Item | Value |
---|---|
geneid | 80727 |
ensemblid | ENSG00000136295.16 |
hgncid | 22222 |
symbol | TTYH3 |
name | tweety family member 3 |
refseq_nuc | NM_025250.3 |
refseq_prot | NP_079526.1 |
ensembl_nuc | ENST00000258796.12 |
ensembl_prot | ENSP00000258796.7 |
mane_status | MANE Select |
chr | chr7 |
start | 2631986 |
end | 2664802 |
strand | + |
ver | v1.2 |
region | chr7:2631986-2664802 |
region5000 | chr7:2626986-2669802 |
regionname0 | TTYH3_chr7_2631986_2664802 |
regionname5000 | TTYH3_chr7_2626986_2669802 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 523 | 383 | 86 | 79 | 164 | 12 | 40 | 116 | TTYH3_chr7_2626986_2669802 | TTYH3 | MAGVS others(518): Show |
chr7 | 2626986 | 2669802 |
a0002 | 0/0 | 523 | 13 | 10 | 3 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | MAGVS others(518): Show |
chr7 | 2626986 | 2669802 |
a0003 | 0/0 | 523 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | MAGVS others(518): Show |
chr7 | 2626986 | 2669802 |
a0004 | 0/0 | 523 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | MAGVS others(518): Show |
chr7 | 2626986 | 2669802 |
a0005 | 0/0 | 523 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | MAGVS others(518): Show |
chr7 | 2626986 | 2669802 |
a0006 | 0/0 | 523 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | MAGVS others(518): Show |
chr7 | 2626986 | 2669802 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1569 | 351 | 83 | 79 | 140 | 11 | 36 | TTYH3_chr7_2626986_2669802 | TTYH3 | ATGGC others(1564): Show |
chr7 | 2626986 | 2669802 | ||
a0001c0002 | 0/0 | 1569 | 18 | 0 | 0 | 18 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | ATGGC others(1564): Show |
chr7 | 2626986 | 2669802 | ||
a0001c0004 | 0/0 | 1569 | 4 | 0 | 0 | 4 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | ATGGC others(1564): Show |
chr7 | 2626986 | 2669802 | ||
a0001c0005 | 0/0 | 1569 | 3 | 3 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | ATGGC others(1564): Show |
chr7 | 2626986 | 2669802 | ||
a0001c0006 | 0/0 | 1569 | 3 | 0 | 0 | 0 | 1 | 2 | TTYH3_chr7_2626986_2669802 | TTYH3 | ATGGC others(1564): Show |
chr7 | 2626986 | 2669802 | ||
a0001c0008 | 0/0 | 1569 | 2 | 0 | 0 | 0 | 0 | 2 | TTYH3_chr7_2626986_2669802 | TTYH3 | ATGGC others(1564): Show |
chr7 | 2626986 | 2669802 | ||
a0001c0012 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | ATGGC others(1564): Show |
chr7 | 2626986 | 2669802 | ||
a0001c0013 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | ATGGC others(1564): Show |
chr7 | 2626986 | 2669802 | ||
a0002c0003 | 0/0 | 1569 | 13 | 10 | 3 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | ATGGC others(1564): Show |
chr7 | 2626986 | 2669802 | ||
a0003c0007 | 0/0 | 1569 | 2 | 0 | 0 | 0 | 2 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | ATGGC others(1564): Show |
chr7 | 2626986 | 2669802 | ||
a0004c0009 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | ATGGC others(1564): Show |
chr7 | 2626986 | 2669802 | ||
a0004c0014 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | ATGGC others(1564): Show |
chr7 | 2626986 | 2669802 | ||
a0005c0010 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | ATGGC others(1564): Show |
chr7 | 2626986 | 2669802 | ||
a0006c0011 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | ATGGC others(1564): Show |
chr7 | 2626986 | 2669802 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4805 | 135 | 19 | 35 | 59 | 5 | 15 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0002 | 0/0 | 4805 | 83 | 2 | 18 | 52 | 0 | 11 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0003 | 0/0 | 4805 | 27 | 9 | 7 | 8 | 1 | 2 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0004 | 0/0 | 4805 | 18 | 0 | 3 | 9 | 3 | 3 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0005 | 0/0 | 4805 | 13 | 13 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0006 | 0/0 | 4805 | 7 | 7 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0007 | 0/0 | 4805 | 7 | 4 | 3 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0009 | 0/0 | 4805 | 5 | 5 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0010 | 0/0 | 4805 | 4 | 0 | 2 | 0 | 2 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0011 | 0/0 | 4805 | 4 | 4 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0012 | 0/0 | 4805 | 3 | 3 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0013 | 0/0 | 4805 | 3 | 2 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0015 | 0/0 | 4805 | 3 | 1 | 2 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0016 | 0/0 | 4805 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0017 | 0/0 | 4805 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0018 | 0/0 | 4805 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0019 | 0/0 | 4805 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0021 | 0/0 | 4805 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0022 | 0/0 | 4805 | 2 | 0 | 2 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0023 | 0/0 | 4805 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0024 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0026 | 0/0 | 4805 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0027 | 0/0 | 4805 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0028 | 0/0 | 4805 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0029 | 0/0 | 4805 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0030 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0031 | 0/0 | 4805 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0032 | 0/0 | 4805 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0033 | 0/0 | 4805 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0034 | 0/0 | 4805 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0036 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0037 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0038 | 0/0 | 4805 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0041 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0042 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0043 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0044 | 0/0 | 4805 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0045 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0046 | 0/0 | 4805 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0047 | 0/0 | 4805 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0048 | 0/0 | 4805 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0050 | 0/0 | 4805 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0051 | 0/0 | 4763 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4758): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0052 | 0/0 | 4805 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0053 | 0/0 | 4805 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0001t0054 | 0/0 | 4790 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4785): Show |
chr7 | 2626986 | 2669802 |
a0001c0002t0001 | 0/0 | 4805 | 17 | 0 | 0 | 17 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0002t0039 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0004t0002 | 0/0 | 4805 | 3 | 0 | 0 | 3 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0004t0025 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0005t0014 | 0/0 | 4805 | 3 | 3 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0006t0002 | 0/0 | 4805 | 3 | 0 | 0 | 0 | 1 | 2 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0008t0002 | 0/0 | 4805 | 2 | 0 | 0 | 0 | 0 | 2 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0012t0001 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0001c0013t0001 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0002c0003t0004 | 0/0 | 4805 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0002c0003t0007 | 0/0 | 4805 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0002c0003t0008 | 0/0 | 4805 | 6 | 6 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0002c0003t0017 | 0/0 | 4805 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0002c0003t0020 | 0/0 | 4805 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0002c0003t0040 | 0/0 | 4805 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0002c0003t0049 | 0/0 | 4805 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0003c0007t0007 | 0/0 | 4805 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0003c0007t0035 | 0/0 | 4805 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0004c0009t0006 | 0/0 | 4805 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0004c0014t0006 | 0/0 | 4805 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0005c0010t0001 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
a0006c0011t0001 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | GCGGA others(4800): Show |
chr7 | 2626986 | 2669802 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0001 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0003g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0006g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0006g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0006g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0006g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0007g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0007g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0007g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0009g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0009g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0009g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0009g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0010g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0010g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0010g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0010g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0011g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0011g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0011g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0012g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0012g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0012g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0013g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0013g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0013g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0015g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0015g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0015g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0016g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0016g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0017g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0018g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0018g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0019g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0019g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0021g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0021g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0022g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0022g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0023g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0023g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0024g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0026g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0027g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0028g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0029g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0030g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0031g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0032g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0033g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0034g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0036g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0037g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0038g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0041g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0042g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0043g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0044g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0045g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0046g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0047g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0048g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0050g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0051g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0052g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0053g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0001t0054g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0002t0039g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0004t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0004t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0004t0025g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0005t0014g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0005t0014g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0005t0014g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0006t0002g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0006t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0008t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0012t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0001c0013t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0002c0003t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0002c0003t0007g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0002c0003t0008g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0002c0003t0008g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0002c0003t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0002c0003t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0002c0003t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0002c0003t0017g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0002c0003t0020g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0002c0003t0040g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0002c0003t0049g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0003c0007t0007g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0003c0007t0035g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0004c0009t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0004c0014t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0005c0010t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
a0006c0011t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0292 | EUR | GBR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | GBR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00140 | hp2 | a0003 | c0007 | t0007 | g0124 | EUR | GBR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00280 | hp1 | a0003 | c0007 | t0035 | g0136 | EUR | FIN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00280 | hp2 | a0001 | c0006 | t0002 | g0247 | EUR | FIN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0315 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0259 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00738 | hp2 | a0001 | c0001 | t0015 | g0254 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0354 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0113 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0309 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0350 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01109 | hp1 | a0002 | c0003 | t0049 | g0182 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01167 | hp2 | a0001 | c0001 | t0007 | g0093 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0288 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01192 | hp1 | a0001 | c0001 | t0007 | g0346 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01243 | hp1 | a0001 | c0001 | t0013 | g0344 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01255 | hp1 | a0002 | c0003 | t0004 | g0187 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01257 | hp1 | a0001 | c0001 | t0031 | g0275 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01361 | hp1 | a0001 | c0001 | t0010 | g0291 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01496 | hp2 | a0002 | c0003 | t0007 | g0083 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0305 | EUR | IBS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01515 | hp2 | a0001 | c0001 | t0010 | g0195 | EUR | IBS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0006 | EUR | IBS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01516 | hp2 | a0001 | c0001 | t0010 | g0196 | EUR | IBS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0304 | EUR | IBS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | IBS | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0183 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0360 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01952 | hp2 | a0001 | c0001 | t0048 | g0159 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01975 | hp1 | a0001 | c0001 | t0022 | g0125 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01978 | hp1 | a0001 | c0001 | t0015 | g0116 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01981 | hp1 | a0001 | c0001 | t0029 | g0257 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02004 | hp1 | a0001 | c0001 | t0044 | g0053 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02004 | hp2 | a0001 | c0001 | t0022 | g0106 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02055 | hp1 | a0001 | c0001 | t0019 | g0228 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02056 | hp2 | a0001 | c0002 | t0039 | g0048 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02145 | hp2 | a0001 | c0001 | t0018 | g0190 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02148 | hp1 | a0001 | c0001 | t0053 | g0120 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02165 | hp2 | a0001 | c0001 | t0043 | g0001 | EAS | CDX | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02258 | hp1 | a0001 | c0001 | t0013 | g0348 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02280 | hp1 | a0001 | c0001 | t0026 | g0100 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02300 | hp1 | a0001 | c0001 | t0046 | g0231 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02300 | hp2 | a0001 | c0001 | t0010 | g0199 | AMR | PEL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02451 | hp1 | a0001 | c0001 | t0009 | g0325 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02451 | hp2 | a0002 | c0003 | t0008 | g0080 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02523 | hp1 | a0001 | c0001 | t0041 | g0021 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0294 | EAS | KHV | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02572 | hp1 | a0001 | c0001 | t0018 | g0189 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02602 | hp1 | a0001 | c0006 | t0002 | g0016 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02615 | hp1 | a0002 | c0003 | t0008 | g0085 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0322 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02622 | hp2 | a0002 | c0003 | t0017 | g0191 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02630 | hp1 | a0001 | c0001 | t0009 | g0141 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0347 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02647 | hp1 | a0001 | c0001 | t0034 | g0281 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02647 | hp2 | a0001 | c0001 | t0032 | g0188 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0280 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0342 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0289 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0286 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0278 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02818 | hp2 | a0001 | c0001 | t0052 | g0333 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0193 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02886 | hp2 | a0004 | c0009 | t0006 | g0224 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02895 | hp2 | a0002 | c0003 | t0020 | g0014 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02896 | hp1 | a0002 | c0003 | t0008 | g0008 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02897 | hp1 | a0002 | c0003 | t0008 | g0008 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02897 | hp2 | a0002 | c0003 | t0020 | g0014 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02922 | hp1 | a0001 | c0001 | t0047 | g0179 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0084 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02965 | hp1 | a0004 | c0014 | t0006 | g0203 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0174 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0160 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0324 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0293 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03017 | hp2 | a0001 | c0001 | t0051 | g0161 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0343 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03098 | hp1 | a0001 | c0001 | t0019 | g0242 | AFR | MSL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0317 | AFR | MSL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03130 | hp1 | a0001 | c0001 | t0011 | g0029 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03130 | hp2 | a0001 | c0001 | t0011 | g0332 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03139 | hp1 | a0001 | c0001 | t0009 | g0323 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03139 | hp2 | a0001 | c0001 | t0011 | g0341 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03209 | hp1 | a0001 | c0001 | t0012 | g0337 | AFR | MSL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03209 | hp2 | a0002 | c0003 | t0008 | g0202 | AFR | MSL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03225 | hp1 | a0001 | c0001 | t0027 | g0101 | AFR | MSL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03453 | hp1 | a0001 | c0001 | t0021 | g0172 | AFR | MSL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0180 | AFR | MSL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03486 | hp1 | a0001 | c0005 | t0014 | g0091 | AFR | MSL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | MSL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03490 | hp2 | a0001 | c0001 | t0038 | g0219 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0295 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03491 | hp2 | a0001 | c0008 | t0002 | g0010 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03492 | hp2 | a0001 | c0008 | t0002 | g0010 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03516 | hp1 | a0001 | c0001 | t0012 | g0320 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | ESN | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0194 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | GWD | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03579 | hp1 | a0001 | c0001 | t0021 | g0173 | AFR | MSL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0181 | AFR | MSL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0359 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0272 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0357 | SAS | STU | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03704 | hp2 | a0001 | c0001 | t0050 | g0127 | SAS | PJL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | BEB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | BEB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03927 | hp1 | a0001 | c0006 | t0002 | g0016 | SAS | BEB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG04115 | hp1 | a0001 | c0001 | t0028 | g0050 | SAS | STU | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG04115 | hp2 | a0001 | c0001 | t0054 | g0126 | SAS | STU | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | STU | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | STU | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | STU | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0327 | SAS | STU | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18522 | hp1 | a0001 | c0001 | t0033 | g0090 | AFR | YRI | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0253 | AFR | YRI | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | CHB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | CHB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18906 | hp1 | a0002 | c0003 | t0040 | g0212 | AFR | YRI | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18906 | hp2 | a0001 | c0001 | t0012 | g0321 | AFR | YRI | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18939 | hp1 | a0001 | c0001 | t0045 | g0296 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18943 | hp1 | a0001 | c0004 | t0025 | g0099 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18945 | hp2 | a0001 | c0012 | t0001 | g0066 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18947 | hp1 | a0001 | c0001 | t0037 | g0072 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18948 | hp2 | a0001 | c0004 | t0002 | g0025 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18950 | hp2 | a0001 | c0001 | t0024 | g0098 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18960 | hp1 | a0001 | c0013 | t0001 | g0336 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18969 | hp2 | a0001 | c0001 | t0036 | g0164 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18973 | hp2 | a0001 | c0001 | t0016 | g0335 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18975 | hp1 | a0001 | c0001 | t0016 | g0358 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0361 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18982 | hp2 | a0005 | c0010 | t0001 | g0073 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18990 | hp1 | a0001 | c0004 | t0002 | g0025 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18994 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0349 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19007 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19012 | hp1 | a0006 | c0011 | t0001 | g0218 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19030 | hp1 | a0001 | c0001 | t0015 | g0178 | AFR | LWK | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19030 | hp2 | a0001 | c0005 | t0014 | g0210 | AFR | LWK | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19043 | hp1 | a0001 | c0001 | t0013 | g0204 | AFR | LWK | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | LWK | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19055 | hp1 | a0001 | c0001 | t0023 | g0134 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19056 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19056 | hp2 | a0001 | c0001 | t0030 | g0329 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0351 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19070 | hp1 | a0001 | c0001 | t0023 | g0133 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19083 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19091 | hp2 | a0001 | c0004 | t0002 | g0269 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | YRI | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | YRI | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA20129 | hp1 | a0002 | c0003 | t0008 | g0081 | AFR | ASW | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | ASW | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0176 | EUR | TSI | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0276 | EUR | TSI | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | GIH | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | GIH | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0290 | AMR | CLM | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02109 | hp2 | a0001 | c0005 | t0014 | g0211 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02486 | hp2 | a0001 | c0001 | t0017 | g0270 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02559 | hp1 | a0001 | c0001 | t0011 | g0029 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0279 | AFR | ACB | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0353 | AFR | MSL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0175 | AFR | USA | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18955 | hp1 | a0001 | c0001 | t0042 | g0163 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | USA | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0177 | AFR | LWK | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | LWK | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0265 | REF | REF | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0162 | REF | REF | TTYH3_chr7_2626986_2669802 | TTYH3 | chr7 | 2626986 | 2669802 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:2632228 | T | G | 1 | a0003 | 2 | HG00140.hp2 HG00280.hp1 |
missense_variant | MODERATE | c.73T>G | p.Trp25Gly | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/14 | 243/4805 | 73/1572 | 25/523 | chr7 | 2632228 | |||
chr7:2649943 | G | A | 1 | a0004 | 2 | HG02886.hp2 HG02965.hp1 |
missense_variant | MODERATE | c.826G>A | p.Ala276Thr | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/14 | 996/4805 | 826/1572 | 276/523 | chr7 | 2649943 | |||
chr7:2649959 | T | A | 1 | a0005 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.842T>A | p.Met281Lys | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/14 | 1012/4805 | 842/1572 | 281/523 | chr7 | 2649959 | |||
chr7:2653005 | A | G | 1 | a0002 | 13 | HG01109.hp1 HG01255.hp1 HG01496.hp2 others(10): Show |
missense_variant | MODERATE | c.1015A>G | p.Thr339Ala | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/14 | 1185/4805 | 1015/1572 | 339/523 | chr7 | 2653005 | |||
chr7:2656107 | G | T | 1 | a0006 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.1036G>T | p.Val346Phe | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 10/14 | 1206/4805 | 1036/1572 | 346/523 | chr7 | 2656107 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:2632209 | G | T | 1 | a0001c0008 | 2 | HG03491.hp2 HG03492.hp2 |
synonymous_variant | LOW | c.54G>T | p.Leu18Leu | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/14 | 224/4805 | 54/1572 | 18/523 | chr7 | 2632209 | |||
chr7:2646891 | C | T | 1 | a0004c0014 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.162C>T | p.Leu54Leu | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 2/14 | 332/4805 | 162/1572 | 54/523 | chr7 | 2646891 | |||
chr7:2647229 | C | T | 1 | a0001c0013 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.381C>T | p.Arg127Arg | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 3/14 | 551/4805 | 381/1572 | 127/523 | chr7 | 2647229 | |||
chr7:2647532 | C | T | 1 | a0001c0004 | 4 | NA18943.hp1 NA18948.hp2 NA18990.hp1 others(1): Show |
synonymous_variant | LOW | c.520C>T | p.Leu174Leu | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 4/14 | 690/4805 | 520/1572 | 174/523 | chr7 | 2647532 | |||
chr7:2647594 | G | T | 1 | a0001c0006 | 3 | HG00280.hp2 HG02602.hp1 HG03927.hp1 |
synonymous_variant | LOW | c.582G>T | p.Ser194Ser | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 4/14 | 752/4805 | 582/1572 | 194/523 | chr7 | 2647594 | |||
chr7:2649942 | C | T | 1 | a0001c0012 | 1 | NA18945.hp2 | synonymous_variant | LOW | c.825C>T | p.Asp275Asp | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/14 | 995/4805 | 825/1572 | 275/523 | chr7 | 2649942 | |||
chr7:2656130 | G | A | 1 | a0001c0005 | 3 | HG02109.hp2 HG03486.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.1059G>A | p.Thr353Thr | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 10/14 | 1229/4805 | 1059/1572 | 353/523 | chr7 | 2656130 | |||
chr7:2658421 | G | A | 1 | a0001c0005 | 3 | HG02109.hp2 HG03486.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.1386G>A | p.Ala462Ala | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 12/14 | 1556/4805 | 1386/1572 | 462/523 | chr7 | 2658421 | |||
chr7:2659000 | G | A | 3 | a0001c0002 a0001c0013 a0005c0010 |
20 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(17): Show |
synonymous_variant | LOW | c.1485G>A | p.Glu495Glu | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/14 | 1655/4805 | 1485/1572 | 495/523 | chr7 | 2659000 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:2632005 | AGCCGGGC others(8): Show |
A | 1 | a0001c0001t0054 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-141_-127delAGCCGG others(9): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/14 | 127 | INFO_REALIGN_3_PRIME | chr7 | 2632005 | |||||
chr7:2632061 | C | A | 4 | a0001c0001t0024 a0001c0001t0026 a0001c0001t0027 others(1): Show |
4 | HG02280.hp1 HG03225.hp1 NA18943.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-95C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/14 | 95 | chr7 | 2632061 | ||||||
chr7:2632072 | C | T | 1 | a0001c0001t0023 | 2 | NA19055.hp1 NA19070.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-84C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/14 | chr7 | 2632072 | |||||||
chr7:2632090 | C | T | 2 | a0001c0001t0022 a0001c0001t0053 |
3 | HG01975.hp1 HG02004.hp2 HG02148.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-66C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/14 | chr7 | 2632090 | |||||||
chr7:2632146 | G | C | 1 | a0001c0001t0016 | 2 | NA18973.hp2 NA18975.hp1 |
5_prime_UTR_variant | MODIFIER | c.-10G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/14 | 10 | chr7 | 2632146 | ||||||
chr7:2632152 | C | T | 1 | a0001c0001t0052 | 1 | HG02818.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-4C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/14 | chr7 | 2632152 | |||||||
chr7:2661837 | G | A | 1 | a0001c0001t0028 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*98G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 98 | chr7 | 2661837 | ||||||
chr7:2661840 | C | T | 1 | a0001c0001t0021 | 2 | HG03453.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*101C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 101 | chr7 | 2661840 | ||||||
chr7:2661851 | CCAGACGC others(35): Show |
C | 1 | a0001c0001t0051 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*116_*157delACGCGT others(36): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 116 | INFO_REALIGN_3_PRIME | chr7 | 2661851 | |||||
chr7:2661929 | G | A | 1 | a0001c0001t0029 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*190G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 190 | chr7 | 2661929 | ||||||
chr7:2662029 | C | T | 2 | a0001c0001t0050 a0002c0003t0049 |
2 | HG01109.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*290C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 290 | chr7 | 2662029 | ||||||
chr7:2662048 | C | T | 1 | a0002c0003t0020 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*309C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 309 | chr7 | 2662048 | ||||||
chr7:2662061 | T | C | 1 | a0001c0001t0030 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 322 | chr7 | 2662061 | ||||||
chr7:2662155 | C | T | 4 | a0001c0001t0011 a0001c0001t0015 a0001c0001t0026 others(1): Show |
9 | HG00738.hp2 HG01978.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*416C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 416 | chr7 | 2662155 | ||||||
chr7:2662192 | G | A | 10 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0012 others(7): Show |
55 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*453G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 453 | chr7 | 2662192 | ||||||
chr7:2662197 | C | T | 1 | a0001c0005t0014 | 3 | HG02109.hp2 HG03486.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*458C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 458 | chr7 | 2662197 | ||||||
chr7:2662250 | C | G | 1 | a0001c0001t0048 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*511C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 511 | chr7 | 2662250 | ||||||
chr7:2662273 | C | T | 1 | a0001c0001t0019 | 2 | HG02055.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*534C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 534 | chr7 | 2662273 | ||||||
chr7:2662435 | C | T | 3 | a0001c0001t0013 a0001c0001t0047 a0001c0005t0014 |
7 | HG01243.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*696C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 696 | chr7 | 2662435 | ||||||
chr7:2662497 | C | T | 1 | a0001c0001t0018 | 2 | HG02145.hp2 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*758C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 758 | chr7 | 2662497 | ||||||
chr7:2662559 | G | A | 2 | a0001c0001t0004 a0002c0003t0004 |
19 | HG00408.hp1 HG00738.hp1 HG01123.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*820G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 820 | chr7 | 2662559 | ||||||
chr7:2662589 | G | A | 1 | a0001c0001t0031 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*850G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 850 | chr7 | 2662589 | ||||||
chr7:2662635 | A | C | 1 | a0001c0001t0046 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*896A>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 896 | chr7 | 2662635 | ||||||
chr7:2662648 | C | T | 10 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0012 others(7): Show |
