Item | Value |
---|---|
geneid | 150465 |
ensemblid | ENSG00000114999.8 |
hgncid | 21586 |
symbol | TTL |
name | tubulin tyrosine ligase |
refseq_nuc | NM_153712.5 |
refseq_prot | NP_714923.1 |
ensembl_nuc | ENST00000233336.7 |
ensembl_prot | ENSP00000233336.5 |
mane_status | MANE Select |
chr | chr2 |
start | 112482156 |
end | 112541739 |
strand | + |
ver | v1.2 |
region | chr2:112482156-112541739 |
region5000 | chr2:112477156-112546739 |
regionname0 | TTL_chr2_112482156_112541739 |
regionname5000 | TTL_chr2_112477156_112546739 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 377 | 345 | 98 | 62 | 143 | 12 | 30 | 110 | TTL_chr2_112477156_112546739 | TTL | MYTFV others(372): Show |
chr2 | 112477156 | 112546739 |
a0002 | 0/0 | 377 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | MYTFV others(372): Show |
chr2 | 112477156 | 112546739 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1131 | 159 | 48 | 30 | 57 | 6 | 18 | TTL_chr2_112477156_112546739 | TTL | ATGTA others(1126): Show |
chr2 | 112477156 | 112546739 | ||
a0001c0002 | 0/0 | 1131 | 103 | 37 | 20 | 34 | 5 | 7 | TTL_chr2_112477156_112546739 | TTL | ATGTA others(1126): Show |
chr2 | 112477156 | 112546739 | ||
a0001c0003 | 0/0 | 1131 | 81 | 13 | 10 | 52 | 1 | 5 | TTL_chr2_112477156_112546739 | TTL | ATGTA others(1126): Show |
chr2 | 112477156 | 112546739 | ||
a0001c0004 | 0/0 | 1131 | 2 | 0 | 2 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | ATGTA others(1126): Show |
chr2 | 112477156 | 112546739 | ||
a0002c0005 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | ATGTA others(1126): Show |
chr2 | 112477156 | 112546739 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 14284 | 53 | 3 | 14 | 23 | 5 | 8 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0004 | 0/0 | 14284 | 10 | 0 | 1 | 9 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0005 | 0/0 | 14267 | 9 | 8 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14262): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0006 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0012 | 0/0 | 14284 | 4 | 0 | 0 | 3 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0013 | 0/0 | 14282 | 4 | 3 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14277): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0015 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0016 | 0/0 | 14285 | 3 | 0 | 0 | 1 | 0 | 2 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0017 | 0/0 | 14283 | 3 | 0 | 0 | 3 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14278): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0023 | 0/0 | 14284 | 3 | 2 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0024 | 0/0 | 14285 | 3 | 2 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0025 | 0/0 | 14282 | 3 | 0 | 3 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14277): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0030 | 0/0 | 14285 | 2 | 1 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0037 | 0/0 | 14282 | 2 | 0 | 1 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14277): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0038 | 0/0 | 14281 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14276): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0044 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0045 | 0/0 | 14284 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0046 | 0/0 | 14267 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14262): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0047 | 0/0 | 14267 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14262): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0048 | 0/0 | 14267 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14262): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0055 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0057 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0058 | 0/0 | 14286 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14281): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0059 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0060 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0061 | 0/0 | 14284 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0062 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0063 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0064 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0065 | 0/0 | 14284 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0066 | 0/0 | 14288 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14283): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0067 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14276): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0068 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0069 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0070 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0071 | 0/0 | 14285 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0072 | 0/0 | 14282 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14277): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0073 | 0/0 | 14284 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0074 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0075 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0076 | 0/0 | 14284 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0077 | 0/0 | 14283 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14278): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0078 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0080 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14276): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0081 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14276): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0082 | 0/0 | 14283 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14278): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0083 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0084 | 0/0 | 14282 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14277): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0085 | 0/0 | 14282 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14277): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0086 | 0/0 | 14285 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0087 | 0/0 | 14283 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14278): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0088 | 0/0 | 14284 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0089 | 0/0 | 14284 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0090 | 0/0 | 14285 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0091 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14276): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0092 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14276): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0093 | 0/0 | 14284 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0094 | 0/0 | 14284 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0095 | 0/0 | 14282 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14277): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0112 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14276): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0113 | 0/0 | 14284 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0114 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0115 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14276): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0116 | 0/0 | 14267 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14262): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0117 | 0/0 | 14266 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14261): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0121 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0123 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14276): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0124 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14276): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0125 | 0/0 | 14284 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0126 | 0/0 | 14281 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14276): Show |
chr2 | 112477156 | 112546739 |
a0001c0001t0127 | 0/0 | 14270 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14265): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0002 | 0/0 | 14285 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0003 | 0/0 | 14284 | 31 | 0 | 9 | 19 | 1 | 2 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0006 | 0/0 | 14285 | 2 | 0 | 1 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0007 | 0/0 | 14288 | 8 | 8 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14283): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0008 | 0/0 | 14282 | 6 | 0 | 1 | 0 | 3 | 2 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14277): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0009 | 0/0 | 14282 | 6 | 4 | 2 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14277): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0011 | 0/0 | 14289 | 4 | 4 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14284): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0014 | 0/0 | 14261 | 3 | 3 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14256): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0015 | 0/0 | 14284 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0018 | 0/0 | 14285 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0019 | 0/0 | 14284 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0022 | 0/0 | 14285 | 3 | 0 | 0 | 3 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0027 | 0/0 | 14288 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14283): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0028 | 0/0 | 14287 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14282): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0029 | 0/0 | 14277 | 2 | 1 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14272): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0031 | 0/0 | 14285 | 2 | 0 | 1 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0034 | 0/0 | 14270 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14265): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0039 | 0/0 | 14284 | 2 | 0 | 1 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0040 | 0/0 | 14289 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14284): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0041 | 0/0 | 14286 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14281): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0042 | 0/0 | 14282 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14277): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0043 | 0/0 | 14282 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14277): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0049 | 0/0 | 14284 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0050 | 0/0 | 14284 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0051 | 0/0 | 14287 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14282): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0052 | 0/0 | 14287 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14282): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0053 | 0/0 | 14284 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0054 | 0/0 | 14282 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14277): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0079 | 0/0 | 14283 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14278): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0097 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0108 | 0/0 | 14284 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0109 | 0/0 | 14283 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14278): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0111 | 0/0 | 14283 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14278): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0118 | 0/0 | 14283 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14278): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0119 | 0/0 | 14277 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14272): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0120 | 0/0 | 14279 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14274): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0122 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0131 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0132 | 0/0 | 14210 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14205): Show |
chr2 | 112477156 | 112546739 |
a0001c0002t0133 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0002 | 0/0 | 14285 | 33 | 8 | 3 | 21 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0003 | 0/0 | 14284 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0006 | 0/0 | 14285 | 6 | 0 | 0 | 6 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0010 | 0/0 | 14285 | 5 | 0 | 0 | 5 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0019 | 0/0 | 14284 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0020 | 0/0 | 14286 | 3 | 0 | 0 | 3 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14281): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0021 | 0/0 | 14286 | 3 | 0 | 0 | 0 | 1 | 2 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14281): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0026 | 0/0 | 14285 | 3 | 0 | 0 | 3 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0032 | 0/0 | 14287 | 2 | 0 | 0 | 1 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14282): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0033 | 0/0 | 14286 | 2 | 0 | 0 | 1 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14281): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0035 | 0/0 | 14284 | 2 | 0 | 1 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0036 | 0/0 | 14285 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0056 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0096 | 0/0 | 14284 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0098 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0099 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0100 | 0/0 | 14284 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0101 | 0/0 | 14285 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0102 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0103 | 0/0 | 14286 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14281): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0104 | 0/0 | 14285 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0105 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0106 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0107 | 0/0 | 14286 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14281): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0110 | 0/0 | 14284 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0128 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0129 | 0/0 | 14284 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0001c0003t0130 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
a0001c0004t0001 | 0/0 | 14284 | 2 | 0 | 2 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14279): Show |
chr2 | 112477156 | 112546739 |
a0002c0005t0018 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | GCTTT others(14280): Show |
chr2 | 112477156 | 112546739 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0004g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0012g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0012g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0012g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0012g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0013g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0013g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0015g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0016g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0016g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0016g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0017g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0017g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0017g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0023g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0023g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0024g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0025g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0025g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0030g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0030g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0037g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0037g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0038g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0038g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0044g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0045g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0046g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0047g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0048g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0055g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0057g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0058g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0059g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0060g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0061g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0062g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0063g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0064g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0065g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0066g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0067g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0068g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0069g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0070g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0071g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0072g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0073g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0074g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0075g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0076g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0077g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0078g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0080g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0081g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0082g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0083g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0084g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0085g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0086g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0087g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0088g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0089g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0090g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0091g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0092g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0093g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0094g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0095g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0112g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0113g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0114g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0115g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0116g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0117g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0121g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0123g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0124g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0125g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0126g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0127g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0006g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0007g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0007g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0008g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0008g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0008g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0008g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0008g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0008g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0009g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0009g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0009g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0011g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0011g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0011g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0014g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0014g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0015g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0015g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0018g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0018g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0019g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0022g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0022g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0022g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0027g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0028g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0028g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0029g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0029g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0031g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0031g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0034g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0034g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0039g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0039g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0040g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0041g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0042g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0043g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0049g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0050g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0051g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0052g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0053g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0054g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0079g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0097g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0108g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0109g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0111g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0118g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0119g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0120g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0122g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0131g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0132g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0133g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0005 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0006g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0010g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0010g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0010g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0010g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0019g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0019g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0020g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0020g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0020g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0021g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0021g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0021g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0026g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0026g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0032g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0032g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0033g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0033g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0035g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0035g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0036g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0056g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0096g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0098g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0099g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0100g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0101g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0102g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0103g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0104g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0105g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0106g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0107g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0110g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0128g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0129g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0130g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0004t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0004t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0002c0005t0018g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00099 | hp2 | a0001 | c0002 | t0008 | g0089 | EUR | GBR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00140 | hp1 | a0001 | c0002 | t0008 | g0070 | EUR | GBR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | GBR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00280 | hp1 | a0001 | c0003 | t0021 | g0174 | EUR | FIN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00280 | hp2 | a0001 | c0002 | t0042 | g0071 | EUR | FIN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00408 | hp1 | a0001 | c0003 | t0105 | g0172 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00423 | hp2 | a0001 | c0003 | t0020 | g0163 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00438 | hp1 | a0001 | c0002 | t0034 | g0297 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00544 | hp1 | a0001 | c0001 | t0078 | g0003 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00544 | hp2 | a0001 | c0003 | t0020 | g0159 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00621 | hp1 | a0001 | c0002 | t0003 | g0136 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00621 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00639 | hp1 | a0001 | c0001 | t0005 | g0054 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00639 | hp2 | a0001 | c0003 | t0101 | g0176 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00673 | hp1 | a0002 | c0005 | t0018 | g0139 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00735 | hp1 | a0001 | c0003 | t0104 | g0152 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00735 | hp2 | a0001 | c0002 | t0003 | g0133 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00738 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00738 | hp2 | a0001 | c0001 | t0025 | g0042 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00741 | hp2 | a0001 | c0003 | t0002 | g0280 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01070 | hp2 | a0001 | c0002 | t0003 | g0115 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01071 | hp1 | a0001 | c0002 | t0003 | g0009 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01074 | hp1 | a0001 | c0003 | t0100 | g0150 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01074 | hp2 | a0001 | c0002 | t0039 | g0059 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01081 | hp1 | a0001 | c0002 | t0006 | g0060 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01081 | hp2 | a0001 | c0002 | t0003 | g0009 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01106 | hp1 | a0001 | c0003 | t0002 | g0177 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01109 | hp1 | a0001 | c0001 | t0013 | g0044 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0132 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01167 | hp2 | a0001 | c0001 | t0024 | g0007 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01168 | hp1 | a0001 | c0003 | t0110 | g0157 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01168 | hp2 | a0001 | c0002 | t0079 | g0134 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01175 | hp1 | a0001 | c0001 | t0030 | g0191 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01243 | hp1 | a0001 | c0001 | t0023 | g0101 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01243 | hp2 | a0001 | c0002 | t0029 | g0187 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01256 | hp2 | a0001 | c0001 | t0025 | g0011 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01257 | hp1 | a0001 | c0002 | t0009 | g0291 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01258 | hp1 | a0001 | c0002 | t0009 | g0292 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01258 | hp2 | a0001 | c0001 | t0025 | g0011 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01261 | hp1 | a0001 | c0002 | t0109 | g0004 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01261 | hp2 | a0001 | c0003 | t0035 | g0178 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01346 | hp1 | a0001 | c0001 | t0046 | g0272 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01358 | hp1 | a0001 | c0002 | t0041 | g0073 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01358 | hp2 | a0001 | c0001 | t0061 | g0261 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01361 | hp1 | a0001 | c0002 | t0031 | g0129 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01361 | hp2 | a0001 | c0001 | t0086 | g0213 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01496 | hp1 | a0001 | c0004 | t0001 | g0246 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01496 | hp2 | a0001 | c0001 | t0071 | g0219 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01516 | hp1 | a0001 | c0002 | t0008 | g0076 | EUR | IBS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01884 | hp1 | a0001 | c0001 | t0123 | g0301 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01884 | hp2 | a0001 | c0002 | t0009 | g0147 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01891 | hp1 | a0001 | c0002 | t0028 | g0097 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01891 | hp2 | a0001 | c0001 | t0038 | g0050 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01928 | hp2 | a0001 | c0004 | t0001 | g0245 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01952 | hp1 | a0001 | c0002 | t0003 | g0277 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01952 | hp2 | a0001 | c0001 | t0089 | g0001 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01975 | hp1 | a0001 | c0003 | t0096 | g0160 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01975 | hp2 | a0001 | c0002 | t0003 | g0119 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01978 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01978 | hp2 | a0001 | c0001 | t0090 | g0224 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01981 | hp1 | a0001 | c0003 | t0103 | g0156 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01981 | hp2 | a0001 | c0001 | t0037 | g0029 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0215 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02004 | hp2 | a0001 | c0002 | t0003 | g0009 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0116 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02040 | hp2 | a0001 | c0001 | t0017 | g0214 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02055 | hp1 | a0001 | c0001 | t0013 | g0033 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02055 | hp2 | a0001 | c0003 | t0102 | g0238 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0283 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02071 | hp2 | a0001 | c0002 | t0003 | g0127 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02080 | hp1 | a0001 | c0003 | t0099 | g0165 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02080 | hp2 | a0001 | c0001 | t0012 | g0047 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02083 | hp1 | a0001 | c0003 | t0002 | g0239 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02083 | hp2 | a0001 | c0001 | t0068 | g0250 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02129 | hp1 | a0001 | c0003 | t0032 | g0231 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02132 | hp2 | a0001 | c0002 | t0003 | g0080 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02135 | hp1 | a0001 | c0002 | t0132 | g0279 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02135 | hp2 | a0001 | c0003 | t0002 | g0282 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02145 | hp1 | a0001 | c0002 | t0053 | g0276 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CDX | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02155 | hp2 | a0001 | c0003 | t0006 | g0057 | EAS | CDX | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02165 | hp2 | a0001 | c0002 | t0131 | g0045 | EAS | CDX | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02257 | hp1 | a0001 | c0001 | t0095 | g0103 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02257 | hp2 | a0001 | c0001 | t0081 | g0113 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02258 | hp2 | a0001 | c0001 | t0124 | g0043 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02280 | hp1 | a0001 | c0002 | t0009 | g0290 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02280 | hp2 | a0001 | c0003 | t0128 | g0028 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02293 | hp1 | a0001 | c0002 | t0008 | g0075 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02300 | hp1 | a0001 | c0002 | t0003 | g0121 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02451 | hp1 | a0001 | c0001 | t0121 | g0041 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02451 | hp2 | a0001 | c0002 | t0054 | g0096 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02523 | hp1 | a0001 | c0001 | t0012 | g0049 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02523 | hp2 | a0001 | c0003 | t0002 | g0179 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02572 | hp2 | a0001 | c0002 | t0007 | g0110 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02602 | hp1 | a0001 | c0001 | t0016 | g0265 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02602 | hp2 | a0001 | c0001 | t0126 | g0026 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02615 | hp1 | a0001 | c0003 | t0002 | g0005 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02615 | hp2 | a0001 | c0002 | t0011 | g0105 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02622 | hp1 | a0001 | c0002 | t0007 | g0008 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02622 | hp2 | a0001 | c0001 | t0067 | g0099 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02630 | hp1 | a0001 | c0003 | t0002 | g0005 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02630 | hp2 | a0001 | c0001 | t0092 | g0210 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02647 | hp1 | a0001 | c0002 | t0051 | g0275 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02647 | hp2 | a0001 | c0002 | t0118 | g0039 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02683 | hp1 | a0001 | c0002 | t0111 | g0235 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02683 | hp2 | a0001 | c0001 | t0093 | g0254 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02698 | hp2 | a0001 | c0002 | t0008 | g0072 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02717 | hp1 | a0001 | c0001 | t0127 | g0010 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02723 | hp1 | a0001 | c0002 | t0120 | g0069 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02723 | hp2 | a0001 | c0001 | t0114 | g0102 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02738 | hp1 | a0001 | c0001 | t0088 | g0237 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02738 | hp2 | a0001 | c0001 | t0016 | g0248 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02809 | hp1 | a0001 | c0001 | t0065 | g0211 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02809 | hp2 | a0001 | c0002 | t0011 | g0109 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02818 | hp1 | a0001 | c0002 | t0011 | g0108 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02818 | hp2 | a0001 | c0001 | t0044 | g0195 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02886 | hp2 | a0001 | c0003 | t0019 | g0114 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02895 | hp1 | a0001 | c0002 | t0027 | g0022 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02895 | hp2 | a0001 | c0002 | t0119 | g0040 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02896 | hp1 | a0001 | c0002 | t0050 | g0233 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02897 | hp1 | a0001 | c0002 | t0027 | g0022 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0052 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02922 | hp1 | a0001 | c0001 | t0072 | g0090 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02922 | hp2 | a0001 | c0002 | t0049 | g0234 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02965 | hp1 | a0001 | c0001 | t0117 | g0035 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02965 | hp2 | a0001 | c0002 | t0007 | g0008 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02970 | hp1 | a0001 | c0001 | t0112 | g0100 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02970 | hp2 | a0001 | c0002 | t0007 | g0106 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02976 | hp1 | a0001 | c0001 | t0030 | g0192 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02976 | hp2 | a0001 | c0001 | t0084 | g0205 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03017 | hp1 | a0001 | c0001 | t0076 | g0003 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03017 | hp2 | a0001 | c0002 | t0008 | g0074 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03041 | hp2 | a0001 | c0001 | t0013 | g0010 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03098 | hp1 | a0001 | c0002 | t0007 | g0104 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03098 | hp2 | a0001 | c0002 | t0133 | g0095 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03130 | hp1 | a0001 | c0003 | t0002 | g0171 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03130 | hp2 | a0001 | c0001 | t0024 | g0007 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03139 | hp1 | a0001 | c0001 | t0073 | g0255 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03139 | hp2 | a0001 | c0002 | t0009 | g0293 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03195 | hp1 | a0001 | c0002 | t0014 | g0083 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03195 | hp2 | a0001 | c0001 | t0038 | g0046 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03209 | hp1 | a0001 | c0002 | t0043 | g0081 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03209 | hp2 | a0001 | c0002 | t0007 | g0008 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03225 | hp1 | a0001 | c0002 | t0011 | g0111 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03225 | hp2 | a0001 | c0003 | t0002 | g0153 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03239 | hp1 | a0001 | c0003 | t0021 | g0167 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03453 | hp1 | a0001 | c0003 | t0019 | g0180 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03453 | hp2 | a0001 | c0002 | t0028 | g0149 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03490 | hp2 | a0001 | c0001 | t0125 | g0031 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03516 | hp1 | a0001 | c0002 | t0014 | g0084 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03516 | hp2 | a0001 | c0002 | t0052 | g0094 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03540 | hp2 | a0001 | c0002 | t0019 | g0093 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03579 | hp1 | a0001 | c0003 | t0002 | g0155 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03579 | hp2 | a0001 | c0002 | t0122 | g0034 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03704 | hp1 | a0001 | c0001 | t0094 | g0241 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03710 | hp2 | a0001 | c0002 | t0003 | g0138 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03927 | hp1 | a0001 | c0002 | t0108 | g0285 | SAS | BEB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03927 | hp2 | a0001 | c0002 | t0040 | g0088 | SAS | BEB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03942 | hp1 | a0001 | c0003 | t0021 | g0168 | SAS | BEB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04115 | hp1 | a0001 | c0001 | t0012 | g0048 | SAS | STU | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04115 | hp2 | a0001 | c0003 | t0033 | g0158 | SAS | STU | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04184 | hp1 | a0001 | c0003 | t0032 | g0183 | SAS | BEB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04199 | hp1 | a0001 | c0001 | t0113 | g0259 | SAS | STU | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04199 | hp2 | a0001 | c0002 | t0003 | g0137 | SAS | STU | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04204 | hp1 | a0001 | c0003 | t0002 | g0161 | SAS | STU | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18522 | hp1 | a0001 | c0003 | t0002 | g0151 | AFR | YRI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18522 | hp2 | a0001 | c0002 | t0009 | g0146 | AFR | YRI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18612 | hp2 | a0001 | c0003 | t0033 | g0240 | EAS | CHB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | YRI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18906 | hp2 | a0001 | c0001 | t0116 | g0067 | AFR | YRI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18939 | hp1 | a0001 | c0002 | t0003 | g0128 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18939 | hp2 | a0001 | c0001 | t0077 | g0257 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18942 | hp1 | a0001 | c0001 | t0082 | g0189 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18942 | hp2 | a0001 | c0003 | t0002 | g0162 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18943 | hp2 | a0001 | c0002 | t0015 | g0122 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18944 | hp2 | a0001 | c0003 | t0002 | g0016 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18945 | hp2 | a0001 | c0003 | t0002 | g0229 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18947 | hp1 | a0001 | c0002 | t0003 | g0131 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18948 | hp1 | a0001 | c0003 | t0010 | g0227 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18948 | hp2 | a0001 | c0003 | t0002 | g0295 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18950 | hp1 | a0001 | c0001 | t0058 | g0212 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18954 | hp1 | a0001 | c0003 | t0036 | g0002 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18954 | hp2 | a0001 | c0001 | t0087 | g0198 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18957 | hp1 | a0001 | c0003 | t0006 | g0012 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18957 | hp2 | a0001 | c0001 | t0063 | g0206 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18960 | hp1 | a0001 | c0001 | t0070 | g0263 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18960 | hp2 | a0001 | c0003 | t0010 | g0025 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18961 | hp1 | a0001 | c0003 | t0002 | g0299 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18961 | hp2 | a0001 | c0002 | t0039 | g0061 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18963 | hp1 | a0001 | c0003 | t0006 | g0065 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18963 | hp2 | a0001 | c0002 | t0034 | g0298 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18964 | hp1 | a0001 | c0002 | t0022 | g0124 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18964 | hp2 | a0001 | c0003 | t0010 | g0025 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18965 | hp1 | a0001 | c0002 | t0031 | g0278 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18968 | hp1 | a0001 | c0001 | t0060 | g0018 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18968 | hp2 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18971 | hp2 | a0001 | c0003 | t0026 | g0006 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18973 | hp1 | a0001 | c0003 | t0003 | g0173 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18973 | hp2 | a0001 | c0002 | t0006 | g0058 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18974 | hp1 | a0001 | c0002 | t0018 | g0120 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18974 | hp2 | a0001 | c0003 | t0002 | g0228 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18979 | hp1 | a0001 | c0002 | t0018 | g0015 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18979 | hp2 | a0001 | c0003 | t0020 | g0230 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18980 | hp1 | a0001 | c0003 | t0026 | g0006 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18980 | hp2 | a0001 | c0002 | t0003 | g0130 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18981 | hp1 | a0001 | c0002 | t0003 | g0185 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18981 | hp2 | a0001 | c0001 | t0069 | g0021 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18985 | hp1 | a0001 | c0003 | t0026 | g0062 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18985 | hp2 | a0001 | c0001 | t0064 | g0197 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18986 | hp1 | a0001 | c0003 | t0002 | g0117 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18986 | hp2 | a0001 | c0002 | t0003 | g0141 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18989 | hp2 | a0001 | c0003 | t0003 | g0175 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18992 | hp1 | a0001 | c0002 | t0003 | g0143 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18992 | hp2 | a0001 | c0001 | t0074 | g0001 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18994 | hp1 | a0001 | c0003 | t0006 | g0066 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18995 | hp1 | a0001 | c0003 | t0098 | g0170 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18995 | hp2 | a0001 | c0001 | t0059 | g0208 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18998 | hp1 | a0001 | c0003 | t0002 | g0225 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18998 | hp2 | a0001 | c0001 | t0017 | g0284 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18999 | hp1 | a0001 | c0001 | t0012 | g0063 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18999 | hp2 | a0001 | c0003 | t0002 | g0236 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19001 | hp1 | a0001 | c0002 | t0022 | g0125 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19001 | hp2 | a0001 | c0001 | t0062 | g0200 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19002 | hp1 | a0001 | c0001 | t0055 | g0001 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19002 | hp2 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19003 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19003 | hp2 | a0001 | c0003 | t0107 | g0181 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19004 | hp2 | a0001 | c0003 | t0036 | g0002 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19005 | hp1 | a0001 | c0001 | t0075 | g0021 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19005 | hp2 | a0001 | c0002 | t0097 | g0004 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19009 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19009 | hp2 | a0001 | c0003 | t0002 | g0226 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19011 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19011 | hp2 | a0001 | c0001 | t0057 | g0218 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19030 | hp1 | a0001 | c0001 | t0047 | g0287 | AFR | LWK | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19030 | hp2 | a0001 | c0001 | t0083 | g0086 | AFR | LWK | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19043 | hp1 | a0001 | c0001 | t0013 | g0032 | AFR | LWK | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0068 | AFR | LWK | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19054 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19056 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19056 | hp2 | a0001 | c0003 | t0002 | g0166 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19057 | hp1 | a0001 | c0002 | t0003 | g0140 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19057 | hp2 | a0001 | c0003 | t0006 | g0064 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19060 | hp1 | a0001 | c0003 | t0010 | g0294 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19065 | hp1 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19066 | hp1 | a0001 | c0001 | t0017 | g0223 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19066 | hp2 | a0001 | c0003 | t0002 | g0154 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19072 | hp1 | a0001 | c0003 | t0056 | g0182 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19072 | hp2 | a0001 | c0001 | t0015 | g0193 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19075 | hp1 | a0001 | c0002 | t0003 | g0123 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19075 | hp2 | a0001 | c0003 | t0002 | g0118 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19077 | hp1 | a0001 | c0002 | t0003 | g0135 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19077 | hp2 | a0001 | c0003 | t0035 | g0281 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19079 | hp1 | a0001 | c0003 | t0006 | g0012 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19079 | hp2 | a0001 | c0002 | t0015 | g0126 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19080 | hp1 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19081 | hp1 | a0001 | c0001 | t0016 | g0203 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19081 | hp2 | a0001 | c0003 | t0002 | g0112 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19084 | hp2 | a0001 | c0003 | t0010 | g0296 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19087 | hp1 | a0001 | c0002 | t0022 | g0142 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19088 | hp1 | a0001 | c0003 | t0002 | g0016 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19090 | hp1 | a0001 | c0002 | t0003 | g0079 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19090 | hp2 | a0001 | c0003 | t0130 | g0006 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19091 | hp1 | a0001 | c0003 | t0106 | g0169 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19091 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19240 | hp1 | a0001 | c0001 | t0066 | g0082 | AFR | YRI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19240 | hp2 | a0001 | c0001 | t0085 | g0289 | AFR | YRI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20129 | hp1 | a0001 | c0002 | t0007 | g0232 | AFR | ASW | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20129 | hp2 | a0001 | c0001 | t0024 | g0007 | AFR | ASW | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20752 | hp2 | a0001 | c0001 | t0037 | g0030 | EUR | TSI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20805 | hp1 | a0001 | c0002 | t0003 | g0015 | EUR | TSI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | TSI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02109 | hp1 | a0001 | c0001 | t0115 | g0098 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02109 | hp2 | a0001 | c0002 | t0014 | g0085 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02486 | hp1 | a0001 | c0001 | t0048 | g0273 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02486 | hp2 | a0001 | c0001 | t0023 | g0013 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0056 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02559 | hp2 | a0001 | c0001 | t0023 | g0013 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03471 | hp1 | a0001 | c0001 | t0045 | g0144 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03471 | hp2 | a0001 | c0003 | t0002 | g0005 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG06807 | hp1 | a0001 | c0002 | t0007 | g0107 | AFR | USA | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG06807 | hp2 | a0001 | c0003 | t0002 | g0164 | AFR | USA | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20300 | hp1 | a0001 | c0002 | t0029 | g0186 | AFR | USA | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20300 | hp2 | a0001 | c0001 | t0080 | g0148 | AFR | USA | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA21309 | hp1 | a0001 | c0003 | t0129 | g0027 | AFR | LWK | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA21309 | hp2 | a0001 | c0001 | t0091 | g0091 | AFR | LWK | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112485925 | C | T | 1 | a0002 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.166C>T | p.Pro56Ser | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/7 | 355/14267 | 166/1134 | 56/377 | chr2 | 112485925 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112494341 | C | T | 1 | a0001c0004 | 2 | HG01496.hp1 HG01928.hp2 |
synonymous_variant | LOW | c.435C>T | p.Asn145Asn | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/7 | 624/14267 | 435/1134 | 145/377 | chr2 | 112494341 | |||
chr2:112501339 | C | T | 3 | a0001c0002 a0001c0003 a0002c0005 |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
splice_region_variant&synonymous_variant | LOW | c.603C>T | p.Ile201Ile | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/7 | 792/14267 | 603/1134 | 201/377 | chr2 | 112501339 | |||
chr2:112520372 | T | C | 1 | a0001c0003 | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
synonymous_variant | LOW | c.966T>C | p.Asp322Asp | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/7 | 1155/14267 | 966/1134 | 322/377 | chr2 | 112520372 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112482172 | C | G | 1 | a0001c0002t0133 | 1 | HG03098.hp2 | 5_prime_UTR_variant | MODIFIER | c.-173C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/7 | 173 | chr2 | 112482172 | ||||||
chr2:112482173 | CCGGCGGG others(68): Show |
C | 1 | a0001c0002t0132 | 1 | HG02135.hp1 | 5_prime_UTR_variant | MODIFIER | c.-154_-80delCGGCGCC others(68): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/7 | 80 | INFO_REALIGN_3_PRIME | chr2 | 112482173 | |||||
chr2:112482234 | G | T | 1 | a0001c0003t0026 | 3 | NA18971.hp2 NA18980.hp1 NA18985.hp1 |
5_prime_UTR_variant | MODIFIER | c.-111G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/7 | 111 | chr2 | 112482234 | ||||||
chr2:112482256 | C | T | 27 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0012 others(24): Show |
54 | HG00639.hp1 HG00738.hp2 HG01074.hp2 others(51): Show |
5_prime_UTR_variant | MODIFIER | c.-89C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/7 | 89 | chr2 | 112482256 | ||||||
chr2:112528915 | T | A | 5 | a0001c0002t0008 a0001c0002t0040 a0001c0002t0041 others(2): Show |
10 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*120T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 120 | chr2 | 112528915 | ||||||
