Item | Value |
---|---|
geneid | 8742 |
ensemblid | ENSG00000239697.12 |
hgncid | 11927 |
symbol | TNFSF12 |
name | TNF superfamily member 12 |
refseq_nuc | NM_003809.3 |
refseq_prot | NP_003800.1 |
ensembl_nuc | ENST00000293825.11 |
ensembl_prot | ENSP00000293825.6 |
mane_status | MANE Select |
chr | chr17 |
start | 7549058 |
end | 7557881 |
strand | + |
ver | v1.2 |
region | chr17:7549058-7557881 |
region5000 | chr17:7544058-7562881 |
regionname0 | TNFSF12_chr17_7549058_7557881 |
regionname5000 | TNFSF12_chr17_7544058_7562881 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 747 | 190 | 30 | 41 | 88 | 4 | 27 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | ATGGC others(742): Show |
chr17 | 7544058 | 7562881 | ||
a0001c0002 | 1/0 | 747 | 153 | 29 | 22 | 85 | 5 | 11 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | ATGGC others(742): Show |
chr17 | 7544058 | 7562881 | ||
a0001c0003 | 0/1 | 747 | 31 | 6 | 15 | 0 | 5 | 4 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | ATGGC others(742): Show |
chr17 | 7544058 | 7562881 | ||
a0001c0004 | 0/0 | 747 | 28 | 1 | 2 | 18 | 2 | 5 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | ATGGC others(742): Show |
chr17 | 7544058 | 7562881 | ||
a0001c0005 | 0/0 | 747 | 17 | 15 | 1 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | ATGGC others(742): Show |
chr17 | 7544058 | 7562881 | ||
a0001c0006 | 0/0 | 747 | 9 | 7 | 1 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | ATGGC others(742): Show |
chr17 | 7544058 | 7562881 | ||
a0001c0007 | 0/0 | 747 | 7 | 7 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | ATGGC others(742): Show |
chr17 | 7544058 | 7562881 | ||
a0001c0008 | 0/0 | 747 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | ATGGC others(742): Show |
chr17 | 7544058 | 7562881 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1377 | 51 | 4 | 12 | 31 | 0 | 4 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0001t0002 | 0/0 | 1377 | 106 | 4 | 20 | 57 | 4 | 21 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0001t0004 | 0/0 | 1377 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0001t0005 | 0/0 | 1377 | 21 | 21 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0001t0007 | 0/0 | 1377 | 8 | 0 | 8 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0001t0008 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0001t0009 | 0/0 | 1377 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0001t0011 | 0/0 | 1377 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0002t0001 | 1/0 | 1377 | 114 | 20 | 19 | 68 | 2 | 4 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0002t0002 | 0/0 | 1377 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0002t0003 | 0/0 | 1377 | 37 | 8 | 3 | 16 | 3 | 7 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0002t0010 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0003t0001 | 0/1 | 1377 | 27 | 2 | 15 | 0 | 5 | 4 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0003t0003 | 0/0 | 1377 | 4 | 4 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0004t0002 | 0/0 | 1377 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0004t0004 | 0/0 | 1377 | 27 | 1 | 2 | 18 | 2 | 4 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0005t0001 | 0/0 | 1377 | 2 | 1 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0005t0003 | 0/0 | 1377 | 8 | 8 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0005t0006 | 0/0 | 1377 | 6 | 5 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0005t0012 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0006t0001 | 0/0 | 1377 | 4 | 4 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0006t0003 | 0/0 | 1377 | 2 | 1 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0006t0006 | 0/0 | 1377 | 3 | 2 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0007t0001 | 0/0 | 1377 | 7 | 7 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
a0001c0008t0003 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | CTCTC others(1372): Show |
chr17 | 7544058 | 7562881 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 23 | 0 | 6 | 14 | 0 | 3 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0001g0006 | 0/0 | 8 | 1 | 3 | 4 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0001g0018 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0001g0031 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0002 | 0/0 | 26 | 1 | 7 | 9 | 3 | 6 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0007 | 0/0 | 11 | 0 | 3 | 5 | 0 | 3 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0017 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0022 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0023 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0035 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0005g0001 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0005g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0005g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0007g0001 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0007g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0009g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0001t0011g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0003 | 0/0 | 19 | 0 | 4 | 14 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0004 | 0/0 | 19 | 0 | 3 | 15 | 1 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0005 | 0/0 | 14 | 4 | 4 | 3 | 1 | 2 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0008 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0013 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0015 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0020 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0028 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0051 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0010 | 0/0 | 7 | 1 | 1 | 2 | 0 | 3 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0011 | 0/0 | 7 | 1 | 1 | 4 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0016 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0033 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0002t0010g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0025 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0062 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0003t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0004t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0004t0004g0012 | 0/0 | 8 | 0 | 0 | 3 | 2 | 3 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0004t0004g0021 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0004t0004g0036 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0004t0004g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0004t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0004t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0004t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0004t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0004t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0004t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0004t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0004t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0004t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0005t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0005t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0005t0003g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0005t0003g0034 