55 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*909C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 909 | chr7 | 2662648 | ||||||
chr7:2662659 | G | A | 2 | a0001c0001t0032 a0001c0001t0033 |
2 | HG02647.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*920G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 920 | chr7 | 2662659 | ||||||
chr7:2662682 | C | T | 14 | a0001c0001t0002 a0001c0001t0041 a0001c0001t0042 others(11): Show |
103 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*943C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 943 | chr7 | 2662682 | ||||||
chr7:2662683 | G | A | 1 | a0003c0007t0035 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*944G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 944 | chr7 | 2662683 | ||||||
chr7:2662716 | C | G | 3 | a0001c0001t0009 a0001c0001t0021 a0002c0003t0040 |
8 | HG02451.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*977C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 977 | chr7 | 2662716 | ||||||
chr7:2662995 | C | G | 1 | a0001c0001t0010 | 4 | HG01361.hp1 HG01515.hp2 HG01516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1256C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 1256 | chr7 | 2662995 | ||||||
chr7:2663064 | T | C | 1 | a0001c0001t0041 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1325T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 1325 | chr7 | 2663064 | ||||||
chr7:2663168 | C | T | 1 | a0001c0001t0047 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1429C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 1429 | chr7 | 2663168 | ||||||
chr7:2663182 | A | G | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(15): Show |
82 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1443A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 1443 | chr7 | 2663182 | ||||||
chr7:2663241 | T | C | 36 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(33): Show |
127 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*1502T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 1502 | chr7 | 2663241 | ||||||
chr7:2663305 | C | G | 1 | a0001c0001t0005 | 13 | HG02055.hp2 HG02559.hp2 HG02717.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1566C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 1566 | chr7 | 2663305 | ||||||
chr7:2663328 | G | A | 1 | a0001c0001t0011 | 4 | HG02559.hp1 HG03130.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1589G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 1589 | chr7 | 2663328 | ||||||
chr7:2663356 | C | T | 1 | a0002c0003t0020 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1617C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 1617 | chr7 | 2663356 | ||||||
chr7:2663361 | C | T | 1 | a0001c0001t0027 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1622C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 1622 | chr7 | 2663361 | ||||||
chr7:2663563 | G | A | 4 | a0001c0001t0011 a0001c0001t0015 a0001c0001t0026 others(1): Show |
9 | HG00738.hp2 HG01978.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1824G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 1824 | chr7 | 2663563 | ||||||
chr7:2663623 | T | C | 7 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0019 others(4): Show |
18 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1884T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 1884 | chr7 | 2663623 | ||||||
chr7:2663678 | C | A | 1 | a0001c0001t0042 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1939C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 1939 | chr7 | 2663678 | ||||||
chr7:2663830 | G | A | 11 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0030 others(8): Show |
54 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2091G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 2091 | chr7 | 2663830 | ||||||
chr7:2663899 | C | T | 2 | a0001c0001t0022 a0001c0001t0037 |
3 | HG01975.hp1 HG02004.hp2 NA18947.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2160C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 2160 | chr7 | 2663899 | ||||||
chr7:2663910 | G | A | 3 | a0001c0001t0006 a0004c0009t0006 a0004c0014t0006 |
9 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2171G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 2171 | chr7 | 2663910 | ||||||
chr7:2663981 | C | A | 1 | a0001c0001t0043 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2242C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 2242 | chr7 | 2663981 | ||||||
chr7:2664006 | G | T | 2 | a0001c0001t0017 a0002c0003t0017 |
2 | HG02486.hp2 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2267G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 2267 | chr7 | 2664006 | ||||||
chr7:2664018 | T | C | 32 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(29): Show |
113 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2279T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 2279 | chr7 | 2664018 | ||||||
chr7:2664319 | T | G | 2 | a0001c0001t0021 a0002c0003t0040 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2580T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 2580 | chr7 | 2664319 | ||||||
chr7:2664345 | G | A | 9 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0030 others(6): Show |
52 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2606G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 2606 | chr7 | 2664345 | ||||||
chr7:2664582 | C | T | 1 | a0001c0001t0045 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2843C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 2843 | chr7 | 2664582 | ||||||
chr7:2664655 | T | C | 1 | a0001c0001t0044 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2916T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 14/14 | 2916 | chr7 | 2664655 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:2632367 | C | T | 1 | a0001c0002t0001g0361 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.123+89C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2632367 | |||||||
chr7:2632383 | C | T | 1 | a0001c0001t0002g0360 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.123+105C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2632383 | |||||||
chr7:2632387 | C | T | 1 | a0001c0001t0002g0359 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.123+109C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2632387 | |||||||
chr7:2632431 | C | T | 93 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0283 others(90): Show |
102 | HG00099.hp2 HG00609.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.123+153C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2632431 | |||||||
chr7:2632581 | C | G | 1 | a0001c0001t0016g0358 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.123+303C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2632581 | |||||||
chr7:2632633 | G | A | 1 | a0001c0001t0002g0031 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.123+355G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2632633 | |||||||
chr7:2632725 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0002g0032 a0001c0001t0002g0034 |
3 | HG01981.hp2 HG01993.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.123+447G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2632725 | |||||||
chr7:2632743 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.123+465G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2632743 | |||||||
chr7:2632788 | G | A | 1 | a0001c0001t0002g0031 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.123+510G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2632788 | |||||||
chr7:2632832 | C | T | 6 | a0001c0001t0001g0274 a0001c0001t0003g0272 a0001c0001t0003g0273 others(3): Show |
6 | HG00741.hp1 HG01257.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+554C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2632832 | |||||||
chr7:2632932 | A | G | 1 | a0001c0001t0017g0270 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.123+654A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2632932 | |||||||
chr7:2633074 | A | G | 1 | a0001c0004t0002g0269 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.123+796A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633074 | |||||||
chr7:2633129 | G | C | 2 | a0001c0001t0005g0036 a0001c0001t0005g0037 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.123+851G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633129 | |||||||
chr7:2633191 | G | A | 1 | a0001c0001t0004g0276 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.123+913G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633191 | |||||||
chr7:2633213 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0022 others(72): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.123+935C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633213 | |||||||
chr7:2633338 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0019 others(207): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.123+1060C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633338 | |||||||
chr7:2633366 | G | T | 1 | a0001c0001t0001g0357 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.123+1088G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633366 | |||||||
chr7:2633421 | G | A | 2 | a0001c0001t0021g0172 a0001c0001t0021g0173 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.123+1143G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633421 | |||||||
chr7:2633432 | C | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(267): Show |
301 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.123+1154C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633432 | |||||||
chr7:2633441 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.123+1163C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633441 | |||||||
chr7:2633472 | G | A | 6 | a0001c0001t0003g0277 a0001c0001t0003g0282 a0001c0001t0005g0278 others(3): Show |
6 | HG02559.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+1194G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633472 | |||||||
chr7:2633487 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.123+1209G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633487 | |||||||
chr7:2633533 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG02015.hp2 NA18939.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.123+1255C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633533 | |||||||
chr7:2633581 | C | G | 1 | a0001c0001t0002g0168 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.123+1303C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633581 | |||||||
chr7:2633654 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(267): Show |
301 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.123+1376C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633654 | |||||||
chr7:2633777 | G | T | 7 | a0001c0001t0003g0206 a0001c0001t0003g0208 a0001c0001t0005g0207 others(4): Show |
7 | HG01081.hp2 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.123+1499G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633777 | |||||||
chr7:2633820 | C | T | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.123+1542C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633820 | |||||||
chr7:2633913 | T | A | 1 | a0001c0002t0001g0039 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.123+1635T>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2633913 | |||||||
chr7:2634224 | G | A | 13 | a0001c0001t0001g0013 a0001c0001t0003g0176 a0001c0001t0003g0206 others(10): Show |
14 | HG00639.hp1 HG01081.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.123+1946G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2634224 | |||||||
chr7:2634406 | C | T | 96 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0283 others(93): Show |
104 | HG00099.hp2 HG00639.hp2 HG01074.hp1 others(101): Show |
intron_variant | MODIFIER | c.123+2128C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2634406 | |||||||
chr7:2634447 | GGGGTGGA others(10): Show |
G | 1 | a0001c0001t0002g0032 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.123+2170_123+2186d others(19): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2634447 | |||||||
chr7:2634465 | A | C | 1 | a0001c0001t0002g0032 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.123+2187A>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2634465 | |||||||
chr7:2634722 | C | T | 2 | a0001c0001t0017g0270 a0002c0003t0020g0014 |
3 | HG02486.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.123+2444C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2634722 | |||||||
chr7:2634733 | C | T | 1 | a0001c0001t0017g0270 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.123+2455C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2634733 | |||||||
chr7:2634882 | G | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0040 others(7): Show |
13 | HG02129.hp1 HG02155.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.123+2604G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2634882 | |||||||
chr7:2634921 | C | T | 1 | a0004c0014t0006g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.123+2643C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2634921 | |||||||
chr7:2634970 | G | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(142): Show |
160 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.123+2692G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2634970 | |||||||
chr7:2635049 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.123+2771C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2635049 | |||||||
chr7:2635088 | G | A | 1 | a0001c0004t0002g0269 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.123+2810G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2635088 | |||||||
chr7:2635232 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.123+2954T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2635232 | |||||||
chr7:2635281 | G | A | 1 | a0004c0014t0006g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.123+3003G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2635281 | |||||||
chr7:2635596 | G | T | 1 | a0004c0014t0006g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.123+3318G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2635596 | |||||||
chr7:2635675 | C | G | 1 | a0001c0001t0001g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.123+3397C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2635675 | |||||||
chr7:2635689 | G | A | 13 | a0001c0001t0001g0184 a0001c0001t0003g0183 a0001c0001t0003g0185 others(10): Show |
13 | HG01109.hp1 HG01192.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.123+3411G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2635689 | |||||||
chr7:2635693 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0007g0093 a0001c0005t0014g0091 |
3 | HG01167.hp2 HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.123+3415G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2635693 | |||||||
chr7:2635759 | C | A | 4 | a0001c0001t0003g0206 a0001c0001t0003g0208 a0001c0001t0005g0207 others(1): Show |
4 | HG01081.hp2 HG02055.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+3481C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2635759 | |||||||
chr7:2635893 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.123+3615C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2635893 | |||||||
chr7:2635985 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.123+3707C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2635985 | |||||||
chr7:2635990 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG00741.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.123+3712G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2635990 | |||||||
chr7:2636012 | C | A | 2 | a0001c0001t0002g0097 a0001c0001t0004g0096 |
2 | NA19005.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.123+3734C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636012 | |||||||
chr7:2636028 | T | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(274): Show |
309 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.123+3750T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636028 | |||||||
chr7:2636052 | T | C | 1 | a0001c0001t0047g0179 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.123+3774T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636052 | |||||||
chr7:2636086 | A | G | 1 | a0001c0001t0003g0030 | 2 | NA19064.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.123+3808A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636086 | |||||||
chr7:2636122 | T | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(272): Show |
307 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.123+3844T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636122 | |||||||
chr7:2636124 | G | A | 1 | a0001c0001t0022g0106 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.123+3846G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636124 | |||||||
chr7:2636191 | G | T | 10 | a0001c0001t0001g0184 a0001c0001t0003g0183 a0001c0001t0003g0185 others(7): Show |
10 | HG01109.hp1 HG01192.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+3913G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636191 | |||||||
chr7:2636198 | G | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(146): Show |
164 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.123+3920G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636198 | |||||||
chr7:2636319 | G | T | 2 | a0001c0001t0017g0270 a0002c0003t0020g0014 |
3 | HG02486.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.123+4041G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636319 | |||||||
chr7:2636397 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.123+4119G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636397 | |||||||
chr7:2636406 | T | C | 1 | a0001c0008t0002g0010 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.123+4128T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636406 | |||||||
chr7:2636412 | G | A | 1 | a0001c0001t0024g0098 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.123+4134G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636412 | |||||||
chr7:2636498 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.123+4220C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636498 | |||||||
chr7:2636543 | A | T | 1 | a0001c0001t0002g0078 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.123+4265A>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636543 | |||||||
chr7:2636548 | C | T | 8 | a0001c0001t0002g0076 a0001c0001t0004g0075 a0001c0001t0037g0072 others(5): Show |