chr2:112528932 | C | T | 4 | a0001c0001t0023 a0001c0001t0024 a0001c0001t0114 others(1): Show |
8 | HG01167.hp2 HG01243.hp1 HG02109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*137C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 137 | chr2 | 112528932 | ||||||
chr2:112528933 | G | A | 2 | a0001c0001t0044 a0001c0001t0045 |
2 | HG02818.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*138G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 138 | chr2 | 112528933 | ||||||
chr2:112528985 | A | G | 134 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(131): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*190A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 190 | chr2 | 112528985 | ||||||
chr2:112529074 | C | T | 1 | a0001c0001t0113 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*279C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 279 | chr2 | 112529074 | ||||||
chr2:112529080 | C | T | 4 | a0001c0001t0023 a0001c0001t0024 a0001c0001t0114 others(1): Show |
8 | HG01167.hp2 HG01243.hp1 HG02109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*285C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 285 | chr2 | 112529080 | ||||||
chr2:112529182 | G | A | 1 | a0001c0002t0040 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*387G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 387 | chr2 | 112529182 | ||||||
chr2:112529337 | C | T | 1 | a0001c0002t0040 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*542C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 542 | chr2 | 112529337 | ||||||
chr2:112529386 | C | A | 4 | a0001c0001t0023 a0001c0001t0024 a0001c0001t0114 others(1): Show |
8 | HG01167.hp2 HG01243.hp1 HG02109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*591C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 591 | chr2 | 112529386 | ||||||
chr2:112529622 | T | A | 2 | a0001c0002t0049 a0001c0002t0050 |
2 | HG02896.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*827T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 827 | chr2 | 112529622 | ||||||
chr2:112529741 | T | C | 2 | a0001c0001t0015 a0001c0002t0015 |
3 | NA18943.hp2 NA19072.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*946T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 946 | chr2 | 112529741 | ||||||
chr2:112529752 | C | G | 117 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(114): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
3_prime_UTR_variant | MODIFIER | c.*957C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 957 | chr2 | 112529752 | ||||||
chr2:112530117 | C | T | 1 | a0001c0001t0112 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1322C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 1322 | chr2 | 112530117 | ||||||
chr2:112530153 | A | G | 4 | a0001c0002t0040 a0001c0002t0049 a0001c0002t0050 others(1): Show |
4 | HG02896.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1358A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 1358 | chr2 | 112530153 | ||||||
chr2:112530387 | A | G | 114 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(111): Show |
286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*1592A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 1592 | chr2 | 112530387 | ||||||
chr2:112530436 | T | C | 1 | a0001c0001t0055 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1641T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 1641 | chr2 | 112530436 | ||||||
chr2:112530608 | G | A | 1 | a0001c0003t0056 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1813G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 1813 | chr2 | 112530608 | ||||||
chr2:112531003 | G | A | 134 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(131): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*2208G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2208 | chr2 | 112531003 | ||||||
chr2:112531011 | C | T | 48 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0095 others(45): Show |
141 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*2216C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2216 | chr2 | 112531011 | ||||||
chr2:112531064 | C | T | 2 | a0001c0001t0093 a0001c0001t0094 |
2 | HG02683.hp2 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2269C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2269 | chr2 | 112531064 | ||||||
chr2:112531065 | G | A | 1 | a0001c0002t0049 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2270G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2270 | chr2 | 112531065 | ||||||
chr2:112531132 | A | G | 5 | a0001c0001t0030 a0001c0001t0038 a0001c0001t0091 others(2): Show |
7 | HG01175.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2337A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2337 | chr2 | 112531132 | ||||||
chr2:112531200 | T | C | 1 | a0001c0002t0014 | 3 | HG02109.hp2 HG03195.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2405T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2405 | chr2 | 112531200 | ||||||
chr2:112531364 | C | G | 1 | a0001c0002t0131 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2569C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2569 | chr2 | 112531364 | ||||||
chr2:112531455 | A | G | 46 | a0001c0001t0006 a0001c0001t0030 a0001c0001t0090 others(43): Show |
137 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*2660A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2660 | chr2 | 112531455 | ||||||
chr2:112531645 | A | AC | 2 | a0001c0001t0024 a0001c0001t0114 |
4 | HG01167.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2850_*2851insC | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2851 | chr2 | 112531645 | ||||||
chr2:112531681 | A | G | 1 | a0001c0002t0133 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2886A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2886 | chr2 | 112531681 | ||||||
chr2:112531893 | A | C | 1 | a0001c0001t0089 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3098A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 3098 | chr2 | 112531893 | ||||||
chr2:112532124 | T | G | 118 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(115): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*3329T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 3329 | chr2 | 112532124 | ||||||
chr2:112532623 | A | T | 1 | a0001c0001t0088 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3828A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 3828 | chr2 | 112532623 | ||||||
chr2:112532630 | A | C | 1 | a0001c0002t0133 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3835A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 3835 | chr2 | 112532630 | ||||||
chr2:112532658 | G | A | 1 | a0001c0002t0040 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3863G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 3863 | chr2 | 112532658 | ||||||
chr2:112532737 | T | G | 133 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(130): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
3_prime_UTR_variant | MODIFIER | c.*3942T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 3942 | chr2 | 112532737 | ||||||
chr2:112532765 | C | CTCTTAAA others(14): Show |
133 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(130): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
3_prime_UTR_variant | MODIFIER | c.*3975_*3976insAAAA others(17): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 3976 | INFO_REALIGN_3_PRIME | chr2 | 112532765 | |||||
chr2:112532824 | G | T | 1 | a0001c0002t0133 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4029G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 4029 | chr2 | 112532824 | ||||||
chr2:112532869 | T | C | 1 | a0001c0002t0097 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4074T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 4074 | chr2 | 112532869 | ||||||
chr2:112533153 | A | C | 2 | a0001c0002t0007 a0001c0002t0011 |
12 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4358A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 4358 | chr2 | 112533153 | ||||||
chr2:112533207 | C | T | 4 | a0001c0002t0008 a0001c0002t0041 a0001c0002t0042 others(1): Show |
9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4412C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 4412 | chr2 | 112533207 | ||||||
chr2:112533301 | A | T | 4 | a0001c0002t0008 a0001c0002t0041 a0001c0002t0042 others(1): Show |
9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4506A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 4506 | chr2 | 112533301 | ||||||
chr2:112533412 | T | G | 1 | a0001c0003t0098 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4617T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 4617 | chr2 | 112533412 | ||||||
chr2:112533630 | G | C | 2 | a0001c0002t0049 a0001c0002t0050 |
2 | HG02896.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4835G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 4835 | chr2 | 112533630 | ||||||
chr2:112533808 | G | A | 45 | a0001c0001t0006 a0001c0001t0030 a0001c0002t0002 others(42): Show |
136 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*5013G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5013 | chr2 | 112533808 | ||||||
chr2:112533896 | T | C | 1 | a0001c0001t0057 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5101T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5101 | chr2 | 112533896 | ||||||
chr2:112534102 | C | T | 116 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(113): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*5307C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5307 | chr2 | 112534102 | ||||||
chr2:112534109 | A | G | 1 | a0001c0002t0040 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5314A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5314 | chr2 | 112534109 | ||||||
chr2:112534182 | C | T | 1 | a0001c0002t0040 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5387C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5387 | chr2 | 112534182 | ||||||
chr2:112534189 | A | G | 6 | a0001c0002t0009 a0001c0002t0029 a0001c0002t0054 others(3): Show |
12 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5394A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5394 | chr2 | 112534189 | ||||||
chr2:112534209 | A | G | 1 | a0001c0003t0036 | 2 | NA18954.hp1 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5414A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5414 | chr2 | 112534209 | ||||||
chr2:112534277 | G | A | 2 | a0001c0001t0013 a0001c0001t0095 |
5 | HG01109.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5482G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5482 | chr2 | 112534277 | ||||||
chr2:112534323 | CAA | C | 10 | a0001c0001t0058 a0001c0001t0059 a0001c0001t0060 others(7): Show |
13 | HG01358.hp2 HG01361.hp1 HG02129.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5549_*5550delAA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5549 | INFO_REALIGN_3_PRIME | chr2 | 112534323 | |||||
chr2:112534323 | CAAA | C | 106 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(103): Show |
286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*5548_*5550delAAA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5548 | INFO_REALIGN_3_PRIME | chr2 | 112534323 | |||||
chr2:112534323 | CAAAA | C | 15 | a0001c0001t0087 a0001c0002t0008 a0001c0002t0009 others(12): Show |
27 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5547_*5550delAAAA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5547 | INFO_REALIGN_3_PRIME | chr2 | 112534323 | |||||
chr2:112534412 | C | G | 1 | a0001c0002t0122 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5617C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5617 | chr2 | 112534412 | ||||||
chr2:112534486 | G | C | 1 | a0001c0001t0114 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5691G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5691 | chr2 | 112534486 | ||||||
chr2:112534701 | A | G | 2 | a0001c0002t0108 a0001c0002t0111 |
2 | HG02683.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5906A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5906 | chr2 | 112534701 | ||||||
chr2:112534817 | C | G | 113 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(110): Show |
285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*6022C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6022 | chr2 | 112534817 | ||||||
chr2:112534872 | CG | C | 13 | a0001c0002t0007 a0001c0002t0009 a0001c0002t0011 others(10): Show |
31 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*6078delG | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6078 | chr2 | 112534872 | ||||||
chr2:112534893 | A | G | 1 | a0001c0002t0040 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6098A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6098 | chr2 | 112534893 | ||||||
chr2:112534966 | G | A | 1 | a0001c0001t0113 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6171G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6171 | chr2 | 112534966 | ||||||
chr2:112535100 | AAGTT | A | 1 | a0001c0002t0014 | 3 | HG02109.hp2 HG03195.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6310_*6313delAGTT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6310 | INFO_REALIGN_3_PRIME | chr2 | 112535100 | |||||
chr2:112535194 | G | T | 133 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(130): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
3_prime_UTR_variant | MODIFIER | c.*6399G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6399 | chr2 | 112535194 | ||||||
chr2:112535204 | A | G | 1 | a0001c0003t0010 | 5 | NA18948.hp1 NA18960.hp2 NA18964.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6409A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6409 | chr2 | 112535204 | ||||||
chr2:112535286 | A | G | 1 | a0001c0001t0086 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6491A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6491 | chr2 | 112535286 | ||||||
chr2:112535303 | C | G | 2 | a0001c0001t0117 a0001c0002t0122 |
2 | HG02965.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6508C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6508 | chr2 | 112535303 | ||||||
chr2:112535305 | G | A | 1 | a0001c0001t0116 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6510G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6510 | chr2 | 112535305 | ||||||
chr2:112535365 | G | A | 4 | a0001c0002t0007 a0001c0002t0011 a0001c0002t0027 others(1): Show |
16 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*6570G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6570 | chr2 | 112535365 | ||||||
chr2:112535396 | A | G | 3 | a0001c0002t0049 a0001c0002t0050 a0001c0002t0133 |
3 | HG02896.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6601A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6601 | chr2 | 112535396 | ||||||
chr2:112535567 | T | TA | 8 | a0001c0002t0007 a0001c0002t0011 a0001c0002t0027 others(5): Show |
20 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*6773dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6774 | INFO_REALIGN_3_PRIME | chr2 | 112535567 | |||||
chr2:112535744 | AT | A | 132 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(129): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
3_prime_UTR_variant | MODIFIER | c.*6957delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6957 | INFO_REALIGN_3_PRIME | chr2 | 112535744 | |||||
chr2:112535771 | A | G | 2 | a0001c0002t0049 a0001c0002t0050 |
2 | HG02896.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6976A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6976 | chr2 | 112535771 | ||||||
chr2:112535820 | T | G | 2 | a0001c0002t0049 a0001c0002t0050 |
2 | HG02896.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7025T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7025 | chr2 | 112535820 | ||||||
chr2:112535934 | A | T | 1 | a0001c0001t0085 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7139A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7139 | chr2 | 112535934 | ||||||
chr2:112535982 | T | G | 57 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0030 others(54): Show |
151 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*7187T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7187 | chr2 | 112535982 | ||||||
chr2:112536004 | C | T | 2 | a0001c0002t0049 a0001c0002t0050 |
2 | HG02896.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7209C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7209 | chr2 | 112536004 | ||||||
chr2:112536045 | G | A | 3 | a0001c0002t0008 a0001c0002t0041 a0001c0002t0042 |
8 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7250G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7250 | chr2 | 112536045 | ||||||
chr2:112536080 | G | A | 1 | a0001c0001t0113 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7285G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7285 | chr2 | 112536080 | ||||||
chr2:112536223 | A | G | 2 | a0001c0001t0046 a0001c0001t0048 |
2 | HG01346.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7428A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7428 | chr2 | 112536223 | ||||||
chr2:112536239 | A | T | 1 | a0001c0001t0037 | 2 | HG01981.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7444A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7444 | chr2 | 112536239 | ||||||
chr2:112536240 | A | T | 8 | a0001c0001t0025 a0001c0001t0037 a0001c0001t0083 others(5): Show |
11 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7445A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7445 | chr2 | 112536240 | ||||||
chr2:112536241 | T | A | 13 | a0001c0001t0066 a0001c0002t0007 a0001c0002t0008 others(10): Show |
30 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*7446T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7446 | chr2 | 112536241 | ||||||
chr2:112536311 | T | G | 1 | a0001c0002t0040 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7516T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7516 | chr2 | 112536311 | ||||||
chr2:112536354 | T | C | 1 | a0001c0001t0124 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7559T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7559 | chr2 | 112536354 | ||||||
chr2:112536408 | A | G | 2 | a0001c0003t0106 a0001c0003t0107 |
2 | NA19003.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7613A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7613 | chr2 | 112536408 | ||||||
chr2:112536429 | A | G | 2 | a0001c0002t0049 a0001c0002t0050 |
2 | HG02896.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7634A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7634 | chr2 | 112536429 | ||||||
chr2:112536721 | C | T | 70 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0030 others(67): Show |
181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*7926C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7926 | chr2 | 112536721 | ||||||
chr2:112536764 | G | A | 63 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0030 others(60): Show |
169 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*7969G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7969 | chr2 | 112536764 | ||||||
chr2:112536919 | A | G | 1 | a0001c0002t0133 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8124A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8124 | chr2 | 112536919 | ||||||
chr2:112537077 | TTTTG | T | 2 | a0001c0002t0029 a0001c0002t0119 |
3 | HG01243.hp2 HG02895.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8303_*8306delTTTG | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8303 | INFO_REALIGN_3_PRIME | chr2 | 112537077 | |||||
chr2:112537161 | A | G | 64 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0030 others(61): Show |
170 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*8366A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8366 | chr2 | 112537161 | ||||||
chr2:112537166 | C | T | 1 | a0001c0001t0082 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8371C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8371 | chr2 | 112537166 | ||||||
chr2:112537179 | T | TA | 64 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0030 others(61): Show |
170 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*8386dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8387 | INFO_REALIGN_3_PRIME | chr2 | 112537179 | |||||
chr2:112537363 | G | T | 3 | a0001c0002t0051 a0001c0002t0052 a0001c0002t0053 |
3 | HG02145.hp1 HG02647.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8568G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8568 | chr2 | 112537363 | ||||||
chr2:112537438 | A | G | 8 | a0001c0001t0066 a0001c0002t0007 a0001c0002t0011 others(5): Show |
20 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*8643A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8643 | chr2 | 112537438 | ||||||
chr2:112537447 | C | T | 1 | a0001c0001t0081 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8652C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8652 | chr2 | 112537447 | ||||||
chr2:112537624 | C | T | 3 | a0001c0001t0023 a0001c0001t0024 a0001c0001t0114 |
7 | HG01167.hp2 HG01243.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8829C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8829 | chr2 | 112537624 | ||||||
chr2:112537710 | C | A | 1 | a0001c0001t0062 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8915C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8915 | chr2 | 112537710 | ||||||
chr2:112537904 | C | G | 1 | a0001c0003t0104 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9109C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9109 | chr2 | 112537904 | ||||||
chr2:112538036 | G | C | 4 | a0001c0001t0038 a0001c0001t0067 a0001c0001t0091 others(1): Show |
5 | HG01891.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9241G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9241 | chr2 | 112538036 | ||||||
chr2:112538046 | A | G | 9 | a0001c0001t0066 a0001c0002t0007 a0001c0002t0011 others(6): Show |
21 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*9251A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9251 | chr2 | 112538046 | ||||||
chr2:112538275 | C | T | 2 | a0001c0001t0046 a0001c0001t0048 |
2 | HG01346.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9480C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9480 | chr2 | 112538275 | ||||||
chr2:112538358 | C | T | 1 | a0001c0001t0081 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9563C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9563 | chr2 | 112538358 | ||||||
chr2:112538421 | A | C | 1 | a0001c0001t0080 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9626A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9626 | chr2 | 112538421 | ||||||
chr2:112538481 | G | A | 36 | a0001c0001t0013 a0001c0001t0062 a0001c0001t0063 others(33): Show |
87 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*9686G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9686 | chr2 | 112538481 | ||||||
chr2:112538526 | C | T | 1 | a0001c0002t0054 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9731C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9731 | chr2 | 112538526 | ||||||
chr2:112538541 | G | A | 26 | a0001c0001t0013 a0001c0001t0062 a0001c0001t0063 others(23): Show |
65 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*9746G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9746 | chr2 | 112538541 | ||||||
chr2:112538626 | G | C | 35 | a0001c0001t0013 a0001c0001t0062 a0001c0001t0063 others(32): Show |
86 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*9831G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9831 | chr2 | 112538626 | ||||||
chr2:112538881 | G | C | 1 | a0001c0001t0068 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10086G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10086 | chr2 | 112538881 | ||||||
chr2:112538883 | C | T | 1 | a0001c0001t0068 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10088C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10088 | chr2 | 112538883 | ||||||
chr2:112538884 | A | G | 1 | a0001c0001t0068 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10089A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10089 | chr2 | 112538884 | ||||||
chr2:112538888 | C | T | 1 | a0001c0003t0103 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10093C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10093 | chr2 | 112538888 | ||||||
chr2:112538914 | A | G | 1 | a0001c0001t0092 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10119A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10119 | chr2 | 112538914 | ||||||
chr2:112538924 | T | C | 1 | a0001c0001t0069 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10129T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10129 | chr2 | 112538924 | ||||||
chr2:112538931 | T | C | 1 | a0001c0003t0130 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10136T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10136 | chr2 | 112538931 | ||||||
chr2:112538955 | A | C | 1 | a0001c0002t0079 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10160A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10160 | chr2 | 112538955 | ||||||
chr2:112538989 | C | T | 1 | a0001c0001t0078 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10194C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10194 | chr2 | 112538989 | ||||||
chr2:112539048 | C | A | 1 | a0001c0001t0070 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10253C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10253 | chr2 | 112539048 | ||||||
chr2:112539111 | T | TA | 12 | a0001c0001t0016 a0001c0001t0025 a0001c0001t0037 others(9): Show |
20 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*10340dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10341 | INFO_REALIGN_3_PRIME | chr2 | 112539111 | |||||
chr2:112539111 | T | TAAA | 7 | a0001c0001t0066 a0001c0001t0127 a0001c0002t0007 others(4): Show |
15 | HG01891.hp1 HG02572.hp2 HG02622.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*10338_*10340dupAA others(1): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10341 | INFO_REALIGN_3_PRIME | chr2 | 112539111 | |||||
chr2:112539111 | T | TAAAA | 2 | a0001c0002t0011 a0001c0002t0027 |
6 | HG02615.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*10337_*10340dupAA others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10341 | INFO_REALIGN_3_PRIME | chr2 | 112539111 | |||||
chr2:112539111 | TA | T | 31 | a0001c0001t0013 a0001c0001t0061 a0001c0001t0062 others(28): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*10340delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10340 | INFO_REALIGN_3_PRIME | chr2 | 112539111 | |||||
chr2:112539111 | TAAAAAAA others(8): Show |
T | 1 | a0001c0002t0034 | 2 | HG00438.hp1 NA18963.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10326_*10340delAA others(13): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10326 | INFO_REALIGN_3_PRIME | chr2 | 112539111 | |||||
chr2:112539162 | A | G | 7 | a0001c0001t0061 a0001c0002t0008 a0001c0002t0041 others(4): Show |
12 | HG00099.hp2 HG00140.hp1 HG01358.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*10367A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10367 | chr2 | 112539162 | ||||||
chr2:112539230 | T | A | 16 | a0001c0001t0062 a0001c0001t0063 a0001c0001t0064 others(13): Show |
51 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*10435T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10435 | chr2 | 112539230 | ||||||
chr2:112539265 | A | G | 7 | a0001c0001t0061 a0001c0002t0008 a0001c0002t0041 others(4): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*10470A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10470 | chr2 | 112539265 | ||||||
