Item | Value |
---|---|
geneid | 121355 |
ensemblid | ENSG00000170627.11 |
hgncid | 26565 |
symbol | GTSF1 |
name | gametocyte specific factor 1 |
refseq_nuc | NM_144594.3 |
refseq_prot | NP_653195.2 |
ensembl_nuc | ENST00000305879.8 |
ensembl_prot | ENSP00000304185.5 |
mane_status | MANE Select |
chr | chr12 |
start | 54455957 |
end | 54473602 |
strand | - |
ver | v1.2 |
region | chr12:54455957-54473602 |
region5000 | chr12:54450957-54478602 |
regionname0 | GTSF1_chr12_54455957_54473602 |
regionname5000 | GTSF1_chr12_54450957_54478602 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 167 | 359 | 88 | 69 | 146 | 14 | 40 | 106 | GTSF1_chr12_54450957_54478602 | GTSF1 | MEETY others(162): Show |
chr12 | 54450957 | 54478602 |
a0002 | 0/0 | 167 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | MEETY others(162): Show |
chr12 | 54450957 | 54478602 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 501 | 357 | 86 | 69 | 146 | 14 | 40 | GTSF1_chr12_54450957_54478602 | GTSF1 | ATGGA others(496): Show |
chr12 | 54450957 | 54478602 | ||
a0001c0002 | 0/0 | 501 | 2 | 2 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | ATGGA others(496): Show |
chr12 | 54450957 | 54478602 | ||
a0002c0003 | 0/0 | 501 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | ATGGA others(496): Show |
chr12 | 54450957 | 54478602 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 807 | 263 | 50 | 49 | 117 | 14 | 31 | GTSF1_chr12_54450957_54478602 | GTSF1 | GTTGC others(802): Show |
chr12 | 54450957 | 54478602 |
a0001c0001t0002 | 0/0 | 807 | 74 | 30 | 17 | 18 | 0 | 9 | GTSF1_chr12_54450957_54478602 | GTSF1 | GTTGC others(802): Show |
chr12 | 54450957 | 54478602 |
a0001c0001t0003 | 0/0 | 807 | 10 | 0 | 3 | 7 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | GTTGC others(802): Show |
chr12 | 54450957 | 54478602 |
a0001c0001t0004 | 0/0 | 807 | 3 | 0 | 0 | 3 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | GTTGC others(802): Show |
chr12 | 54450957 | 54478602 |
a0001c0001t0005 | 0/0 | 807 | 3 | 3 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | GTTGC others(802): Show |
chr12 | 54450957 | 54478602 |
a0001c0001t0006 | 0/0 | 807 | 2 | 2 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | GTTGC others(802): Show |
chr12 | 54450957 | 54478602 |
a0001c0001t0007 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | GTTGC others(802): Show |
chr12 | 54450957 | 54478602 |
a0001c0001t0008 | 0/0 | 807 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | GTTGC others(802): Show |
chr12 | 54450957 | 54478602 |
a0001c0002t0002 | 0/0 | 807 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | GTTGC others(802): Show |
chr12 | 54450957 | 54478602 |
a0001c0002t0003 | 0/0 | 807 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | GTTGC others(802): Show |
chr12 | 54450957 | 54478602 |
a0002c0003t0003 | 0/0 | 807 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | GTTGC others(802): Show |
chr12 | 54450957 | 54478602 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 36 | 0 | 4 | 29 | 1 | 2 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0002 | 0/0 | 27 | 3 | 11 | 8 | 2 | 3 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0003 | 0/0 | 26 | 1 | 1 | 18 | 1 | 5 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0005 | 0/0 | 19 | 0 | 4 | 15 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0006 | 0/0 | 16 | 2 | 7 | 0 | 4 | 3 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0007 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0009 | 0/0 | 8 | 0 | 0 | 3 | 0 | 5 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0013 | 0/0 | 4 | 1 | 0 | 0 | 3 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0004 | 0/0 | 26 | 3 | 10 | 11 | 0 | 2 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0008 | 0/0 | 9 | 8 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0003g0010 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0004g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0005g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0006g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0001c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
a0002c0003t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00735 | hp1 | a0002 | c0003 | t0003 | g0072 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | IBS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | MSL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0141 | AFR | MSL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | STU | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | STU | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | YRI | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18946 | hp1 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | LWK | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19082 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | YRI | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA19240 | hp2 | a0001 | c0002 | t0003 | g0140 | AFR | YRI | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ASW | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | ASW | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | TSI | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | MSL | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | LWK | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0033 | REF | REF | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0044 | REF | REF | GTSF1_chr12_54450957_54478602 | GTSF1 | chr12 | 54450957 | 54478602 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:54462164 | C | T | 1 | a0002 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.337G>A | p.Glu113Lys | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/9 | 423/807 | 337/504 | 113/167 | chr12 | 54462164 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:54462153 | G | A | 1 | a0001c0002 | 2 | NA19240.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.348C>T | p.Ser116Ser | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/9 | 434/807 | 348/504 | 116/167 | chr12 | 54462153 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:54456026 | G | C | 1 | a0001c0001t0005 | 3 | HG02622.hp2 HG03041.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*148C>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 9/9 | 3083 | chr12 | 54456026 | ||||||
chr12:54456092 | T | G | 3 | a0001c0001t0002 a0001c0001t0006 a0001c0002t0002 |
77 | HG00733.hp2 HG00741.hp2 HG01074.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*82A>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 9/9 | 3017 | chr12 | 54456092 | ||||||
chr12:54456119 | A | G | 1 | a0001c0001t0008 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 9/9 | 2990 | chr12 | 54456119 | ||||||