8 | HG00558.hp2 HG02071.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+4270C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636548 | |||||||
chr7:2636558 | C | G | 2 | a0001c0001t0021g0172 a0001c0001t0021g0173 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.123+4280C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636558 | |||||||
chr7:2636570 | T | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(272): Show |
307 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.123+4292T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636570 | |||||||
chr7:2636587 | A | G | 1 | a0001c0001t0002g0266 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.123+4309A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636587 | |||||||
chr7:2636760 | C | G | 1 | a0004c0014t0006g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.123+4482C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636760 | |||||||
chr7:2636774 | G | A | 40 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0095 others(37): Show |
40 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.123+4496G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2636774 | |||||||
chr7:2636803 | T | TG | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(271): Show |
306 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.123+4529dupG | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2636803 | ||||||
chr7:2637086 | A | G | 4 | a0001c0001t0003g0176 a0001c0001t0007g0174 a0001c0001t0007g0175 others(1): Show |
4 | HG02970.hp1 HG06807.hp2 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+4808A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2637086 | |||||||
chr7:2637107 | C | T | 3 | a0001c0001t0015g0178 a0001c0001t0021g0172 a0001c0001t0021g0173 |
3 | HG03453.hp1 HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.123+4829C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2637107 | |||||||
chr7:2637120 | C | G | 161 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(158): Show |
177 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.123+4842C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2637120 | |||||||
chr7:2637294 | C | T | 1 | a0001c0001t0001g0352 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.123+5016C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2637294 | |||||||
chr7:2637500 | C | A | 4 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0352 others(1): Show |
4 | HG03041.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+5222C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2637500 | |||||||
chr7:2637516 | G | C | 1 | a0001c0001t0002g0031 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.123+5238G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2637516 | |||||||
chr7:2637517 | C | T | 1 | a0003c0007t0035g0136 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.123+5239C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2637517 | |||||||
chr7:2637577 | T | C | 1 | a0001c0001t0016g0358 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.123+5299T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2637577 | |||||||
chr7:2637781 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.123+5503G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2637781 | |||||||
chr7:2637929 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.123+5651G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2637929 | |||||||
chr7:2637930 | G | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0192 a0001c0001t0005g0193 others(2): Show |
6 | HG00639.hp1 HG02145.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+5652G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2637930 | |||||||
chr7:2637994 | C | T | 1 | a0001c0001t0003g0351 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.123+5716C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2637994 | |||||||
chr7:2638020 | C | A | 1 | a0002c0003t0049g0182 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.123+5742C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638020 | |||||||
chr7:2638023 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(82): Show |
99 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.123+5745T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638023 | |||||||
chr7:2638058 | T | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(146): Show |
165 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.123+5780T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638058 | |||||||
chr7:2638156 | C | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(147): Show |
166 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.123+5878C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638156 | |||||||
chr7:2638178 | C | A | 1 | a0001c0005t0014g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.123+5900C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638178 | |||||||
chr7:2638366 | G | A | 1 | a0001c0001t0002g0109 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.123+6088G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638366 | |||||||
chr7:2638447 | C | T | 2 | a0001c0001t0021g0172 a0001c0001t0021g0173 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.123+6169C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638447 | |||||||
chr7:2638513 | G | A | 39 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(36): Show |
41 | HG00099.hp2 HG01074.hp1 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.123+6235G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638513 | |||||||
chr7:2638521 | C | T | 1 | a0001c0001t0001g0013 | 2 | HG00639.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.123+6243C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638521 | |||||||
chr7:2638535 | G | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(119): Show |
138 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.123+6257G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638535 | |||||||
chr7:2638540 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(147): Show |
166 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.123+6262T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638540 | |||||||
chr7:2638542 | T | G | 1 | a0001c0001t0016g0358 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.123+6264T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638542 | |||||||
chr7:2638543 | G | T | 1 | a0001c0001t0016g0358 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.123+6265G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638543 | |||||||
chr7:2638606 | G | C | 3 | a0001c0001t0001g0214 a0001c0001t0002g0215 a0001c0002t0001g0213 |
3 | HG00408.hp2 NA18999.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.123+6328G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638606 | |||||||
chr7:2638636 | G | A | 1 | a0004c0014t0006g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.123+6358G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638636 | |||||||
chr7:2638662 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0002g0069 a0001c0002t0001g0067 others(3): Show |
7 | HG00438.hp2 HG02135.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+6384C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638662 | |||||||
chr7:2638663 | G | A | 1 | a0001c0001t0017g0270 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.123+6385G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638663 | |||||||
chr7:2638680 | C | G | 1 | a0001c0001t0001g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.123+6402C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638680 | |||||||
chr7:2638755 | T | G | 1 | a0001c0001t0002g0216 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.123+6477T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638755 | |||||||
chr7:2638773 | G | T | 2 | a0001c0005t0014g0210 a0001c0005t0014g0211 |
2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.123+6495G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638773 | |||||||
chr7:2638790 | C | T | 5 | a0001c0001t0003g0206 a0001c0001t0003g0208 a0001c0001t0005g0207 others(2): Show |
5 | HG01081.hp2 HG02055.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+6512C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638790 | |||||||
chr7:2638799 | C | G | 1 | a0001c0001t0015g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.123+6521C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638799 | |||||||
chr7:2638914 | T | C | 1 | a0001c0001t0002g0217 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.123+6636T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638914 | |||||||
chr7:2638948 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.123+6670C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2638948 | |||||||
chr7:2639115 | T | C | 1 | a0004c0014t0006g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.123+6837T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639115 | |||||||
chr7:2639222 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.123+6944C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639222 | |||||||
chr7:2639238 | C | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(144): Show |
161 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.123+6960C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639238 | |||||||
chr7:2639364 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.123+7086G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639364 | |||||||
chr7:2639393 | C | T | 2 | a0001c0001t0047g0179 a0002c0003t0020g0014 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.123+7115C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639393 | |||||||
chr7:2639394 | G | A | 2 | a0001c0001t0024g0098 a0001c0004t0025g0099 |
2 | NA18943.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.123+7116G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639394 | |||||||
chr7:2639397 | A | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(150): Show |
168 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.123+7119A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639397 | |||||||
chr7:2639409 | C | T | 1 | a0001c0001t0002g0350 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.123+7131C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639409 | |||||||
chr7:2639474 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.123+7196C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639474 | |||||||
chr7:2639506 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.123+7228C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639506 | |||||||
chr7:2639521 | G | A | 1 | a0001c0001t0003g0277 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+7243G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639521 | |||||||
chr7:2639585 | C | T | 1 | a0001c0001t0001g0013 | 2 | HG00639.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.124-7268C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639585 | |||||||
chr7:2639604 | C | T | 2 | a0001c0001t0002g0065 a0001c0001t0002g0078 |
2 | HG00597.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.124-7249C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639604 | |||||||
chr7:2639639 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG00639.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.124-7214G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639639 | |||||||
chr7:2639645 | G | A | 11 | a0001c0001t0001g0184 a0001c0001t0003g0183 a0001c0001t0003g0185 others(8): Show |
11 | HG01109.hp1 HG01192.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.124-7208G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639645 | |||||||
chr7:2639662 | C | T | 5 | a0001c0001t0003g0206 a0001c0001t0003g0208 a0001c0001t0005g0207 others(2): Show |
5 | HG01081.hp2 HG02055.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-7191C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639662 | |||||||
chr7:2639714 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.124-7139G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639714 | |||||||
chr7:2639728 | T | G | 6 | a0001c0001t0001g0082 a0002c0003t0007g0083 a0002c0003t0008g0008 others(3): Show |
7 | HG01496.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-7125T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639728 | |||||||
chr7:2639731 | C | T | 1 | a0002c0003t0008g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.124-7122C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639731 | |||||||
chr7:2639815 | C | T | 82 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0283 others(79): Show |
90 | HG00099.hp2 HG00609.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.124-7038C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639815 | |||||||
chr7:2639833 | C | T | 1 | a0001c0001t0002g0263 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.124-7020C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639833 | |||||||
chr7:2639916 | C | T | 3 | a0001c0001t0001g0260 a0001c0001t0002g0261 a0001c0001t0002g0262 |
3 | HG02040.hp1 NA18954.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.124-6937C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639916 | |||||||
chr7:2639942 | C | G | 1 | a0001c0001t0003g0349 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.124-6911C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639942 | |||||||
chr7:2639975 | C | A | 5 | a0001c0001t0005g0084 a0002c0003t0008g0008 a0002c0003t0008g0080 others(2): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-6878C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2639975 | |||||||
chr7:2640020 | C | T | 104 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(101): Show |
112 | HG00408.hp1 HG00609.hp2 HG00642.hp2 others(109): Show |
intron_variant | MODIFIER | c.124-6833C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640020 | |||||||
chr7:2640062 | C | T | 1 | a0001c0002t0001g0077 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.124-6791C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640062 | |||||||
chr7:2640092 | C | T | 2 | a0001c0001t0021g0172 a0001c0001t0021g0173 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.124-6761C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640092 | |||||||
chr7:2640136 | G | A | 356 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(353): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.124-6717G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640136 | |||||||
chr7:2640142 | C | T | 1 | a0001c0001t0002g0252 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.124-6711C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640142 | |||||||
chr7:2640150 | C | T | 4 | a0001c0001t0013g0348 a0001c0001t0017g0270 a0002c0003t0007g0083 others(1): Show |
4 | HG01496.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-6703C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640150 | |||||||
chr7:2640173 | G | A | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(150): Show |
170 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.124-6680G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640173 | |||||||
chr7:2640219 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.124-6634C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640219 | |||||||
chr7:2640223 | A | G | 32 | a0001c0001t0001g0082 a0001c0001t0001g0095 a0001c0001t0001g0105 others(29): Show |
33 | HG00741.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.124-6630A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640223 | |||||||
chr7:2640279 | A | T | 7 | a0001c0001t0001g0082 a0001c0001t0005g0084 a0001c0001t0007g0177 others(4): Show |
8 | HG01496.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-6574A>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640279 | |||||||
chr7:2640286 | C | T | 7 | a0001c0001t0001g0107 a0001c0001t0002g0114 a0001c0001t0002g0130 others(4): Show |
7 | HG00544.hp2 HG00558.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-6567C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640286 | |||||||
chr7:2640287 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0308 |
2 | HG01346.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.124-6566G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640287 | |||||||
chr7:2640370 | C | G | 7 | a0001c0001t0003g0328 a0001c0001t0003g0330 a0001c0001t0003g0351 others(4): Show |
7 | HG02280.hp1 HG03225.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-6483C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640370 | |||||||
chr7:2640371 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.124-6482G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640371 | |||||||
chr7:2640390 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.124-6463G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640390 | |||||||
chr7:2640392 | C | T | 1 | a0001c0001t0002g0251 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.124-6461C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640392 | |||||||
chr7:2640396 | G | A | 3 | a0001c0001t0001g0192 a0001c0001t0005g0193 a0001c0001t0005g0194 |
3 | HG02886.hp1 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.124-6457G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640396 | |||||||
chr7:2640403 | T | G | 1 | a0001c0001t0005g0205 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.124-6450T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640403 | |||||||
chr7:2640403 | T | TG | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(104): Show |
121 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.124-6442dupG | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2640403 | ||||||
chr7:2640405 | G | T | 16 | a0001c0001t0001g0302 a0001c0001t0001g0304 a0001c0001t0001g0305 others(13): Show |
18 | HG01074.hp1 HG01074.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.124-6448G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640405 | |||||||
chr7:2640455 | C | T | 8 | a0001c0001t0001g0326 a0001c0001t0009g0322 a0001c0001t0009g0323 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-6398C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640455 | |||||||
chr7:2640476 | C | T | 1 | a0001c0001t0003g0315 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.124-6377C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640476 | |||||||
chr7:2640579 | C | T | 2 | a0001c0001t0021g0172 a0001c0001t0021g0173 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.124-6274C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640579 | |||||||
chr7:2640616 | G | A | 2 | a0001c0001t0021g0172 a0001c0001t0021g0173 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.124-6237G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640616 | |||||||