chr2:112539293 | C | T | 41 | a0001c0001t0013 a0001c0001t0062 a0001c0001t0063 others(38): Show |
100 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*10498C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10498 | chr2 | 112539293 | ||||||
chr2:112539378 | TTAA | T | 18 | a0001c0001t0025 a0001c0001t0037 a0001c0001t0038 others(15): Show |
22 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*10586_*10588delAT others(1): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10586 | INFO_REALIGN_3_PRIME | chr2 | 112539378 | |||||
chr2:112539425 | T | C | 1 | a0001c0001t0059 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10630T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10630 | chr2 | 112539425 | ||||||
chr2:112539577 | T | TG | 3 | a0001c0003t0021 a0001c0003t0102 a0001c0003t0103 |
5 | HG00280.hp1 HG01981.hp1 HG02055.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*10783dupG | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10784 | INFO_REALIGN_3_PRIME | chr2 | 112539577 | |||||
chr2:112539757 | C | G | 1 | a0001c0001t0076 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10962C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10962 | chr2 | 112539757 | ||||||
chr2:112539794 | T | A | 36 | a0001c0001t0013 a0001c0001t0062 a0001c0001t0063 others(33): Show |
89 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*10999T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10999 | chr2 | 112539794 | ||||||
chr2:112539994 | C | T | 1 | a0001c0003t0101 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11199C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11199 | chr2 | 112539994 | ||||||
chr2:112540089 | T | C | 9 | a0001c0001t0066 a0001c0001t0127 a0001c0002t0007 others(6): Show |
21 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*11294T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11294 | chr2 | 112540089 | ||||||
chr2:112540192 | CT | C | 1 | a0001c0001t0017 | 3 | HG02040.hp2 NA18998.hp2 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11400delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11400 | INFO_REALIGN_3_PRIME | chr2 | 112540192 | |||||
chr2:112540199 | C | T | 36 | a0001c0001t0013 a0001c0001t0062 a0001c0001t0063 others(33): Show |
89 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*11404C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11404 | chr2 | 112540199 | ||||||
chr2:112540208 | C | G | 2 | a0001c0001t0127 a0001c0002t0052 |
2 | HG02717.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11413C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11413 | chr2 | 112540208 | ||||||
chr2:112540273 | A | C | 1 | a0001c0001t0075 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11478A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11478 | chr2 | 112540273 | ||||||
chr2:112540419 | A | G | 5 | a0001c0001t0066 a0001c0002t0007 a0001c0002t0011 others(2): Show |
17 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*11624A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11624 | chr2 | 112540419 | ||||||
chr2:112540433 | C | CA | 15 | a0001c0001t0066 a0001c0001t0072 a0001c0001t0080 others(12): Show |
26 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*11654dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11655 | INFO_REALIGN_3_PRIME | chr2 | 112540433 | |||||
chr2:112540433 | CA | C | 64 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0013 others(61): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*11654delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11654 | INFO_REALIGN_3_PRIME | chr2 | 112540433 | |||||
chr2:112540441 | A | C | 31 | a0001c0001t0013 a0001c0001t0061 a0001c0001t0062 others(28): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*11646A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11646 | chr2 | 112540441 | ||||||
chr2:112540445 | A | G | 22 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0015 others(19): Show |
78 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*11650A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11650 | chr2 | 112540445 | ||||||
chr2:112540447 | AAAG | A | 24 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0015 others(21): Show |
81 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*11654_*11656delAG others(1): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11654 | INFO_REALIGN_3_PRIME | chr2 | 112540447 | |||||
chr2:112540448 | A | G | 3 | a0001c0001t0001 a0001c0001t0068 a0001c0002t0131 |
4 | HG00438.hp2 HG02083.hp2 HG02165.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11653A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11653 | chr2 | 112540448 | ||||||
chr2:112540450 | G | A | 3 | a0001c0001t0001 a0001c0001t0068 a0001c0002t0131 |
4 | HG00438.hp2 HG02083.hp2 HG02165.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11655G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11655 | chr2 | 112540450 | ||||||
chr2:112540608 | A | G | 1 | a0001c0001t0074 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11813A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11813 | chr2 | 112540608 | ||||||
chr2:112540743 | CTT | C | 3 | a0001c0002t0014 a0001c0002t0029 a0001c0002t0119 |
6 | HG01243.hp2 HG02109.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*11952_*11953delTT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11952 | INFO_REALIGN_3_PRIME | chr2 | 112540743 | |||||
chr2:112540783 | G | T | 1 | a0001c0001t0073 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11988G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11988 | chr2 | 112540783 | ||||||
chr2:112540910 | T | C | 1 | a0001c0001t0071 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12115T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12115 | chr2 | 112540910 | ||||||
chr2:112541009 | T | C | 55 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0015 others(52): Show |
132 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*12214T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12214 | chr2 | 112541009 | ||||||
chr2:112541053 | A | G | 5 | a0001c0002t0009 a0001c0002t0014 a0001c0002t0029 others(2): Show |
13 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*12258A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12258 | chr2 | 112541053 | ||||||
chr2:112541106 | A | G | 1 | a0001c0002t0040 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12311A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12311 | chr2 | 112541106 | ||||||
chr2:112541214 | G | A | 3 | a0001c0002t0019 a0001c0003t0019 a0001c0003t0129 |
4 | HG02886.hp2 HG03453.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*12419G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12419 | chr2 | 112541214 | ||||||
chr2:112541239 | A | G | 5 | a0001c0002t0009 a0001c0002t0014 a0001c0002t0029 others(2): Show |
13 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*12444A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12444 | chr2 | 112541239 | ||||||
chr2:112541251 | C | G | 49 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0015 others(46): Show |
118 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*12456C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12456 | chr2 | 112541251 | ||||||
chr2:112541326 | C | A | 1 | a0001c0002t0040 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12531C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12531 | chr2 | 112541326 | ||||||
chr2:112541330 | T | C | 1 | a0001c0003t0026 | 3 | NA18971.hp2 NA18980.hp1 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12535T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12535 | chr2 | 112541330 | ||||||
chr2:112541431 | T | C | 3 | a0001c0001t0046 a0001c0001t0048 a0001c0002t0040 |
3 | HG01346.hp1 HG02486.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12636T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12636 | chr2 | 112541431 | ||||||
chr2:112541560 | CAG | C | 2 | a0001c0001t0013 a0001c0001t0095 |
5 | HG01109.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*12766_*12767delAG | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12766 | chr2 | 112541560 | ||||||
chr2:112541592 | T | C | 1 | a0001c0001t0089 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12797T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12797 | chr2 | 112541592 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112482520 | C | T | 1 | a0001c0001t0123g0301 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.157+19C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482520 | |||||||
chr2:112482551 | G | T | 1 | a0001c0001t0001g0300 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.157+50G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482551 | |||||||
chr2:112482606 | T | C | 71 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0087 others(68): Show |
74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.157+105T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482606 | |||||||
chr2:112482702 | C | T | 1 | a0001c0003t0002g0299 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.157+201C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482702 | |||||||
chr2:112482762 | A | G | 1 | a0001c0002t0008g0089 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.157+261A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482762 | |||||||
chr2:112482773 | C | G | 2 | a0001c0002t0034g0297 a0001c0002t0034g0298 |
2 | HG00438.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.157+272C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482773 | |||||||
chr2:112482794 | C | T | 1 | a0001c0003t0010g0025 | 2 | NA18960.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.157+293C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482794 | |||||||
chr2:112482820 | C | A | 2 | a0001c0001t0072g0090 a0001c0001t0091g0091 |
2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.157+319C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482820 | |||||||
chr2:112482847 | G | GTCCGCCG others(13): Show |
1 | a0001c0001t0001g0087 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.157+352_157+371dup others(20): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 112482847 | ||||||
chr2:112482853 | C | G | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.157+352C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482853 | |||||||
chr2:112482862 | C | CGCTGG | 4 | a0001c0003t0002g0295 a0001c0003t0010g0025 a0001c0003t0010g0294 others(1): Show |
5 | NA18948.hp2 NA18960.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+363_157+364ins others(5): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 112482862 | ||||||
chr2:112482867 | C | G | 4 | a0001c0003t0002g0295 a0001c0003t0010g0025 a0001c0003t0010g0294 others(1): Show |
5 | NA18948.hp2 NA18960.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+366C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482867 | |||||||
chr2:112482985 | C | T | 4 | a0001c0002t0009g0290 a0001c0002t0009g0291 a0001c0002t0009g0292 others(1): Show |
4 | HG01257.hp1 HG01258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+484C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482985 | |||||||
chr2:112482990 | C | A | 1 | a0001c0001t0123g0301 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.157+489C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482990 | |||||||
chr2:112482990 | C | T | 1 | a0001c0001t0085g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.157+489C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482990 | |||||||
chr2:112483127 | T | A | 1 | a0001c0001t0126g0026 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.157+626T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112483127 | |||||||
chr2:112483340 | G | C | 52 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(49): Show |
55 | HG00639.hp1 HG00738.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.157+839G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112483340 | |||||||
chr2:112483344 | G | T | 28 | a0001c0001t0005g0051 a0001c0001t0005g0052 a0001c0001t0005g0053 others(25): Show |
30 | HG00639.hp1 HG01074.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.157+843G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112483344 | |||||||
chr2:112483385 | C | T | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.157+884C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112483385 | |||||||
chr2:112484210 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.158-1707C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484210 | |||||||
chr2:112484234 | G | GT | 13 | a0001c0001t0001g0286 a0001c0001t0004g0283 a0001c0001t0013g0044 others(10): Show |
13 | HG00741.hp2 HG01109.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.158-1668dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 112484234 | ||||||
chr2:112484234 | GT | G | 12 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0087 others(9): Show |
12 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-1668delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 112484234 | ||||||
chr2:112484302 | C | T | 4 | a0001c0001t0083g0086 a0001c0002t0014g0083 a0001c0002t0014g0084 others(1): Show |
4 | HG02109.hp2 HG03195.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-1615C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484302 | |||||||
chr2:112484354 | C | T | 1 | a0001c0001t0124g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.158-1563C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484354 | |||||||
chr2:112484408 | C | T | 4 | a0001c0001t0083g0086 a0001c0002t0014g0083 a0001c0002t0014g0084 others(1): Show |
4 | HG02109.hp2 HG03195.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-1509C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484408 | |||||||
chr2:112484466 | T | G | 1 | a0001c0002t0019g0093 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.158-1451T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484466 | |||||||
chr2:112484645 | C | G | 3 | a0001c0002t0019g0093 a0001c0002t0051g0275 a0001c0002t0053g0276 |
3 | HG02145.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.158-1272C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484645 | |||||||
chr2:112484688 | A | G | 2 | a0001c0001t0025g0011 a0001c0001t0025g0042 |
3 | HG00738.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.158-1229A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484688 | |||||||
chr2:112484781 | C | G | 1 | a0001c0002t0019g0093 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.158-1136C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484781 | |||||||
chr2:112484988 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.158-929C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484988 | |||||||
chr2:112485050 | A | G | 3 | a0001c0002t0019g0093 a0001c0002t0051g0275 a0001c0002t0053g0276 |
3 | HG02145.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.158-867A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112485050 | |||||||
chr2:112485711 | A | G | 2 | a0001c0001t0066g0082 a0001c0002t0043g0081 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.158-206A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112485711 | |||||||
chr2:112485744 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(222): Show |
249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.158-173G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112485744 | |||||||
chr2:112485877 | G | GGGGCTGA others(17): Show |
30 | a0001c0001t0006g0056 a0001c0001t0023g0013 a0001c0001t0023g0101 others(27): Show |
35 | HG01167.hp2 HG01243.hp1 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.158-40_158-39insGG others(22): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112485877 | |||||||
chr2:112486113 | A | G | 1 | a0001c0003t0002g0236 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.236+118A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486113 | |||||||
chr2:112486137 | G | A | 1 | a0001c0001t0088g0237 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.236+142G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486137 | |||||||
chr2:112486197 | A | G | 2 | a0001c0001t0083g0086 a0001c0001t0121g0041 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.236+202A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486197 | |||||||
chr2:112486222 | T | A | 12 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0066g0082 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+227T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486222 | |||||||
chr2:112486345 | C | G | 2 | a0001c0002t0108g0285 a0001c0002t0111g0235 |
2 | HG02683.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.236+350C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486345 | |||||||
chr2:112486355 | C | G | 2 | a0001c0002t0049g0234 a0001c0002t0050g0233 |
2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.236+360C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486355 | |||||||
chr2:112486438 | T | C | 1 | a0001c0001t0006g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.236+443T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486438 | |||||||
chr2:112486447 | A | T | 2 | a0001c0002t0049g0234 a0001c0002t0050g0233 |
2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.236+452A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486447 | |||||||
chr2:112486675 | G | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(284): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.236+680G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486675 | |||||||
chr2:112486682 | G | C | 2 | a0001c0001t0072g0090 a0001c0001t0085g0289 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.236+687G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486682 | |||||||
chr2:112486721 | C | T | 12 | a0001c0001t0012g0063 a0001c0003t0002g0225 a0001c0003t0002g0226 others(9): Show |
13 | HG02129.hp1 NA18945.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.236+726C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486721 | |||||||
chr2:112486759 | G | A | 1 | a0001c0003t0002g0112 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.236+764G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486759 | |||||||
chr2:112486946 | C | T | 1 | a0001c0002t0053g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+951C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486946 | |||||||
chr2:112487064 | G | A | 1 | a0001c0001t0081g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.236+1069G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487064 | |||||||
chr2:112487092 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(126): Show |
143 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.236+1097C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487092 | |||||||
chr2:112487093 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(126): Show |
143 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.236+1098A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487093 | |||||||
chr2:112487170 | C | T | 1 | a0001c0003t0128g0028 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.236+1175C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487170 | |||||||
chr2:112487383 | A | G | 13 | a0001c0001t0001g0087 a0001c0002t0008g0070 a0001c0002t0008g0072 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.236+1388A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487383 | |||||||
chr2:112487556 | G | A | 1 | a0001c0001t0066g0082 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.236+1561G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487556 | |||||||
chr2:112487866 | T | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(286): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.236+1871T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487866 | |||||||
chr2:112487870 | T | G | 1 | a0001c0001t0005g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.236+1875T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487870 | |||||||
chr2:112488084 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(299): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.236+2089A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488084 | |||||||
chr2:112488150 | C | T | 2 | a0001c0002t0003g0184 a0001c0002t0003g0185 |
2 | NA18981.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.236+2155C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488150 | |||||||
chr2:112488434 | G | A | 12 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+2439G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488434 | |||||||
chr2:112488483 | C | T | 1 | a0001c0002t0053g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+2488C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488483 | |||||||
chr2:112488588 | T | C | 1 | a0001c0003t0019g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.236+2593T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488588 | |||||||
chr2:112488766 | AG | A | 8 | a0001c0001t0072g0090 a0001c0001t0094g0241 a0001c0002t0003g0115 others(5): Show |
8 | HG01070.hp2 HG02040.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+2772delG | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488766 | |||||||
chr2:112488767 | G | A | 281 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(278): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.236+2772G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488767 | |||||||
chr2:112488859 | C | T | 71 | a0001c0003t0002g0002 a0001c0003t0002g0005 a0001c0003t0002g0016 others(68): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.236+2864C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488859 | |||||||
chr2:112488960 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.236+2965G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488960 | |||||||
chr2:112489032 | A | C | 1 | a0001c0002t0003g0080 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.236+3037A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489032 | |||||||
chr2:112489085 | T | C | 1 | a0001c0001t0001g0243 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.236+3090T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489085 | |||||||
chr2:112489197 | C | T | 1 | a0001c0001t0090g0224 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.236+3202C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489197 | |||||||
chr2:112489273 | C | T | 1 | a0001c0001t0048g0273 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.236+3278C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489273 | |||||||
chr2:112489283 | C | G | 2 | a0001c0001t0046g0272 a0001c0001t0048g0273 |
2 | HG01346.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.236+3288C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489283 | |||||||
chr2:112489370 | A | C | 12 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+3375A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489370 | |||||||
chr2:112489396 | C | T | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.236+3401C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489396 | |||||||
chr2:112489444 | G | T | 1 | a0001c0001t0017g0223 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.236+3449G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489444 | |||||||
chr2:112489462 | A | C | 3 | a0001c0003t0002g0239 a0001c0003t0032g0183 a0001c0003t0033g0240 |
3 | HG02083.hp1 HG04184.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.236+3467A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489462 | |||||||
chr2:112489726 | G | C | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.236+3731G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489726 | |||||||
chr2:112489912 | A | T | 1 | a0001c0001t0038g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.236+3917A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489912 | |||||||
chr2:112490039 | G | T | 4 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(1): Show |
4 | HG01891.hp1 HG02647.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+4044G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490039 | |||||||
chr2:112490043 | C | G | 69 | a0001c0003t0002g0002 a0001c0003t0002g0005 a0001c0003t0002g0016 others(66): Show |
79 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.236+4048C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490043 | |||||||
chr2:112490059 | C | T | 12 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(9): Show |
12 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+4064C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490059 | |||||||
chr2:112490178 | G | A | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.237-3965G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490178 | |||||||
chr2:112490213 | C | T | 12 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(9): Show |
12 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.237-3930C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490213 | |||||||
chr2:112490291 | G | A | 1 | a0001c0002t0052g0094 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.237-3852G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490291 | |||||||
chr2:112490410 | C | A | 1 | a0001c0001t0094g0241 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.237-3733C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490410 | |||||||
chr2:112490559 | T | A | 2 | a0001c0002t0118g0039 a0001c0002t0120g0069 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.237-3584T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490559 | |||||||
chr2:112490568 | C | CT | 15 | a0001c0001t0001g0024 a0001c0001t0001g0078 a0001c0001t0001g0092 others(12): Show |
16 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.237-3553dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 112490568 | ||||||
chr2:112490568 | CT | C | 29 | a0001c0001t0001g0190 a0001c0001t0082g0189 a0001c0002t0003g0143 others(26): Show |
32 | HG01257.hp1 HG01891.hp1 HG02135.hp1 others(29): Show |
intron_variant | MODIFIER | c.237-3553delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 112490568 | ||||||
chr2:112490568 | CTT | C | 67 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(64): Show |
71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.237-3554_237-3553d others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 112490568 | ||||||
chr2:112490568 | CTTTTTT | C | 64 | a0001c0003t0002g0002 a0001c0003t0002g0005 a0001c0003t0002g0016 others(61): Show |
74 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.237-3558_237-3553d others(8): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 112490568 | ||||||
chr2:112490571 | T | C | 2 | a0001c0002t0049g0234 a0001c0002t0050g0233 |
2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.237-3572T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490571 | |||||||
chr2:112490655 | C | T | 18 | a0001c0001t0001g0001 a0001c0001t0004g0001 a0001c0001t0004g0215 others(15): Show |
21 | HG01361.hp2 HG01496.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.237-3488C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490655 | |||||||
chr2:112490675 | G | A | 1 | a0001c0003t0002g0299 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.237-3468G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490675 | |||||||
chr2:112490727 | A | G | 12 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-3416A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490727 | |||||||
chr2:112490784 | G | A | 3 | a0001c0002t0029g0186 a0001c0002t0029g0187 a0001c0002t0119g0040 |
3 | HG01243.hp2 HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.237-3359G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490784 | |||||||
chr2:112490938 | C | G | 12 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(9): Show |
12 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.237-3205C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490938 | |||||||