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0005t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0005t0006g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0005t0006g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0005t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0005t0012g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0006t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0006t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0006t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0006t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0006t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0006t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0006t0006g0027 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0007t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0007t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
a0001c0008t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0003 | g0114 | EUR | GBR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0005 | EUR | GBR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0069 | EUR | FIN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | FIN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0064 | EUR | FIN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00544 | hp1 | a0001 | c0004 | t0004 | g0021 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00544 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00558 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00597 | hp1 | a0001 | c0002 | t0003 | g0110 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00673 | hp2 | a0001 | c0004 | t0004 | g0036 | EAS | CHS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00733 | hp1 | a0001 | c0003 | t0001 | g0057 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0154 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01070 | hp1 | a0001 | c0002 | t0003 | g0010 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01071 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01081 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0055 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0056 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01167 | hp1 | a0001 | c0005 | t0006 | g0039 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0149 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01168 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01169 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01175 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0068 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01192 | hp1 | a0001 | c0003 | t0001 | g0025 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01192 | hp2 | a0001 | c0004 | t0004 | g0164 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01243 | hp1 | a0001 | c0004 | t0004 | g0166 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01243 | hp2 | a0001 | c0006 | t0006 | g0027 | AMR | PUR | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0024 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01256 | hp1 | a0001 | c0003 | t0001 | g0058 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01257 | hp1 | a0001 | c0003 | t0001 | g0025 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0059 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01358 | hp1 | a0001 | c0003 | t0001 | g0066 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01516 | hp1 | a0001 | c0002 | t0003 | g0113 | EUR | IBS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01516 | hp2 | a0001 | c0004 | t0004 | g0012 | EUR | IBS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01517 | hp1 | a0001 | c0002 | t0003 | g0112 | EUR | IBS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0037 | EUR | IBS | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01884 | hp1 | a0001 | c0005 | t0003 | g0019 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01884 | hp2 | a0001 | c0007 | t0001 | g0014 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01934 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01952 | hp1 | a0001 | c0003 | t0001 | g0060 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0024 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01981 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01993 | hp2 | a0001 | c0001 | t0007 | g0006 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02074 | hp2 | a0001 | c0002 | t0003 | g0111 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02135 | hp2 | a0001 | c0002 | t0003 | g0011 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02145 | hp1 | a0001 | c0002 | t0003 | g0033 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0067 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02148 | hp1 | a0001 | c0003 | t0001 | g0063 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0156 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CDX | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02257 | hp2 | a0001 | c0008 | t0003 | g0026 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02258 | hp1 | a0001 | c0002 | t0010 | g0038 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02280 | hp1 | a0001 | c0005 | t0006 | g0039 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02523 | hp1 | a0001 | c0004 | t0004 | g0012 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02572 | hp1 | a0001 | c0007 | t0001 | g0014 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02615 | hp2 | a0001 | c0005 | t0012 | g0140 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02622 | hp1 | a0001 | c0007 | t0001 | g0013 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0072 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02647 | hp1 | a0001 | c0005 | t0003 | g0019 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02647 | hp2 | a0001 | c0005 | t0006 | g0029 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02683 | hp1 | a0001 | c0001 | t0009 | g0002 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02698 | hp1 | a0001 | c0002 | t0003 | g0010 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02717 | hp1 | a0001 | c0006 | t0006 | g0027 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02717 | hp2 | a0001 | c0005 | t0003 | g0019 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02723 | hp2 | a0001 | c0005 | t0006 | g0029 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02735 | hp1 | a0001 | c0004 | t0004 | g0012 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02735 | hp2 | a0001 | c0004 | t0004 | g0012 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02738 | hp1 | a0001 | c0003 | t0001 | g0070 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02809 | hp1 | a0001 | c0006 | t0001 | g0078 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02818 | hp2 | a0001 | c0005 | t0001 | g0019 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02886 | hp2 | a0001 | c0005 | t0003 | g0034 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02895 | hp1 | a0001 | c0002 | t0003 | g0026 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02896 | hp1 | a0001 | c0003 | t0003 | g0014 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02896 | hp2 | a0001 | c0002 | t0003 | g0026 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02897 | hp2 | a0001 | c0003 | t0003 | g0013 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02922 | hp1 | a0001 | c0005 | t0003 | g0034 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02970 | hp1 | a0001 | c0006 | t0001 | g0084 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0098 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0094 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02976 | hp2 | a0001 | c0006 | t0001 | g0079 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03017 | hp1 | a0001 | c0002 | t0003 | g0011 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | MSL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | MSL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0081 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03209 | hp1 | a0001 | c0005 | t0003 | g0115 | AFR | MSL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03209 | hp2 | a0001 | c0007 | t0001 | g0014 | AFR | MSL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03225 | hp1 | a0001 | c0007 | t0001 | g0014 | AFR | MSL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | MSL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03239 | hp1 | a0001 | c0003 | t0001 | g0054 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | MSL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03453 | hp2 | a0001 | c0004 | t0004 | g0162 | AFR | MSL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0086 | AFR | MSL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | MSL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | ESN | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03540 | hp1 | a0001 | c0007 | t0001 | g0013 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03579 | hp1 | a0001 | c0003 | t0003 | g0085 | AFR | MSL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | MSL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03654 | hp1 | a0001 | c0002 | t0003 | g0109 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | STU | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03688 | hp2 | a0001 | c0006 | t0003 | g0077 | SAS | STU | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03831 | hp1 | a0001 | c0002 | t0003 | g0010 | SAS | BEB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03831 | hp2 | a0001 | c0002 | t0003 | g0107 | SAS | BEB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | BEB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0025 | SAS | BEB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | BEB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03927 | hp2 | a0001 | c0002 | t0003 | g0010 | SAS | BEB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03942 | hp1 | a0001 | c0004 | t0004 | g0021 | SAS | BEB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | BEB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG04115 | hp1 | a0001 | c0001 | t0011 | g0032 | SAS | STU | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | STU | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | BEB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG04184 | hp2 | a0001 | c0003 | t0001 | g0065 | SAS | BEB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | STU | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | STU | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG04204 | hp1 | a0001 | c0002 | t0003 | g0108 | SAS | STU | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG04204 | hp2 | a0001 | c0004 | t0004 | g0012 | SAS | STU | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | STU | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | STU | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18522 | hp1 | a0001 | c0005 | t0006 | g0029 | AFR | YRI | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18522 | hp2 | a0001 | c0005 | t0003 | g0034 | AFR | YRI | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18612 | hp2 | a0001 | c0004 | t0004 | g0036 | EAS | CHB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18747 | hp1 | a0001 | c0002 | t0003 | g0010 | EAS | CHB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | CHB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18906 | hp1 | a0001 | c0006 | t0001 | g0083 | AFR | YRI | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | YRI | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18946 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18948 | hp1 | a0001 | c0004 | t0004 | g0053 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18956 | hp2 | a0001 | c0005 | t0001 | g0165 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18957 | hp2 | a0001 | c0004 | t0004 | g0021 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18961 | hp1 | a0001 | c0004 | t0004 | g0158 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18963 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18967 | hp1 | a0001 | c0004 | t0004 | g0161 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18975 | hp2 | a0001 | c0004 | t0004 | g0012 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18980 | hp1 | a0001 | c0004 | t0004 | g0012 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18983 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18984 | hp1 | a0001 | c0004 | t0004 | g0021 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18992 | hp2 | a0001 | c0004 | t0004 | g0163 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18994 | hp2 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18995 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18997 | hp1 | a0001 | c0004 | t0004 | g0155 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19004 | hp1 | a0001 | c0004 | t0004 | g0053 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19011 | hp1 | a0001 | c0004 | t0004 | g0159 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19030 | hp2 | a0001 | c0003 | t0003 | g0082 | AFR | LWK | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19055 | hp1 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19057 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19060 | hp1 | a0001 | c0004 | t0004 | g0021 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19066 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19067 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19077 | hp2 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19080 | hp2 | a0001 | c0004 | t0004 | g0160 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19091 | hp2 | a0001 | c0004 | t0004 | g0036 | EAS | JPT | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0041 | AFR | YRI | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | YRI | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | ASW | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ASW | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA20752 | hp1 | a0001 | c0004 | t0004 | g0012 | EUR | TSI | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0023 | EUR | TSI | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA20805 | hp1 | a0001 | c0003 | t0001 | g0037 | EUR | TSI | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0024 | EUR | TSI | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA20905 | hp1 | a0001 | c0004 | t0002 | g0157 | SAS | GIH | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0071 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02109 | hp2 | a0001 | c0002 | t0003 | g0011 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02486 | hp2 | a0001 | c0005 | t0006 | g0090 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG02559 | hp2 | a0001 | c0006 | t0006 | g0027 | AFR | ACB | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | MSL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | MSL | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG06807 | hp1 | a0001 | c0005 | t0003 | g0019 | AFR | USA | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
HG06807 | hp2 | a0001 | c0007 | t0001 | g0013 | AFR | USA | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA20300 | hp1 | a0001 | c0002 | t0003 | g0014 | AFR | USA | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | USA | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | LWK | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
NA21309 | hp2 | a0001 | c0006 | t0003 | g0076 | AFR | LWK | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0062 | REF | REF | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0013 | REF | REF | TNFSF12_chr17_7544058_7562881 | TNFSF12 | chr17 | 7544058 | 7562881 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:7557881 | A | G | 1 | a0001 | 1 | HG02258.hp1 | splice_region_variant | LOW | c.*531A>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 7/7 | chr17 | 7557881 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:7549225 | C | T | 2 | a0001c0004 a0001c0005 |
45 | HG00544.hp1 HG00673.hp2 HG01167.hp1 others(42): Show |
synonymous_variant | LOW | c.72C>T | p.Leu24Leu | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 1/7 | 168/1377 | 72/750 | 24/249 | chr17 | 7549225 | |||
chr17:7550188 | C | A | 2 | a0001c0003 a0001c0006 |
39 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(36): Show |
synonymous_variant | LOW | c.276C>A | p.Arg92Arg | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 3/7 | 372/1377 | 276/750 | 92/249 | chr17 | 7550188 | |||
chr17:7557197 | G | A | 1 | a0001c0008 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.597G>A | p.Ala199Ala | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 7/7 | 693/1377 | 597/750 | 199/249 | chr17 | 7557197 | |||
chr17:7557200 | G | C | 3 | a0001c0001 a0001c0004 a0001c0006 |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
synonymous_variant | LOW | c.600G>C | p.Ala200Ala | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 7/7 | 696/1377 | 600/750 | 200/249 | chr17 | 7557200 | |||
chr17:7557242 | G | T | 1 | a0001c0007 | 7 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
synonymous_variant | LOW | c.642G>T | p.Gly214Gly | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 7/7 | 738/1377 | 642/750 | 214/249 | chr17 | 7557242 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:7549066 | G | A | 2 | a0001c0001t0005 a0001c0001t0008 |
22 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-88G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 1/7 | 88 | chr17 | 7549066 | ||||||
chr17:7557368 | G | A | 4 | a0001c0001t0002 a0001c0001t0009 a0001c0002t0002 others(1): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*18G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 7/7 | 18 | chr17 | 7557368 | ||||||
chr17:7557415 | C | T | 1 | a0001c0005t0012 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*65C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 7/7 | 65 | chr17 | 7557415 | ||||||
chr17:7557426 | G | A | 1 | a0001c0001t0007 | 8 | HG01074.hp2 HG01081.hp1 HG01168.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*76G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 7/7 | 76 | chr17 | 7557426 | ||||||
chr17:7557441 | G | A | 2 | a0001c0001t0004 a0001c0004t0004 |
28 | HG00544.hp1 HG00673.hp2 HG01192.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*91G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 7/7 | 91 | chr17 | 7557441 | ||||||
chr17:7557589 | C | G | 2 | a0001c0005t0006 a0001c0006t0006 |
9 | HG01167.hp1 HG01243.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*239C>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 7/7 | 239 | chr17 | 7557589 | ||||||
chr17:7557595 | A | G | 1 | a0001c0001t0011 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*245A>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 7/7 | 245 | chr17 | 7557595 | ||||||
chr17:7557640 | G | T | 8 | a0001c0001t0004 a0001c0002t0003 a0001c0003t0003 others(5): Show |
81 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*290G>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 7/7 | 290 | chr17 | 7557640 | ||||||
chr17:7557716 | T | C | 1 | a0001c0001t0008 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*366T>C | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 7/7 | 366 | chr17 | 7557716 | ||||||
chr17:7557817 | T | G | 1 | a0001c0001t0009 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*467T>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 7/7 | 467 | chr17 | 7557817 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:7549435 | G | A | 20 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0037 others(17): Show |
25 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.160-39G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 1/6 | chr17 | 7549435 | |||||||
chr17:7549589 | G | A | 4 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(1): Show |
4 | HG02630.hp2 HG03139.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+68G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 2/6 | chr17 | 7549589 | |||||||
chr17:7549660 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(148): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.207+139C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 2/6 | chr17 | 7549660 | |||||||
chr17:7549970 | G | GC | 6 | a0001c0002t0001g0028 a0001c0002t0001g0038 a0001c0002t0001g0087 others(3): Show |
8 | HG00639.hp1 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-147dupC | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 7549970 | ||||||
chr17:7550292 | G | A | 3 | a0001c0005t0006g0029 a0001c0005t0006g0039 a0001c0005t0006g0090 |
6 | HG01167.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+97G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 3/6 | chr17 | 7550292 | |||||||
chr17:7550455 | C | G | 6 | a0001c0002t0001g0028 a0001c0002t0001g0038 a0001c0002t0001g0087 others(3): Show |
