Item | Value |
---|---|
geneid | 8458 |
ensemblid | ENSG00000116830.12 |
hgncid | 12398 |
symbol | TTF2 |
name | transcription termination factor 2 |
refseq_nuc | NM_003594.4 |
refseq_prot | NP_003585.3 |
ensembl_nuc | ENST00000369466.9 |
ensembl_prot | ENSP00000358478.3 |
mane_status | MANE Select |
chr | chr1 |
start | 117060326 |
end | 117107453 |
strand | + |
ver | v1.2 |
region | chr1:117060326-117107453 |
region5000 | chr1:117055326-117112453 |
regionname0 | TTF2_chr1_117060326_117107453 |
regionname5000 | TTF2_chr1_117055326_117112453 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1162 | 153 | 58 | 26 | 45 | 6 | 17 | 37 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0002 | 0/0 | 1162 | 137 | 12 | 45 | 60 | 7 | 13 | 37 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0003 | 0/0 | 1162 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0004 | 0/0 | 1162 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0005 | 0/0 | 1162 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0006 | 0/0 | 1162 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0007 | 0/0 | 1162 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0008 | 0/0 | 1162 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0009 | 0/0 | 1162 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0010 | 0/0 | 1162 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0011 | 0/0 | 1162 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0012 | 0/0 | 1162 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0013 | 0/0 | 1162 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0014 | 0/0 | 1162 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0015 | 0/0 | 1162 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0016 | 0/0 | 1162 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0017 | 0/0 | 1162 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0018 | 0/0 | 1162 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0019 | 0/0 | 1162 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0020 | 0/0 | 1162 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
a0021 | 0/1 | 1162 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | MEEVR others(1157): Show |
chr1 | 117055326 | 117112453 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 1/0 | 3486 | 95 | 35 | 21 | 23 | 6 | 9 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0001c0003 | 0/0 | 3486 | 48 | 14 | 5 | 21 | 0 | 8 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0001c0004 | 0/0 | 3486 | 6 | 6 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0001c0007 | 0/0 | 3486 | 3 | 3 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0001c0018 | 0/0 | 3486 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0002c0001 | 0/0 | 3486 | 131 | 8 | 43 | 60 | 7 | 13 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0002c0013 | 0/0 | 3486 | 2 | 2 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0002c0027 | 0/0 | 3486 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0002c0028 | 0/0 | 3486 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0002c0031 | 0/0 | 3486 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0002c0035 | 0/0 | 3486 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0003c0006 | 0/0 | 3486 | 3 | 3 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0003c0008 | 0/0 | 3486 | 3 | 3 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0003c0010 | 0/0 | 3486 | 2 | 2 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0003c0017 | 0/0 | 3486 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0004c0005 | 0/0 | 3486 | 5 | 5 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0005c0014 | 0/0 | 3486 | 2 | 2 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0005c0036 | 0/0 | 3486 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0006c0009 | 0/0 | 3486 | 2 | 2 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0006c0015 | 0/0 | 3486 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0007c0012 | 0/0 | 3486 | 2 | 0 | 0 | 0 | 1 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0008c0011 | 0/0 | 3486 | 2 | 2 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0009c0023 | 0/0 | 3486 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0009c0025 | 0/0 | 3486 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0010c0021 | 0/0 | 3486 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0011c0032 | 0/0 | 3486 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0012c0030 | 0/0 | 3486 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0013c0022 | 0/0 | 3486 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0014c0016 | 0/0 | 3486 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0015c0019 | 0/0 | 3486 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0016c0020 | 0/0 | 3486 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0017c0034 | 0/0 | 3486 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0018c0029 | 0/0 | 3486 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0019c0033 | 0/0 | 3486 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0020c0024 | 0/0 | 3486 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 | ||
a0021c0026 | 0/1 | 3486 | 1 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | ATGGA others(3481): Show |
chr1 | 117055326 | 117112453 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 9439 | 22 | 0 | 6 | 15 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0002 | 0/0 | 9439 | 14 | 2 | 4 | 4 | 1 | 3 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0003 | 0/0 | 9427 | 15 | 3 | 6 | 1 | 2 | 3 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0004 | 0/0 | 9439 | 13 | 7 | 3 | 0 | 2 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0007 | 0/0 | 9427 | 5 | 5 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0008 | 0/0 | 9440 | 4 | 4 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0010 | 0/0 | 9440 | 5 | 5 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0011 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0015 | 0/0 | 9440 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0017 | 0/0 | 9439 | 2 | 0 | 0 | 2 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0018 | 0/0 | 9440 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0019 | 0/0 | 9428 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9423): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0022 | 0/0 | 9439 | 1 | 0 | 0 | 0 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0027 | 0/0 | 9439 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0029 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0034 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0035 | 0/0 | 9440 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0043 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0050 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9421): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0051 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0061 | 1/0 | 9439 | 1 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0063 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0002t0067 | 0/0 | 9429 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9424): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0004 | 0/0 | 9439 | 17 | 3 | 3 | 9 | 0 | 2 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0006 | 0/0 | 9426 | 13 | 1 | 0 | 8 | 0 | 4 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9421): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0007 | 0/0 | 9427 | 3 | 2 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0010 | 0/0 | 9440 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0011 | 0/0 | 9439 | 2 | 2 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0014 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0021 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0022 | 0/0 | 9439 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0023 | 0/0 | 9428 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9423): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0024 | 0/0 | 9427 | 2 | 1 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0053 | 0/0 | 9439 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0059 | 0/0 | 9441 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9436): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0062 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0069 | 0/0 | 9427 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0070 | 0/0 | 9426 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9421): Show |
chr1 | 117055326 | 117112453 |