chr2:112490999 | C | T | 1 | a0001c0001t0004g0220 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.237-3144C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490999 | |||||||
chr2:112491055 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.237-3088G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112491055 | |||||||
chr2:112491096 | A | G | 12 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-3047A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112491096 | |||||||
chr2:112491125 | G | A | 2 | a0001c0003t0100g0150 a0001c0003t0128g0028 |
2 | HG01074.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.237-3018G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112491125 | |||||||
chr2:112491390 | T | C | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.237-2753T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112491390 | |||||||
chr2:112491545 | T | C | 3 | a0001c0002t0014g0083 a0001c0002t0014g0084 a0001c0002t0014g0085 |
3 | HG02109.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.237-2598T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112491545 | |||||||
chr2:112491743 | A | G | 3 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 |
3 | HG01891.hp1 HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.237-2400A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112491743 | |||||||
chr2:112491768 | A | G | 3 | a0001c0002t0029g0186 a0001c0002t0029g0187 a0001c0002t0119g0040 |
3 | HG01243.hp2 HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.237-2375A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112491768 | |||||||
chr2:112492056 | C | T | 1 | a0001c0002t0108g0285 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.237-2087C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492056 | |||||||
chr2:112492259 | T | C | 1 | a0001c0002t0051g0275 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.237-1884T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492259 | |||||||
chr2:112492274 | G | A | 1 | a0001c0001t0080g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.237-1869G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492274 | |||||||
chr2:112492354 | G | A | 2 | a0001c0002t0009g0290 a0001c0002t0054g0096 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.237-1789G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492354 | |||||||
chr2:112492444 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.237-1699G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492444 | |||||||
chr2:112492742 | T | A | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.237-1401T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492742 | |||||||
chr2:112492783 | C | T | 71 | a0001c0003t0002g0002 a0001c0003t0002g0005 a0001c0003t0002g0016 others(68): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.237-1360C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492783 | |||||||
chr2:112492904 | A | T | 1 | a0001c0001t0058g0212 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.237-1239A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492904 | |||||||
chr2:112492952 | T | C | 54 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(51): Show |
58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.237-1191T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492952 | |||||||
chr2:112493135 | T | G | 51 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(48): Show |
55 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.237-1008T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493135 | |||||||
chr2:112493160 | G | A | 54 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(51): Show |
58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.237-983G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493160 | |||||||
chr2:112493212 | G | A | 1 | a0001c0002t0028g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.237-931G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493212 | |||||||
chr2:112493215 | C | G | 1 | a0001c0002t0049g0234 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237-928C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493215 | |||||||
chr2:112493355 | T | TA | 78 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(75): Show |
88 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.237-774dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 112493355 | ||||||
chr2:112493423 | C | T | 180 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(177): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.237-720C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493423 | |||||||
chr2:112493570 | A | T | 1 | a0001c0001t0081g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.237-573A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493570 | |||||||
chr2:112493571 | T | C | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.237-572T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493571 | |||||||
chr2:112493582 | G | A | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.237-561G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493582 | |||||||
chr2:112493764 | C | G | 1 | a0001c0001t0083g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.237-379C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493764 | |||||||
chr2:112493826 | A | G | 7 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(4): Show |
7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-317A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493826 | |||||||
chr2:112493966 | C | T | 1 | a0001c0002t0053g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-177C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493966 | |||||||
chr2:112494134 | A | T | 4 | a0001c0001t0013g0010 a0001c0001t0013g0033 a0001c0001t0013g0044 others(1): Show |
4 | HG01109.hp1 HG02055.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-9A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112494134 | |||||||
chr2:112494445 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.469+70C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494445 | |||||||
chr2:112494467 | G | A | 1 | a0001c0002t0003g0119 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.469+92G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494467 | |||||||
chr2:112494540 | T | C | 7 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(4): Show |
7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+165T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494540 | |||||||
chr2:112494685 | T | C | 1 | a0001c0002t0119g0040 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.469+310T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494685 | |||||||
chr2:112494713 | CT | C | 3 | a0001c0001t0072g0090 a0001c0001t0080g0148 a0001c0001t0085g0289 |
3 | HG02922.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.469+339delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494713 | |||||||
chr2:112494762 | C | G | 1 | a0001c0003t0002g0112 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.469+387C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494762 | |||||||
chr2:112494826 | A | G | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.469+451A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494826 | |||||||
chr2:112494849 | C | T | 1 | a0001c0002t0009g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.469+474C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494849 | |||||||
chr2:112494888 | T | C | 7 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(4): Show |
7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+513T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494888 | |||||||
chr2:112495011 | G | A | 7 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(4): Show |
7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+636G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495011 | |||||||
chr2:112495148 | A | G | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.469+773A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495148 | |||||||
chr2:112495188 | T | C | 1 | a0001c0003t0002g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.469+813T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495188 | |||||||
chr2:112495250 | C | T | 1 | a0001c0001t0125g0031 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.469+875C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495250 | |||||||
chr2:112495421 | A | G | 12 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.469+1046A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495421 | |||||||
chr2:112495482 | T | C | 1 | a0001c0001t0083g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.469+1107T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495482 | |||||||
chr2:112495601 | G | A | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.469+1226G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495601 | |||||||
chr2:112495613 | C | T | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.469+1238C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495613 | |||||||
chr2:112495657 | C | T | 5 | a0001c0001t0005g0051 a0001c0001t0005g0052 a0001c0001t0005g0053 others(2): Show |
5 | HG00639.hp1 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+1282C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495657 | |||||||
chr2:112495675 | G | A | 155 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(152): Show |
172 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.469+1300G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495675 | |||||||
chr2:112495728 | T | C | 2 | a0001c0001t0030g0191 a0001c0001t0030g0192 |
2 | HG01175.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.469+1353T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495728 | |||||||
chr2:112495764 | G | A | 71 | a0001c0003t0002g0002 a0001c0003t0002g0005 a0001c0003t0002g0016 others(68): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.469+1389G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495764 | |||||||
chr2:112495846 | T | TA | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.469+1481dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112495846 | ||||||
chr2:112495962 | G | C | 2 | a0001c0001t0046g0272 a0001c0001t0048g0273 |
2 | HG01346.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.469+1587G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495962 | |||||||
chr2:112495974 | A | G | 1 | a0001c0002t0122g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.469+1599A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495974 | |||||||
chr2:112496108 | C | T | 12 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.469+1733C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496108 | |||||||
chr2:112496194 | C | A | 5 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.469+1819C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496194 | |||||||
chr2:112496569 | A | G | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.469+2194A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496569 | |||||||
chr2:112496665 | C | CTG | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(68): Show |
82 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.469+2332_469+2333d others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | ||||||
chr2:112496665 | C | CTGTG | 20 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0207 others(17): Show |
22 | HG00438.hp2 HG00673.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.469+2330_469+2333d others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | ||||||
chr2:112496665 | C | CTGTGTG | 10 | a0001c0001t0012g0063 a0001c0001t0013g0010 a0001c0001t0013g0033 others(7): Show |
10 | HG01109.hp1 HG01496.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.469+2328_469+2333d others(8): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | ||||||
chr2:112496665 | CTG | C | 57 | a0001c0001t0001g0077 a0001c0001t0001g0244 a0001c0001t0001g0268 others(54): Show |
67 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.469+2332_469+2333d others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | ||||||
chr2:112496665 | CTGTG | C | 16 | a0001c0001t0001g0286 a0001c0002t0007g0104 a0001c0002t0008g0070 others(13): Show |
16 | HG00140.hp1 HG00280.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.469+2330_469+2333d others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | ||||||
chr2:112496665 | CTGTGTG | C | 4 | a0001c0002t0133g0095 a0001c0003t0002g0225 a0001c0003t0100g0150 others(1): Show |
4 | HG01074.hp1 HG02280.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.469+2328_469+2333d others(8): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | ||||||
chr2:112496665 | CTGTGTGT others(1): Show |
C | 4 | a0001c0002t0027g0022 a0001c0002t0118g0039 a0001c0002t0120g0069 others(1): Show |
5 | HG00735.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.469+2326_469+2333d others(10): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | ||||||
chr2:112496665 | CTGTGTGT others(3): Show |
C | 5 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+2324_469+2333d others(12): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | ||||||
chr2:112496665 | CTGTGTGT others(5): Show |
C | 3 | a0001c0002t0009g0291 a0001c0002t0009g0292 a0001c0002t0122g0034 |
3 | HG01257.hp1 HG01258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.469+2322_469+2333d others(14): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | ||||||
chr2:112496665 | CTGTGTGT others(7): Show |
C | 6 | a0001c0001t0001g0247 a0001c0001t0001g0274 a0001c0001t0015g0193 others(3): Show |
6 | HG01256.hp1 HG01346.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+2320_469+2333d others(16): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | ||||||
chr2:112496665 | CTGTGTGT others(11): Show |
C | 1 | a0001c0001t0038g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.469+2316_469+2333d others(20): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | ||||||
chr2:112496697 | G | A | 1 | a0001c0001t0016g0248 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.469+2322G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496697 | |||||||
chr2:112496698 | TGTGTGTG others(4): Show |
T | 2 | a0001c0001t0016g0248 a0001c0002t0018g0120 |
2 | HG02738.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.469+2324_469+2334d others(13): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496698 | |||||||
chr2:112496700 | TGTGTGTG others(2): Show |
T | 14 | a0001c0002t0003g0004 a0001c0002t0003g0116 a0001c0002t0003g0119 others(11): Show |
15 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.469+2326_469+2334d others(11): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496700 | |||||||
chr2:112496702 | TGTGTGTA | T | 38 | a0001c0002t0002g0132 a0001c0002t0003g0009 a0001c0002t0003g0014 others(35): Show |
41 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.469+2328_469+2334d others(9): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496702 | |||||||
chr2:112496703 | G | A | 1 | a0001c0001t0124g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.469+2328G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496703 | |||||||
chr2:112496706 | TGTA | T | 4 | a0001c0001t0038g0046 a0001c0003t0006g0065 a0001c0003t0021g0168 others(1): Show |
4 | HG02055.hp2 HG03195.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.469+2332_469+2334d others(5): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496706 | |||||||
chr2:112496708 | T | TGTA | 4 | a0001c0001t0037g0029 a0001c0001t0069g0021 a0001c0001t0075g0021 others(1): Show |
4 | HG01361.hp2 HG01981.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.469+2333_469+2334i others(5): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496708 | |||||||
chr2:112496709 | A | T | 6 | a0001c0001t0037g0029 a0001c0001t0069g0021 a0001c0001t0075g0021 others(3): Show |
6 | HG01361.hp2 HG01981.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+2334A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496709 | |||||||
chr2:112496710 | T | A | 58 | a0001c0001t0038g0046 a0001c0002t0002g0132 a0001c0002t0003g0004 others(55): Show |
62 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.469+2335T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496710 | |||||||
chr2:112496790 | C | G | 7 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(4): Show |
7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+2415C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496790 | |||||||
chr2:112496815 | C | T | 1 | a0001c0001t0065g0211 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.469+2440C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496815 | |||||||
chr2:112496817 | C | G | 7 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(4): Show |
7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+2442C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496817 | |||||||
chr2:112496946 | G | A | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.469+2571G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496946 | |||||||
chr2:112497062 | C | T | 173 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(170): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.469+2687C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497062 | |||||||
chr2:112497064 | C | T | 2 | a0001c0002t0034g0297 a0001c0002t0034g0298 |
2 | HG00438.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.469+2689C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497064 | |||||||
chr2:112497121 | C | T | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.469+2746C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497121 | |||||||
chr2:112497216 | G | A | 1 | a0001c0002t0049g0234 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.469+2841G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497216 | |||||||
chr2:112497292 | C | T | 1 | a0001c0003t0002g0154 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.469+2917C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497292 | |||||||
chr2:112497467 | C | T | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.469+3092C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497467 | |||||||
chr2:112497543 | A | G | 1 | a0001c0002t0003g0141 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.469+3168A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497543 | |||||||
chr2:112497629 | G | A | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.469+3254G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497629 | |||||||
chr2:112497637 | T | G | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.469+3262T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497637 | |||||||
chr2:112497760 | A | G | 1 | a0001c0002t0053g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.469+3385A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497760 | |||||||
chr2:112497802 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.470-3404A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497802 | |||||||
chr2:112497840 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0266 a0001c0001t0001g0267 |
4 | HG01928.hp1 HG01993.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.470-3366C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497840 | |||||||
chr2:112497920 | A | G | 1 | a0001c0002t0008g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.470-3286A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497920 | |||||||
chr2:112497925 | C | G | 1 | a0001c0002t0053g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.470-3281C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497925 | |||||||
chr2:112498269 | G | A | 6 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.470-2937G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498269 | |||||||
chr2:112498278 | G | T | 1 | a0001c0002t0133g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.470-2928G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498278 | |||||||
chr2:112498331 | A | C | 19 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(16): Show |
19 | HG01109.hp1 HG01257.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.470-2875A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498331 | |||||||
chr2:112498343 | C | G | 2 | a0001c0002t0028g0097 a0001c0002t0028g0149 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.470-2863C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498343 | |||||||
chr2:112498484 | C | T | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.470-2722C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498484 | |||||||
chr2:112498570 | T | C | 2 | a0001c0002t0118g0039 a0001c0002t0120g0069 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.470-2636T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498570 | |||||||
chr2:112498600 | T | G | 1 | a0001c0002t0003g0121 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.470-2606T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498600 | |||||||
chr2:112498675 | G | A | 2 | a0001c0001t0001g0262 a0001c0002t0040g0088 |
2 | HG02132.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.470-2531G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498675 | |||||||
chr2:112498719 | C | T | 1 | a0001c0001t0013g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.470-2487C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498719 | |||||||
chr2:112498773 | C | T | 12 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.470-2433C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498773 | |||||||
chr2:112498777 | C | T | 2 | a0001c0002t0009g0291 a0001c0002t0009g0292 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.470-2429C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498777 | |||||||
chr2:112498787 | C | T | 1 | a0001c0002t0122g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.470-2419C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498787 | |||||||
chr2:112498838 | C | T | 1 | a0001c0001t0005g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.470-2368C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498838 | |||||||
chr2:112498921 | C | T | 71 | a0001c0003t0002g0002 a0001c0003t0002g0005 a0001c0003t0002g0016 others(68): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.470-2285C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498921 | |||||||
chr2:112499088 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.470-2118G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499088 | |||||||
chr2:112499184 | G | A | 12 | a0001c0002t0003g0014 a0001c0002t0003g0123 a0001c0002t0003g0127 others(9): Show |
13 | HG00438.hp1 HG02071.hp2 NA18939.hp1 others(10): Show |
intron_variant | MODIFIER | c.470-2022G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499184 | |||||||
chr2:112499255 | T | A | 8 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(5): Show |
8 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-1951T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499255 | |||||||
chr2:112499294 | T | A | 1 | a0001c0001t0125g0031 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.470-1912T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499294 | |||||||
chr2:112499374 | C | T | 8 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(5): Show |
8 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-1832C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499374 | |||||||
chr2:112499398 | G | A | 1 | a0001c0003t0002g0118 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.470-1808G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499398 | |||||||
chr2:112499404 | C | G | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.470-1802C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499404 | |||||||
chr2:112499705 | A | T | 7 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(4): Show |
7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.470-1501A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499705 | |||||||
chr2:112499880 | G | C | 1 | a0001c0002t0053g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.470-1326G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499880 | |||||||
chr2:112499950 | A | G | 2 | a0001c0002t0118g0039 a0001c0002t0120g0069 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.470-1256A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499950 | |||||||
chr2:112500041 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.470-1165C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500041 | |||||||
chr2:112500139 | A | G | 1 | a0001c0002t0003g0140 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.470-1067A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500139 | |||||||
chr2:112500196 | A | G | 2 | a0001c0002t0049g0234 a0001c0002t0050g0233 |
2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.470-1010A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500196 | |||||||
chr2:112500235 | G | A | 71 | a0001c0003t0002g0002 a0001c0003t0002g0005 a0001c0003t0002g0016 others(68): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.470-971G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500235 | |||||||
chr2:112500238 | CA | C | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.470-966delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112500238 | ||||||
chr2:112500242 | A | G | 3 | a0001c0003t0002g0177 a0001c0003t0035g0178 a0001c0003t0101g0176 |
3 | HG00639.hp2 HG01106.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.470-964A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500242 | |||||||
chr2:112500527 | C | T | 3 | a0001c0002t0014g0083 a0001c0002t0014g0084 a0001c0002t0014g0085 |
3 | HG02109.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.470-679C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500527 | |||||||
chr2:112500572 | AAAAC | A | 5 | a0001c0001t0005g0051 a0001c0001t0005g0052 a0001c0001t0005g0053 others(2): Show |
5 | HG00639.hp1 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-618_470-615del others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112500572 | ||||||
chr2:112500775 | A | G | 1 | a0001c0002t0028g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.470-431A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500775 | |||||||
chr2:112500783 | A | G | 8 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(5): Show |
8 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-423A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500783 | |||||||
chr2:112500902 | A | C | 79 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(76): Show |
89 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.470-304A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500902 | |||||||
chr2:112501094 | G | A | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.470-112G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112501094 | |||||||
chr2:112501371 | T | C | 2 | a0001c0002t0118g0039 a0001c0002t0120g0069 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.605+30T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501371 | |||||||
chr2:112501498 | C | T | 1 | a0001c0001t0123g0301 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.605+157C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501498 | |||||||
chr2:112501641 | A | G | 1 | a0001c0002t0008g0072 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.605+300A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501641 | |||||||
chr2:112501642 | T | C | 1 | a0001c0002t0008g0072 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.605+301T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501642 | |||||||
chr2:112501643 | G | A | 1 | a0001c0002t0008g0072 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.605+302G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501643 | |||||||
chr2:112501782 | A | T | 1 | a0001c0003t0020g0230 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.605+441A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501782 | |||||||
