |||||||
chr9:114792222 | TGTACACA others(1): Show |
T | 1 | a0002c0003t0020g0028 | 3 | HG02486.hp2 HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.301+177_301+184del others(8): Show |
TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792222 | |||||||
chr9:114792223 | G | A | 1 | a0002c0003t0016g0151 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.301+184C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792223 | |||||||
chr9:114792224 | T | C | 1 | a0002c0003t0016g0151 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.301+183A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792224 | |||||||
chr9:114792224 | T | TAC | 4 | a0001c0002t0002g0001 a0001c0002t0002g0032 a0001c0002t0002g0083 others(1): Show |
8 | HG00738.hp1 HG01074.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.301+181_301+182dup others(2): Show |
TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792224 | |||||||
chr9:114792224 | TAC | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0006g0009 others(9): Show |
17 | HG01175.hp1 HG01515.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.301+181_301+182del others(2): Show |
TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792224 | |||||||
chr9:114792224 | TACAC | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0050 others(21): Show |
64 | HG00099.hp2 HG00544.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.301+179_301+182del others(4): Show |
TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792224 | |||||||
chr9:114792224 | TACACAC | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0022 others(15): Show |
37 | HG00099.hp1 HG00323.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.301+177_301+182del others(6): Show |
TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792224 | |||||||
chr9:114792224 | TACACACA others(1): Show |
T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0004g0144 others(10): Show |
24 | HG01123.hp1 HG01496.hp2 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.301+175_301+182del others(8): Show |
TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792224 | |||||||
chr9:114792224 | TACACACA others(3): Show |
T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0027 others(46): Show |
144 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.301+173_301+182del others(10): Show |
TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792224 | |||||||
chr9:114792224 | TACACACA others(5): Show |
T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0008g0141 others(1): Show |
14 | HG00738.hp2 NA18953.hp2 NA18954.hp1 others(11): Show |
intron_variant | MODIFIER | c.301+171_301+182del others(12): Show |
TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792224 | |||||||
chr9:114792224 | TACACACA others(7): Show |
T | 2 | a0001c0001t0001g0002 a0001c0001t0009g0018 |
2 | NA19011.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.301+169_301+182del others(14): Show |
TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792224 | |||||||
chr9:114792224 | TACACACA others(13): Show |
T | 5 | a0001c0001t0011g0012 a0001c0001t0011g0038 a0001c0001t0011g0120 others(2): Show |
11 | HG01109.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.301+163_301+182del others(20): Show |
TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 3/3 | chr9 | 114792224 | |||||||
chr9:114792511 | C | T | 1 | a0001c0001t0001g0033 | 3 | HG03669.hp2 HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.254-57G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 2/3 | chr9 | 114792511 | |||||||
chr9:114792558 | A | C | 1 | a0001c0001t0026g0042 | 2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.254-104T>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 2/3 | chr9 | 114792558 | |||||||
chr9:114792603 | T | C | 8 | a0002c0003t0015g0052 a0002c0003t0015g0089 a0002c0003t0015g0147 others(5): Show |
9 | HG00558.hp1 HG02027.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.254-149A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 2/3 | chr9 | 114792603 | |||||||
chr9:114792619 | G | A | 3 | a0001c0001t0007g0008 a0001c0001t0007g0041 a0001c0001t0007g0074 |
12 | HG01884.hp2 HG02257.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.254-165C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 2/3 | chr9 | 114792619 | |||||||
chr9:114792712 | C | T | 1 | a0001c0001t0003g0043 | 2 | NA18974.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.254-258G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 2/3 | chr9 | 114792712 | |||||||
chr9:114792802 | C | G | 1 | a0001c0002t0002g0106 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.254-348G>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 2/3 | chr9 | 114792802 | |||||||
chr9:114792881 | C | T | 1 | a0001c0001t0006g0059 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.254-427G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 2/3 | chr9 | 114792881 | |||||||
chr9:114793298 | G | A | 1 | a0001c0001t0026g0042 | 2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.253+228C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 2/3 | chr9 | 114793298 | |||||||
chr9:114793494 | C | T | 17 | a0001c0001t0003g0005 a0001c0001t0003g0029 a0001c0001t0003g0030 others(14): Show |
43 | HG00423.hp1 HG00438.hp1 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.253+32G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 2/3 | chr9 | 114793494 | |||||||
chr9:114793782 | T | C | 1 | a0001c0002t0005g0082 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.211-214A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114793782 | |||||||
chr9:114793824 | C | T | 9 | a0002c0003t0015g0052 a0002c0003t0015g0089 a0002c0003t0015g0147 others(6): Show |
12 | HG00558.hp1 HG02027.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.211-256G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114793824 | |||||||
chr9:114793884 | T | A | 1 | a0003c0004t0042g0054 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.211-316A>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114793884 | |||||||