chr12:54456133 | C | G | 6 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(3): Show |
18 | HG00735.hp1 HG01346.hp1 HG01891.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*41G>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 9/9 | 2976 | chr12 | 54456133 | ||||||
chr12:54473597 | A | G | 2 | a0001c0001t0004 a0001c0001t0007 |
4 | HG02040.hp1 HG02071.hp2 NA18946.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-81T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/9 | 2349 | chr12 | 54473597 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:54456352 | T | C | 12 | a0001c0001t0002g0004 a0001c0001t0002g0123 a0001c0001t0002g0124 others(9): Show |
37 | HG00733.hp2 HG00741.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.*21-199A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54456352 | |||||||
chr12:54456449 | G | A | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.*21-296C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54456449 | |||||||
chr12:54456479 | T | C | 1 | a0001c0001t0002g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*21-326A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54456479 | |||||||
chr12:54456486 | C | G | 1 | a0001c0001t0002g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*21-333G>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54456486 | |||||||
chr12:54456683 | C | G | 1 | a0001c0001t0002g0145 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.*21-530G>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54456683 | |||||||
chr12:54456698 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0008g0141 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*21-545G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54456698 | |||||||
chr12:54456893 | T | G | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 |
3 | HG01192.hp2 HG04199.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.*21-740A>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54456893 | |||||||
chr12:54456955 | C | T | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.*21-802G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54456955 | |||||||
chr12:54456999 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0065 a0001c0001t0001g0066 |
3 | HG00741.hp1 HG02300.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.*21-846G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54456999 | |||||||
chr12:54457323 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.*21-1170G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54457323 | |||||||
chr12:54457391 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.*21-1238A>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54457391 | |||||||
chr12:54457415 | A | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(5): Show |
21 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.*21-1262T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54457415 | |||||||
chr12:54457697 | C | T | 1 | a0001c0001t0006g0021 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.*20+1392G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54457697 | |||||||
chr12:54457787 | T | TA | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.*20+1301dupT | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54457787 | |||||||
chr12:54457912 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.*20+1177A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54457912 | |||||||
chr12:54458021 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0008g0141 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*20+1068T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458021 | |||||||
chr12:54458073 | G | A | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.*20+1016C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458073 | |||||||
chr12:54458131 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.*20+958G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458131 | |||||||
chr12:54458228 | G | C | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.*20+861C>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458228 | |||||||
chr12:54458336 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.*20+753C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458336 | |||||||
chr12:54458442 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.*20+647C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458442 | |||||||
chr12:54458474 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*20+615G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458474 | |||||||
chr12:54458532 | C | A | 1 | a0001c0001t0002g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*20+557G>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458532 | |||||||
chr12:54458573 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.*20+516A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458573 | |||||||
chr12:54458618 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.*20+471G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458618 | |||||||
chr12:54458807 | T | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0144 others(3): Show |
8 | HG02280.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.*20+282A>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458807 | |||||||
chr12:54458808 | G | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0144 others(3): Show |
8 | HG02280.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.*20+281C>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458808 | |||||||
chr12:54458809 | A | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0144 others(3): Show |
8 | HG02280.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.*20+280T>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458809 | |||||||
chr12:54458811 | A | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0144 others(3): Show |
8 | HG02280.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.*20+278T>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458811 | |||||||
chr12:54458813 | ATC | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0144 others(3): Show |
8 | HG02280.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.*20+274_*20+275del others(2): Show |
GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458813 | |||||||
chr12:54458818 | G | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0144 others(3): Show |
8 | HG02280.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.*20+271C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458818 | |||||||
chr12:54458832 | T | TA | 12 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0049 others(9): Show |