chr2:112501835 | C | T | 1 | a0001c0002t0028g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.605+494C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501835 | |||||||
chr2:112501866 | CA | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(129): Show |
146 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.605+544delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 112501866 | ||||||
chr2:112501866 | CAAAA | C | 158 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(155): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.605+541_605+544del others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 112501866 | ||||||
chr2:112501866 | CAAAAA | C | 8 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(5): Show |
8 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.605+540_605+544del others(5): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 112501866 | ||||||
chr2:112501887 | C | A | 7 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(4): Show |
7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.605+546C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501887 | |||||||
chr2:112501896 | A | G | 180 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(177): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.605+555A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501896 | |||||||
chr2:112501944 | C | T | 1 | a0001c0001t0114g0102 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.605+603C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501944 | |||||||
chr2:112502162 | A | G | 66 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(63): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.606-750A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112502162 | |||||||
chr2:112502637 | C | CA | 15 | a0001c0001t0012g0047 a0001c0001t0016g0248 a0001c0001t0037g0029 others(12): Show |
15 | HG01243.hp2 HG01361.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.606-259dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 112502637 | ||||||
chr2:112502637 | CA | C | 74 | a0001c0001t0115g0098 a0001c0002t0019g0093 a0001c0002t0028g0097 others(71): Show |
84 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.606-259delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 112502637 | ||||||
chr2:112502661 | AT | A | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.606-244delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 112502661 | ||||||
chr2:112502872 | T | C | 1 | a0001c0002t0003g0130 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.606-40T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112502872 | |||||||
chr2:112503284 | T | G | 95 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(92): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.875+103T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503284 | |||||||
chr2:112503387 | A | ATG | 15 | a0001c0001t0126g0026 a0001c0002t0007g0008 a0001c0002t0007g0104 others(12): Show |
18 | HG02572.hp2 HG02602.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.875+222_875+223dup others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503387 | ||||||
chr2:112503387 | A | G | 1 | a0001c0002t0133g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.875+206A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503387 | |||||||
chr2:112503401 | G | A | 1 | a0001c0002t0053g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.875+220G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503401 | |||||||
chr2:112503401 | G | GTA | 12 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.875+221_875+222ins others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503401 | ||||||
chr2:112503401 | G | GTATA | 5 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(2): Show |
5 | HG01891.hp1 HG03098.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.875+221_875+222ins others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503401 | ||||||
chr2:112503403 | G | A | 20 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(17): Show |
20 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.875+222G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503403 | |||||||
chr2:112503403 | G | GTA | 8 | a0001c0001t0001g0256 a0001c0002t0009g0146 a0001c0002t0009g0147 others(5): Show |
8 | HG00140.hp2 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.875+238_875+239dup others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | ||||||
chr2:112503403 | G | GTATA | 54 | a0001c0001t0065g0211 a0001c0001t0073g0255 a0001c0002t0002g0132 others(51): Show |
59 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.875+236_875+239dup others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | ||||||
chr2:112503403 | G | GTATATA | 59 | a0001c0002t0003g0079 a0001c0002t0003g0080 a0001c0002t0003g0131 others(56): Show |
67 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.875+234_875+239dup others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | ||||||
chr2:112503403 | G | GTATATAT others(1): Show |
6 | a0001c0003t0002g0239 a0001c0003t0006g0064 a0001c0003t0010g0294 others(3): Show |
6 | HG02055.hp2 HG02083.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.875+232_875+239dup others(8): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | ||||||
chr2:112503403 | G | GTATATAT others(3): Show |
1 | a0001c0003t0019g0180 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+230_875+239dup others(10): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | ||||||
chr2:112503403 | G | GTGTATA | 4 | a0001c0003t0002g0112 a0001c0003t0002g0154 a0001c0003t0021g0167 others(1): Show |
4 | HG02280.hp2 HG03239.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.875+223_875+224ins others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | ||||||
chr2:112503403 | G | GTGTATAT others(1): Show |
3 | a0001c0003t0002g0229 a0001c0003t0006g0012 a0001c0003t0006g0065 |
4 | NA18945.hp2 NA18957.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.875+223_875+224ins others(8): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | ||||||
chr2:112503403 | GTA | G | 3 | a0001c0001t0030g0191 a0001c0001t0030g0192 a0001c0001t0092g0210 |
3 | HG01175.hp1 HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.875+238_875+239del others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | ||||||
chr2:112503405 | A | G | 12 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(9): Show |
12 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.875+224A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503405 | |||||||
chr2:112503429 | T | A | 15 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(12): Show |
18 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.875+248T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503429 | |||||||
chr2:112503458 | A | G | 95 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(92): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.875+277A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503458 | |||||||
chr2:112503483 | G | C | 1 | a0001c0001t0001g0270 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.875+302G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503483 | |||||||
chr2:112503490 | A | G | 2 | a0001c0002t0006g0060 a0001c0002t0039g0059 |
2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.875+309A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503490 | |||||||
chr2:112503577 | G | A | 1 | a0001c0002t0133g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.875+396G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503577 | |||||||
chr2:112503658 | C | CT | 15 | a0001c0001t0013g0033 a0001c0002t0008g0070 a0001c0002t0008g0072 others(12): Show |
15 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.875+497dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503658 | ||||||
chr2:112503658 | CT | C | 98 | a0001c0001t0012g0049 a0001c0001t0015g0193 a0001c0001t0038g0046 others(95): Show |
110 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.875+497delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503658 | ||||||
chr2:112503658 | CTT | C | 6 | a0001c0002t0011g0111 a0001c0002t0049g0234 a0001c0002t0118g0039 others(3): Show |
6 | HG02647.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+496_875+497del others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503658 | ||||||
chr2:112503700 | TA | T | 71 | a0001c0003t0002g0002 a0001c0003t0002g0005 a0001c0003t0002g0016 others(68): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.875+520delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503700 | |||||||
chr2:112503775 | T | G | 1 | a0001c0001t0077g0257 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.875+594T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503775 | |||||||
chr2:112503805 | C | CT | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(128): Show |
141 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.875+644dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503805 | ||||||
chr2:112503805 | CT | C | 75 | a0001c0002t0007g0008 a0001c0002t0011g0105 a0001c0002t0027g0022 others(72): Show |
85 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.875+644delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503805 | ||||||
chr2:112503805 | CTT | C | 7 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(4): Show |
7 | HG01891.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.875+643_875+644del others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503805 | ||||||
chr2:112503805 | CTTT | C | 49 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(46): Show |
53 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.875+642_875+644del others(3): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503805 | ||||||
chr2:112503805 | CTTTTT | C | 11 | a0001c0002t0008g0070 a0001c0002t0008g0074 a0001c0002t0008g0075 others(8): Show |
11 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(8): Show |
intron_variant | MODIFIER | c.875+640_875+644del others(5): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503805 | ||||||
chr2:112503902 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.875+721C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503902 | |||||||
chr2:112503962 | C | A | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.875+781C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503962 | |||||||
chr2:112503997 | T | C | 1 | a0001c0001t0117g0035 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.875+816T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503997 | |||||||
chr2:112504082 | C | T | 7 | a0001c0002t0007g0104 a0001c0002t0007g0106 a0001c0002t0007g0110 others(4): Show |
7 | HG02572.hp2 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.875+901C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504082 | |||||||
chr2:112504107 | T | G | 1 | a0001c0001t0091g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.875+926T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504107 | |||||||
chr2:112504111 | A | G | 66 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(63): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.875+930A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504111 | |||||||
chr2:112504182 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(94): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.875+1001A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504182 | |||||||
chr2:112504286 | G | A | 12 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.875+1105G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504286 | |||||||
chr2:112504349 | A | C | 1 | a0001c0002t0003g0130 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.875+1168A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504349 | |||||||
chr2:112504383 | C | T | 1 | a0001c0001t0080g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.875+1202C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504383 | |||||||
chr2:112504449 | A | G | 1 | a0001c0003t0002g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.875+1268A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504449 | |||||||
chr2:112504513 | G | A | 89 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(86): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.875+1332G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504513 | |||||||
chr2:112504522 | G | A | 1 | a0001c0003t0103g0156 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.875+1341G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504522 | |||||||
chr2:112504738 | C | T | 55 | a0001c0001t0066g0082 a0001c0002t0002g0132 a0001c0002t0003g0004 others(52): Show |
59 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.875+1557C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504738 | |||||||
chr2:112504739 | G | A | 35 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(32): Show |
38 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.875+1558G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504739 | |||||||
chr2:112504818 | A | G | 12 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.875+1637A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504818 | |||||||
chr2:112504820 | G | T | 180 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(177): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.875+1639G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504820 | |||||||
chr2:112504842 | G | T | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.875+1661G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504842 | |||||||
chr2:112505168 | A | G | 54 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(51): Show |
58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.875+1987A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505168 | |||||||
chr2:112505246 | T | G | 1 | a0001c0003t0099g0165 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.875+2065T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505246 | |||||||
chr2:112505284 | A | T | 1 | a0002c0005t0018g0139 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.875+2103A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505284 | |||||||
chr2:112505290 | C | T | 1 | a0001c0001t0088g0237 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.875+2109C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505290 | |||||||
chr2:112505310 | T | C | 95 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(92): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.875+2129T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505310 | |||||||
chr2:112505390 | G | A | 1 | a0001c0002t0051g0275 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.875+2209G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505390 | |||||||
chr2:112505497 | G | T | 1 | a0001c0003t0002g0228 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.875+2316G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505497 | |||||||
chr2:112505515 | T | G | 2 | a0001c0001t0072g0090 a0001c0001t0085g0289 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.875+2334T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505515 | |||||||
chr2:112505567 | C | T | 1 | a0001c0001t0081g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.875+2386C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505567 | |||||||
chr2:112505580 | G | A | 1 | a0001c0002t0053g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.875+2399G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505580 | |||||||
chr2:112505595 | C | G | 1 | a0001c0002t0133g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.875+2414C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505595 | |||||||
chr2:112505611 | CTGTT | C | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.875+2434_875+2437d others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112505611 | ||||||
chr2:112505712 | T | G | 1 | a0001c0001t0005g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.875+2531T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505712 | |||||||
chr2:112505738 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.875+2557A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505738 | |||||||
chr2:112505753 | G | A | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.875+2572G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505753 | |||||||
chr2:112505846 | T | C | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.875+2665T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505846 | |||||||
chr2:112505864 | C | T | 56 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(53): Show |
60 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.875+2683C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505864 | |||||||
chr2:112505977 | T | A | 1 | a0001c0002t0108g0285 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.875+2796T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505977 | |||||||
chr2:112506103 | T | C | 92 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(89): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.875+2922T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506103 | |||||||
chr2:112506299 | C | A | 16 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(13): Show |
19 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.875+3118C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506299 | |||||||
chr2:112506299 | C | T | 11 | a0001c0002t0008g0070 a0001c0002t0008g0074 a0001c0002t0008g0075 others(8): Show |
11 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(8): Show |
intron_variant | MODIFIER | c.875+3118C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506299 | |||||||
chr2:112506423 | T | C | 79 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(76): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.875+3242T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506423 | |||||||
chr2:112506424 | C | T | 76 | a0001c0002t0007g0104 a0001c0002t0007g0106 a0001c0002t0007g0110 others(73): Show |
86 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.875+3243C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506424 | |||||||
chr2:112506429 | G | T | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.875+3248G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506429 | |||||||
chr2:112506522 | A | G | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.875+3341A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506522 | |||||||
chr2:112506599 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.875+3418T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506599 | |||||||
chr2:112506616 | A | C | 3 | a0001c0001t0025g0011 a0001c0001t0025g0042 a0001c0001t0125g0031 |
4 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.875+3435A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506616 | |||||||
chr2:112506652 | C | T | 1 | a0001c0001t0006g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.875+3471C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506652 | |||||||
chr2:112506693 | T | A | 8 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(5): Show |
8 | HG01109.hp1 HG01346.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.875+3512T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506693 | |||||||
chr2:112506703 | C | G | 12 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.875+3522C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506703 | |||||||
chr2:112506731 | C | T | 8 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(5): Show |
8 | HG01109.hp1 HG01346.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.875+3550C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506731 | |||||||
chr2:112506757 | G | C | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.875+3576G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506757 | |||||||
chr2:112506833 | T | G | 1 | a0001c0002t0133g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.875+3652T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506833 | |||||||
chr2:112506945 | A | G | 95 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(92): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.875+3764A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506945 | |||||||
chr2:112506974 | C | A | 12 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(9): Show |
15 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.875+3793C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506974 | |||||||
chr2:112506987 | A | G | 1 | a0001c0003t0019g0180 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+3806A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506987 | |||||||
chr2:112507012 | G | T | 2 | a0001c0001t0001g0209 a0001c0002t0040g0088 |
2 | HG03927.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.875+3831G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507012 | |||||||
chr2:112507027 | A | G | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.875+3846A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507027 | |||||||
chr2:112507053 | C | T | 1 | a0001c0003t0021g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.875+3872C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507053 | |||||||
chr2:112507103 | A | T | 1 | a0001c0002t0008g0075 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.875+3922A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507103 | |||||||
chr2:112507118 | G | A | 1 | a0001c0002t0008g0089 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.875+3937G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507118 | |||||||
chr2:112507223 | G | A | 1 | a0001c0001t0077g0257 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.875+4042G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507223 | |||||||
chr2:112507286 | T | G | 2 | a0001c0001t0001g0286 a0001c0001t0068g0250 |
2 | HG02083.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.875+4105T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507286 | |||||||
chr2:112507388 | G | A | 1 | a0001c0003t0110g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.875+4207G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507388 | |||||||
chr2:112507602 | A | G | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.875+4421A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507602 | |||||||
chr2:112507769 | A | G | 2 | a0001c0003t0100g0150 a0001c0003t0128g0028 |
2 | HG01074.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.875+4588A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507769 | |||||||
chr2:112507856 | T | G | 6 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.875+4675T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507856 | |||||||
chr2:112507943 | T | C | 95 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(92): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.875+4762T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507943 | |||||||
chr2:112508161 | G | T | 2 | a0001c0002t0009g0146 a0001c0002t0009g0147 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.875+4980G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508161 | |||||||
chr2:112508172 | G | C | 1 | a0001c0002t0003g0143 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.875+4991G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508172 | |||||||
chr2:112508175 | G | A | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.875+4994G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508175 | |||||||
chr2:112508306 | T | C | 3 | a0001c0002t0029g0186 a0001c0002t0029g0187 a0001c0002t0119g0040 |
3 | HG01243.hp2 HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.875+5125T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508306 | |||||||
chr2:112508321 | T | C | 2 | a0001c0001t0072g0090 a0001c0001t0085g0289 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.875+5140T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508321 | |||||||
chr2:112508456 | C | G | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.875+5275C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508456 | |||||||
chr2:112508607 | C | T | 2 | a0001c0001t0046g0272 a0001c0001t0048g0273 |
2 | HG01346.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.875+5426C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508607 | |||||||
chr2:112508615 | G | C | 7 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(4): Show |
7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.875+5434G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508615 | |||||||
chr2:112508635 | G | A | 2 | a0001c0002t0015g0122 a0001c0002t0015g0126 |
2 | NA18943.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.875+5454G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508635 | |||||||
chr2:112508643 | C | T | 94 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(91): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.875+5462C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508643 | |||||||
chr2:112508666 | C | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(112): Show |
126 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.875+5485C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508666 | |||||||
chr2:112508686 | C | G | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.875+5505C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508686 | |||||||
chr2:112508770 | G | A | 71 | a0001c0003t0002g0002 a0001c0003t0002g0005 a0001c0003t0002g0016 others(68): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.875+5589G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508770 | |||||||
chr2:112508998 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.875+5817A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508998 | |||||||
chr2:112509014 | TGTTA | T | 54 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(51): Show |
58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.875+5837_875+5840d others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112509014 | ||||||
chr2:112509073 | T | C | 182 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(179): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.875+5892T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509073 | |||||||
chr2:112509093 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.875+5912C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509093 | |||||||
chr2:112509100 | T | G | 179 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(176): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.875+5919T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509100 | |||||||
chr2:112509102 | G | A | 12 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(9): Show |
12 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.875+5921G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509102 | |||||||
chr2:112509169 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.875+5988C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509169 | |||||||
chr2:112509169 | C | T | 1 | a0001c0001t0095g0103 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.875+5988C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509169 | |||||||
chr2:112509170 | G | A | 2 | a0001c0003t0010g0025 a0001c0003t0010g0296 |
3 | NA18960.hp2 NA18964.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.875+5989G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509170 | |||||||
chr2:112509240 | A | G | 51 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(48): Show |
55 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.875+6059A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509240 | |||||||
chr2:112509349 | C | G | 55 | a0001c0001t0001g0242 a0001c0002t0002g0132 a0001c0002t0003g0004 others(52): Show |
59 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.875+6168C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509349 | |||||||
chr2:112509358 | T | C | 1 | a0001c0002t0003g0277 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.875+6177T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509358 | |||||||