8 | HG00639.hp1 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+260C>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 3/6 | chr17 | 7550455 | |||||||
chr17:7550539 | A | G | 3 | a0001c0002t0001g0168 a0001c0002t0001g0169 a0001c0002t0001g0170 |
3 | NA18944.hp1 NA18947.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.284-260A>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 3/6 | chr17 | 7550539 | |||||||
chr17:7550593 | C | T | 1 | a0001c0001t0002g0167 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.284-206C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 3/6 | chr17 | 7550593 | |||||||
chr17:7550602 | C | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0106 a0001c0001t0002g0002 others(105): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.284-197C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 3/6 | chr17 | 7550602 | |||||||
chr17:7550714 | C | T | 6 | a0001c0002t0001g0028 a0001c0002t0001g0038 a0001c0002t0001g0087 others(3): Show |
8 | HG00639.hp1 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.284-85C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 3/6 | chr17 | 7550714 | |||||||
chr17:7550764 | C | T | 3 | a0001c0003t0001g0086 a0001c0003t0003g0085 a0001c0006t0006g0027 |
5 | HG01243.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-35C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 3/6 | chr17 | 7550764 | |||||||
chr17:7550772 | G | A | 1 | a0001c0001t0002g0091 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.284-27G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 3/6 | chr17 | 7550772 | |||||||
chr17:7550934 | A | G | 6 | a0001c0002t0001g0028 a0001c0002t0001g0038 a0001c0002t0001g0087 others(3): Show |
8 | HG00639.hp1 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.338-9A>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 4/6 | chr17 | 7550934 | |||||||
chr17:7551170 | G | A | 6 | a0001c0002t0001g0028 a0001c0002t0001g0038 a0001c0002t0001g0087 others(3): Show |
8 | HG00639.hp1 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.373+192G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7551170 | |||||||
chr17:7551211 | C | G | 16 | a0001c0001t0004g0156 a0001c0004t0002g0157 a0001c0004t0004g0012 others(13): Show |
30 | HG00544.hp1 HG00673.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.373+233C>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7551211 | |||||||
chr17:7551271 | G | A | 1 | a0001c0001t0002g0103 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.373+293G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7551271 | |||||||
chr17:7551279 | G | A | 3 | a0001c0002t0001g0045 a0001c0002t0001g0104 a0001c0002t0001g0105 |
4 | NA18957.hp1 NA19074.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.373+301G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7551279 | |||||||
chr17:7551502 | C | T | 1 | a0001c0002t0003g0154 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.373+524C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7551502 | |||||||
chr17:7551854 | C | T | 1 | a0001c0003t0001g0071 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.373+876C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7551854 | |||||||
chr17:7551930 | C | T | 2 | a0001c0001t0002g0152 a0001c0001t0002g0153 |
2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.373+952C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7551930 | |||||||
chr17:7552074 | C | T | 21 | a0001c0003t0001g0024 a0001c0003t0001g0025 a0001c0003t0001g0037 others(18): Show |
26 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.373+1096C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7552074 | |||||||
chr17:7552112 | C | T | 3 | a0001c0001t0002g0052 a0001c0001t0002g0150 a0001c0001t0002g0151 |
4 | HG01346.hp1 HG01993.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.373+1134C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7552112 | |||||||
chr17:7552219 | C | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0099 others(104): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.373+1241C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7552219 | |||||||
chr17:7552270 | G | A | 3 | a0001c0005t0006g0029 a0001c0005t0006g0039 a0001c0005t0006g0090 |
6 | HG01167.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.373+1292G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7552270 | |||||||
chr17:7552293 | C | T | 3 | a0001c0002t0003g0112 a0001c0002t0003g0113 a0001c0002t0003g0114 |
3 | HG00099.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.373+1315C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7552293 | |||||||
chr17:7552327 | C | CT | 26 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0032 others(23): Show |
44 | HG00099.hp2 HG00558.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.373+1367dupT | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7552327 | ||||||
chr17:7552327 | CT | C | 14 | a0001c0001t0001g0093 a0001c0001t0004g0156 a0001c0001t0005g0092 others(11): Show |
28 | HG00544.hp1 HG00673.hp2 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.373+1367delT | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7552327 | ||||||
chr17:7552380 | T | A | 5 | a0001c0002t0001g0028 a0001c0002t0001g0038 a0001c0002t0001g0087 others(2): Show |
7 | HG00639.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.373+1402T>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7552380 | |||||||
chr17:7552390 | C | T | 45 | a0001c0001t0001g0005 a0001c0001t0002g0146 a0001c0001t0004g0156 others(42): Show |
130 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.373+1412C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7552390 | |||||||
chr17:7552484 | C | G | 46 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0009 others(43): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.373+1506C>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7552484 | |||||||
chr17:7552617 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
380 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(377): Show |
intron_variant | MODIFIER | c.373+1639T>C | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7552617 | |||||||
chr17:7552666 | G | A | 1 | a0001c0003t0003g0085 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.373+1688G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7552666 | |||||||
chr17:7552704 | A | G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(29): Show |
86 | HG00423.hp2 HG00735.hp2 HG01074.hp2 others(83): Show |
intron_variant | MODIFIER | c.373+1726A>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7552704 | |||||||
chr17:7552781 | C | T | 1 | a0001c0001t0005g0098 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.373+1803C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7552781 | |||||||
chr17:7552906 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.373+1928C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7552906 | |||||||
chr17:7552917 | T | C | 1 | a0001c0001t0002g0116 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.373+1939T>C | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7552917 | |||||||