16 | HG01517.hp1 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.*20+256dupT | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458832 | |||||||
chr12:54458832 | T | TAA | 4 | a0001c0001t0001g0142 a0001c0001t0004g0014 a0001c0001t0007g0039 others(1): Show |
6 | HG02040.hp1 HG02071.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.*20+255_*20+256dup others(2): Show |
GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 8/8 | chr12 | 54458832 | |||||||
chr12:54459640 | T | C | 1 | a0001c0001t0002g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.488-515A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459640 | |||||||
chr12:54459653 | C | T | 2 | a0001c0001t0004g0014 a0001c0001t0007g0039 |
4 | HG02040.hp1 HG02071.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-528G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459653 | |||||||
chr12:54459655 | C | A | 1 | a0001c0001t0008g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.488-530G>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459655 | |||||||
chr12:54459709 | ACTGATAT others(308): Show |
A | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.487+353_488-585del | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459709 | |||||||
chr12:54459721 | C | T | 10 | a0001c0001t0002g0004 a0001c0001t0002g0123 a0001c0001t0002g0124 others(7): Show |
35 | HG00733.hp2 HG00741.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.488-596G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459721 | |||||||
chr12:54459722 | C | CT | 18 | a0001c0001t0001g0028 a0001c0001t0001g0042 a0001c0001t0001g0048 others(15): Show |
19 | HG00673.hp2 HG01106.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.488-598dupA | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459722 | |||||||
chr12:54459722 | CT | C | 17 | a0001c0001t0001g0016 a0001c0001t0001g0092 a0001c0001t0001g0098 others(14): Show |
45 | HG00733.hp2 HG00741.hp2 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.488-598delA | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459722 | |||||||
chr12:54459724 | T | C | 1 | a0001c0001t0002g0128 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.488-599A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459724 | |||||||
chr12:54459749 | C | T | 2 | a0001c0001t0005g0020 a0001c0001t0005g0040 |
3 | HG02622.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.488-624G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459749 | |||||||
chr12:54459789 | G | C | 1 | a0001c0001t0001g0030 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.487+588C>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459789 | |||||||
chr12:54459819 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.487+558G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459819 | |||||||
chr12:54459852 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.487+525T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459852 | |||||||
chr12:54459854 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.487+523C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459854 | |||||||
chr12:54459927 | C | T | 1 | a0001c0001t0003g0026 | 2 | NA19063.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.487+450G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459927 | |||||||
chr12:54459928 | G | T | 1 | a0001c0001t0001g0024 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.487+449C>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459928 | |||||||
chr12:54459936 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.487+441G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459936 | |||||||
chr12:54459994 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.487+383C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 7/8 | chr12 | 54459994 | |||||||
chr12:54460719 | T | A | 2 | a0001c0001t0005g0020 a0001c0001t0005g0040 |
3 | HG02622.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.393-248A>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54460719 | |||||||
chr12:54460815 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.393-344G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54460815 | |||||||
chr12:54460821 | C | G | 1 | a0001c0001t0006g0021 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.393-350G>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54460821 | |||||||
chr12:54460863 | C | T | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.393-392G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54460863 | |||||||
chr12:54460887 | T | G | 1 | a0001c0001t0001g0025 | 2 | HG01192.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.393-416A>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54460887 | |||||||
chr12:54461018 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.393-547G>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54461018 | |||||||
chr12:54461027 | T | C | 4 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(1): Show |
4 | HG02572.hp2 HG02622.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.393-556A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54461027 | |||||||
chr12:54461049 | G | C | 1 | a0001c0001t0002g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.393-578C>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54461049 | |||||||
chr12:54461078 | A | G | 2 | a0001c0001t0002g0136 a0001c0001t0002g0139 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.393-607T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54461078 | |||||||
chr12:54461080 | G | A | 2 | a0001c0001t0002g0136 a0001c0001t0002g0139 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.393-609C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54461080 | |||||||
chr12:54461089 | C | T | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.393-618G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54461089 | |||||||
chr12:54461182 | C | A | 1 | a0001c0001t0008g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.393-711G>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54461182 | |||||||
chr12:54461306 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(128): Show |
320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.392+803T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54461306 | |||||||
chr12:54461388 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0088 |
6 | NA18942.hp1 NA18968.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.392+721T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54461388 | |||||||
chr12:54461442 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.392+667C>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54461442 | |||||||