chr2:112509383 | C | G | 1 | a0001c0001t0001g0251 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.875+6202C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509383 | |||||||
chr2:112509418 | T | C | 54 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(51): Show |
58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.875+6237T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509418 | |||||||
chr2:112509496 | G | T | 2 | a0001c0001t0024g0007 a0001c0001t0114g0102 |
4 | HG01167.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.875+6315G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509496 | |||||||
chr2:112509547 | C | T | 11 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(8): Show |
11 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(8): Show |
intron_variant | MODIFIER | c.875+6366C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509547 | |||||||
chr2:112509550 | A | G | 2 | a0001c0002t0003g0137 a0001c0002t0003g0138 |
2 | HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.875+6369A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509550 | |||||||
chr2:112509560 | T | C | 1 | a0001c0003t0033g0158 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.875+6379T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509560 | |||||||
chr2:112509589 | T | C | 95 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(92): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.875+6408T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509589 | |||||||
chr2:112509660 | G | A | 1 | a0001c0001t0086g0213 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.875+6479G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509660 | |||||||
chr2:112509663 | C | G | 1 | a0001c0002t0133g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.875+6482C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509663 | |||||||
chr2:112509669 | C | T | 2 | a0001c0001t0005g0037 a0001c0001t0005g0038 |
2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.875+6488C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509669 | |||||||
chr2:112509674 | C | T | 1 | a0001c0002t0133g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.875+6493C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509674 | |||||||
chr2:112509702 | G | C | 5 | a0001c0002t0003g0009 a0001c0002t0003g0115 a0001c0002t0003g0121 others(2): Show |
7 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.875+6521G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509702 | |||||||
chr2:112509774 | C | T | 1 | a0001c0001t0016g0203 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.875+6593C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509774 | |||||||
chr2:112509793 | G | T | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.875+6612G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509793 | |||||||
chr2:112509861 | T | C | 1 | a0001c0003t0020g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.875+6680T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509861 | |||||||
chr2:112509886 | G | A | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.875+6705G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509886 | |||||||
chr2:112509914 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.875+6733G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509914 | |||||||
chr2:112509923 | C | T | 8 | a0001c0001t0005g0051 a0001c0001t0005g0052 a0001c0001t0005g0053 others(5): Show |
8 | HG00639.hp1 HG02717.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.875+6742C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509923 | |||||||
chr2:112509963 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.875+6782A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509963 | |||||||
chr2:112509964 | C | G | 1 | a0001c0002t0008g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.875+6783C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509964 | |||||||
chr2:112510228 | C | T | 1 | a0001c0002t0043g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.875+7047C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510228 | |||||||
chr2:112510319 | G | T | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.875+7138G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510319 | |||||||
chr2:112510352 | C | T | 1 | a0001c0001t0059g0208 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.875+7171C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510352 | |||||||
chr2:112510507 | T | C | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.875+7326T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510507 | |||||||
chr2:112510541 | G | A | 1 | a0001c0003t0128g0028 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.875+7360G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510541 | |||||||
chr2:112510659 | C | T | 4 | a0001c0001t0013g0010 a0001c0001t0013g0033 a0001c0001t0013g0044 others(1): Show |
4 | HG01109.hp1 HG02055.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.875+7478C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510659 | |||||||
chr2:112510824 | C | G | 1 | a0001c0002t0122g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.875+7643C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510824 | |||||||
chr2:112510828 | A | G | 1 | a0001c0002t0052g0094 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.875+7647A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510828 | |||||||
chr2:112510940 | A | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0274 |
2 | HG01256.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.875+7759A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510940 | |||||||
chr2:112510943 | G | T | 1 | a0001c0003t0129g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.875+7762G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510943 | |||||||
chr2:112511091 | T | C | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.875+7910T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511091 | |||||||
chr2:112511319 | T | C | 2 | a0001c0002t0003g0079 a0001c0002t0003g0080 |
2 | HG02132.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.875+8138T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511319 | |||||||
chr2:112511470 | T | G | 1 | a0001c0002t0027g0022 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.875+8289T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511470 | |||||||
chr2:112511506 | A | G | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.875+8325A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511506 | |||||||
chr2:112511611 | C | T | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.875+8430C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511611 | |||||||
chr2:112511754 | A | G | 1 | a0001c0003t0020g0163 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.876-8528A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511754 | |||||||
chr2:112511817 | C | T | 1 | a0001c0001t0112g0100 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.876-8465C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511817 | |||||||
chr2:112511823 | A | G | 54 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(51): Show |
58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.876-8459A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511823 | |||||||
chr2:112511982 | C | CATTCT | 93 | a0001c0001t0001g0269 a0001c0002t0002g0132 a0001c0002t0003g0004 others(90): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.876-8282_876-8278d others(7): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112511982 | ||||||
chr2:112511982 | C | CATTCTAT others(3): Show |
1 | a0001c0002t0003g0128 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.876-8287_876-8278d others(12): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112511982 | ||||||
chr2:112512027 | T | C | 3 | a0001c0003t0002g0177 a0001c0003t0035g0178 a0001c0003t0101g0176 |
3 | HG00639.hp2 HG01106.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.876-8255T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512027 | |||||||
chr2:112512057 | A | T | 1 | a0001c0002t0052g0094 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.876-8225A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512057 | |||||||
chr2:112512129 | C | T | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-8153C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512129 | |||||||
chr2:112512324 | G | A | 12 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.876-7958G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512324 | |||||||
chr2:112512331 | C | T | 1 | a0001c0001t0080g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.876-7951C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512331 | |||||||
chr2:112512339 | T | G | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.876-7943T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512339 | |||||||
chr2:112512348 | C | T | 7 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(4): Show |
7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.876-7934C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512348 | |||||||
chr2:112512407 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0202 |
2 | NA19080.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.876-7875C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512407 | |||||||
chr2:112512484 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.876-7798G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512484 | |||||||
chr2:112512514 | G | A | 1 | a0001c0002t0131g0045 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.876-7768G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512514 | |||||||
chr2:112512625 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.876-7657G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512625 | |||||||
chr2:112512643 | C | T | 54 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(51): Show |
58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.876-7639C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512643 | |||||||
chr2:112512657 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.876-7625A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512657 | |||||||
chr2:112512787 | C | T | 12 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(9): Show |
12 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.876-7495C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512787 | |||||||
chr2:112512937 | G | A | 1 | a0001c0002t0053g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.876-7345G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512937 | |||||||
chr2:112513022 | G | A | 54 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(51): Show |
58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.876-7260G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513022 | |||||||
chr2:112513172 | A | G | 3 | a0001c0002t0029g0186 a0001c0002t0029g0187 a0001c0002t0119g0040 |
3 | HG01243.hp2 HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.876-7110A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513172 | |||||||
chr2:112513215 | G | A | 54 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(51): Show |
58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.876-7067G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513215 | |||||||
chr2:112513337 | C | T | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.876-6945C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513337 | |||||||
chr2:112513452 | A | G | 1 | a0001c0003t0021g0167 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.876-6830A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513452 | |||||||
chr2:112513457 | T | C | 1 | a0001c0001t0115g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.876-6825T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513457 | |||||||
chr2:112513541 | G | T | 3 | a0001c0002t0014g0083 a0001c0002t0014g0084 a0001c0002t0014g0085 |
3 | HG02109.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.876-6741G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513541 | |||||||
chr2:112513569 | A | G | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.876-6713A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513569 | |||||||
chr2:112513571 | A | ATATAAAT others(35): Show |
3 | a0001c0002t0022g0124 a0001c0003t0002g0112 a0001c0003t0002g0154 |
3 | NA18964.hp1 NA19066.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.876-6689_876-6648d others(44): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112513571 | ||||||
chr2:112513575 | AAATATTT others(53): Show |
A | 2 | a0001c0002t0049g0234 a0001c0002t0050g0233 |
2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.876-6683_876-6624d others(62): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112513575 | ||||||
chr2:112513587 | A | T | 1 | a0001c0003t0033g0158 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.876-6695A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513587 | |||||||
chr2:112513617 | AAATATTT others(11): Show |
A | 1 | a0001c0003t0104g0152 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.876-6647_876-6630d others(20): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112513617 | ||||||
chr2:112513626 | T | C | 2 | a0001c0001t0025g0011 a0001c0001t0025g0042 |
3 | HG00738.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.876-6656T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513626 | |||||||
chr2:112513628 | C | CAAGTATA others(17): Show |
1 | a0001c0002t0133g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.876-6648_876-6647i others(26): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112513628 | ||||||
chr2:112513635 | G | A | 177 | a0001c0001t0013g0010 a0001c0001t0013g0032 a0001c0001t0013g0033 others(174): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.876-6647G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513635 | |||||||
chr2:112513817 | G | T | 1 | a0001c0001t0001g0266 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.876-6465G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513817 | |||||||
chr2:112513832 | C | A | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-6450C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513832 | |||||||
chr2:112513879 | G | T | 1 | a0001c0002t0003g0130 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.876-6403G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513879 | |||||||
chr2:112513929 | A | G | 1 | a0001c0002t0043g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.876-6353A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513929 | |||||||
chr2:112514110 | G | A | 3 | a0001c0001t0001g0087 a0001c0003t0002g0112 a0001c0003t0002g0154 |
3 | HG01516.hp2 NA19066.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.876-6172G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112514110 | |||||||
chr2:112514227 | G | A | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.876-6055G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112514227 | |||||||
chr2:112514274 | C | T | 14 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(11): Show |
17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.876-6008C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112514274 | |||||||
chr2:112514326 | G | C | 1 | a0001c0001t0123g0301 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.876-5956G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112514326 | |||||||
chr2:112514369 | A | G | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-5913A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112514369 | |||||||
chr2:112514381 | C | CAA | 70 | a0001c0003t0002g0002 a0001c0003t0002g0005 a0001c0003t0002g0016 others(67): Show |
80 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.876-5889_876-5888d others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112514381 | ||||||
chr2:112514381 | CA | C | 7 | a0001c0001t0006g0056 a0001c0001t0023g0013 a0001c0001t0023g0101 others(4): Show |
10 | HG01167.hp2 HG01243.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.876-5888delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112514381 | ||||||
chr2:112514631 | T | A | 6 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-5651T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112514631 | |||||||
chr2:112514815 | T | A | 1 | a0001c0002t0050g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.876-5467T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112514815 | |||||||
chr2:112515045 | G | A | 6 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-5237G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112515045 | |||||||
chr2:112515347 | T | A | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-4935T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112515347 | |||||||
chr2:112515392 | G | C | 1 | a0001c0001t0001g0251 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.876-4890G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112515392 | |||||||
chr2:112515454 | AAGT | A | 95 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(92): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.876-4823_876-4821d others(5): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515454 | ||||||
chr2:112515510 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0266 a0001c0001t0001g0267 |
4 | HG01928.hp1 HG01993.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.876-4772T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112515510 | |||||||
chr2:112515676 | G | A | 6 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-4606G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112515676 | |||||||
chr2:112515803 | C | T | 1 | a0001c0001t0061g0261 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.876-4479C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112515803 | |||||||
chr2:112515901 | C | G | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.876-4381C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112515901 | |||||||
chr2:112515948 | G | GAATA | 9 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0051 others(6): Show |
10 | HG00639.hp1 HG01243.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.876-4286_876-4283d others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | ||||||
chr2:112515948 | G | GAATAAAT others(1): Show |
3 | a0001c0001t0006g0056 a0001c0001t0024g0007 a0001c0001t0123g0301 |
5 | HG01167.hp2 HG01884.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.876-4290_876-4283d others(10): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | ||||||
chr2:112515948 | G | GAATAAAT others(5): Show |
1 | a0001c0001t0005g0068 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.876-4294_876-4283d others(14): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | ||||||
chr2:112515948 | G | GAATAAAT others(9): Show |
3 | a0001c0001t0047g0287 a0001c0001t0085g0289 a0001c0001t0114g0102 |
3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.876-4298_876-4283d others(18): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | ||||||
chr2:112515948 | GAATA | G | 19 | a0001c0001t0001g0244 a0001c0001t0001g0247 a0001c0001t0001g0249 others(16): Show |
19 | HG01256.hp1 HG01891.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.876-4286_876-4283d others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | ||||||
chr2:112515948 | GAATAAAT others(1): Show |
G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(90): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.876-4290_876-4283d others(10): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | ||||||
chr2:112515948 | GAATAAAT others(5): Show |
G | 2 | a0001c0001t0030g0192 a0001c0001t0084g0205 |
2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.876-4294_876-4283d others(14): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | ||||||
chr2:112515948 | GAATAAAT others(9): Show |
G | 1 | a0001c0001t0080g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.876-4298_876-4283d others(18): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | ||||||
chr2:112515948 | GAATAAAT others(13): Show |
G | 4 | a0001c0001t0025g0011 a0001c0001t0025g0042 a0001c0002t0118g0039 others(1): Show |
5 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.876-4302_876-4283d others(22): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | ||||||
chr2:112515948 | GAATAAAT others(17): Show |
G | 170 | a0001c0001t0001g0199 a0001c0001t0001g0204 a0001c0001t0001g0262 others(167): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.876-4306_876-4283d others(26): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | ||||||
chr2:112516042 | G | A | 1 | a0001c0001t0063g0206 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.876-4240G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516042 | |||||||
chr2:112516210 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.876-4072C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516210 | |||||||
chr2:112516256 | A | G | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.876-4026A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516256 | |||||||
chr2:112516314 | C | A | 1 | a0001c0001t0063g0206 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.876-3968C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516314 | |||||||
chr2:112516510 | C | T | 1 | a0001c0002t0009g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.876-3772C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516510 | |||||||
chr2:112516535 | A | G | 2 | a0001c0001t0046g0272 a0001c0001t0048g0273 |
2 | HG01346.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.876-3747A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516535 | |||||||
chr2:112516629 | G | T | 2 | a0001c0001t0046g0272 a0001c0001t0048g0273 |
2 | HG01346.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.876-3653G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516629 | |||||||
chr2:112516712 | C | T | 13 | a0001c0002t0003g0004 a0001c0002t0003g0116 a0001c0002t0003g0119 others(10): Show |
14 | HG00621.hp1 HG00735.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.876-3570C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516712 | |||||||
chr2:112516801 | A | G | 72 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(69): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.876-3481A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516801 | |||||||
chr2:112516902 | A | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(300): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.876-3380A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516902 | |||||||
chr2:112517073 | C | G | 2 | a0001c0002t0049g0234 a0001c0002t0050g0233 |
2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.876-3209C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517073 | |||||||
chr2:112517156 | C | CA | 17 | a0001c0001t0001g0274 a0001c0001t0001g0300 a0001c0001t0005g0036 others(14): Show |
17 | HG00741.hp1 HG01346.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.876-3103dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517156 | ||||||
chr2:112517156 | CA | C | 17 | a0001c0001t0004g0217 a0001c0001t0005g0054 a0001c0001t0082g0189 others(14): Show |
18 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.876-3103delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517156 | ||||||
chr2:112517156 | CAA | C | 18 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(15): Show |
20 | HG00280.hp2 HG01257.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.876-3104_876-3103d others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517156 | ||||||
chr2:112517156 | CAAA | C | 53 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(50): Show |
57 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.876-3105_876-3103d others(5): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517156 | ||||||
chr2:112517156 | CAAAAAAA | C | 72 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(69): Show |
82 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.876-3109_876-3103d others(9): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517156 | ||||||
chr2:112517156 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0006g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.876-3114_876-3103d others(14): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517156 | ||||||
chr2:112517309 | G | A | 1 | a0001c0002t0133g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.876-2973G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517309 | |||||||
chr2:112517336 | C | A | 1 | a0001c0002t0133g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.876-2946C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517336 | |||||||
chr2:112517351 | G | A | 2 | a0001c0001t0044g0195 a0001c0001t0045g0144 |
2 | HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.876-2931G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517351 | |||||||
chr2:112517438 | G | A | 2 | a0001c0003t0096g0160 a0001c0003t0103g0156 |
2 | HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.876-2844G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517438 | |||||||
chr2:112517441 | GT | G | 9 | a0001c0003t0002g0002 a0001c0003t0002g0118 a0001c0003t0002g0179 others(6): Show |
12 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.876-2838delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517441 | ||||||
chr2:112517540 | T | G | 1 | a0001c0001t0004g0215 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.876-2742T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517540 | |||||||
chr2:112517542 | T | C | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-2740T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517542 | |||||||
chr2:112517543 | C | G | 1 | a0001c0003t0002g0179 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.876-2739C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517543 | |||||||
chr2:112517575 | C | T | 1 | a0001c0003t0002g0166 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.876-2707C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517575 | |||||||
chr2:112517762 | A | G | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-2520A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517762 | |||||||
chr2:112517953 | C | CT | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.876-2320dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517953 | ||||||
chr2:112518015 | G | A | 6 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-2267G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518015 | |||||||
chr2:112518104 | G | A | 1 | a0001c0002t0007g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.876-2178G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518104 | |||||||
chr2:112518135 | AT | A | 152 | a0001c0001t0005g0052 a0001c0002t0002g0132 a0001c0002t0003g0004 others(149): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.876-2127delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112518135 | ||||||
chr2:112518142 | T | C | 11 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(8): Show |
14 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.876-2140T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518142 | |||||||
chr2:112518331 | A | AT | 83 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(80): Show |
93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.876-1939dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112518331 | ||||||
chr2:112518540 | C | T | 7 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(4): Show |
7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.876-1742C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518540 | |||||||
chr2:112518678 | C | CT | 170 | a0001c0001t0001g0267 a0001c0001t0013g0010 a0001c0001t0013g0032 others(167): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.876-1590dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112518678 | ||||||