chr17:7553022 | C | CCTTT | 3 | a0001c0004t0004g0012 a0001c0004t0004g0021 a0001c0004t0004g0163 |
14 | HG00544.hp1 HG01516.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.373+2045_373+2048d others(6): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553022 | ||||||
chr17:7553022 | CCTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0131 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.373+2045_373+2057d others(15): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7553022 | |||||||
chr17:7553023 | C | CT | 12 | a0001c0002t0001g0011 a0001c0002t0001g0014 a0001c0002t0001g0073 others(9): Show |
23 | HG00099.hp1 HG00597.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.373+2084dupT | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553023 | C | CTT | 7 | a0001c0002t0001g0074 a0001c0002t0003g0016 a0001c0002t0003g0026 others(4): Show |
13 | HG00558.hp1 HG00741.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.373+2083_373+2084d others(4): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553023 | C | CTTTCT | 6 | a0001c0004t0002g0157 a0001c0004t0004g0036 a0001c0004t0004g0158 others(3): Show |
8 | HG00673.hp2 HG01192.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.373+2048_373+2049i others(7): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553023 | C | CTTTTT | 3 | a0001c0005t0001g0019 a0001c0005t0003g0019 a0001c0005t0012g0140 |
6 | HG01884.hp1 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.373+2080_373+2084d others(7): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553023 | CTTTTTTT others(1): Show |
C | 16 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0093 others(13): Show |
27 | HG00323.hp2 HG00735.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.373+2077_373+2084d others(10): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553023 | CTTTTTTT others(2): Show |
C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0030 others(23): Show |
74 | HG00423.hp2 HG00733.hp1 HG01074.hp1 others(71): Show |
intron_variant | MODIFIER | c.373+2076_373+2084d others(11): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553023 | CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0001g0040 a0001c0001t0005g0040 a0001c0001t0005g0094 others(3): Show |
6 | HG01081.hp2 HG01106.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.373+2075_373+2084d others(12): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553023 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0005g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.373+2074_373+2084d others(13): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553023 | CTTTTTTT others(5): Show |
C | 14 | a0001c0001t0001g0044 a0001c0001t0002g0022 a0001c0001t0002g0023 others(11): Show |
23 | HG01256.hp2 HG01361.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.373+2073_373+2084d others(14): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553023 | CTTTTTTT others(6): Show |
C | 39 | a0001c0001t0001g0099 a0001c0001t0002g0002 a0001c0001t0002g0007 others(36): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.373+2072_373+2084d others(15): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553023 | CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0002g0101 a0001c0001t0002g0103 a0001c0001t0002g0117 others(2): Show |
5 | HG00558.hp2 HG02922.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.373+2071_373+2084d others(16): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553023 | CTTTTTTT others(8): Show |
C | 2 | a0001c0004t0004g0155 a0001c0005t0006g0090 |
2 | HG02486.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.373+2070_373+2084d others(17): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553023 | CTTTTTTT others(13): Show |
C | 3 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0139 |
3 | NA19010.hp1 NA19083.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.373+2065_373+2084d others(22): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553023 | CTTTTTTT others(14): Show |
C | 21 | a0001c0001t0001g0005 a0001c0001t0002g0146 a0001c0002t0001g0003 others(18): Show |
92 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.373+2064_373+2084d others(23): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553023 | CTTTTTTT others(15): Show |
C | 2 | a0001c0002t0001g0133 a0001c0002t0001g0134 |
2 | NA18954.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.373+2063_373+2084d others(24): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7553023 | ||||||
chr17:7553036 | T | C | 1 | a0001c0001t0004g0156 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.373+2058T>C | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7553036 | |||||||
chr17:7553042 | T | C | 1 | a0001c0004t0004g0155 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.373+2064T>C | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7553042 | |||||||
chr17:7553064 | T | A | 102 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0099 others(99): Show |
251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.373+2086T>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7553064 | |||||||
chr17:7553172 | C | T | 26 | a0001c0001t0001g0005 a0001c0001t0002g0146 a0001c0002t0001g0003 others(23): Show |
97 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.373+2194C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7553172 | |||||||
chr17:7553206 | C | T | 3 | a0001c0006t0001g0079 a0001c0006t0003g0076 a0001c0006t0003g0077 |
3 | HG02976.hp2 HG03688.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.373+2228C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7553206 | |||||||
chr17:7553686 | A | T | 3 | a0001c0005t0006g0029 a0001c0005t0006g0039 a0001c0005t0006g0090 |
6 | HG01167.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.373+2708A>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7553686 | |||||||
chr17:7554035 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(89): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.374-2743G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554035 | |||||||
chr17:7554058 | G | A | 1 | a0001c0001t0002g0046 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.374-2720G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554058 | |||||||
chr17:7554104 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
377 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(374): Show |
intron_variant | MODIFIER | c.374-2674T>C | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554104 | |||||||
chr17:7554104 | T | G | 1 | a0001c0006t0006g0027 | 3 | HG01243.hp2 HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.374-2674T>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554104 | |||||||
chr17:7554151 | A | G | 2 | a0001c0004t0004g0162 a0001c0004t0004g0166 |
2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.374-2627A>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554151 | |||||||
chr17:7554307 | C | CT | 14 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0003g0010 others(11): Show |
31 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.374-2447dupT | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7554307 | ||||||