chr12:54461624 | C | G | 1 | a0001c0001t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.392+485G>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54461624 | |||||||
chr12:54461794 | G | A | 2 | a0001c0001t0002g0136 a0001c0001t0002g0139 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.392+315C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54461794 | |||||||
chr12:54461891 | C | T | 3 | a0001c0001t0002g0041 a0001c0001t0005g0020 a0001c0001t0005g0040 |
4 | HG02622.hp2 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.392+218G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 6/8 | chr12 | 54461891 | |||||||
chr12:54462182 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.329-10C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 5/8 | chr12 | 54462182 | |||||||
chr12:54462268 | A | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0144 others(1): Show |
6 | HG02280.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-96T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 5/8 | chr12 | 54462268 | |||||||
chr12:54462303 | TCCTG | T | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.329-135_329-132del others(4): Show |
GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 5/8 | chr12 | 54462303 | |||||||
chr12:54462352 | C | T | 11 | a0001c0001t0002g0004 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
36 | HG00733.hp2 HG00741.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.329-180G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 5/8 | chr12 | 54462352 | |||||||
chr12:54462439 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0117 |
3 | HG01167.hp2 HG01169.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.328+203T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 5/8 | chr12 | 54462439 | |||||||
chr12:54462521 | A | C | 1 | a0001c0001t0002g0126 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.328+121T>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 5/8 | chr12 | 54462521 | |||||||
chr12:54462574 | T | C | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.328+68A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 5/8 | chr12 | 54462574 | |||||||
chr12:54462751 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.245-26T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 4/8 | chr12 | 54462751 | |||||||
chr12:54462940 | G | T | 2 | a0001c0001t0005g0020 a0001c0001t0005g0040 |
3 | HG02622.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.245-215C>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 4/8 | chr12 | 54462940 | |||||||
chr12:54463011 | A | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0144 |
5 | HG02280.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+160T>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 4/8 | chr12 | 54463011 | |||||||
chr12:54463086 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.244+85G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 4/8 | chr12 | 54463086 | |||||||
chr12:54463359 | A | G | 1 | a0001c0001t0008g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.118-62T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 3/8 | chr12 | 54463359 | |||||||
chr12:54463739 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.118-442A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 3/8 | chr12 | 54463739 | |||||||
chr12:54464004 | A | G | 1 | a0001c0001t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.118-707T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 3/8 | chr12 | 54464004 | |||||||
chr12:54464047 | G | A | 3 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0133 |
3 | HG02572.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.118-750C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 3/8 | chr12 | 54464047 | |||||||
chr12:54464080 | T | G | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.118-783A>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 3/8 | chr12 | 54464080 | |||||||
chr12:54464132 | T | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0144 |
5 | HG02280.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-835A>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 3/8 | chr12 | 54464132 | |||||||
chr12:54464221 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0086 a0001c0001t0001g0112 |
4 | NA18955.hp1 NA18974.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+846T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 3/8 | chr12 | 54464221 | |||||||
chr12:54464416 | T | C | 1 | a0001c0001t0001g0017 | 3 | NA18962.hp2 NA18966.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.117+651A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 3/8 | chr12 | 54464416 | |||||||
chr12:54464610 | C | T | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.117+457G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 3/8 | chr12 | 54464610 | |||||||
chr12:54464769 | G | C | 2 | a0001c0001t0004g0014 a0001c0001t0007g0039 |
4 | HG02040.hp1 HG02071.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+298C>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 3/8 | chr12 | 54464769 | |||||||
chr12:54464814 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.117+253C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 3/8 | chr12 | 54464814 | |||||||
chr12:54464855 | G | T | 1 | a0001c0001t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+212C>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 3/8 | chr12 | 54464855 | |||||||
chr12:54464856 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.117+211A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 3/8 | chr12 | 54464856 | |||||||
chr12:54465006 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.117+61A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 3/8 | chr12 | 54465006 | |||||||
chr12:54465201 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.17-34T>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54465201 | |||||||
chr12:54465346 | A | T | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.17-179T>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54465346 | |||||||
chr12:54465597 | A | G | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.17-430T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54465597 | |||||||
chr12:54465655 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.17-488G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54465655 | |||||||
chr12:54465701 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.17-534A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54465701 | |||||||
chr12:54465712 | T | C | 1 | a0001c0001t0006g0021 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.17-545A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54465712 | |||||||