chr9:114793980 | G | A | 1 | a0001c0001t0006g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.211-412C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114793980 | |||||||
chr9:114794111 | C | T | 1 | a0002c0003t0015g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.211-543G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114794111 | |||||||
chr9:114794285 | C | G | 1 | a0001c0002t0036g0116 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.211-717G>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114794285 | |||||||
chr9:114794521 | C | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0022 others(11): Show |
51 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.211-953G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114794521 | |||||||
chr9:114794831 | C | T | 2 | a0001c0001t0006g0025 a0001c0001t0006g0093 |
4 | HG01192.hp1 HG01934.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-1263G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114794831 | |||||||
chr9:114794895 | T | C | 1 | a0002c0003t0020g0028 | 3 | HG02486.hp2 HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.211-1327A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114794895 | |||||||
chr9:114795013 | C | T | 1 | a0001c0001t0001g0050 | 2 | HG00099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.211-1445G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795013 | |||||||
chr9:114795223 | C | T | 1 | a0001c0001t0001g0022 | 4 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-1655G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795223 | |||||||
chr9:114795301 | A | C | 3 | a0002c0003t0016g0125 a0002c0003t0016g0151 a0002c0003t0016g0152 |
3 | HG02074.hp1 NA18947.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.211-1733T>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795301 | |||||||
chr9:114795371 | G | A | 3 | a0001c0001t0007g0008 a0001c0001t0007g0041 a0001c0001t0007g0074 |
12 | HG01884.hp2 HG02257.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.211-1803C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795371 | |||||||
chr9:114795428 | A | G | 1 | a0001c0001t0009g0064 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.211-1860T>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795428 | |||||||
chr9:114795499 | A | T | 1 | a0001c0002t0010g0105 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.211-1931T>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795499 | |||||||
chr9:114795592 | G | T | 11 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0053 others(8): Show |
30 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.211-2024C>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795592 | |||||||
chr9:114795706 | G | A | 19 | a0001c0001t0003g0043 a0001c0001t0003g0092 a0001c0001t0011g0120 others(16): Show |
44 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.211-2138C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795706 | |||||||
chr9:114795717 | T | A | 1 | a0001c0002t0002g0111 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.211-2149A>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795717 | |||||||
chr9:114795739 | A | G | 1 | a0001c0001t0003g0088 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.211-2171T>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795739 | |||||||
chr9:114795750 | C | T | 6 | a0001c0001t0011g0012 a0001c0001t0011g0038 a0001c0001t0014g0036 others(3): Show |
13 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.211-2182G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795750 | |||||||
chr9:114795794 | C | T | 1 | a0001c0001t0003g0087 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.211-2226G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795794 | |||||||
chr9:114795811 | G | A | 3 | a0002c0003t0015g0147 a0002c0003t0016g0151 a0002c0003t0016g0152 |
3 | HG02074.hp1 HG02074.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.211-2243C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795811 | |||||||
chr9:114795844 | G | A | 1 | a0001c0002t0002g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.211-2276C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795844 | |||||||
chr9:114795925 | G | A | 2 | a0001c0001t0006g0023 a0001c0001t0041g0061 |
4 | HG01109.hp2 HG03225.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-2357C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795925 | |||||||
chr9:114795981 | C | T | 2 | a0001c0001t0004g0011 a0001c0001t0004g0146 |
7 | HG02258.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.211-2413G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114795981 | |||||||
chr9:114796034 | C | T | 1 | a0001c0001t0004g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.211-2466G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114796034 | |||||||
chr9:114796188 | C | T | 1 | a0001c0002t0002g0045 | 2 | NA18942.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.211-2620G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114796188 | |||||||
chr9:114796423 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.211-2855G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114796423 | |||||||
chr9:114796575 | G | A | 1 | a0001c0002t0002g0083 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.211-3007C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114796575 | |||||||
chr9:114796737 | C | T | 1 | a0001c0002t0005g0128 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.211-3169G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114796737 | |||||||
chr9:114796738 | G | A | 1 | a0001c0001t0007g0008 | 9 | HG01884.hp2 HG02257.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.211-3170C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114796738 | |||||||
chr9:114796822 | T | C | 1 | a0001c0001t0006g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.211-3254A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114796822 | |||||||
chr9:114796835 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0136 |