chr17:7554307 | CT | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.374-2447delT | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7554307 | ||||||
chr17:7554307 | CTT | C | 8 | a0001c0001t0001g0030 a0001c0001t0002g0047 a0001c0001t0002g0152 others(5): Show |
10 | HG01167.hp2 HG01975.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.374-2448_374-2447d others(4): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7554307 | ||||||
chr17:7554307 | CTTTTTTT | C | 15 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0008 others(12): Show |
71 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.374-2453_374-2447d others(9): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7554307 | ||||||
chr17:7554307 | CTTTTTTT others(1): Show |
C | 5 | a0001c0002t0001g0133 a0001c0002t0001g0135 a0001c0005t0006g0029 others(2): Show |
8 | HG01167.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.374-2454_374-2447d others(10): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7554307 | ||||||
chr17:7554336 | T | C | 5 | a0001c0005t0001g0019 a0001c0005t0003g0019 a0001c0005t0003g0034 others(2): Show |
10 | HG01884.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.374-2442T>C | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554336 | |||||||
chr17:7554337 | G | A | 1 | a0001c0002t0003g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.374-2441G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554337 | |||||||
chr17:7554368 | T | C | 5 | a0001c0005t0001g0019 a0001c0005t0003g0019 a0001c0005t0003g0034 others(2): Show |
10 | HG01884.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.374-2410T>C | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554368 | |||||||
chr17:7554376 | C | T | 57 | a0001c0001t0001g0099 a0001c0001t0002g0002 a0001c0001t0002g0007 others(54): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.374-2402C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554376 | |||||||
chr17:7554383 | G | A | 2 | a0001c0001t0002g0048 a0001c0001t0002g0116 |
3 | HG00642.hp1 HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.374-2395G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554383 | |||||||
chr17:7554387 | T | C | 2 | a0001c0001t0002g0048 a0001c0001t0002g0116 |
3 | HG00642.hp1 HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.374-2391T>C | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554387 | |||||||
chr17:7554462 | C | A | 59 | a0001c0001t0001g0099 a0001c0001t0002g0002 a0001c0001t0002g0007 others(56): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.374-2316C>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554462 | |||||||
chr17:7554471 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.374-2307G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554471 | |||||||
chr17:7554474 | T | C | 64 | a0001c0001t0001g0099 a0001c0001t0002g0002 a0001c0001t0002g0007 others(61): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.374-2304T>C | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554474 | |||||||
chr17:7554547 | C | T | 15 | a0001c0001t0004g0156 a0001c0004t0002g0157 a0001c0004t0004g0012 others(12): Show |
29 | HG00544.hp1 HG00673.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.374-2231C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554547 | |||||||
chr17:7554693 | C | T | 1 | a0001c0002t0001g0100 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.374-2085C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554693 | |||||||
chr17:7554764 | GCCA | G | 47 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0009 others(44): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.374-2009_374-2007d others(5): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7554764 | ||||||
chr17:7554794 | G | T | 64 | a0001c0001t0001g0005 a0001c0001t0004g0156 a0001c0002t0001g0003 others(61): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.374-1984G>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554794 | |||||||
chr17:7554832 | G | T | 65 | a0001c0001t0001g0005 a0001c0001t0002g0123 a0001c0001t0004g0156 others(62): Show |
155 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.374-1946G>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554832 | |||||||
chr17:7554833 | C | G | 65 | a0001c0001t0001g0005 a0001c0001t0002g0123 a0001c0001t0004g0156 others(62): Show |
155 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.374-1945C>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554833 | |||||||
chr17:7554853 | G | A | 2 | a0001c0003t0001g0058 a0001c0003t0001g0059 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.374-1925G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554853 | |||||||
chr17:7554897 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
380 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(377): Show |
intron_variant | MODIFIER | c.374-1881G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7554897 | |||||||
chr17:7555147 | C | CA | 126 | a0001c0001t0001g0005 a0001c0001t0001g0099 a0001c0001t0002g0002 others(123): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.374-1622dupA | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555147 | ||||||
chr17:7555259 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.374-1519C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7555259 | |||||||
chr17:7555265 | A | T | 64 | a0001c0001t0001g0005 a0001c0001t0004g0156 a0001c0002t0001g0003 others(61): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.374-1513A>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7555265 | |||||||
chr17:7555350 | C | T | 1 | a0001c0002t0001g0028 | 3 | HG00639.hp1 HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.374-1428C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7555350 | |||||||
chr17:7555478 | A | G | 24 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0074 others(21): Show |
29 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.374-1300A>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7555478 | |||||||
chr17:7555565 | C | T | 1 | a0001c0002t0001g0137 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.374-1213C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7555565 | |||||||
chr17:7555709 | C | T | 3 | a0001c0001t0005g0042 a0001c0001t0005g0092 a0001c0001t0005g0094 |
4 | HG02630.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.374-1069C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7555709 | |||||||
chr17:7555710 | G | C | 2 | a0001c0001t0005g0041 a0001c0001t0008g0041 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.374-1068G>C | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7555710 | |||||||
chr17:7555745 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
377 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(374): Show |
intron_variant | MODIFIER | c.374-1033A>G | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7555745 | |||||||
chr17:7555972 | C | CGTTTTTT | 10 | a0001c0001t0001g0099 a0001c0002t0001g0028 a0001c0002t0001g0038 others(7): Show |