chr12:54465751 | TG | T | 2 | a0001c0001t0004g0014 a0001c0001t0007g0039 |
4 | HG02040.hp1 HG02071.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-585delC | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54465751 | |||||||
chr12:54465833 | A | G | 22 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(19): Show |
41 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.17-666T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54465833 | |||||||
chr12:54465861 | T | C | 21 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(18): Show |
39 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.17-694A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54465861 | |||||||
chr12:54465947 | T | C | 2 | a0001c0001t0001g0142 a0001c0001t0008g0141 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.17-780A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54465947 | |||||||
chr12:54465956 | A | C | 1 | a0001c0001t0002g0124 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.17-789T>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54465956 | |||||||
chr12:54466017 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.17-850A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54466017 | |||||||
chr12:54466204 | G | C | 2 | a0001c0001t0001g0142 a0001c0001t0008g0141 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.17-1037C>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54466204 | |||||||
chr12:54466397 | A | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(5): Show |
21 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.17-1230T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54466397 | |||||||
chr12:54466398 | T | A | 3 | a0001c0001t0002g0041 a0001c0001t0005g0020 a0001c0001t0005g0040 |
4 | HG02622.hp2 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-1231A>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54466398 | |||||||
chr12:54466786 | A | G | 2 | a0001c0001t0004g0014 a0001c0001t0007g0039 |
4 | HG02040.hp1 HG02071.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-1619T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54466786 | |||||||
chr12:54466816 | C | CT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(91): Show |
240 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.17-1650dupA | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54466816 | |||||||
chr12:54466816 | C | CTT | 6 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0114 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.17-1651_17-1650dup others(2): Show |
GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54466816 | |||||||
chr12:54466816 | C | CTTT | 10 | a0001c0001t0002g0004 a0001c0001t0002g0123 a0001c0001t0002g0124 others(7): Show |
35 | HG00733.hp2 HG00741.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.17-1652_17-1650dup others(3): Show |
GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54466816 | |||||||
chr12:54466816 | CT | C | 17 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(14): Show |
34 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(31): Show |
intron_variant | MODIFIER | c.17-1650delA | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54466816 | |||||||
chr12:54466835 | T | A | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.17-1668A>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54466835 | |||||||
chr12:54466838 | CAG | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02148.hp2 NA18940.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.17-1673_17-1672del others(2): Show |
GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54466838 | |||||||
chr12:54466940 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.17-1773C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54466940 | |||||||
chr12:54466985 | T | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(5): Show |
21 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.17-1818A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54466985 | |||||||
chr12:54467049 | CT | C | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.17-1883delA | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467049 | |||||||
chr12:54467089 | A | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
19 | HG00323.hp1 HG01074.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.17-1922T>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467089 | |||||||
chr12:54467134 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.17-1967G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467134 | |||||||
chr12:54467270 | T | C | 2 | a0001c0001t0004g0014 a0001c0001t0007g0039 |
4 | HG02040.hp1 HG02071.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-2103A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467270 | |||||||
chr12:54467275 | G | A | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.17-2108C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467275 | |||||||
chr12:54467306 | G | GT | 5 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0016 others(2): Show |
28 | HG00408.hp2 HG00423.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.17-2140dupA | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467306 | |||||||
chr12:54467318 | T | G | 1 | a0001c0001t0001g0066 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.17-2151A>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467318 | |||||||
chr12:54467322 | G | GT | 7 | a0001c0001t0001g0038 a0001c0001t0001g0085 a0001c0001t0001g0142 others(4): Show |
8 | HG02145.hp1 HG02280.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.17-2156dupA | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467322 | |||||||
chr12:54467322 | G | GTT | 12 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(9): Show |
27 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(24): Show |
intron_variant | MODIFIER | c.17-2157_17-2156dup others(2): Show |
GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467322 | |||||||
chr12:54467329 | T | G | 1 | a0001c0001t0002g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.17-2162A>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467329 | |||||||
chr12:54467355 | T | C | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.17-2188A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467355 | |||||||
chr12:54467371 | G | C | 1 | a0001c0001t0001g0076 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.17-2204C>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467371 | |||||||
chr12:54467377 | C | T | 4 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(1): Show |
4 | HG02572.hp2 HG02622.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-2210G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467377 | |||||||