3 | HG00099.hp1 HG01433.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.211-3267T>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114796835 | |||||||
chr9:114797304 | T | C | 5 | a0001c0002t0002g0150 a0002c0003t0015g0052 a0002c0003t0015g0147 others(2): Show |
6 | HG02074.hp1 HG02074.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-3736A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114797304 | |||||||
chr9:114797349 | A | C | 1 | a0001c0001t0006g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.211-3781T>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114797349 | |||||||
chr9:114797395 | C | T | 1 | a0001c0001t0006g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.211-3827G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114797395 | |||||||
chr9:114797456 | G | C | 1 | a0001c0001t0004g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.211-3888C>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114797456 | |||||||
chr9:114797565 | A | G | 2 | a0001c0002t0002g0103 a0001c0002t0002g0113 |
2 | HG02027.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.211-3997T>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114797565 | |||||||
chr9:114797683 | T | A | 13 | a0001c0001t0006g0009 a0001c0001t0006g0023 a0001c0001t0006g0025 others(10): Show |
26 | HG01109.hp2 HG01192.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.211-4115A>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114797683 | |||||||
chr9:114797726 | T | TCATGG | 5 | a0001c0002t0002g0150 a0002c0003t0015g0052 a0002c0003t0015g0147 others(2): Show |
6 | HG02074.hp1 HG02074.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-4163_211-4159d others(7): Show |
TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114797726 | |||||||
chr9:114797949 | A | T | 1 | a0001c0002t0002g0102 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.211-4381T>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114797949 | |||||||
chr9:114797985 | A | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0022 others(12): Show |
52 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.211-4417T>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114797985 | |||||||
chr9:114798039 | A | G | 1 | a0001c0001t0003g0029 | 3 | HG02602.hp1 HG02735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.211-4471T>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114798039 | |||||||
chr9:114798258 | G | T | 4 | a0001c0001t0004g0006 a0001c0001t0004g0035 a0001c0001t0004g0053 others(1): Show |
18 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.211-4690C>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114798258 | |||||||
chr9:114798315 | T | C | 1 | a0001c0002t0002g0100 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.211-4747A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114798315 | |||||||
chr9:114798340 | G | A | 1 | a0001c0001t0022g0085 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.211-4772C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114798340 | |||||||
chr9:114798374 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.211-4806A>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114798374 | |||||||
chr9:114798514 | C | T | 1 | a0001c0001t0009g0137 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.211-4946G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114798514 | |||||||
chr9:114798537 | G | T | 1 | a0001c0001t0018g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.211-4969C>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114798537 | |||||||
chr9:114798622 | C | T | 5 | a0001c0002t0002g0150 a0002c0003t0015g0052 a0002c0003t0015g0147 others(2): Show |
6 | HG02074.hp1 HG02074.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-5054G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114798622 | |||||||
chr9:114798680 | A | G | 30 | a0001c0001t0001g0027 a0001c0001t0003g0005 a0001c0001t0003g0029 others(27): Show |
65 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.211-5112T>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114798680 | |||||||
chr9:114798702 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0022 others(12): Show |
52 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.211-5134G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114798702 | |||||||
chr9:114798747 | T | C | 1 | a0001c0002t0002g0112 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.211-5179A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114798747 | |||||||
chr9:114798812 | T | G | 1 | a0001c0002t0002g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.211-5244A>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114798812 | |||||||
chr9:114799068 | G | A | 1 | a0001c0001t0012g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.211-5500C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114799068 | |||||||
chr9:114799184 | T | C | 1 | a0001c0002t0010g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.211-5616A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114799184 | |||||||
chr9:114799221 | T | C | 5 | a0001c0002t0002g0150 a0002c0003t0015g0052 a0002c0003t0015g0147 others(2): Show |
6 | HG02074.hp1 HG02074.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-5653A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114799221 | |||||||
chr9:114799260 | G | A | 1 | a0001c0001t0007g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.211-5692C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114799260 | |||||||
chr9:114799390 | T | C | 1 | a0001c0001t0006g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.211-5822A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114799390 | |||||||
chr9:114799594 | G | A | 1 | a0001c0001t0011g0038 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.211-6026C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114799594 | |||||||
chr9:114799711 | G | A | 1 | a0001c0002t0002g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.210+6092C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114799711 | |||||||