chr7:2640648 | G | A | 1 | a0001c0001t0004g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.124-6205G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640648 | |||||||
chr7:2640680 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.124-6173G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640680 | |||||||
chr7:2640688 | G | A | 3 | a0001c0001t0017g0270 a0002c0003t0004g0187 a0002c0003t0017g0191 |
3 | HG01255.hp1 HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.124-6165G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640688 | |||||||
chr7:2640714 | G | A | 1 | a0002c0003t0008g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.124-6139G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640714 | |||||||
chr7:2640767 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.124-6086G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640767 | |||||||
chr7:2640778 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.124-6075C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640778 | |||||||
chr7:2640781 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(125): Show |
145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.124-6072C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640781 | |||||||
chr7:2640786 | G | GTGTCC | 253 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(250): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.124-6065_124-6064i others(7): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2640786 | ||||||
chr7:2640849 | G | A | 2 | a0001c0004t0002g0269 a0001c0004t0025g0099 |
2 | NA18943.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.124-6004G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2640849 | |||||||
chr7:2641021 | G | A | 1 | a0004c0009t0006g0224 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.124-5832G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641021 | |||||||
chr7:2641022 | G | A | 1 | a0001c0001t0002g0359 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.124-5831G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641022 | |||||||
chr7:2641072 | G | T | 1 | a0002c0003t0008g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.124-5781G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641072 | |||||||
chr7:2641201 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.124-5652C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641201 | |||||||
chr7:2641201 | C | T | 4 | a0001c0001t0017g0270 a0002c0003t0004g0187 a0002c0003t0017g0191 others(1): Show |
5 | HG01255.hp1 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-5652C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641201 | |||||||
chr7:2641212 | T | C | 2 | a0001c0001t0002g0023 a0001c0001t0002g0031 |
3 | HG00438.hp1 NA18952.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.124-5641T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641212 | |||||||
chr7:2641219 | G | C | 1 | a0002c0003t0008g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.124-5634G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641219 | |||||||
chr7:2641220 | G | C | 1 | a0002c0003t0008g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.124-5633G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641220 | |||||||
chr7:2641260 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.124-5593G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641260 | |||||||
chr7:2641288 | G | C | 1 | a0001c0001t0001g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.124-5565G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641288 | |||||||
chr7:2641477 | C | T | 1 | a0002c0003t0020g0014 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.124-5376C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641477 | |||||||
chr7:2641525 | C | T | 3 | a0001c0001t0017g0270 a0002c0003t0004g0187 a0002c0003t0017g0191 |
3 | HG01255.hp1 HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.124-5328C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641525 | |||||||
chr7:2641701 | G | T | 3 | a0001c0001t0024g0098 a0001c0001t0026g0100 a0001c0001t0027g0101 |
3 | HG02280.hp1 HG03225.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.124-5152G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641701 | |||||||
chr7:2641760 | T | C | 1 | a0004c0009t0006g0224 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.124-5093T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641760 | |||||||
chr7:2641802 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0023g0133 a0001c0001t0023g0134 |
3 | NA19004.hp1 NA19055.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.124-5051C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641802 | |||||||
chr7:2641803 | G | A | 2 | a0001c0001t0021g0172 a0001c0001t0021g0173 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.124-5050G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641803 | |||||||
chr7:2641808 | C | T | 1 | a0001c0001t0001g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.124-5045C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641808 | |||||||
chr7:2641846 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0002g0055 |
3 | HG02129.hp1 HG02273.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.124-5007C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641846 | |||||||
chr7:2641936 | C | T | 1 | a0002c0003t0020g0014 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.124-4917C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2641936 | |||||||
chr7:2642044 | C | G | 32 | a0001c0001t0001g0056 a0001c0001t0001g0079 a0001c0001t0001g0107 others(29): Show |
32 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.124-4809C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642044 | |||||||
chr7:2642073 | G | T | 6 | a0001c0001t0003g0206 a0001c0001t0003g0208 a0001c0001t0005g0207 others(3): Show |
6 | HG01081.hp2 HG02055.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-4780G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642073 | |||||||
chr7:2642076 | G | A | 6 | a0001c0001t0003g0206 a0001c0001t0003g0208 a0001c0001t0005g0207 others(3): Show |
6 | HG01081.hp2 HG02055.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-4777G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642076 | |||||||
chr7:2642085 | A | G | 1 | a0001c0001t0001g0306 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.124-4768A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642085 | |||||||
chr7:2642125 | G | A | 1 | a0001c0001t0001g0357 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.124-4728G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642125 | |||||||
chr7:2642177 | T | C | 1 | a0002c0003t0020g0014 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.124-4676T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642177 | |||||||
chr7:2642237 | AT | A | 7 | a0001c0001t0003g0206 a0001c0001t0003g0208 a0001c0001t0005g0207 others(4): Show |
7 | HG01081.hp2 HG02055.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-4609delT | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2642237 | ||||||
chr7:2642238 | T | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0260 a0001c0002t0001g0067 others(3): Show |
7 | HG00438.hp2 HG02135.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-4615T>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642238 | |||||||
chr7:2642245 | A | T | 1 | a0001c0001t0002g0023 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.124-4608A>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642245 | |||||||
chr7:2642277 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.124-4576C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642277 | |||||||
chr7:2642307 | C | T | 80 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0063 others(77): Show |
83 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.124-4546C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642307 | |||||||
chr7:2642346 | G | T | 1 | a0001c0001t0012g0321 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.124-4507G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642346 | |||||||
chr7:2642371 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.124-4482G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642371 | |||||||
chr7:2642537 | C | CA | 103 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0046 others(100): Show |
109 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.124-4294dupA | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2642537 | ||||||
chr7:2642537 | C | CAA | 9 | a0001c0001t0001g0013 a0001c0001t0001g0287 a0001c0001t0002g0044 others(6): Show |
10 | HG00639.hp1 HG01106.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.124-4295_124-4294d others(4): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2642537 | ||||||
chr7:2642556 | A | G | 7 | a0001c0001t0001g0082 a0001c0001t0001g0104 a0001c0001t0001g0105 others(4): Show |
7 | HG01496.hp1 HG02257.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-4297A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642556 | |||||||
chr7:2642598 | T | C | 93 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0063 others(90): Show |
96 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(93): Show |
intron_variant | MODIFIER | c.124-4255T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642598 | |||||||
chr7:2642745 | T | C | 1 | a0001c0008t0002g0010 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.124-4108T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642745 | |||||||
chr7:2642748 | C | CT | 9 | a0001c0001t0001g0258 a0001c0001t0001g0264 a0001c0001t0009g0324 others(6): Show |
10 | HG00438.hp2 HG02451.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.124-4087dupT | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2642748 | ||||||
chr7:2642748 | CT | C | 23 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0056 others(20): Show |
25 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.124-4087delT | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2642748 | ||||||
chr7:2642753 | T | C | 3 | a0001c0001t0005g0193 a0001c0001t0005g0194 a0001c0001t0005g0205 |
3 | HG02809.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.124-4100T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2642753 | |||||||
chr7:2643024 | C | G | 1 | a0001c0001t0001g0355 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.124-3829C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643024 | |||||||
chr7:2643149 | A | G | 1 | a0004c0014t0006g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.124-3704A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643149 | |||||||
chr7:2643208 | A | C | 1 | a0002c0003t0020g0014 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.124-3645A>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643208 | |||||||
chr7:2643216 | T | G | 1 | a0001c0001t0002g0229 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.124-3637T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643216 | |||||||
chr7:2643227 | T | C | 1 | a0001c0001t0002g0229 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.124-3626T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643227 | |||||||
chr7:2643333 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(239): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.124-3520C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643333 | |||||||
chr7:2643349 | T | C | 1 | a0004c0009t0006g0224 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.124-3504T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643349 | |||||||
chr7:2643354 | C | CA | 101 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0041 others(98): Show |
107 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.124-3480dupA | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2643354 | ||||||
chr7:2643354 | C | CAA | 27 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0153 others(24): Show |
29 | HG00738.hp1 HG00741.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.124-3481_124-3480d others(4): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2643354 | ||||||
chr7:2643354 | CA | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0104 others(7): Show |
11 | HG00639.hp1 HG01257.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.124-3480delA | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2643354 | ||||||
chr7:2643356 | A | C | 1 | a0001c0001t0007g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.124-3497A>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643356 | |||||||
chr7:2643357 | A | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0104 others(4): Show |
8 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-3496A>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643357 | |||||||
chr7:2643375 | C | T | 2 | a0001c0001t0018g0189 a0001c0001t0018g0190 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.124-3478C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643375 | |||||||
chr7:2643537 | C | T | 1 | a0001c0001t0015g0254 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.124-3316C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643537 | |||||||
chr7:2643551 | C | T | 7 | a0001c0001t0001g0082 a0001c0001t0001g0104 a0001c0001t0001g0105 others(4): Show |
7 | HG02257.hp1 HG02809.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-3302C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643551 | |||||||
chr7:2643618 | A | G | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3235A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643618 | |||||||
chr7:2643619 | G | T | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3234G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643619 | |||||||
chr7:2643621 | G | C | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3232G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643621 | |||||||
chr7:2643623 | C | G | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3230C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643623 | |||||||
chr7:2643624 | G | A | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3229G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643624 | |||||||
chr7:2643627 | C | G | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3226C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643627 | |||||||
chr7:2643628 | T | C | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3225T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643628 | |||||||
chr7:2643634 | C | T | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3219C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643634 | |||||||
chr7:2643636 | C | T | 1 | a0001c0001t0015g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124-3217C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643636 | |||||||
chr7:2643640 | G | A | 1 | a0004c0014t0006g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.124-3213G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643640 | |||||||
chr7:2643640 | G | C | 1 | a0001c0001t0001g0013 | 2 | HG00639.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.124-3213G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643640 | |||||||
chr7:2643641 | A | G | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3212A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643641 | |||||||
chr7:2643642 | T | G | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3211T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643642 | |||||||
chr7:2643643 | C | G | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3210C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643643 | |||||||
chr7:2643645 | T | A | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3208T>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643645 | |||||||
chr7:2643652 | C | G | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3201C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643652 | |||||||
chr7:2643660 | T | G | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3193T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643660 | |||||||
chr7:2643662 | T | C | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3191T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643662 | |||||||
chr7:2643664 | T | G | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3189T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643664 | |||||||
chr7:2643668 | T | C | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3185T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643668 | |||||||
chr7:2643670 | T | G | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3183T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643670 | |||||||
chr7:2643674 | T | G | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3179T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643674 | |||||||
chr7:2643675 | C | A | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3178C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643675 | |||||||
chr7:2643676 | C | G | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3177C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643676 | |||||||
chr7:2643678 | T | C | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3175T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643678 | |||||||
chr7:2643680 | T | C | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3173T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643680 | |||||||
chr7:2643681 | T | G | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3172T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643681 | |||||||
chr7:2643693 | A | C | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3160A>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643693 | |||||||
chr7:2643694 | G | C | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3159G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643694 | |||||||
chr7:2643695 | T | A | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3158T>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643695 | |||||||
chr7:2643698 | G | C | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3155G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643698 | |||||||
chr7:2643700 | G | C | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3153G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643700 | |||||||
chr7:2643701 | T | C | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3152T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643701 | |||||||
chr7:2643702 | G | A | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3151G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643702 | |||||||