chr12:54467433 | G | C | 1 | a0001c0001t0002g0132 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.17-2266C>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467433 | |||||||
chr12:54467435 | C | T | 1 | a0001c0002t0002g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.17-2268G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467435 | |||||||
chr12:54467610 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.17-2443G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467610 | |||||||
chr12:54467821 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.17-2654G>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467821 | |||||||
chr12:54467842 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.17-2675G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467842 | |||||||
chr12:54467920 | C | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0018 others(32): Show |
88 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.17-2753G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467920 | |||||||
chr12:54467922 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0002g0082 |
2 | NA18953.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.17-2755G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54467922 | |||||||
chr12:54468151 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.17-2984T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54468151 | |||||||
chr12:54468183 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0002g0111 |
4 | HG00735.hp2 HG00738.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-3016C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54468183 | |||||||
chr12:54468416 | C | T | 2 | a0001c0001t0004g0014 a0001c0001t0007g0039 |
4 | HG02040.hp1 HG02071.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+2817G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54468416 | |||||||
chr12:54468436 | C | G | 1 | a0001c0001t0001g0080 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.16+2797G>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54468436 | |||||||
chr12:54468445 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.16+2788T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54468445 | |||||||
chr12:54468451 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.16+2782G>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54468451 | |||||||
chr12:54468597 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.16+2636T>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54468597 | |||||||
chr12:54468682 | G | A | 1 | a0001c0001t0008g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.16+2551C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54468682 | |||||||
chr12:54468772 | G | C | 1 | a0001c0001t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.16+2461C>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54468772 | |||||||
chr12:54468944 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.16+2289T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54468944 | |||||||
chr12:54468980 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.16+2253C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54468980 | |||||||
chr12:54469110 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0002g0136 a0001c0001t0008g0141 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.16+2123G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469110 | |||||||
chr12:54469111 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.16+2122C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469111 | |||||||
chr12:54469152 | T | C | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.16+2081A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469152 | |||||||
chr12:54469267 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.16+1966G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469267 | |||||||
chr12:54469324 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(5): Show |
21 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.16+1909C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469324 | |||||||
chr12:54469357 | C | A | 37 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(34): Show |
81 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.16+1876G>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469357 | |||||||
chr12:54469366 | C | T | 8 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0142 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.16+1867G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469366 | |||||||
chr12:54469369 | A | G | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.16+1864T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469369 | |||||||
chr12:54469413 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
12 | HG00408.hp1 HG00544.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.16+1820C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469413 | |||||||
chr12:54469441 | CT | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
359 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(356): Show |
intron_variant | MODIFIER | c.16+1791delA | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469441 | |||||||
chr12:54469549 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.16+1684C>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469549 | |||||||
chr12:54469614 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.16+1619C>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469614 | |||||||
chr12:54469687 | C | CA | 22 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(19): Show |
28 | HG00733.hp2 HG00741.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.16+1545dupT | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469687 | |||||||
chr12:54469687 | C | CAA | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0068 others(3): Show |
9 | HG01891.hp1 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.16+1544_16+1545dup others(2): Show |
GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469687 | |||||||
chr12:54469687 | C | CAAA | 11 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(8): Show |
24 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(21): Show |
intron_variant | MODIFIER | c.16+1543_16+1545dup others(3): Show |
GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469687 | |||||||
chr12:54469687 | CA | C | 12 | a0001c0001t0001g0012 a0001c0001t0001g0075 a0001c0001t0001g0076 others(9): Show |
21 | HG00735.hp1 HG01167.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.16+1545delT | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469687 | |||||||
chr12:54469770 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.16+1463G>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469770 | |||||||