a0001c0003t0071 | 0/0 | 9427 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0001c0004t0001 | 0/0 | 9439 | 4 | 4 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0001c0004t0015 | 0/0 | 9440 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0001c0004t0054 | 0/0 | 9440 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0001c0007t0003 | 0/0 | 9427 | 3 | 3 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0001c0018t0001 | 0/0 | 9439 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0001 | 0/0 | 9439 | 44 | 0 | 6 | 32 | 1 | 5 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0002 | 0/0 | 9439 | 20 | 1 | 12 | 6 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0003 | 0/0 | 9427 | 10 | 1 | 5 | 1 | 1 | 2 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0005 | 0/0 | 9440 | 22 | 3 | 8 | 7 | 2 | 2 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0008 | 0/0 | 9440 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0009 | 0/0 | 9427 | 7 | 0 | 6 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0012 | 0/0 | 9438 | 4 | 0 | 1 | 3 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9433): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0013 | 0/0 | 9439 | 3 | 0 | 0 | 3 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0018 | 0/0 | 9440 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0019 | 0/0 | 9428 | 1 | 0 | 0 | 0 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9423): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0020 | 0/0 | 9439 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0025 | 0/0 | 9439 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0026 | 0/0 | 9440 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0030 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0031 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0033 | 0/0 | 9439 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0036 | 0/0 | 9439 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0037 | 0/0 | 9439 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0038 | 0/0 | 9439 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0039 | 0/0 | 9439 | 1 | 0 | 0 | 0 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0040 | 0/0 | 9439 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0041 | 0/0 | 9438 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9433): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0042 | 0/0 | 9440 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0044 | 0/0 | 9429 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9424): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0046 | 0/0 | 9427 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0047 | 0/0 | 9426 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9421): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0048 | 0/0 | 9426 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9421): Show |
chr1 | 117055326 | 117112453 |
a0002c0001t0049 | 0/0 | 9429 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9424): Show |
chr1 | 117055326 | 117112453 |
a0002c0013t0016 | 0/0 | 9439 | 2 | 2 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0027t0028 | 0/0 | 9440 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0002c0028t0032 | 0/0 | 9438 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9433): Show |
chr1 | 117055326 | 117112453 |
a0002c0031t0002 | 0/0 | 9439 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0002c0035t0065 | 0/0 | 9440 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0003c0006t0003 | 0/0 | 9427 | 2 | 2 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0003c0006t0045 | 0/0 | 9428 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9423): Show |
chr1 | 117055326 | 117112453 |
a0003c0008t0014 | 0/0 | 9439 | 2 | 2 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0003c0008t0021 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0003c0010t0052 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0003c0010t0064 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0003c0017t0001 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0004c0005t0003 | 0/0 | 9427 | 3 | 3 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0004c0005t0007 | 0/0 | 9427 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0004c0005t0008 | 0/0 | 9440 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0005c0014t0007 | 0/0 | 9427 | 2 | 2 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0005c0036t0057 | 0/0 | 9440 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0006c0009t0004 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0006c0009t0072 | 0/0 | 9457 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9452): Show |
chr1 | 117055326 | 117112453 |
a0006c0015t0011 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0007c0012t0003 | 0/0 | 9427 | 2 | 0 | 0 | 0 | 1 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0008c0011t0011 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0008c0011t0058 | 0/0 | 9440 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0009c0023t0001 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0009c0025t0066 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0010c0021t0060 | 0/0 | 9439 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0011c0032t0003 | 0/0 | 9427 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9422): Show |
chr1 | 117055326 | 117112453 |
a0012c0030t0020 | 0/0 | 9439 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0013c0022t0005 | 0/0 | 9440 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0014c0016t0068 | 0/0 | 9428 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9423): Show |
chr1 | 117055326 | 117112453 |
a0015c0019t0008 | 0/0 | 9440 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0016c0020t0056 | 0/0 | 9439 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0017c0034t0023 | 0/0 | 9428 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9423): Show |
chr1 | 117055326 | 117112453 |
a0018c0029t0001 | 0/0 | 9439 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0019c0033t0004 | 0/0 | 9439 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
a0020c0024t0055 | 0/0 | 9440 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9435): Show |
chr1 | 117055326 | 117112453 |
a0021c0026t0002 | 0/1 | 9439 | 1 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | GAACT others(9434): Show |
chr1 | 117055326 | 117112453 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0002g0012 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0003g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0004g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0008g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0010g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0010g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0015g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0017g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0018g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0019g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0022g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0027g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0029g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0034g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0035g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0043g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0050g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0051g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0061g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0063g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0002t0067g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0006g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0006g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0006g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0010g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0011g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0011g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0014g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0021g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0022g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0023g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0024g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0024g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0053g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0059g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0062g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0069g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0070g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0003t0071g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0004t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0004t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0004t0015g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0004t0054g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0007t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0007t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0007t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0001c0018t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0001 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0002g0002 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0002g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0005g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0005g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0005g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0005g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0005g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0005g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0005g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0005g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0009g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0009g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0009g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0009g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0012g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0012g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0012g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0012g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0013g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0013g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0018g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0019g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0020g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0025g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0026g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0030g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0031g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0033g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0036g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0037g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0038g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0039g