chr9:114799780 | T | C | 1 | a0001c0002t0002g0115 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.210+6023A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114799780 | |||||||
chr9:114799910 | T | G | 3 | a0001c0001t0003g0029 a0001c0001t0003g0095 a0001c0002t0002g0096 |
5 | HG02602.hp1 HG02735.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+5893A>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114799910 | |||||||
chr9:114799920 | A | T | 1 | a0001c0002t0002g0100 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.210+5883T>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114799920 | |||||||
chr9:114800328 | C | T | 1 | a0001c0001t0007g0008 | 9 | HG01884.hp2 HG02257.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+5475G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114800328 | |||||||
chr9:114800373 | G | A | 1 | a0001c0002t0002g0100 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.210+5430C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114800373 | |||||||
chr9:114800519 | A | C | 1 | a0001c0002t0002g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.210+5284T>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114800519 | |||||||
chr9:114800622 | T | C | 1 | a0001c0001t0004g0053 | 2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.210+5181A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114800622 | |||||||
chr9:114800715 | G | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.210+5088C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114800715 | |||||||
chr9:114800926 | G | C | 1 | a0001c0002t0002g0100 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.210+4877C>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114800926 | |||||||
chr9:114800927 | C | G | 1 | a0001c0002t0002g0100 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.210+4876G>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114800927 | |||||||
chr9:114800928 | C | T | 1 | a0001c0001t0007g0008 | 9 | HG01884.hp2 HG02257.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+4875G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114800928 | |||||||
chr9:114800974 | G | A | 1 | a0001c0002t0002g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.210+4829C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114800974 | |||||||
chr9:114801017 | G | A | 1 | a0001c0001t0014g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.210+4786C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114801017 | |||||||
chr9:114801183 | G | T | 1 | a0001c0001t0017g0026 | 3 | HG01256.hp2 HG01258.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.210+4620C>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114801183 | |||||||
chr9:114801207 | T | G | 1 | a0001c0001t0006g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.210+4596A>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114801207 | |||||||
chr9:114801275 | G | A | 19 | a0001c0001t0001g0027 a0001c0001t0003g0005 a0001c0001t0003g0029 others(16): Show |
46 | HG00558.hp1 HG01255.hp2 HG01256.hp2 others(43): Show |
intron_variant | MODIFIER | c.210+4528C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114801275 | |||||||
chr9:114801355 | C | G | 3 | a0001c0002t0002g0150 a0002c0003t0016g0151 a0002c0003t0016g0152 |
3 | HG02074.hp1 NA18949.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.210+4448G>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114801355 | |||||||
chr9:114801395 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.210+4408C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114801395 | |||||||
chr9:114801407 | T | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.210+4396A>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114801407 | |||||||
chr9:114801546 | C | T | 1 | a0001c0002t0002g0078 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.210+4257G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114801546 | |||||||
chr9:114801667 | G | A | 1 | a0001c0001t0009g0076 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.210+4136C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114801667 | |||||||
chr9:114801854 | G | A | 1 | a0001c0001t0011g0038 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.210+3949C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114801854 | |||||||
chr9:114802011 | T | G | 1 | a0001c0001t0006g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.210+3792A>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114802011 | |||||||
chr9:114802276 | G | A | 1 | a0003c0004t0042g0054 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.210+3527C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114802276 | |||||||
chr9:114802398 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.210+3405C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114802398 | |||||||
chr9:114802410 | G | A | 1 | a0001c0002t0005g0047 | 2 | NA18957.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.210+3393C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114802410 | |||||||
chr9:114802595 | T | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.210+3208A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114802595 | |||||||
chr9:114802683 | T | A | 1 | a0001c0002t0002g0123 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.210+3120A>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114802683 | |||||||
chr9:114802743 | CTGGTATA others(22): Show |
C | 1 | a0001c0002t0002g0032 | 3 | NA18979.hp1 NA18980.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.210+3031_210+3059d others(31): Show |
TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114802743 | |||||||
chr9:114802773 | T | A | 1 | a0001c0002t0002g0032 | 3 | NA18979.hp1 NA18980.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.210+3030A>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114802773 | |||||||
chr9:114803158 | G | A | 1 | a0003c0004t0042g0054 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.210+2645C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114803158 | |||||||