chr12:54469798 | C | A | 1 | a0001c0001t0002g0132 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.16+1435G>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469798 | |||||||
chr12:54469846 | G | A | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.16+1387C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469846 | |||||||
chr12:54469926 | A | G | 3 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0133 |
3 | HG02572.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.16+1307T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54469926 | |||||||
chr12:54470227 | T | G | 4 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(1): Show |
4 | HG02572.hp2 HG02622.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+1006A>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54470227 | |||||||
chr12:54470722 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.16+511C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54470722 | |||||||
chr12:54470900 | T | G | 1 | a0001c0002t0003g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.16+333A>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54470900 | |||||||
chr12:54470971 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.16+262T>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54470971 | |||||||
chr12:54471030 | CCTTTTCA others(11): Show |
C | 1 | a0001c0001t0001g0042 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.16+185_16+202delTC others(16): Show |
GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54471030 | |||||||
chr12:54471088 | T | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0116 |
3 | HG01243.hp2 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.16+145A>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54471088 | |||||||
chr12:54471188 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.16+45C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 2/8 | chr12 | 54471188 | |||||||
chr12:54471481 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-29-204A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54471481 | |||||||
chr12:54471585 | C | T | 2 | a0001c0002t0002g0143 a0001c0002t0003g0140 |
2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-29-308G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54471585 | |||||||
chr12:54471620 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-29-343A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54471620 | |||||||
chr12:54471667 | C | A | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.-29-390G>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54471667 | |||||||
chr12:54471741 | T | C | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.-29-464A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54471741 | |||||||
chr12:54471869 | A | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0040 |
3 | HG02622.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-29-592T>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54471869 | |||||||
chr12:54471869 | AC | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(67): Show |
201 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-29-593delG | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54471869 | |||||||
chr12:54471880 | AAAAC | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0117 |
3 | HG01167.hp2 HG01169.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-29-607_-29-604del others(4): Show |
GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54471880 | |||||||
chr12:54472069 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-29-792A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54472069 | |||||||
chr12:54472113 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-29-836C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54472113 | |||||||
chr12:54472135 | GCAGGTTA others(1): Show |
G | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.-29-866_-29-859del others(8): Show |
GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54472135 | |||||||
chr12:54472204 | C | T | 37 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(34): Show |
81 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-29-927G>A | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54472204 | |||||||
chr12:54472285 | C | A | 2 | a0001c0001t0004g0014 a0001c0001t0007g0039 |
4 | HG02040.hp1 HG02071.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-1008G>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54472285 | |||||||
chr12:54472423 | G | A | 4 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(1): Show |
4 | HG02572.hp2 HG02622.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+1123C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54472423 | |||||||
chr12:54472468 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-30+1078C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54472468 | |||||||
chr12:54472501 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(5): Show |
21 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30+1045C>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54472501 | |||||||
chr12:54472650 | C | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(5): Show |
21 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30+896G>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54472650 | |||||||
chr12:54473185 | T | G | 18 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.-30+361A>C | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54473185 | |||||||
chr12:54473207 | T | C | 11 | a0001c0001t0002g0004 a0001c0001t0002g0123 a0001c0001t0002g0124 others(8): Show |
36 | HG00733.hp2 HG00741.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-30+339A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54473207 | |||||||
chr12:54473354 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-30+192A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54473354 | |||||||
chr12:54473400 | A | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(17): Show |
37 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.-30+146T>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54473400 | |||||||
chr12:54473467 | T | A | 20 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(17): Show |
37 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.-30+79A>T | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54473467 | |||||||
chr12:54473491 | T | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0144 others(1): Show |
6 | HG02280.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30+55A>G | GTSF1 | ENSG00000170627.11 | transcript | ENST00000305879.8 | protein_coding | 1/8 | chr12 | 54473491 |