chr7:2643703 | G | T | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3150G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643703 | |||||||
chr7:2643707 | G | C | 1 | a0001c0001t0002g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.124-3146G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643707 | |||||||
chr7:2643714 | C | T | 1 | a0006c0011t0001g0218 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.124-3139C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643714 | |||||||
chr7:2643768 | C | T | 5 | a0001c0001t0003g0206 a0001c0001t0003g0208 a0001c0001t0005g0207 others(2): Show |
5 | HG01081.hp2 HG02055.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-3085C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643768 | |||||||
chr7:2643794 | G | T | 1 | a0001c0001t0002g0216 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.124-3059G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643794 | |||||||
chr7:2643802 | C | T | 1 | a0001c0008t0002g0010 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.124-3051C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643802 | |||||||
chr7:2643811 | C | CAGCGGGG others(1): Show |
95 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0063 others(92): Show |
101 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.124-3041_124-3040i others(10): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2643811 | ||||||
chr7:2643811 | C | CAGCGGGT | 117 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0056 others(114): Show |
133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.124-3041_124-3040i others(9): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2643811 | ||||||
chr7:2643816 | G | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0028 others(216): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.124-3037G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643816 | |||||||
chr7:2643835 | C | T | 3 | a0001c0001t0004g0115 a0001c0001t0004g0129 a0001c0001t0004g0131 |
3 | NA18962.hp1 NA19007.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.124-3018C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2643835 | |||||||
chr7:2644002 | A | C | 1 | a0001c0001t0002g0359 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.124-2851A>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644002 | |||||||
chr7:2644042 | C | T | 2 | a0001c0001t0009g0323 a0004c0014t0006g0203 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.124-2811C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644042 | |||||||
chr7:2644253 | C | T | 3 | a0001c0001t0018g0189 a0001c0001t0018g0190 a0002c0003t0008g0202 |
3 | HG02145.hp2 HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.124-2600C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644253 | |||||||
chr7:2644264 | G | A | 1 | a0001c0001t0001g0340 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.124-2589G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644264 | |||||||
chr7:2644394 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.124-2459C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644394 | |||||||
chr7:2644436 | C | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(135): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.124-2417C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644436 | |||||||
chr7:2644673 | CT | C | 3 | a0001c0001t0017g0270 a0002c0003t0004g0187 a0002c0003t0017g0191 |
3 | HG01255.hp1 HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.124-2179delT | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644673 | |||||||
chr7:2644766 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0171 |
2 | NA18939.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.124-2087C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644766 | |||||||
chr7:2644810 | G | A | 4 | a0001c0001t0005g0193 a0001c0001t0005g0194 a0001c0001t0005g0205 others(1): Show |
4 | HG02809.hp1 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-2043G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644810 | |||||||
chr7:2644826 | G | A | 1 | a0002c0003t0007g0083 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.124-2027G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644826 | |||||||
chr7:2644829 | G | C | 1 | a0001c0001t0003g0233 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.124-2024G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644829 | |||||||
chr7:2644832 | C | T | 1 | a0001c0001t0015g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124-2021C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644832 | |||||||
chr7:2644921 | G | A | 8 | a0001c0001t0001g0082 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG02257.hp1 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-1932G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644921 | |||||||
chr7:2644939 | A | T | 1 | a0001c0002t0001g0271 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.124-1914A>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644939 | |||||||
chr7:2644969 | C | G | 62 | a0001c0001t0001g0028 a0001c0001t0001g0143 a0001c0001t0001g0144 others(59): Show |
64 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.124-1884C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2644969 | |||||||
chr7:2645055 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.124-1798C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2645055 | |||||||
chr7:2645069 | G | A | 2 | a0001c0001t0002g0017 a0001c0001t0002g0234 |
3 | HG01256.hp2 HG01258.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.124-1784G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2645069 | |||||||
chr7:2645073 | G | GTGTGCCT others(40): Show |
1 | a0001c0001t0002g0359 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.124-1744_124-1743i others(49): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2645073 | ||||||
chr7:2645126 | C | A | 1 | a0001c0001t0030g0329 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.124-1727C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2645126 | |||||||
chr7:2645127 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0004g0096 a0001c0001t0030g0329 |
3 | NA18988.hp1 NA19056.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.124-1726A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2645127 | |||||||
chr7:2645143 | A | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
16 | HG00423.hp2 HG00597.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.124-1710A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2645143 | |||||||
chr7:2645246 | C | T | 1 | a0004c0014t0006g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.124-1607C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2645246 | |||||||
chr7:2645247 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG00639.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.124-1606G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2645247 | |||||||
chr7:2645283 | T | G | 1 | a0001c0001t0002g0249 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.124-1570T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2645283 | |||||||
chr7:2645358 | C | T | 11 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0287 others(8): Show |
12 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.124-1495C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2645358 | |||||||
chr7:2645426 | G | A | 1 | a0004c0009t0006g0224 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.124-1427G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2645426 | |||||||
chr7:2645496 | GGACAGGG others(33): Show |
G | 1 | a0001c0001t0001g0339 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.124-1355_124-1316d others(42): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2645496 | ||||||
chr7:2645549 | C | T | 1 | a0002c0003t0049g0182 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.124-1304C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2645549 | |||||||
chr7:2645604 | G | A | 1 | a0002c0003t0040g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.124-1249G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2645604 | |||||||
chr7:2645735 | G | C | 8 | a0001c0001t0001g0082 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG02257.hp1 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-1118G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2645735 | |||||||
chr7:2646019 | CT | C | 86 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(83): Show |
89 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(86): Show |
intron_variant | MODIFIER | c.124-821delT | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 2646019 | ||||||
chr7:2646217 | G | A | 4 | a0001c0001t0005g0193 a0001c0001t0005g0194 a0001c0001t0005g0205 others(1): Show |
4 | HG02809.hp1 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-636G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2646217 | |||||||
chr7:2646382 | T | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0104 others(6): Show |
10 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.124-471T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2646382 | |||||||
chr7:2646425 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(224): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.124-428T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2646425 | |||||||
chr7:2646508 | T | C | 3 | a0001c0001t0006g0253 a0001c0001t0019g0228 a0001c0001t0019g0242 |
3 | HG02055.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.124-345T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2646508 | |||||||
chr7:2646576 | C | G | 81 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(78): Show |
84 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.124-277C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2646576 | |||||||
chr7:2646587 | A | G | 3 | a0001c0001t0006g0253 a0001c0001t0019g0228 a0001c0001t0019g0242 |
3 | HG02055.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.124-266A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2646587 | |||||||
chr7:2646604 | C | G | 1 | a0001c0001t0002g0216 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.124-249C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2646604 | |||||||
chr7:2646743 | G | A | 3 | a0001c0001t0017g0270 a0002c0003t0004g0187 a0002c0003t0017g0191 |
3 | HG01255.hp1 HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.124-110G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2646743 | |||||||
chr7:2646768 | C | G | 4 | a0001c0001t0005g0193 a0001c0001t0005g0194 a0001c0001t0005g0205 others(1): Show |
4 | HG02809.hp1 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-85C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2646768 | |||||||
chr7:2646778 | T | C | 2 | a0001c0001t0002g0307 a0001c0001t0003g0233 |
2 | NA19009.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.124-75T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2646778 | |||||||
chr7:2646821 | C | A | 82 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(79): Show |
85 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.124-32C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 1/13 | chr7 | 2646821 | |||||||
chr7:2647111 | G | C | 1 | a0001c0001t0002g0310 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.294-31G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 2/13 | chr7 | 2647111 | |||||||
chr7:2647127 | G | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(253): Show |
280 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.294-15G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 2/13 | chr7 | 2647127 | |||||||
chr7:2647284 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0005g0193 a0001c0001t0005g0194 others(1): Show |
5 | HG00639.hp1 HG02145.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+31A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 3/13 | chr7 | 2647284 | |||||||
chr7:2647315 | C | T | 1 | a0001c0001t0050g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.405+62C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 3/13 | chr7 | 2647315 | |||||||
chr7:2647378 | C | CG | 7 | a0001c0001t0001g0144 a0001c0001t0002g0168 a0001c0001t0002g0356 others(4): Show |
7 | HG00423.hp1 HG00438.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.406-37dupG | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 2647378 | ||||||
chr7:2647402 | C | T | 2 | a0001c0001t0021g0172 a0001c0001t0021g0173 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.406-16C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 3/13 | chr7 | 2647402 | |||||||
chr7:2647665 | G | C | 1 | a0001c0001t0002g0020 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.626+27G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 4/13 | chr7 | 2647665 | |||||||
chr7:2647666 | C | G | 1 | a0001c0001t0002g0020 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.626+28C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 4/13 | chr7 | 2647666 | |||||||
chr7:2647700 | A | G | 4 | a0001c0001t0001g0287 a0001c0001t0018g0189 a0001c0001t0018g0190 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+62A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 4/13 | chr7 | 2647700 | |||||||
chr7:2647862 | C | T | 1 | a0001c0001t0004g0075 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.627-97C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 4/13 | chr7 | 2647862 | |||||||
chr7:2648080 | G | A | 1 | a0004c0014t0006g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.722+26G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648080 | |||||||
chr7:2648093 | G | A | 1 | a0004c0014t0006g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.722+39G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648093 | |||||||
chr7:2648163 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.722+109C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648163 | |||||||
chr7:2648221 | G | A | 1 | a0001c0001t0003g0052 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.722+167G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648221 | |||||||
chr7:2648300 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.722+246G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648300 | |||||||
chr7:2648304 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.722+250C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648304 | |||||||
chr7:2648505 | G | GC | 8 | a0001c0001t0001g0082 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG02257.hp1 HG02809.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.722+451_722+452ins others(1): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648505 | |||||||
chr7:2648556 | C | T | 80 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(77): Show |
83 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.722+502C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648556 | |||||||
chr7:2648588 | G | C | 3 | a0001c0001t0018g0189 a0001c0001t0018g0190 a0002c0003t0008g0202 |
3 | HG02145.hp2 HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.722+534G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648588 | |||||||
chr7:2648664 | G | A | 1 | a0001c0012t0001g0066 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.722+610G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648664 | |||||||
chr7:2648706 | C | T | 5 | a0001c0001t0003g0206 a0001c0001t0003g0208 a0001c0001t0005g0207 others(2): Show |
5 | HG01081.hp2 HG02055.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.722+652C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648706 | |||||||
chr7:2648875 | T | G | 1 | a0001c0001t0001g0051 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.723-692T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648875 | |||||||
chr7:2648883 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.723-684T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648883 | |||||||
chr7:2648886 | T | G | 1 | a0001c0001t0001g0051 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.723-681T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648886 | |||||||
chr7:2648905 | T | C | 1 | a0002c0003t0008g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.723-662T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648905 | |||||||
chr7:2648905 | TGCAGTGG others(12): Show |
T | 3 | a0001c0005t0014g0091 a0002c0003t0017g0191 a0004c0009t0006g0224 |
3 | HG02622.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.723-605_723-587del others(19): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr7 | 2648905 | ||||||
chr7:2648919 | G | A | 1 | a0002c0003t0008g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.723-648G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648919 | |||||||
chr7:2648924 | C | CGCAGTGG others(13): Show |
1 | a0001c0001t0015g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.723-630_723-629ins others(20): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr7 | 2648924 | ||||||
chr7:2648924 | C | T | 1 | a0002c0003t0008g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.723-643C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648924 | |||||||
chr7:2648935 | G | GTGGGGCC others(12): Show |
1 | a0001c0001t0015g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.723-614_723-613ins others(19): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr7 | 2648935 | ||||||
chr7:2648935 | G | GTGGGGCC others(31): Show |
214 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0028 others(211): Show |
234 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.723-595_723-594ins others(38): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr7 | 2648935 | ||||||
chr7:2648935 | G | GTGGGGCC others(31): Show |
2 | a0001c0001t0002g0220 a0001c0001t0002g0241 |
2 | HG00544.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.723-606_723-605ins others(38): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr7 | 2648935 | ||||||
chr7:2648940 | G | GCCCGCAG others(31): Show |
1 | a0001c0001t0028g0050 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.723-595_723-594ins others(38): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr7 | 2648940 | ||||||
chr7:2648972 | T | TATGGGGC others(30): Show |
1 | a0001c0001t0001g0339 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.723-595_723-594ins others(37): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648972 | |||||||
chr7:2648973 | G | GTGGGGCC others(69): Show |
4 | a0001c0001t0002g0020 a0001c0001t0002g0097 a0001c0001t0002g0223 others(1): Show |
5 | NA18940.hp2 NA18975.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.723-587_723-586ins others(76): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr7 | 2648973 | ||||||