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0040g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0041g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0042g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0044g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0046g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0047g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0048g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0001t0049g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0013t0016g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0013t0016g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0027t0028g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0028t0032g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0031t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0002c0035t0065g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0003c0006t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0003c0006t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0003c0006t0045g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0003c0008t0014g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0003c0008t0014g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0003c0008t0021g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0003c0010t0052g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0003c0010t0064g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0003c0017t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0004c0005t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0004c0005t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0004c0005t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0004c0005t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0004c0005t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0005c0014t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0005c0014t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0005c0036t0057g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0006c0009t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0006c0009t0072g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0006c0015t0011g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0007c0012t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0007c0012t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0008c0011t0011g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0008c0011t0058g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0009c0023t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0009c0025t0066g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0010c0021t0060g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0011c0032t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0012c0030t0020g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0013c0022t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0014c0016t0068g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0015c0019t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0016c0020t0056g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0017c0034t0023g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0018c0029t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0019c0033t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0020c0024t0055g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
a0021c0026t0002g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0039 | g0001 | EUR | GBR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0012 | EUR | GBR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00280 | hp1 | a0002 | c0001 | t0001 | g0229 | EUR | FIN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00280 | hp2 | a0001 | c0002 | t0004 | g0053 | EUR | FIN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00323 | hp1 | a0001 | c0002 | t0022 | g0046 | EUR | FIN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00323 | hp2 | a0007 | c0012 | t0003 | g0093 | EUR | FIN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00408 | hp1 | a0002 | c0001 | t0013 | g0022 | EAS | CHS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | CHS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00438 | hp1 | a0002 | c0001 | t0001 | g0022 | EAS | CHS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | CHS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00544 | hp1 | a0002 | c0001 | t0001 | g0226 | EAS | CHS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | CHS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00558 | hp1 | a0002 | c0001 | t0001 | g0240 | EAS | CHS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00558 | hp2 | a0002 | c0001 | t0001 | g0204 | EAS | CHS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00597 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00597 | hp2 | a0002 | c0001 | t0005 | g0009 | EAS | CHS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00621 | hp1 | a0002 | c0001 | t0001 | g0028 | EAS | CHS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00621 | hp2 | a0002 | c0001 | t0026 | g0255 | EAS | CHS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00639 | hp1 | a0002 | c0001 | t0002 | g0225 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00639 | hp2 | a0002 | c0001 | t0040 | g0220 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00642 | hp1 | a0001 | c0003 | t0004 | g0134 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00733 | hp1 | a0001 | c0002 | t0003 | g0088 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00733 | hp2 | a0002 | c0001 | t0002 | g0251 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00735 | hp1 | a0002 | c0001 | t0020 | g0203 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0085 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00738 | hp1 | a0002 | c0001 | t0009 | g0004 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00738 | hp2 | a0002 | c0031 | t0002 | g0029 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00741 | hp1 | a0001 | c0002 | t0004 | g0011 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0099 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01069 | hp2 | a0002 | c0001 | t0002 | g0005 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01070 | hp2 | a0002 | c0001 | t0041 | g0005 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01071 | hp2 | a0002 | c0001 | t0002 | g0005 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01074 | hp1 | a0002 | c0001 | t0002 | g0025 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01074 | hp2 | a0002 | c0001 | t0002 | g0005 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01081 | hp1 | a0002 | c0001 | t0002 | g0002 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0069 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01106 | hp1 | a0001 | c0002 | t0004 | g0052 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01106 | hp2 | a0002 | c0001 | t0005 | g0258 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01109 | hp1 | a0001 | c0002 | t0003 | g0067 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01109 | hp2 | a0002 | c0001 | t0003 | g0215 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01167 | hp1 | a0002 | c0001 | t0009 | g0023 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01167 | hp2 | a0002 | c0001 | t0001 | g0113 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01168 | hp1 | a0002 | c0001 | t0003 | g0214 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01168 | hp2 | a0002 | c0001 | t0002 | g0233 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01169 | hp1 | a0002 | c0001 | t0009 | g0023 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01169 | hp2 | a0002 | c0001 | t0002 | g0222 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01175 | hp1 | a0002 | c0001 | t0012 | g0221 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01175 | hp2 | a0001 | c0002 | t0004 | g0047 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01243 | hp1 | a0010 | c0021 | t0060 | g0013 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01243 | hp2 | a0001 | c0002 | t0035 | g0083 | AMR | PUR | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01256 | hp1 | a0011 | c0032 | t0003 | g0227 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01256 | hp2 | a0002 | c0001 | t0049 | g0004 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01257 | hp1 | a0012 | c0030 | t0020 | g0208 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01257 | hp2 | a0002 | c0001 | t0001 | g0228 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01261 | hp1 | a0002 | c0001 | t0009 | g0004 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01261 | hp2 | a0002 | c0001 | t0003 | g0218 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01358 | hp1 | a0002 | c0001 | t0005 | g0244 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01358 | hp2 | a0001 | c0002 | t0003 | g0072 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01361 | hp1 | a0002 | c0001 | t0002 | g0249 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01361 | hp2 | a0001 | c0002 | t0003 | g0250 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01433 | hp1 | a0001 | c0003 | t0024 | g0122 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01433 | hp2 | a0002 | c0001 | t0005 | g0024 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01496 | hp1 | a0002 | c0001 | t0005 | g0024 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01496 | hp2 | a0001 | c0003 | t0071 | g0135 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01515 | hp1 | a0001 | c0002 | t0004 | g0011 | EUR | IBS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01515 | hp2 | a0002 | c0001 | t0005 | g0032 | EUR | IBS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01516 | hp1 | a0001 | c0002 | t0003 | g0019 | EUR | IBS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01516 | hp2 | a0002 | c0001 | t0019 | g0027 | EUR | IBS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01517 | hp1 | a0001 | c0002 | t0003 | g0019 | EUR | IBS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01517 | hp2 | a0002 | c0001 | t0005 | g0032 | EUR | IBS | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01884 | hp1 | a0005 | c0036 | t0057 | g0153 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01884 | hp2 | a0001 | c0002 | t0051 | g0073 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01891 | hp1 | a0001 | c0002 | t0010 | g0060 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01891 | hp2 | a0008 | c0011 | t0011 | g0040 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01934 | hp1 | a0002 | c0001 | t0002 | g0002 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0086 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01943 | hp1 | a0001 | c0003 | t0004 | g0144 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01943 | hp2 | a0002 | c0001 | t0005 | g0033 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01952 | hp1 | a0002 | c0001 | t0001 | g0207 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01952 | hp2 | a0002 | c0001 | t0001 | g0247 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01975 | hp1 | a0002 | c0001 | t0005 | g0033 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01975 | hp2 | a0002 | c0001 | t0009 | g0004 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0105 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01978 | hp2 | a0002 | c0001 | t0003 | g0248 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01981 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01981 | hp2 | a0002 | c0001 | t0002 | g0002 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01993 | hp1 | a0002 | c0001 | t0009 | g0027 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02004 | hp1 | a0002 | c0001 | t0005 | g0260 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02004 | hp2 | a0002 | c0001 | t0003 | g0200 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02015 | hp1 | a0002 | c0001 | t0037 | g0199 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02015 | hp2 | a0013 | c0022 | t0005 | g0091 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02040 | hp1 | a0002 | c0001 | t0003 | g0230 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02040 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02055 | hp1 | a0001 | c0002 | t0007 | g0058 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02055 | hp2 | a0009 | c0023 | t0001 | g0187 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0028 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02056 | hp2 | a0001 | c0002 | t0003 | g0175 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02083 | hp1 | a0001 | c0003 | t0006 | g0132 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02083 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02129 | hp1 | a0002 | c0001 | t0005 | g0009 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02129 | hp2 | a0002 | c0001 | t0033 | g0236 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02132 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02135 | hp1 | a0002 | c0001 | t0001 | g0219 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02145 | hp1 | a0001 | c0004 | t0001 | g0181 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02145 | hp2 | a0003 | c0006 | t0045 | g0191 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02165 | hp1 | a0002 | c0001 | t0005 | g0030 | EAS | CDX | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02165 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | CDX | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02257 | hp1 | a0001 | c0002 | t0010 | g0042 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02257 | hp2 | a0003 | c0017 | t0001 | g0190 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02258 | hp1 | a0001 | c0002 | t0043 | g0192 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02258 | hp2 | a0001 | c0004 | t0001 | g0170 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02273 | hp1 | a0002 | c0001 | t0005 | g0262 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0162 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02280 | hp1 | a0001 | c0003 | t0007 | g0014 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02280 | hp2 | a0001 | c0002 | t0008 | g0194 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02293 | hp1 | a0001 | c0003 | t0004 | g0146 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02293 | hp2 | a0001 | c0002 | t0027 | g0180 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02300 | hp1 | a0002 | c0001 | t0046 | g0004 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02300 | hp2 | a0002 | c0035 | t0065 | g0125 | AMR | PEL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02451 | hp1 | a0002 | c0028 | t0032 | g0198 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02451 | hp2 | a0001 | c0002 | t0010 | g0048 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02523 | hp1 | a0002 | c0001 | t0002 | g0002 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02523 | hp2 | a0002 | c0001 | t0001 | g0184 | EAS | KHV | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02572 | hp1 | a0001 | c0002 | t0004 | g0059 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02572 | hp2 | a0001 | c0002 | t0010 | g0010 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02602 | hp1 | a0001 | c0003 | t0022 | g0147 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02602 | hp2 | a0002 | c0001 | t0001 | g0241 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02615 | hp1 | a0001 | c0004 | t0001 | g0167 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02615 | hp2 | a0001 | c0003 | t0004 | g0015 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02622 | hp1 | a0014 | c0016 | t0068 | g0064 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02622 | hp2 | a0001 | c0003 | t0004 | g0118 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02630 | hp1 | a0001 | c0002 | t0003 | g0177 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02630 | hp2 | a0001 | c0002 | t0063 | g0062 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02647 | hp1 | a0004 | c0005 | t0007 | g0041 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02647 | hp2 | a0001 | c0002 | t0004 | g0056 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02698 | hp1 | a0002 | c0001 | t0044 | g0231 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02698 | hp2 | a0001 | c0003 | t0004 | g0018 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02717 | hp1 | a0001 | c0002 | t0008 | g0169 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02717 | hp2 | a0001 | c0003 | t0014 | g0123 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02723 | hp1 | a0003 | c0008 | t0014 | g0116 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02723 | hp2 | a0009 | c0025 | t0066 | g0037 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02735 | hp1 | a0001 | c0003 | t0023 | g0127 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02735 | hp2 | a0002 | c0001 | t0009 | g0201 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02738 | hp1 | a0007 | c0012 | t0003 | g0094 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02738 | hp2 | a0002 | c0001 | t0001 | g0234 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02809 | hp1 | a0002 | c0013 | t0016 | g0211 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02809 | hp2 | a0001 | c0002 | t0004 | g0061 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02818 | hp1 | a0001 | c0002 | t0008 | g0264 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02818 | hp2 | a0002 | c0001 | t0031 | g0265 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02886 | hp1 | a0002 | c0001 | t0030 | g0213 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02886 | hp2 | a0002 | c0013 | t0016 | g0210 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02895 | hp1 | a0001 | c0007 | t0003 | g0160 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02895 | hp2 | a0004 | c0005 | t0003 | g0111 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02896 | hp1 | a0002 | c0001 | t0005 | g0008 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02896 | hp2 | a0001 | c0003 | t0004 | g0015 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02897 | hp1 | a0002 | c0001 | t0005 | g0008 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02897 | hp2 | a0001 | c0007 | t0003 | g0172 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02922 | hp1 | a0004 | c0005 | t0003 | g0109 | AFR | ESN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02922 | hp2 | a0001 | c0003 | t0069 | g0014 | AFR | ESN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02965 | hp1 | a0003 | c0006 | t0003 | g0188 | AFR | ESN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02965 | hp2 | a0006 | c0009 | t0072 | g0066 | AFR | ESN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02970 | hp1 | a0001 | c0002 | t0007 | g0055 | AFR | ESN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02970 | hp2 | a0005 | c0014 | t0007 | g0154 | AFR | ESN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02976 | hp1 | a0001 | c0002 | t0007 | g0057 | AFR | ESN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02976 | hp2 | a0002 | c0001 | t0042 | g0259 | AFR | ESN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03017 | hp1 | a0002 | c0001 | t0003 | g0202 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0163 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03041 | hp1 | a0001 | c0003 | t0006 | g0152 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03041 | hp2 | a0001 | c0004 | t0001 | g0179 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03098 | hp1 | a0015 | c0019 | t0008 | g0171 | AFR | MSL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03098 | hp2 | a0001 | c0003 | t0062 | g0124 | AFR | MSL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03130 | hp1 | a0001 | c0002 | t0010 | g0010 | AFR | ESN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03130 | hp2 | a0001 | c0004 | t0015 | g0164 | AFR | ESN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03139 | hp1 | a0006 | c0009 | t0004 | g0065 | AFR | ESN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03139 | hp2 | a0003 | c0010 | t0052 | g0266 | AFR | ESN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03195 | hp1 | a0001 | c0002 | t0004 | g0051 | AFR | ESN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0193 | AFR | ESN | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03209 | hp1 | a0001 | c0003 | t0021 | g0119 | AFR | MSL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03209 | hp2 | a0004 | c0005 | t0003 | g0110 | AFR | MSL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03225 | hp1 | a0003 | c0008 | t0021 | g0115 | AFR | MSL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03225 | hp2 | a0016 | c0020 | t0056 | g0112 | AFR | MSL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03453 | hp1 | a0004 | c0005 | t0008 | g0108 | AFR | MSL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03453 | hp2 | a0001 | c0002 | t0004 | g0267 | AFR | MSL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03486 | hp1 | a0006 | c0015 | t0011 | g0063 | AFR | MSL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03486 | hp2 | a0001 | c0002 | t0007 | g0035 | AFR | MSL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03490 | hp1 | a0001 | c0003 | t0006 | g0016 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03490 | hp2 | a0001 | c0002 | t0003 | g0098 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03491 | hp1 | a0017 | c0034 | t0023 | g0157 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0070 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0068 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03492 | hp2 | a0001 | c0003 | t0006 | g0016 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03540 | hp1 | a0001 | c0002 | t0029 | g0074 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03540 | hp2 | a0001 | c0002 | t0003 | g0263 | AFR | GWD | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03579 | hp1 | a0002 | c0001 | t0005 | g0008 | AFR | MSL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03579 | hp2 | a0001 | c0002 | t0004 | g0013 | AFR | MSL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03669 | hp1 | a0002 | c0001 | t0001 | g0026 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03669 | hp2 | a0001 | c0003 | t0006 | g0017 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03704 | hp1 | a0002 | c0001 | t0036 | g0001 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0087 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03710 | hp1 | a0001 | c0002 | t0004 | g0054 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03710 | hp2 | a0001 | c0002 | t0003 | g0080 | SAS | PJL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03831 | hp1 | a0001 | c0002 | t0018 | g0084 | SAS | BEB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03831 | hp2 | a0002 | c0001 | t0018 | g0031 | SAS | BEB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03834 | hp1 | a0001 | c0002 | t0003 | g0078 | SAS | BEB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03834 | hp2 | a0002 | c0001 | t0005 | g0223 | SAS | BEB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG04184 | hp1 | a0001 | c0003 | t0006 | g0148 | SAS | BEB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG04184 | hp2 | a0002 | c0001 | t0005 | g0224 | SAS | BEB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG04199 | hp1 | a0002 | c0001 | t0001 | g0232 | SAS | STU | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG04199 | hp2 | a0001 | c0003 | t0004 | g0018 | SAS | STU | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18522 | hp1 | a0001 | c0002 | t0050 | g0178 | AFR | YRI | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18522 | hp2 | a0003 | c0010 | t0064 | g0045 | AFR | YRI | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | CHB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18747 | hp2 | a0001 | c0003 | t0070 | g0141 | EAS | CHB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18906 | hp1 | a0001 | c0002 | t0034 | g0176 | AFR | YRI | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18906 | hp2 | a0001 | c0003 | t0007 | g0120 | AFR | YRI | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18939 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18939 | hp2 | a0002 | c0001 | t0002 | g0077 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18941 | hp1 | a0002 | c0001 | t0001 | g0216 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18941 | hp2 | a0001 | c0003 | t0006 | g0006 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18942 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18944 | hp1 | a0002 | c0001 | t0001 | g0239 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18944 | hp2 | a0001 | c0003 | t0004 | g0126 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18945 | hp2 | a0001 | c0003 | t0006 | g0006 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18947 | hp1 | a0001 | c0018 | t0001 | g0168 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18947 | hp2 | a0002 | c0001 | t0001 | g0235 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18948 | hp1 | a0002 | c0001 | t0002 | g0025 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18948 | hp2 | a0001 | c0003 | t0007 | g0139 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18949 | hp1 | a0001 | c0002 | t0019 | g0107 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18949 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18950 | hp1 | a0001 | c0003 | t0004 | g0130 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18951 | hp2 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18954 | hp1 | a0002 | c0001 | t0001 | g0245 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18954 | hp2 | a0001 | c0003 | t0006 | g0142 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18964 | hp1 | a0002 | c0001 | t0005 | g0030 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18964 | hp2 | a0001 | c0003 | t0004 | g0129 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18969 | hp1 | a0001 | c0003 | t0006 | g0006 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18969 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18970 | hp1 | a0002 | c0001 | t0005 | g0009 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18970 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18971 | hp1 | a0002 | c0001 | t0048 | g0252 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18971 | hp2 | a0002 | c0001 | t0013 | g0007 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18975 | hp1 | a0002 | c0001 | t0025 | g0243 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18975 | hp2 | a0002 | c0001 | t0012 | g0257 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18978 | hp1 | a0001 | c0003 | t0006 | g0150 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18978 | hp2 | a0001 | c0003 | t0004 | g0149 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18982 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18984 | hp1 | a0002 | c0001 | t0012 | g0237 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18984 | hp2 | a0002 | c0001 | t0012 | g0158 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18985 | hp1 | a0001 | c0002 | t0017 | g0021 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18985 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18994 | hp1 | a0001 | c0003 | t0004 | g0136 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA18994 | hp2 | a0018 | c0029 | t0001 | g0206 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19009 | hp1 | a0002 | c0001 | t0008 | g0001 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19009 | hp2 | a0002 | c0001 | t0005 | g0254 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19010 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19011 | hp1 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19030 | hp1 | a0003 | c0006 | t0003 | g0189 | AFR | LWK | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19030 | hp2 | a0001 | c0002 | t0008 | g0106 | AFR | LWK | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19043 | hp1 | a0008 | c0011 | t0058 | g0038 | AFR | LWK | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19043 | hp2 | a0001 | c0002 | t0004 | g0050 | AFR | LWK | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19054 | hp1 | a0002 | c0001 | t0038 | g0197 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19054 | hp2 | a0001 | c0003 | t0004 | g0145 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19056 | hp2 | a0002 | c0001 | t0013 | g0007 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19058 | hp2 | a0002 | c0001 | t0001 | g0185 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19062 | hp1 | a0002 | c0001 | t0001 | g0031 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19063 | hp1 | a0002 | c0001 | t0001 | g0246 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19063 | hp2 | a0001 | c0003 | t0006 | g0017 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19066 | hp1 | a0001 | c0003 | t0004 | g0131 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19066 | hp2 | a0002 | c0001 | t0005 | g0256 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19067 | hp1 | a0001 | c0003 | t0059 | g0138 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19067 | hp2 | a0001 | c0002 | t0017 | g0021 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19079 | hp1 | a0001 | c0003 | t0004 | g0137 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19079 | hp2 | a0002 | c0001 | t0001 | g0159 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19081 | hp1 | a0002 | c0001 | t0047 | g0217 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19081 | hp2 | a0019 | c0033 | t0004 | g0133 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19082 | hp2 | a0001 | c0003 | t0004 | g0143 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19084 | hp1 | a0001 | c0003 | t0053 | g0128 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19084 | hp2 | a0002 | c0001 | t0001 | g0242 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19085 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19085 | hp2 | a0001 | c0003 | t0006 | g0140 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19089 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19240 | hp1 | a0005 | c0014 | t0007 | g0155 | AFR | YRI | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA19240 | hp2 | a0020 | c0024 | t0055 | g0036 | AFR | YRI | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA20129 | hp1 | a0001 | c0003 | t0010 | g0156 | AFR | ASW | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA20129 | hp2 | a0002 | c0001 | t0003 | g0261 | AFR | ASW | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA20805 | hp1 | a0002 | c0001 | t0002 | g0209 | EUR | TSI | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA20805 | hp2 | a0002 | c0001 | t0003 | g0205 | EUR | TSI | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA20905 | hp1 | a0002 | c0001 | t0003 | g0238 | SAS | GIH | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA20905 | hp2 | a0002 | c0001 | t0001 | g0253 | SAS | GIH | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01123 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG01123 | hp2 | a0001 | c0002 | t0003 | g0082 | AMR | CLM | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02109 | hp1 | a0001 | c0007 | t0003 | g0166 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02109 | hp2 | a0001 | c0002 | t0067 | g0039 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02486 | hp1 | a0001 | c0003 | t0011 | g0121 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02486 | hp2 | a0001 | c0002 | t0007 | g0049 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG02559 | hp2 | a0001 | c0004 | t0054 | g0034 | AFR | ACB | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03471 | hp1 | a0001 | c0003 | t0011 | g0151 | AFR | MSL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG03471 | hp2 | a0003 | c0008 | t0014 | g0117 | AFR | MSL | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG06807 | hp1 | a0001 | c0003 | t0024 | g0114 | AFR | USA | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
HG06807 | hp2 | a0002 | c0027 | t0028 | g0212 | AFR | USA | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA20300 | hp1 | a0001 | c0002 | t0011 | g0043 | AFR | USA | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA20300 | hp2 | a0002 | c0001 | t0002 | g0029 | AFR | USA | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0071 | AFR | LWK | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
NA21309 | hp2 | a0001 | c0002 | t0015 | g0195 | AFR | LWK | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
homoSapiens | chm13v2 | a0021 | c0026 | t0002 | g0196 | REF | REF | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
homoSapiens | grch38p0 | a0001 | c0002 | t0061 | g0044 | REF | REF | TTF2_chr1_117055326_117112453 | TTF2 | chr1 | 117055326 | 117112453 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:117060509 | G | A | 2 | a0006 a0014 |
4 | HG02622.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
missense_variant | MODERATE | c.83G>A | p.Ser28Asn | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/23 | 104/9439 | 83/3489 | 28/1162 | chr1 | 117060509 | |||
chr1:117074976 | A | G | 1 | a0005 | 3 | HG01884.hp1 HG02970.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.392A>G | p.Lys131Arg | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 5/23 | 413/9439 | 392/3489 | 131/1162 | chr1 | 117074976 | |||
chr1:117075065 | C | G | 1 | a0011 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.481C>G | p.Gln161Glu | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 5/23 | 502/9439 | 481/3489 | 161/1162 | chr1 | 117075065 | |||
chr1:117075083 | A | G | 4 | a0002 a0011 a0012 others(1): Show |
140 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(137): Show |
missense_variant | MODERATE | c.499A>G | p.Lys167Glu | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 5/23 | 520/9439 | 499/3489 | 167/1162 | chr1 | 117075083 | |||
chr1:117075222 | A | G | 2 | a0004 a0014 |
6 | HG02622.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
missense_variant | MODERATE | c.638A>G | p.Lys213Arg | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 5/23 | 659/9439 | 638/3489 | 213/1162 | chr1 | 117075222 | |||
chr1:117075351 | A | G | 2 | a0009 a0020 |
3 | HG02055.hp2 HG02723.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.767A>G | p.Glu256Gly | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 5/23 | 788/9439 | 767/3489 | 256/1162 | chr1 | 117075351 | |||
chr1:117075402 | G | C | 1 | a0003 | 9 | HG02145.hp2 HG02257.hp2 HG02723.hp1 others(6): Show |
missense_variant | MODERATE | c.818G>C | p.Ser273Thr | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 5/23 | 839/9439 | 818/3489 | 273/1162 | chr1 | 117075402 | |||
chr1:117076700 | A | G | 1 | a0013 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.1450A>G | p.Thr484Ala | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 7/23 | 1471/9439 | 1450/3489 | 484/1162 | chr1 | 117076700 | |||
chr1:117076733 | C | T | 1 | a0010 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.1483C>T | p.Leu495Phe | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 7/23 | 1504/9439 | 1483/3489 | 495/1162 | chr1 | 117076733 | |||
chr1:117077984 | C | T | 1 | a0012 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.1642C>T | p.Arg548Cys | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 8/23 | 1663/9439 | 1642/3489 | 548/1162 | chr1 | 117077984 | |||
chr1:117084101 | C | T | 1 | a0017 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.1987C>T | p.Arg663Trp | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/23 | 2008/9439 | 1987/3489 | 663/1162 | chr1 | 117084101 | |||
chr1:117090602 | A | G | 1 | a0018 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.2567A>G | p.Asn856Ser | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 15/23 | 2588/9439 | 2567/3489 | 856/1162 | chr1 | 117090602 | |||
chr1:117091885 | G | A | 1 | a0008 | 2 | HG01891.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.2740G>A | p.Val914Ile | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 17/23 | 2761/9439 | 2740/3489 | 914/1162 | chr1 | 117091885 | |||
chr1:117092791 | A | G | 1 | a0007 | 2 | HG00323.hp2 HG02738.hp1 |
missense_variant | MODERATE | c.2866A>G | p.Ser956Gly | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/23 | 2887/9439 | 2866/3489 | 956/1162 | chr1 | 117092791 | |||
chr1:117092869 | G | C | 1 | a0019 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.2944G>C | p.Glu982Gln | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/23 | 2965/9439 | 2944/3489 | 982/1162 | chr1 | 117092869 | |||
chr1:117101416 | A | T | 1 | a0015 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.3381A>T | p.Leu1127Phe | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 3402/9439 | 3381/3489 | 1127/1162 | chr1 | 117101416 | |||
chr1:117101498 | G | C | 2 | a0016 a0020 |
2 | HG03225.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.3463G>C | p.Asp1155His | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 3484/9439 | 3463/3489 | 1155/1162 | chr1 | 117101498 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:117060534 | G | T | 7 | a0001c0003 a0002c0035 a0003c0008 others(4): Show |
57 | HG00642.hp1 HG01433.hp1 HG01496.hp2 others(54): Show |
synonymous_variant | LOW | c.108G>T | p.Thr36Thr | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/23 | 129/9439 | 108/3489 | 36/1162 | chr1 | 117060534 | |||
chr1:117075445 | C | T | 9 | a0002c0001 a0002c0013 a0002c0027 others(6): Show |
140 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(137): Show |
synonymous_variant | LOW | c.861C>T | p.Asn287Asn | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 5/23 | 882/9439 | 861/3489 | 287/1162 | chr1 | 117075445 | |||
chr1:117075691 | C | G | 1 | a0002c0031 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.1107C>G | p.Pro369Pro | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 5/23 | 1128/9439 | 1107/3489 | 369/1162 | chr1 | 117075691 | |||
chr1:117075845 | C | T | 2 | a0003c0008 a0003c0010 |
5 | HG02723.hp1 HG03139.hp2 HG03225.hp1 others(2): Show |
synonymous_variant | LOW | c.1261C>T | p.Leu421Leu | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 5/23 | 1282/9439 | 1261/3489 | 421/1162 | chr1 | 117075845 | |||
chr1:117076678 | G | A | 1 | a0001c0007 | 3 | HG02109.hp1 HG02895.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.1428G>A | p.Gln476Gln | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 7/23 | 1449/9439 | 1428/3489 | 476/1162 | chr1 | 117076678 | |||
chr1:117086474 | C | T | 2 | a0009c0025 a0020c0024 |
2 | HG02723.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.2112C>T | p.Pro704Pro | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/23 | 2133/9439 | 2112/3489 | 704/1162 | chr1 | 117086474 | |||
chr1:117091878 | C | T | 2 | a0002c0013 a0002c0028 |
3 | HG02451.hp1 HG02809.hp1 HG02886.hp2 |
synonymous_variant | LOW | c.2733C>T | p.Ser911Ser | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 17/23 | 2754/9439 | 2733/3489 | 911/1162 | chr1 | 117091878 | |||