chr2:112518678 | C | CTT | 8 | a0001c0001t0046g0272 a0001c0001t0048g0273 a0001c0002t0019g0093 others(5): Show |
8 | HG01346.hp1 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.876-1591_876-1590d others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112518678 | ||||||
chr2:112518800 | G | A | 1 | a0001c0001t0077g0257 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.876-1482G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518800 | |||||||
chr2:112518955 | G | A | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-1327G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518955 | |||||||
chr2:112518962 | A | C | 9 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(6): Show |
9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.876-1320A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518962 | |||||||
chr2:112518971 | G | A | 6 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-1311G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518971 | |||||||
chr2:112519030 | C | T | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.876-1252C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519030 | |||||||
chr2:112519053 | C | G | 15 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(12): Show |
18 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.876-1229C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519053 | |||||||
chr2:112519111 | G | GGGAAGAT others(318): Show |
1 | a0001c0002t0050g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.876-1160_876-1159i others(327): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112519111 | ||||||
chr2:112519139 | A | G | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-1143A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519139 | |||||||
chr2:112519193 | G | T | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.876-1089G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519193 | |||||||
chr2:112519245 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.876-1037A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519245 | |||||||
chr2:112519288 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0270 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.876-994C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519288 | |||||||
chr2:112519322 | T | C | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-960T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519322 | |||||||
chr2:112519448 | C | A | 1 | a0001c0003t0002g0229 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.876-834C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519448 | |||||||
chr2:112519493 | G | T | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-789G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519493 | |||||||
chr2:112519550 | G | GT | 18 | a0001c0001t0001g0087 a0001c0001t0001g0190 a0001c0001t0001g0249 others(15): Show |
18 | HG00621.hp1 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.876-711dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112519550 | ||||||
chr2:112519550 | GT | G | 15 | a0001c0001t0001g0199 a0001c0001t0005g0054 a0001c0002t0008g0075 others(12): Show |
15 | HG00639.hp1 HG01243.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.876-711delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112519550 | ||||||
chr2:112519550 | GTT | G | 11 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(8): Show |
11 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(8): Show |
intron_variant | MODIFIER | c.876-712_876-711del others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112519550 | ||||||
chr2:112519550 | GTTT | G | 91 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(88): Show |
104 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.876-713_876-711del others(3): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112519550 | ||||||
chr2:112519559 | T | G | 6 | a0001c0002t0019g0093 a0001c0002t0028g0097 a0001c0002t0028g0149 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-723T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519559 | |||||||
chr2:112519625 | A | G | 22 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(19): Show |
25 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(22): Show |
intron_variant | MODIFIER | c.876-657A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519625 | |||||||
chr2:112519640 | G | A | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.876-642G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519640 | |||||||
chr2:112519759 | A | G | 1 | a0001c0001t0058g0212 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.876-523A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519759 | |||||||
chr2:112519859 | G | C | 168 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(165): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-423G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519859 | |||||||
chr2:112519920 | C | T | 66 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(63): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.876-362C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519920 | |||||||
chr2:112519928 | C | T | 73 | a0001c0002t0049g0234 a0001c0002t0050g0233 a0001c0003t0002g0002 others(70): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.876-354C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519928 | |||||||
chr2:112519977 | A | G | 11 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(8): Show |
14 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.876-305A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519977 | |||||||
chr2:112520022 | C | T | 1 | a0001c0001t0006g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.876-260C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112520022 | |||||||
chr2:112520071 | C | G | 59 | a0001c0001t0001g0018 a0001c0001t0001g0196 a0001c0001t0001g0199 others(56): Show |
63 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.876-211C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112520071 | |||||||
chr2:112520130 | C | CA | 19 | a0001c0001t0001g0274 a0001c0001t0013g0010 a0001c0001t0013g0032 others(16): Show |
21 | HG01109.hp1 HG01167.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.876-132dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112520130 | ||||||
chr2:112520130 | CA | C | 95 | a0001c0001t0001g0247 a0001c0001t0004g0217 a0001c0001t0015g0193 others(92): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.876-132delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112520130 | ||||||
chr2:112520209 | T | C | 1 | a0001c0001t0095g0103 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.876-73T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112520209 | |||||||
chr2:112520260 | C | A | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.876-22C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112520260 | |||||||
chr2:112520273 | G | T | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.876-9G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112520273 | |||||||
chr2:112520613 | T | C | 1 | a0001c0001t0123g0301 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1019+188T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520613 | |||||||
chr2:112520614 | A | T | 159 | a0001c0001t0072g0090 a0001c0001t0080g0148 a0001c0001t0123g0301 others(156): Show |
176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1019+189A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520614 | |||||||
chr2:112520615 | G | GTA | 159 | a0001c0001t0072g0090 a0001c0001t0080g0148 a0001c0001t0123g0301 others(156): Show |
176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1019+190_1019+191i others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520615 | |||||||
chr2:112520616 | G | A | 159 | a0001c0001t0072g0090 a0001c0001t0080g0148 a0001c0001t0123g0301 others(156): Show |
176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1019+191G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520616 | |||||||
chr2:112520734 | C | A | 158 | a0001c0002t0002g0132 a0001c0002t0003g0004 a0001c0002t0003g0009 others(155): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1019+309C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520734 | |||||||
chr2:112520778 | C | T | 2 | a0001c0003t0010g0227 a0001c0003t0010g0294 |
2 | NA18948.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1019+353C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520778 | |||||||
chr2:112520792 | C | T | 1 | a0001c0004t0001g0246 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1019+367C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520792 | |||||||
chr2:112520954 | G | A | 1 | a0001c0003t0019g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1019+529G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520954 | |||||||
chr2:112521118 | G | A | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1019+693G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521118 | |||||||
chr2:112521123 | C | T | 3 | a0001c0001t0061g0261 a0001c0001t0065g0211 a0001c0001t0073g0255 |
3 | HG01358.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1019+698C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521123 | |||||||
chr2:112521140 | G | A | 1 | a0001c0002t0133g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1019+715G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521140 | |||||||
chr2:112521176 | G | A | 1 | a0001c0001t0080g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1019+751G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521176 | |||||||
chr2:112521186 | G | A | 2 | a0001c0002t0040g0088 a0001c0002t0049g0234 |
2 | HG02922.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1019+761G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521186 | |||||||
chr2:112521287 | C | T | 1 | a0001c0002t0008g0072 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1019+862C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521287 | |||||||
chr2:112521410 | C | G | 1 | a0001c0001t0016g0265 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1019+985C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521410 | |||||||
chr2:112521415 | G | A | 1 | a0001c0001t0113g0259 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1019+990G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521415 | |||||||
chr2:112521534 | C | G | 1 | a0001c0003t0104g0152 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1019+1109C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521534 | |||||||
chr2:112521563 | C | G | 1 | a0001c0001t0112g0100 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1019+1138C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521563 | |||||||
chr2:112521621 | C | T | 1 | a0001c0003t0002g0154 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1019+1196C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521621 | |||||||
chr2:112521737 | A | G | 2 | a0001c0003t0002g0295 a0001c0003t0032g0231 |
2 | HG02129.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1019+1312A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521737 | |||||||
chr2:112521857 | C | T | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1019+1432C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521857 | |||||||
chr2:112521903 | A | G | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1019+1478A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521903 | |||||||
chr2:112521922 | C | T | 1 | a0001c0001t0081g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1019+1497C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521922 | |||||||
chr2:112521937 | A | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(280): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1019+1512A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521937 | |||||||
chr2:112522042 | T | G | 1 | a0001c0003t0098g0170 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1019+1617T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522042 | |||||||
chr2:112522045 | C | T | 1 | a0001c0002t0003g0135 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1019+1620C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522045 | |||||||
chr2:112522204 | G | T | 1 | a0001c0001t0013g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1019+1779G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522204 | |||||||
chr2:112522310 | A | G | 1 | a0001c0002t0027g0022 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1019+1885A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522310 | |||||||
chr2:112522311 | T | C | 1 | a0001c0002t0027g0022 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1019+1886T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522311 | |||||||
chr2:112522420 | AACCGACA others(2): Show |
A | 3 | a0001c0002t0051g0275 a0001c0002t0052g0094 a0001c0002t0053g0276 |
3 | HG02145.hp1 HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1019+1998_1019+200 others(13): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112522420 | ||||||
chr2:112522676 | C | G | 9 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(6): Show |
9 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1019+2251C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522676 | |||||||
chr2:112522694 | A | G | 1 | a0001c0002t0049g0234 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1019+2269A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522694 | |||||||
chr2:112522776 | C | T | 1 | a0001c0003t0035g0178 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1019+2351C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522776 | |||||||
chr2:112523006 | A | G | 8 | a0001c0002t0003g0009 a0001c0002t0003g0115 a0001c0002t0003g0121 others(5): Show |
10 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1019+2581A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523006 | |||||||
chr2:112523032 | C | T | 2 | a0001c0003t0106g0169 a0001c0003t0107g0181 |
2 | NA19003.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1019+2607C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523032 | |||||||
chr2:112523052 | C | T | 1 | a0001c0002t0050g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1019+2627C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523052 | |||||||
chr2:112523176 | C | G | 1 | a0001c0002t0133g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1019+2751C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523176 | |||||||
chr2:112523238 | G | C | 1 | a0001c0001t0001g0300 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1019+2813G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523238 | |||||||
chr2:112523303 | C | T | 128 | a0001c0001t0006g0056 a0001c0001t0013g0010 a0001c0001t0013g0032 others(125): Show |
142 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1019+2878C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523303 | |||||||
chr2:112523314 | C | T | 1 | a0001c0001t0025g0042 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1019+2889C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523314 | |||||||
chr2:112523332 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(267): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1019+2907C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523332 | |||||||
chr2:112523350 | C | CTG | 7 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0013g0032 others(4): Show |
7 | HG02896.hp1 HG02922.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.1019+2947_1019+294 others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523350 | ||||||
chr2:112523350 | C | CTGTG | 241 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(238): Show |
265 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1019+2945_1019+294 others(8): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523350 | ||||||
chr2:112523350 | C | CTGTGTG | 25 | a0001c0001t0001g0274 a0001c0001t0023g0013 a0001c0001t0023g0101 others(22): Show |
29 | HG00438.hp1 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.1019+2943_1019+294 others(10): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523350 | ||||||
chr2:112523350 | C | CTGTGTGT others(1): Show |
12 | a0001c0001t0016g0248 a0001c0001t0065g0211 a0001c0002t0008g0070 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1019+2941_1019+294 others(12): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523350 | ||||||
chr2:112523350 | C | CTGTGTGT others(3): Show |
12 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(9): Show |
15 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1019+2939_1019+294 others(14): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523350 | ||||||
chr2:112523350 | C | CTGTGTGT others(17): Show |
1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1019+2948_1019+294 others(28): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523350 | ||||||
chr2:112523469 | CCTGTCAC others(14): Show |
C | 1 | a0001c0002t0133g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1019+3086_1019+310 others(25): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523469 | ||||||
chr2:112523514 | G | C | 1 | a0001c0001t0073g0255 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1019+3089G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523514 | |||||||
chr2:112523546 | G | A | 3 | a0001c0001t0001g0253 a0001c0001t0001g0258 a0001c0001t0088g0237 |
3 | HG01257.hp2 HG02738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1019+3121G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523546 | |||||||
chr2:112523769 | A | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(254): Show |
285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.1019+3344A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523769 | |||||||
chr2:112523770 | GT | G | 55 | a0001c0001t0005g0051 a0001c0001t0005g0052 a0001c0001t0005g0053 others(52): Show |
58 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.1019+3356delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523770 | ||||||
chr2:112523770 | GTT | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(253): Show |
284 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1019+3355_1019+335 others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523770 | ||||||
chr2:112524197 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1019+3772A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524197 | |||||||
chr2:112524491 | C | T | 1 | a0001c0001t0112g0100 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1019+4066C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524491 | |||||||
chr2:112524579 | A | G | 8 | a0001c0002t0003g0009 a0001c0002t0003g0115 a0001c0002t0003g0121 others(5): Show |
10 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1020-4102A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524579 | |||||||
chr2:112524644 | A | T | 1 | a0001c0001t0072g0090 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1020-4037A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524644 | |||||||
chr2:112524666 | A | G | 10 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(7): Show |
10 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1020-4015A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524666 | |||||||
chr2:112524728 | C | T | 1 | a0001c0002t0003g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1020-3953C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524728 | |||||||
chr2:112524923 | C | T | 13 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(10): Show |
16 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1020-3758C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524923 | |||||||
chr2:112524924 | A | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(300): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1020-3757A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524924 | |||||||
chr2:112524941 | T | C | 1 | a0001c0002t0053g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1020-3740T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524941 | |||||||
chr2:112524944 | A | G | 7 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(4): Show |
7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1020-3737A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524944 | |||||||
chr2:112525222 | G | T | 9 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(6): Show |
9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020-3459G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525222 | |||||||
chr2:112525271 | C | T | 128 | a0001c0001t0006g0056 a0001c0001t0013g0010 a0001c0001t0013g0032 others(125): Show |
142 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1020-3410C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525271 | |||||||
chr2:112525385 | A | G | 2 | a0001c0002t0049g0234 a0001c0002t0050g0233 |
2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1020-3296A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525385 | |||||||
chr2:112525465 | G | A | 9 | a0001c0001t0005g0051 a0001c0001t0005g0052 a0001c0001t0005g0053 others(6): Show |
9 | HG00639.hp1 HG02717.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020-3216G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525465 | |||||||
chr2:112525474 | C | T | 10 | a0001c0002t0003g0014 a0001c0002t0003g0123 a0001c0002t0003g0127 others(7): Show |
11 | HG00438.hp1 HG02071.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.1020-3207C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525474 | |||||||
chr2:112525514 | G | A | 8 | a0001c0002t0003g0009 a0001c0002t0003g0115 a0001c0002t0003g0121 others(5): Show |
10 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1020-3167G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525514 | |||||||
chr2:112525631 | A | G | 10 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(7): Show |
10 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1020-3050A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525631 | |||||||
chr2:112525726 | C | T | 1 | a0001c0001t0115g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1020-2955C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525726 | |||||||
chr2:112525727 | G | A | 1 | a0001c0001t0083g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1020-2954G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525727 | |||||||
chr2:112525727 | G | T | 1 | a0001c0003t0002g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1020-2954G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525727 | |||||||
chr2:112525927 | C | T | 2 | a0001c0001t0024g0007 a0001c0001t0114g0102 |
4 | HG01167.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020-2754C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525927 | |||||||
chr2:112526024 | T | A | 1 | a0001c0002t0133g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1020-2657T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526024 | |||||||
chr2:112526032 | TA | T | 13 | a0001c0002t0007g0008 a0001c0002t0007g0104 a0001c0002t0007g0106 others(10): Show |
16 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1020-2648delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526032 | |||||||
chr2:112526036 | G | T | 2 | a0001c0002t0049g0234 a0001c0002t0050g0233 |
2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1020-2645G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526036 | |||||||
chr2:112526249 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1020-2432T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526249 | |||||||
chr2:112526628 | G | A | 9 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(6): Show |
9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020-2053G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526628 | |||||||
chr2:112526767 | T | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(108): Show |
122 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1020-1914T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526767 | |||||||
chr2:112526988 | G | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(295): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1020-1693G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526988 | |||||||
chr2:112526999 | A | G | 2 | a0001c0002t0049g0234 a0001c0002t0050g0233 |
2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1020-1682A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526999 | |||||||
chr2:112527169 | C | T | 2 | a0001c0001t0093g0254 a0001c0001t0094g0241 |
2 | HG02683.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1020-1512C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527169 | |||||||
chr2:112527218 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(265): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1020-1463G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527218 | |||||||
chr2:112527219 | C | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(265): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1020-1462C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527219 | |||||||
chr2:112527283 | G | T | 1 | a0001c0003t0105g0172 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1020-1398G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527283 | |||||||
chr2:112527446 | C | G | 1 | a0001c0001t0080g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1020-1235C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527446 | |||||||
chr2:112527468 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1020-1213A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527468 | |||||||
chr2:112527495 | G | T | 8 | a0001c0001t0005g0051 a0001c0001t0005g0052 a0001c0001t0005g0053 others(5): Show |
8 | HG00639.hp1 HG02717.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1020-1186G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527495 | |||||||
chr2:112527499 | G | T | 9 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(6): Show |
9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020-1182G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527499 | |||||||
chr2:112527501 | A | G | 1 | a0001c0001t0081g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1020-1180A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527501 | |||||||
chr2:112527676 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1020-1005C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527676 | |||||||
chr2:112528044 | G | A | 10 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(7): Show |
10 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1020-637G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528044 | |||||||
chr2:112528173 | G | A | 1 | a0001c0002t0003g0140 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1020-508G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528173 | |||||||
chr2:112528219 | G | A | 12 | a0001c0002t0009g0146 a0001c0002t0009g0147 a0001c0002t0009g0290 others(9): Show |
12 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1020-462G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528219 | |||||||
chr2:112528327 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1020-354C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528327 | |||||||
chr2:112528371 | G | C | 1 | a0001c0002t0011g0111 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1020-310G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528371 | |||||||
chr2:112528446 | A | G | 9 | a0001c0002t0008g0070 a0001c0002t0008g0072 a0001c0002t0008g0074 others(6): Show |
9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020-235A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528446 | |||||||
chr2:112528468 | G | A | 1 | a0001c0002t0040g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1020-213G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528468 | |||||||
chr2:112528618 | T | G | 1 | a0001c0002t0122g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1020-63T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528618 |