chr7:2648973 | G | GTGGGGCC others(12): Show |
1 | a0001c0001t0001g0122 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.723-587_723-586ins others(19): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr7 | 2648973 | ||||||
chr7:2648973 | G | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0028 others(215): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.723-594G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2648973 | |||||||
chr7:2649004 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(245): Show |
272 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.723-563T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2649004 | |||||||
chr7:2649065 | C | T | 1 | a0001c0001t0015g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.723-502C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2649065 | |||||||
chr7:2649103 | G | C | 1 | a0001c0001t0003g0349 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.723-464G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2649103 | |||||||
chr7:2649126 | G | A | 1 | a0001c0001t0003g0317 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.723-441G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2649126 | |||||||
chr7:2649235 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0028 others(221): Show |
245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.723-332G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2649235 | |||||||
chr7:2649244 | C | G | 1 | a0001c0001t0001g0339 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.723-323C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2649244 | |||||||
chr7:2649377 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(245): Show |
272 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.723-190T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2649377 | |||||||
chr7:2649430 | G | T | 3 | a0001c0001t0004g0115 a0001c0001t0004g0129 a0001c0001t0004g0131 |
3 | NA18962.hp1 NA19007.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.723-137G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2649430 | |||||||
chr7:2649479 | C | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | HG02257.hp1 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.723-88C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2649479 | |||||||
chr7:2649553 | T | C | 10 | a0001c0001t0005g0084 a0001c0001t0017g0270 a0002c0003t0004g0187 others(7): Show |
12 | HG01255.hp1 HG01496.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.723-14T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 5/13 | chr7 | 2649553 | |||||||
chr7:2649748 | C | T | 1 | a0001c0001t0003g0349 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.795+109C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 6/13 | chr7 | 2649748 | |||||||
chr7:2649838 | A | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(246): Show |
273 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.796-75A>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 6/13 | chr7 | 2649838 | |||||||
chr7:2649840 | G | A | 1 | a0001c0001t0044g0053 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.796-73G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 6/13 | chr7 | 2649840 | |||||||
chr7:2650250 | G | A | 2 | a0001c0001t0026g0100 a0001c0001t0027g0101 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.871+262G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2650250 | |||||||
chr7:2650317 | C | T | 2 | a0001c0001t0002g0109 a0001c0001t0054g0126 |
2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.871+329C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2650317 | |||||||
chr7:2650471 | C | T | 6 | a0001c0001t0003g0206 a0001c0001t0003g0208 a0001c0001t0005g0207 others(3): Show |
6 | HG01081.hp2 HG02055.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.871+483C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2650471 | |||||||
chr7:2650532 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0038 others(120): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.871+544C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2650532 | |||||||
chr7:2650560 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.871+572A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2650560 | |||||||
chr7:2650595 | G | A | 1 | a0001c0001t0007g0346 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.871+607G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2650595 | |||||||
chr7:2650646 | C | G | 1 | a0001c0001t0003g0317 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.871+658C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2650646 | |||||||
chr7:2650687 | T | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(243): Show |
271 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.871+699T>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2650687 | |||||||
chr7:2650758 | A | G | 1 | a0004c0014t0006g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.871+770A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2650758 | |||||||
chr7:2650767 | G | A | 1 | a0001c0001t0002g0266 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.871+779G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2650767 | |||||||
chr7:2650894 | G | T | 2 | a0001c0001t0018g0189 a0001c0001t0018g0190 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.871+906G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2650894 | |||||||
chr7:2651045 | G | A | 2 | a0004c0009t0006g0224 a0004c0014t0006g0203 |
2 | HG02886.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.871+1057G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651045 | |||||||
chr7:2651069 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.871+1081C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651069 | |||||||
chr7:2651130 | C | G | 1 | a0001c0001t0001g0013 | 2 | HG00639.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.872-1057C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651130 | |||||||
chr7:2651247 | A | T | 1 | a0001c0001t0002g0252 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.872-940A>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651247 | |||||||
chr7:2651356 | C | T | 1 | a0001c0001t0019g0242 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.872-831C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651356 | |||||||
chr7:2651380 | G | A | 5 | a0001c0001t0003g0206 a0001c0001t0003g0208 a0001c0001t0005g0207 others(2): Show |
5 | HG01081.hp2 HG02055.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.872-807G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651380 | |||||||
chr7:2651411 | G | A | 1 | a0002c0003t0020g0014 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.872-776G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651411 | |||||||
chr7:2651527 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0192 |
3 | HG00741.hp2 HG01891.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.872-660C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651527 | |||||||
chr7:2651564 | C | T | 8 | a0001c0001t0003g0206 a0001c0001t0003g0208 a0001c0001t0005g0207 others(5): Show |
8 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.872-623C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651564 | |||||||
chr7:2651567 | C | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(108): Show |
125 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.872-620C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651567 | |||||||
chr7:2651574 | A | T | 1 | a0001c0001t0002g0252 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.872-613A>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651574 | |||||||
chr7:2651628 | C | T | 1 | a0001c0001t0028g0050 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.872-559C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651628 | |||||||
chr7:2651654 | C | T | 22 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0095 others(19): Show |
22 | HG00099.hp1 HG00733.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.872-533C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651654 | |||||||
chr7:2651674 | C | T | 1 | a0001c0001t0002g0252 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.872-513C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651674 | |||||||
chr7:2651687 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.872-500G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651687 | |||||||
chr7:2651724 | T | C | 1 | a0001c0001t0004g0294 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.872-463T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651724 | |||||||
chr7:2651743 | G | GT | 7 | a0001c0001t0001g0028 a0001c0001t0001g0151 a0001c0001t0001g0331 others(4): Show |
8 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.872-435dupT | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 2651743 | ||||||
chr7:2651867 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.872-320C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651867 | |||||||
chr7:2651937 | C | T | 2 | a0001c0001t0021g0172 a0001c0001t0021g0173 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.872-250C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651937 | |||||||
chr7:2651959 | C | A | 5 | a0001c0001t0002g0015 a0001c0001t0002g0021 a0001c0001t0002g0076 others(2): Show |
6 | HG00558.hp2 HG02071.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.872-228C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651959 | |||||||
chr7:2651976 | G | A | 84 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0063 others(81): Show |
87 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.872-211G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2651976 | |||||||
chr7:2652063 | A | G | 7 | a0001c0001t0005g0084 a0002c0003t0007g0083 a0002c0003t0008g0008 others(4): Show |
9 | HG01496.hp2 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.872-124A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2652063 | |||||||
chr7:2652102 | A | G | 86 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0063 others(83): Show |
89 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(86): Show |
intron_variant | MODIFIER | c.872-85A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2652102 | |||||||
chr7:2652108 | G | A | 1 | a0001c0001t0004g0075 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.872-79G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 7/13 | chr7 | 2652108 | |||||||
chr7:2652415 | A | C | 1 | a0001c0001t0015g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.927+173A>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 8/13 | chr7 | 2652415 | |||||||
chr7:2652450 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0007g0175 |
2 | HG04184.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.927+208C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 8/13 | chr7 | 2652450 | |||||||
chr7:2652455 | G | A | 1 | a0002c0003t0008g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.927+213G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 8/13 | chr7 | 2652455 | |||||||
chr7:2652566 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0248 a0001c0001t0002g0001 others(54): Show |
70 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.927+324G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 8/13 | chr7 | 2652566 | |||||||
chr7:2652596 | C | T | 5 | a0001c0001t0005g0084 a0002c0003t0008g0008 a0002c0003t0008g0080 others(2): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-322C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 8/13 | chr7 | 2652596 | |||||||
chr7:2652743 | T | C | 10 | a0001c0001t0001g0013 a0001c0001t0005g0193 a0001c0001t0005g0194 others(7): Show |
11 | HG00639.hp1 HG01109.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.928-175T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 8/13 | chr7 | 2652743 | |||||||
chr7:2652800 | G | T | 2 | a0001c0001t0002g0087 a0001c0001t0004g0096 |
2 | NA18951.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.928-118G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 8/13 | chr7 | 2652800 | |||||||
chr7:2652844 | G | C | 1 | a0001c0001t0001g0009 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.928-74G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 8/13 | chr7 | 2652844 | |||||||
chr7:2652857 | G | C | 1 | a0001c0001t0013g0348 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.928-61G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 8/13 | chr7 | 2652857 | |||||||
chr7:2652874 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.928-44C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 8/13 | chr7 | 2652874 | |||||||
chr7:2653172 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0019 others(83): Show |
96 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.1020+162C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653172 | |||||||
chr7:2653472 | G | T | 3 | a0001c0001t0015g0178 a0001c0001t0026g0100 a0001c0001t0027g0101 |
3 | HG02280.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1020+462G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653472 | |||||||
chr7:2653540 | G | A | 1 | a0001c0002t0039g0048 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1020+530G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653540 | |||||||
chr7:2653564 | T | TA | 6 | a0001c0001t0001g0339 a0001c0001t0015g0116 a0001c0001t0015g0178 others(3): Show |
6 | HG00738.hp2 HG01978.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1020+561dupA | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 2653564 | ||||||
chr7:2653588 | C | A | 7 | a0001c0001t0006g0004 a0001c0001t0006g0253 a0001c0001t0006g0342 others(4): Show |
9 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020+578C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653588 | |||||||
chr7:2653612 | C | T | 45 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0283 others(42): Show |
47 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1020+602C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653612 | |||||||
chr7:2653662 | A | G | 1 | a0002c0003t0020g0014 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1020+652A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653662 | |||||||
chr7:2653710 | T | C | 1 | a0001c0001t0001g0339 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1020+700T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653710 | |||||||
chr7:2653811 | G | A | 1 | a0001c0001t0012g0337 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1020+801G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653811 | |||||||
chr7:2653819 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0331 a0001c0001t0052g0333 |
4 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020+809C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653819 | |||||||
chr7:2653820 | G | A | 3 | a0001c0001t0021g0172 a0001c0001t0021g0173 a0002c0003t0040g0212 |
3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1020+810G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653820 | |||||||
chr7:2653946 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0331 a0001c0001t0052g0333 |
4 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020+936C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653946 | |||||||
chr7:2653947 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1020+937G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653947 | |||||||
chr7:2653964 | C | A | 1 | a0001c0001t0001g0033 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1020+954C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653964 | |||||||
chr7:2653964 | C | T | 10 | a0001c0001t0006g0004 a0001c0001t0006g0253 a0001c0001t0006g0342 others(7): Show |
12 | HG02109.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1020+954C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653964 | |||||||
chr7:2653978 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1020+968C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2653978 | |||||||
chr7:2654007 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1020+997G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2654007 | |||||||
chr7:2654009 | CTGTGGGC others(5): Show |
C | 1 | a0001c0001t0007g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1020+1006_1020+101 others(16): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 2654009 | ||||||
chr7:2654130 | C | T | 3 | a0001c0005t0014g0091 a0001c0005t0014g0210 a0001c0005t0014g0211 |
3 | HG02109.hp2 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1020+1120C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2654130 | |||||||
chr7:2654202 | C | A | 3 | a0001c0005t0014g0091 a0001c0005t0014g0210 a0001c0005t0014g0211 |
3 | HG02109.hp2 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1020+1192C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2654202 | |||||||
chr7:2654288 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(188): Show |
207 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.1020+1278A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2654288 | |||||||
chr7:2654414 | A | G | 2 | a0002c0003t0008g0080 a0002c0003t0008g0081 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1020+1404A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2654414 | |||||||
chr7:2654415 | T | C | 2 | a0001c0001t0001g0292 a0001c0001t0007g0113 |
2 | HG00099.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1020+1405T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2654415 | |||||||
chr7:2654422 | G | GTA | 8 | a0001c0001t0001g0339 a0001c0001t0006g0004 a0001c0001t0006g0342 others(5): Show |
10 | HG01192.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1020+1423_1020+142 others(6): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 2654422 | ||||||
chr7:2654456 | A | T | 169 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(166): Show |
184 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.1020+1446A>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2654456 | |||||||
chr7:2654457 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1020+1447A>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2654457 | |||||||
chr7:2654478 | TACAC | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(101): Show |
114 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1020+1480_1020+148 others(8): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 2654478 | ||||||
chr7:2654563 | C | G | 1 | a0001c0001t0052g0333 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1021-1529C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2654563 | |||||||