chr1:117092778 | G | A | 3 | a0002c0013 a0002c0028 a0006c0015 |
4 | HG02451.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
synonymous_variant | LOW | c.2853G>A | p.Leu951Leu | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/23 | 2874/9439 | 2853/3489 | 951/1162 | chr1 | 117092778 | |||
chr1:117095344 | A | G | 4 | a0001c0004 a0003c0017 a0005c0036 others(1): Show |
9 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
synonymous_variant | LOW | c.3012A>G | p.Gln1004Gln | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 19/23 | 3033/9439 | 3012/3489 | 1004/1162 | chr1 | 117095344 | |||
chr1:117097368 | C | G | 1 | a0002c0028 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.3204C>G | p.Leu1068Leu | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/23 | 3225/9439 | 3204/3489 | 1068/1162 | chr1 | 117097368 | |||
chr1:117097374 | C | T | 2 | a0002c0027 a0016c0020 |
2 | HG03225.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.3210C>T | p.Ala1070Ala | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/23 | 3231/9439 | 3210/3489 | 1070/1162 | chr1 | 117097374 | |||
chr1:117101479 | C | T | 1 | a0001c0018 | 1 | NA18947.hp1 | synonymous_variant | LOW | c.3444C>T | p.Val1148Val | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 3465/9439 | 3444/3489 | 1148/1162 | chr1 | 117101479 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:117060338 | C | A | 63 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0003 others(60): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
5_prime_UTR_variant | MODIFIER | c.-9C>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 1/23 | 9 | chr1 | 117060338 | ||||||
chr1:117060343 | C | A | 1 | a0003c0010t0052 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-4C>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 1/23 | 4 | chr1 | 117060343 | ||||||
chr1:117101628 | A | G | 2 | a0001c0003t0014 a0003c0008t0014 |
3 | HG02717.hp2 HG02723.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*104A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 104 | chr1 | 117101628 | ||||||
chr1:117101862 | C | T | 1 | a0006c0009t0072 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*338C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 338 | chr1 | 117101862 | ||||||
chr1:117101977 | A | G | 2 | a0002c0001t0020 a0012c0030t0020 |
2 | HG00735.hp1 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*453A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 453 | chr1 | 117101977 | ||||||
chr1:117102002 | C | T | 1 | a0001c0002t0051 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*478C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 478 | chr1 | 117102002 | ||||||
chr1:117102291 | T | C | 1 | a0002c0001t0025 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*767T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 767 | chr1 | 117102291 | ||||||
chr1:117102315 | TCCCTGCA others(4): Show |
T | 31 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0019 others(28): Show |
86 | HG00323.hp2 HG00733.hp1 HG00738.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*803_*813delCCCTGC others(5): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 803 | INFO_REALIGN_3_PRIME | chr1 | 117102315 | |||||
chr1:117102739 | C | CCAATCCA others(21): Show |
1 | a0006c0009t0072 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1266_*1293dupTTGG others(24): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 1294 | INFO_REALIGN_3_PRIME | chr1 | 117102739 | |||||
chr1:117102789 | A | G | 2 | a0001c0002t0043 a0009c0025t0066 |
2 | HG02258.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1265A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 1265 | chr1 | 117102789 | ||||||
chr1:117102866 | A | C | 1 | a0001c0002t0050 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1342A>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 1342 | chr1 | 117102866 | ||||||
chr1:117102964 | A | T | 1 | a0002c0001t0042 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1440A>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 1440 | chr1 | 117102964 | ||||||
chr1:117102971 | T | C | 1 | a0001c0003t0053 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1447T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 1447 | chr1 | 117102971 | ||||||
chr1:117103012 | T | C | 53 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0011 others(50): Show |
132 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*1488T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 1488 | chr1 | 117103012 | ||||||
chr1:117103122 | A | G | 13 | a0001c0002t0002 a0001c0002t0018 a0001c0002t0022 others(10): Show |
45 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1598A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 1598 | chr1 | 117103122 | ||||||
chr1:117103159 | A | G | 1 | a0002c0001t0038 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1635A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 1635 | chr1 | 117103159 | ||||||
chr1:117103168 | A | G | 3 | a0001c0003t0071 a0002c0001t0009 a0002c0001t0049 |
9 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1644A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 1644 | chr1 | 117103168 | ||||||
chr1:117103293 | G | T | 2 | a0002c0013t0016 a0002c0028t0032 |
3 | HG02451.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1769G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 1769 | chr1 | 117103293 | ||||||
chr1:117103676 | C | A | 2 | a0016c0020t0056 a0020c0024t0055 |
2 | HG03225.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2152C>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 2152 | chr1 | 117103676 | ||||||
chr1:117103736 | C | T | 2 | a0002c0001t0030 a0002c0001t0031 |
2 | HG02818.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2212C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 2212 | chr1 | 117103736 | ||||||
chr1:117103939 | G | A | 1 | a0005c0036t0057 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2415G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 2415 | chr1 | 117103939 | ||||||
chr1:117103951 | C | CA | 10 | a0001c0002t0015 a0001c0002t0018 a0001c0002t0067 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02300.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2448dupA | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 2449 | INFO_REALIGN_3_PRIME | chr1 | 117103951 | |||||
chr1:117103951 | CA | C | 10 | a0001c0002t0019 a0001c0003t0021 a0002c0001t0012 others(7): Show |
13 | HG01070.hp2 HG01175.hp1 HG01516.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2448delA | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 2448 | INFO_REALIGN_3_PRIME | chr1 | 117103951 | |||||
chr1:117103951 | CAA | C | 21 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0050 others(18): Show |
76 | HG00323.hp2 HG00733.hp1 HG00738.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2447_*2448delAA | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 2447 | INFO_REALIGN_3_PRIME | chr1 | 117103951 | |||||
chr1:117103971 | A | G | 3 | a0001c0002t0003 a0003c0010t0052 a0003c0010t0064 |
3 | HG03139.hp2 HG03834.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2447A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 2447 | chr1 | 117103971 | ||||||
chr1:117103975 | G | A | 1 | a0001c0003t0069 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2451G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 2451 | chr1 | 117103975 | ||||||
chr1:117104185 | C | A | 1 | a0002c0001t0033 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2661C>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 2661 | chr1 | 117104185 | ||||||
chr1:117104274 | T | G | 1 | a0010c0021t0060 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2750T>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 2750 | chr1 | 117104274 | ||||||
chr1:117104321 | T | C | 1 | a0001c0002t0017 | 2 | NA18985.hp1 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2797T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 2797 | chr1 | 117104321 | ||||||
chr1:117104520 | G | A | 1 | a0001c0002t0034 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2996G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 2996 | chr1 | 117104520 | ||||||
chr1:117104754 | G | A | 1 | a0002c0001t0046 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3230G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 3230 | chr1 | 117104754 | ||||||
chr1:117104808 | G | T | 3 | a0002c0001t0048 a0006c0009t0072 a0016c0020t0056 |
3 | HG02965.hp2 HG03225.hp2 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3284G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 3284 | chr1 | 117104808 | ||||||
chr1:117104990 | C | T | 101 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0003 others(98): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*3466C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 3466 | chr1 | 117104990 | ||||||
chr1:117105049 | A | T | 1 | a0002c0001t0037 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3525A>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 3525 | chr1 | 117105049 | ||||||
chr1:117105216 | T | A | 1 | a0002c0001t0039 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3692T>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 3692 | chr1 | 117105216 | ||||||
chr1:117105259 | T | C | 1 | a0006c0009t0072 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3735T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 3735 | chr1 | 117105259 | ||||||
chr1:117105334 | T | C | 1 | a0002c0001t0013 | 3 | HG00408.hp1 NA18971.hp2 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3810T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 3810 | chr1 | 117105334 | ||||||