chr9:114803241 | C | G | 1 | a0001c0001t0006g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.210+2562G>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114803241 | |||||||
chr9:114803286 | G | A | 1 | a0001c0001t0012g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.210+2517C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114803286 | |||||||
chr9:114803287 | C | T | 1 | a0001c0001t0012g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.210+2516G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114803287 | |||||||
chr9:114803289 | T | C | 1 | a0001c0001t0012g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.210+2514A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114803289 | |||||||
chr9:114803292 | G | A | 1 | a0001c0001t0008g0098 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.210+2511C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114803292 | |||||||
chr9:114803423 | T | C | 1 | a0001c0001t0003g0124 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.210+2380A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114803423 | |||||||
chr9:114803476 | T | C | 2 | a0001c0002t0002g0126 a0002c0003t0016g0125 |
2 | NA18947.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.210+2327A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114803476 | |||||||
chr9:114804004 | G | A | 1 | a0001c0001t0026g0042 | 2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.210+1799C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804004 | |||||||
chr9:114804053 | C | A | 1 | a0001c0001t0006g0099 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.210+1750G>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804053 | |||||||
chr9:114804111 | C | A | 3 | a0001c0002t0002g0150 a0002c0003t0016g0151 a0002c0003t0016g0152 |
3 | HG02074.hp1 NA18949.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.210+1692G>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804111 | |||||||
chr9:114804139 | A | C | 2 | a0001c0001t0006g0133 a0001c0001t0026g0042 |
3 | HG01891.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.210+1664T>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804139 | |||||||
chr9:114804160 | A | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.210+1643T>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804160 | |||||||
chr9:114804276 | G | A | 1 | a0001c0001t0012g0127 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.210+1527C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804276 | |||||||
chr9:114804291 | G | A | 1 | a0001c0001t0007g0008 | 9 | HG01884.hp2 HG02257.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+1512C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804291 | |||||||
chr9:114804394 | T | C | 1 | a0001c0002t0005g0128 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.210+1409A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804394 | |||||||
chr9:114804701 | A | G | 1 | a0001c0002t0005g0077 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.210+1102T>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804701 | |||||||
chr9:114804733 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0048 others(24): Show |
100 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.210+1070G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804733 | |||||||
chr9:114804741 | C | T | 9 | a0001c0001t0006g0023 a0001c0001t0006g0040 a0001c0001t0006g0059 others(6): Show |
13 | HG01109.hp2 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.210+1062G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804741 | |||||||
chr9:114804768 | T | G | 1 | a0001c0001t0001g0048 | 2 | NA18975.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.210+1035A>C | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804768 | |||||||
chr9:114804786 | G | A | 1 | a0001c0002t0005g0129 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.210+1017C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804786 | |||||||
chr9:114804843 | G | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0136 |
6 | HG00099.hp1 HG01070.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+960C>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804843 | |||||||
chr9:114804857 | T | C | 30 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0022 others(27): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.210+946A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114804857 | |||||||
chr9:114805057 | G | A | 1 | a0001c0001t0003g0131 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.210+746C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114805057 | |||||||
chr9:114805143 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.210+660G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114805143 | |||||||
chr9:114805367 | G | A | 1 | a0001c0001t0035g0132 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.210+436C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114805367 | |||||||
chr9:114805428 | T | C | 1 | a0001c0001t0006g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.210+375A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114805428 | |||||||
chr9:114805477 | G | A | 1 | a0001c0002t0010g0134 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.210+326C>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114805477 | |||||||
chr9:114805527 | C | T | 5 | a0001c0001t0011g0012 a0001c0001t0011g0038 a0001c0001t0014g0036 others(2): Show |
12 | HG01109.hp1 HG01496.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.210+276G>A | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114805527 | |||||||
chr9:114805697 | T | C | 1 | a0001c0002t0002g0135 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.210+106A>G | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114805697 | |||||||
chr9:114805769 | C | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0022 others(26): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.210+34G>T | TNFSF15 | ENSG00000181634.8 | transcript | ENST00000374045.5 | protein_coding | 1/3 | chr9 | 114805769 |