chr7:2654620 | G | A | 10 | a0001c0001t0006g0004 a0001c0001t0006g0253 a0001c0001t0006g0342 others(7): Show |
12 | HG02109.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1021-1472G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2654620 | |||||||
chr7:2654709 | C | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(123): Show |
138 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1021-1383C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2654709 | |||||||
chr7:2654818 | T | C | 58 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0169 others(55): Show |
60 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1021-1274T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2654818 | |||||||
chr7:2654894 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(94): Show |
106 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1021-1198C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2654894 | |||||||
chr7:2655108 | C | T | 1 | a0001c0001t0003g0353 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1021-984C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655108 | |||||||
chr7:2655144 | T | C | 2 | a0001c0001t0005g0084 a0002c0003t0007g0083 |
2 | HG01496.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1021-948T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655144 | |||||||
chr7:2655154 | G | T | 103 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(100): Show |
113 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1021-938G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655154 | |||||||
chr7:2655168 | A | G | 5 | a0001c0001t0001g0092 a0001c0001t0001g0151 a0001c0001t0001g0284 others(2): Show |
5 | HG01243.hp2 HG02109.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1021-924A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655168 | |||||||
chr7:2655188 | C | T | 1 | a0001c0001t0005g0084 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1021-904C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655188 | |||||||
chr7:2655200 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0165 |
3 | HG03239.hp2 HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1021-892G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655200 | |||||||
chr7:2655222 | C | T | 6 | a0001c0001t0001g0245 a0001c0001t0002g0078 a0001c0001t0002g0215 others(3): Show |
6 | NA18946.hp2 NA18960.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021-870C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655222 | |||||||
chr7:2655232 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1021-860C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655232 | |||||||
chr7:2655261 | T | G | 3 | a0001c0001t0011g0029 a0001c0001t0011g0332 a0001c0001t0011g0341 |
4 | HG02559.hp1 HG03130.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021-831T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655261 | |||||||
chr7:2655308 | G | T | 1 | a0001c0001t0004g0295 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1021-784G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655308 | |||||||
chr7:2655401 | C | T | 1 | a0001c0001t0004g0295 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1021-691C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655401 | |||||||
chr7:2655591 | T | G | 9 | a0001c0001t0011g0029 a0001c0001t0011g0332 a0001c0001t0011g0341 others(6): Show |
10 | HG00738.hp2 HG01978.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1021-501T>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655591 | |||||||
chr7:2655762 | C | T | 3 | a0001c0001t0009g0141 a0001c0001t0021g0172 a0001c0001t0021g0173 |
3 | HG02630.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1021-330C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655762 | |||||||
chr7:2655827 | G | A | 1 | a0001c0005t0014g0210 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1021-265G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655827 | |||||||
chr7:2655983 | G | A | 50 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0354 others(47): Show |
52 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1021-109G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2655983 | |||||||
chr7:2656075 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1021-17C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 9/13 | chr7 | 2656075 | |||||||
chr7:2656316 | G | A | 6 | a0001c0001t0006g0004 a0001c0001t0006g0253 a0001c0001t0006g0342 others(3): Show |
8 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114-82G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 10/13 | chr7 | 2656316 | |||||||
chr7:2656347 | C | T | 2 | a0001c0001t0018g0189 a0001c0001t0018g0190 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1114-51C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 10/13 | chr7 | 2656347 | |||||||
chr7:2656363 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0171 |
2 | NA18939.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1114-35T>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 10/13 | chr7 | 2656363 | |||||||
chr7:2656744 | C | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1250+210C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2656744 | |||||||
chr7:2656759 | G | A | 5 | a0001c0001t0015g0116 a0001c0001t0015g0178 a0001c0001t0015g0254 others(2): Show |
5 | HG00738.hp2 HG01978.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250+225G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2656759 | |||||||
chr7:2656772 | G | T | 1 | a0001c0001t0007g0346 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1250+238G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2656772 | |||||||
chr7:2656906 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0165 |
3 | HG03239.hp2 HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1250+372G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2656906 | |||||||
chr7:2657021 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(88): Show |
102 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1250+487G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2657021 | |||||||
chr7:2657060 | G | A | 1 | a0002c0003t0040g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1250+526G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2657060 | |||||||
chr7:2657306 | C | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(174): Show |
193 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.1250+772C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2657306 | |||||||
chr7:2657313 | G | C | 2 | a0001c0001t0013g0348 a0001c0001t0047g0179 |
2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1250+779G>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2657313 | |||||||
chr7:2657365 | A | G | 3 | a0001c0001t0018g0189 a0001c0001t0018g0190 a0002c0003t0008g0202 |
3 | HG02145.hp2 HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1250+831A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2657365 | |||||||
chr7:2657413 | GTGGTGGT others(2): Show |
G | 7 | a0001c0001t0001g0287 a0001c0001t0006g0004 a0001c0001t0006g0253 others(4): Show |
9 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1251-867_1251-859d others(11): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 2657413 | ||||||
chr7:2657416 | GTGGTGA | G | 170 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(167): Show |
183 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1251-849_1251-844d others(8): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 2657416 | ||||||
chr7:2657422 | A | ATGGTGAT others(38): Show |
4 | a0002c0003t0008g0008 a0002c0003t0008g0080 a0002c0003t0008g0081 others(1): Show |
5 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251-850_1251-849i others(47): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 2657422 | ||||||
chr7:2657637 | G | A | 1 | a0001c0001t0009g0323 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1251-649G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2657637 | |||||||
chr7:2657715 | G | A | 4 | a0001c0001t0002g0023 a0001c0001t0002g0044 a0001c0001t0002g0087 others(1): Show |
5 | HG00438.hp1 HG04204.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1251-571G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2657715 | |||||||
chr7:2657802 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1251-484G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2657802 | |||||||
chr7:2657843 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1251-443C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2657843 | |||||||
chr7:2658044 | C | G | 1 | a0001c0001t0001g0103 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1251-242C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2658044 | |||||||
chr7:2658145 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1251-141C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2658145 | |||||||
chr7:2658169 | G | A | 1 | a0002c0003t0008g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1251-117G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2658169 | |||||||
chr7:2658235 | C | G | 1 | a0001c0001t0002g0026 | 2 | NA18964.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1251-51C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2658235 | |||||||
chr7:2658247 | G | T | 48 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0003g0030 others(45): Show |
50 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1251-39G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 11/13 | chr7 | 2658247 | |||||||
chr7:2658495 | C | T | 5 | a0001c0001t0002g0026 a0001c0001t0002g0031 a0001c0001t0002g0114 others(2): Show |
6 | NA18951.hp1 NA18954.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.1424+36C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 12/13 | chr7 | 2658495 | |||||||
chr7:2658517 | G | T | 1 | a0001c0001t0002g0268 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1424+58G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 12/13 | chr7 | 2658517 | |||||||
chr7:2658518 | G | A | 5 | a0001c0001t0002g0078 a0001c0001t0002g0215 a0001c0001t0002g0221 others(2): Show |
5 | NA18946.hp2 NA18967.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1424+59G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 12/13 | chr7 | 2658518 | |||||||
chr7:2658618 | G | T | 1 | a0001c0001t0029g0257 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1424+159G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 12/13 | chr7 | 2658618 | |||||||
chr7:2658728 | C | T | 2 | a0001c0001t0016g0335 a0001c0001t0016g0358 |
2 | NA18973.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1425-212C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 12/13 | chr7 | 2658728 | |||||||
chr7:2658825 | A | C | 9 | a0001c0001t0011g0029 a0001c0001t0011g0332 a0001c0001t0011g0341 others(6): Show |
10 | HG00738.hp2 HG01978.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1425-115A>C | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 12/13 | chr7 | 2658825 | |||||||
chr7:2659077 | C | G | 1 | a0001c0001t0003g0183 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1500+62C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2659077 | |||||||
chr7:2659208 | C | T | 7 | a0001c0001t0013g0204 a0001c0001t0013g0344 a0001c0001t0013g0348 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1500+193C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2659208 | |||||||
chr7:2659477 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0029g0257 |
2 | HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1500+462G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2659477 | |||||||
chr7:2659890 | A | ACT | 5 | a0001c0001t0002g0215 a0002c0003t0008g0008 a0002c0003t0008g0080 others(2): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1500+894_1500+895d others(4): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 2659890 | ||||||
chr7:2660053 | C | G | 1 | a0001c0001t0007g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1500+1038C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660053 | |||||||
chr7:2660114 | C | A | 3 | a0001c0001t0005g0205 a0001c0001t0021g0172 a0001c0001t0021g0173 |
3 | HG02809.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1500+1099C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660114 | |||||||
chr7:2660114 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1500+1099C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660114 | |||||||
chr7:2660138 | G | T | 1 | a0001c0001t0003g0328 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1500+1123G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660138 | |||||||
chr7:2660149 | G | T | 1 | a0002c0003t0020g0014 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1500+1134G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660149 | |||||||
chr7:2660254 | C | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0225 |
2 | HG02027.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1500+1239C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660254 | |||||||
chr7:2660350 | C | T | 5 | a0002c0003t0008g0008 a0002c0003t0008g0080 a0002c0003t0008g0081 others(2): Show |
7 | HG02451.hp2 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1501-1318C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660350 | |||||||
chr7:2660355 | A | G | 61 | a0001c0001t0003g0030 a0001c0001t0003g0052 a0001c0001t0003g0145 others(58): Show |
65 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.1501-1313A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660355 | |||||||
chr7:2660358 | C | T | 5 | a0001c0001t0007g0093 a0001c0001t0007g0174 a0001c0001t0007g0175 others(2): Show |
5 | HG01167.hp2 HG01192.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1501-1310C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660358 | |||||||
chr7:2660565 | G | A | 1 | a0001c0001t0003g0314 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1501-1103G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660565 | |||||||
chr7:2660583 | C | T | 2 | a0001c0001t0013g0348 a0001c0001t0047g0179 |
2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1501-1085C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660583 | |||||||
chr7:2660620 | G | A | 1 | a0001c0001t0038g0219 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1501-1048G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660620 | |||||||
chr7:2660628 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1501-1040G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660628 | |||||||
chr7:2660653 | C | T | 3 | a0001c0001t0018g0189 a0001c0001t0018g0190 a0002c0003t0008g0202 |
3 | HG02145.hp2 HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1501-1015C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660653 | |||||||
chr7:2660743 | G | T | 3 | a0001c0001t0018g0189 a0001c0001t0018g0190 a0002c0003t0008g0202 |
3 | HG02145.hp2 HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1501-925G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660743 | |||||||
chr7:2660837 | C | G | 3 | a0001c0001t0011g0029 a0001c0001t0011g0332 a0001c0001t0011g0341 |
4 | HG02559.hp1 HG03130.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1501-831C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660837 | |||||||
chr7:2660877 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1501-791A>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660877 | |||||||
chr7:2660952 | C | T | 3 | a0001c0001t0018g0189 a0001c0001t0018g0190 a0002c0003t0008g0202 |
3 | HG02145.hp2 HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1501-716C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2660952 | |||||||
chr7:2661042 | A | T | 1 | a0001c0001t0017g0270 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1501-626A>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2661042 | |||||||
chr7:2661066 | C | G | 55 | a0001c0001t0001g0264 a0001c0001t0001g0312 a0001c0001t0003g0030 others(52): Show |
57 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1501-602C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2661066 | |||||||
chr7:2661072 | C | T | 1 | a0002c0003t0049g0182 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1501-596C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2661072 | |||||||
chr7:2661132 | G | T | 6 | a0001c0001t0006g0004 a0001c0001t0006g0342 a0001c0001t0006g0343 others(3): Show |
8 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1501-536G>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2661132 | |||||||
chr7:2661230 | C | T | 3 | a0001c0001t0011g0029 a0001c0001t0011g0332 a0001c0001t0011g0341 |
4 | HG02559.hp1 HG03130.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1501-438C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2661230 | |||||||
chr7:2661258 | G | A | 3 | a0001c0001t0009g0322 a0001c0001t0009g0324 a0001c0001t0009g0325 |
3 | HG02451.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1501-410G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2661258 | |||||||
chr7:2661263 | C | G | 3 | a0001c0001t0011g0029 a0001c0001t0011g0332 a0001c0001t0011g0341 |
4 | HG02559.hp1 HG03130.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1501-405C>G | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2661263 | |||||||
chr7:2661367 | C | T | 1 | a0001c0001t0005g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1501-301C>T | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2661367 | |||||||
chr7:2661392 | G | A | 1 | a0002c0003t0049g0182 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1501-276G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2661392 | |||||||
chr7:2661400 | CCCT | C | 4 | a0001c0001t0004g0006 a0001c0001t0004g0150 a0001c0001t0004g0288 others(1): Show |
5 | HG00738.hp1 HG01123.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1501-263_1501-261d others(5): Show |
TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 2661400 | ||||||
chr7:2661566 | C | A | 15 | a0001c0001t0006g0004 a0001c0001t0006g0342 a0001c0001t0006g0343 others(12): Show |
17 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1501-102C>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2661566 | |||||||
chr7:2661577 | G | A | 2 | a0001c0001t0001g0264 a0001c0001t0001g0312 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1501-91G>A | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | chr7 | 2661577 | |||||||
chr7:2661648 | TC | T | 4 | a0001c0001t0013g0204 a0001c0001t0013g0344 a0001c0001t0013g0348 others(1): Show |
4 | HG01243.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1501-15delC | TTYH3 | ENSG00000136295.16 | transcript | ENST00000258796.12 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 2661648 |