13 | HG00639.hp1 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.374-805_374-799dup others(7): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555972 | ||||||
chr17:7555973 | G | GTTTTTT | 2 | a0001c0004t0004g0012 a0001c0004t0004g0036 |
11 | HG00673.hp2 HG01516.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.374-802_374-797dup others(6): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555973 | G | GTTTTTTG others(1): Show |
29 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0023 others(26): Show |
73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.374-799_374-798ins others(8): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555973 | G | GTTTTTTG others(2): Show |
15 | a0001c0001t0002g0007 a0001c0001t0002g0035 a0001c0001t0002g0102 others(12): Show |
27 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.374-799_374-798ins others(9): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555973 | G | GTTTTTTG others(3): Show |
1 | a0001c0001t0002g0050 | 2 | HG02129.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.374-799_374-798ins others(10): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555973 | G | GTTTTTTG others(4): Show |
1 | a0001c0001t0002g0145 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.374-799_374-798ins others(11): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555973 | G | GTTTTTTT | 10 | a0001c0001t0004g0156 a0001c0004t0004g0021 a0001c0004t0004g0053 others(7): Show |
15 | HG00544.hp1 HG01192.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.374-803_374-797dup others(7): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555973 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0002g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.374-798_374-797ins others(10): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555973 | G | GTTTTTTT others(5): Show |
2 | a0001c0002t0001g0135 a0001c0002t0001g0168 |
2 | NA18947.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.374-797_374-796ins others(12): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555973 | G | GTTTTTTT others(6): Show |
2 | a0001c0002t0001g0008 a0001c0002t0001g0169 |
12 | HG00642.hp2 HG02040.hp1 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.374-797_374-796ins others(13): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555973 | G | GTTTTTTT others(7): Show |
4 | a0001c0002t0001g0003 a0001c0002t0001g0134 a0001c0002t0001g0147 others(1): Show |
22 | HG01069.hp1 HG01106.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.374-797_374-796ins others(14): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555973 | G | GTTTTTTT others(8): Show |
10 | a0001c0002t0001g0004 a0001c0002t0001g0072 a0001c0002t0001g0073 others(7): Show |
29 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.374-797_374-796ins others(15): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555973 | G | GTTTTTTT others(9): Show |
9 | a0001c0002t0001g0015 a0001c0002t0001g0139 a0001c0002t0001g0148 others(6): Show |
17 | HG00323.hp2 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.374-797_374-796ins others(16): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555973 | G | GTTTTTTT others(10): Show |
7 | a0001c0002t0001g0136 a0001c0003t0001g0025 a0001c0003t0001g0056 others(4): Show |
9 | HG00733.hp1 HG01106.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.374-797_374-796ins others(17): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555973 | G | GTTTTTTT others(11): Show |
3 | a0001c0003t0001g0067 a0001c0003t0001g0070 a0001c0003t0001g0071 |
3 | HG01123.hp1 HG02145.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.374-797_374-796ins others(18): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555973 | G | GTTTTTTT others(13): Show |
1 | a0001c0003t0001g0060 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.374-797_374-796ins others(20): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555973 | ||||||
chr17:7555975 | T | TTTTTG | 7 | a0001c0001t0001g0005 a0001c0001t0002g0127 a0001c0002t0001g0005 others(4): Show |
21 | HG00099.hp2 HG00423.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.374-799_374-798ins others(5): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555975 | ||||||
chr17:7555976 | T | TTTTG | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0030 others(30): Show |
85 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(82): Show |
intron_variant | MODIFIER | c.374-799_374-798ins others(4): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555976 | ||||||
chr17:7555977 | T | TTTGTTTT others(3): Show |
2 | a0001c0001t0002g0120 a0001c0001t0002g0124 |
2 | NA18950.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.374-799_374-798ins others(10): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555977 | ||||||
chr17:7555978 | T | TTGTTTTT others(2): Show |
3 | a0001c0001t0002g0017 a0001c0001t0002g0022 a0001c0001t0002g0123 |
11 | HG00621.hp2 NA18940.hp1 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.374-799_374-798ins others(9): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555978 | ||||||
chr17:7555979 | T | TGTTTTTG | 4 | a0001c0001t0001g0018 a0001c0001t0001g0093 a0001c0001t0001g0095 others(1): Show |
8 | HG00423.hp2 HG01928.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.374-799_374-798ins others(7): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7555979 | |||||||
chr17:7555979 | T | TGTTTTTT others(1): Show |
2 | a0001c0002t0001g0051 a0001c0002t0001g0104 |
3 | HG01433.hp1 HG02027.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.374-799_374-798ins others(8): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7555979 | |||||||
chr17:7555982 | G | GT | 24 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0003g0010 others(21): Show |
45 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.374-781dupT | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555982 | ||||||
chr17:7555982 | G | GTT | 35 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(32): Show |
99 | HG00099.hp2 HG00423.hp1 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.374-782_374-781dup others(2): Show |
TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 7555982 | ||||||
chr17:7555982 | G | T | 126 | a0001c0001t0001g0018 a0001c0001t0001g0093 a0001c0001t0001g0095 others(123): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.374-796G>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7555982 | |||||||
chr17:7556121 | C | T | 4 | a0001c0004t0004g0053 a0001c0004t0004g0159 a0001c0004t0004g0160 others(1): Show |
5 | NA18948.hp1 NA18967.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.374-657C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7556121 | |||||||
chr17:7556618 | C | T | 1 | a0001c0003t0001g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.374-160C>T | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 5/6 | chr17 | 7556618 | |||||||
chr17:7556940 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.498+38G>A | TNFSF12 | ENSG00000239697.12 | transcript | ENST00000293825.11 | protein_coding | 6/6 | chr17 | 7556940 |