chr1:117105536 | G | C | 1 | a0002c0001t0038 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4012G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 4012 | chr1 | 117105536 | ||||||
chr1:117105545 | C | T | 1 | a0001c0002t0063 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4021C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 4021 | chr1 | 117105545 | ||||||
chr1:117105647 | G | A | 23 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0019 others(20): Show |
66 | HG00323.hp2 HG00733.hp1 HG00738.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*4123G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 4123 | chr1 | 117105647 | ||||||
chr1:117105794 | T | A | 1 | a0002c0001t0030 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4270T>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 4270 | chr1 | 117105794 | ||||||
chr1:117106008 | T | G | 1 | a0002c0001t0036 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4484T>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 4484 | chr1 | 117106008 | ||||||
chr1:117106079 | T | C | 2 | a0005c0036t0057 a0008c0011t0058 |
2 | HG01884.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4555T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 4555 | chr1 | 117106079 | ||||||
chr1:117106262 | G | T | 1 | a0001c0002t0051 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4738G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 4738 | chr1 | 117106262 | ||||||
chr1:117106273 | G | GA | 40 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0008 others(37): Show |
111 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*4762dupA | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 4763 | INFO_REALIGN_3_PRIME | chr1 | 117106273 | |||||
chr1:117106407 | G | C | 1 | a0001c0003t0062 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4883G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 4883 | chr1 | 117106407 | ||||||
chr1:117106496 | T | C | 1 | a0002c0001t0026 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4972T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 4972 | chr1 | 117106496 | ||||||
chr1:117106502 | G | A | 1 | a0001c0003t0024 | 2 | HG01433.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4978G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 4978 | chr1 | 117106502 | ||||||
chr1:117106893 | G | C | 1 | a0016c0020t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5369G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 5369 | chr1 | 117106893 | ||||||
chr1:117106971 | A | G | 1 | a0001c0003t0070 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5447A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 5447 | chr1 | 117106971 | ||||||
chr1:117107344 | A | T | 1 | a0002c0001t0040 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5820A>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 23/23 | 5820 | chr1 | 117107344 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:117060404 | G | T | 2 | a0001c0002t0004g0267 a0003c0010t0052g0266 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.28+30G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 1/22 | chr1 | 117060404 | |||||||
chr1:117060566 | G | T | 195 | a0001c0002t0001g0020 a0001c0002t0001g0162 a0001c0002t0001g0163 others(192): Show |
238 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.131+9G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117060566 | |||||||
chr1:117060720 | T | A | 1 | a0002c0001t0001g0113 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.131+163T>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117060720 | |||||||
chr1:117060888 | C | T | 3 | a0001c0002t0004g0013 a0010c0021t0060g0013 a0016c0020t0056g0112 |
3 | HG01243.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.131+331C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117060888 | |||||||
chr1:117060977 | T | A | 51 | a0001c0003t0004g0015 a0001c0003t0004g0018 a0001c0003t0004g0118 others(48): Show |
57 | HG00642.hp1 HG01433.hp1 HG01496.hp2 others(54): Show |
intron_variant | MODIFIER | c.131+420T>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117060977 | |||||||
chr1:117061023 | C | G | 190 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(187): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.131+466C>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117061023 | |||||||
chr1:117061080 | G | A | 6 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0002t0002g0070 others(3): Show |
6 | HG01081.hp2 HG01109.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.131+523G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117061080 | |||||||
chr1:117061183 | G | A | 51 | a0001c0003t0004g0015 a0001c0003t0004g0018 a0001c0003t0004g0118 others(48): Show |
57 | HG00642.hp1 HG01433.hp1 HG01496.hp2 others(54): Show |
intron_variant | MODIFIER | c.131+626G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117061183 | |||||||
chr1:117061187 | C | T | 51 | a0001c0003t0004g0015 a0001c0003t0004g0018 a0001c0003t0004g0118 others(48): Show |
57 | HG00642.hp1 HG01433.hp1 HG01496.hp2 others(54): Show |
intron_variant | MODIFIER | c.131+630C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117061187 | |||||||
chr1:117061234 | T | TA | 50 | a0001c0003t0004g0015 a0001c0003t0004g0018 a0001c0003t0004g0118 others(47): Show |
56 | HG00642.hp1 HG01433.hp1 HG01496.hp2 others(53): Show |
intron_variant | MODIFIER | c.131+685dupA | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 117061234 | ||||||
chr1:117061245 | G | T | 4 | a0006c0009t0004g0065 a0006c0009t0072g0066 a0006c0015t0011g0063 others(1): Show |
4 | HG02622.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.131+688G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117061245 | |||||||
chr1:117061249 | A | G | 51 | a0001c0003t0004g0015 a0001c0003t0004g0018 a0001c0003t0004g0118 others(48): Show |
57 | HG00642.hp1 HG01433.hp1 HG01496.hp2 others(54): Show |
intron_variant | MODIFIER | c.131+692A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117061249 | |||||||
chr1:117061270 | T | A | 1 | a0001c0004t0054g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131+713T>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117061270 | |||||||
chr1:117061584 | G | A | 8 | a0001c0002t0007g0035 a0001c0002t0067g0039 a0001c0004t0054g0034 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.132-803G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117061584 | |||||||
chr1:117061615 | C | T | 1 | a0002c0001t0031g0265 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.132-772C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117061615 | |||||||
chr1:117061939 | G | C | 4 | a0006c0009t0004g0065 a0006c0009t0072g0066 a0006c0015t0011g0063 others(1): Show |
4 | HG02622.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.132-448G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117061939 | |||||||
chr1:117061948 | C | T | 51 | a0001c0003t0004g0015 a0001c0003t0004g0018 a0001c0003t0004g0118 others(48): Show |
57 | HG00642.hp1 HG01433.hp1 HG01496.hp2 others(54): Show |
intron_variant | MODIFIER | c.132-439C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117061948 | |||||||
chr1:117061994 | G | A | 52 | a0001c0003t0004g0015 a0001c0003t0004g0018 a0001c0003t0004g0118 others(49): Show |
58 | HG00642.hp1 HG01433.hp1 HG01496.hp2 others(55): Show |
intron_variant | MODIFIER | c.132-393G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117061994 | |||||||
chr1:117062039 | G | T | 6 | a0001c0003t0006g0152 a0001c0003t0010g0156 a0001c0003t0011g0151 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.132-348G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117062039 | |||||||
chr1:117062076 | C | T | 2 | a0001c0002t0003g0263 a0001c0002t0008g0264 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.132-311C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117062076 | |||||||
chr1:117062105 | G | A | 1 | a0001c0002t0051g0073 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.132-282G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117062105 | |||||||
chr1:117062109 | G | A | 1 | a0001c0002t0029g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.132-278G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117062109 | |||||||
chr1:117062233 | A | G | 31 | a0001c0003t0004g0018 a0001c0003t0004g0126 a0001c0003t0004g0129 others(28): Show |
36 | HG00642.hp1 HG01496.hp2 HG01943.hp1 others(33): Show |
intron_variant | MODIFIER | c.132-154A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 2/22 | chr1 | 117062233 | |||||||
chr1:117062508 | CT | C | 40 | a0001c0002t0001g0020 a0001c0002t0001g0162 a0001c0002t0001g0163 others(37): Show |
43 | HG00408.hp2 HG00544.hp2 HG01516.hp1 others(40): Show |
intron_variant | MODIFIER | c.218+49delT | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117062508 | ||||||
chr1:117062518 | T | C | 1 | a0002c0001t0001g0159 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.218+45T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117062518 | |||||||
chr1:117062590 | AT | A | 2 | a0001c0002t0010g0010 a0001c0002t0010g0042 |
3 | HG02257.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.218+120delT | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117062590 | ||||||
chr1:117062714 | G | A | 51 | a0001c0003t0004g0015 a0001c0003t0004g0018 a0001c0003t0004g0118 others(48): Show |
57 | HG00642.hp1 HG01433.hp1 HG01496.hp2 others(54): Show |
intron_variant | MODIFIER | c.218+241G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117062714 | |||||||
chr1:117062822 | A | G | 103 | a0001c0002t0003g0250 a0002c0001t0001g0001 a0002c0001t0001g0002 others(100): Show |
137 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.218+349A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117062822 | |||||||
chr1:117063579 | A | C | 28 | a0001c0002t0003g0193 a0001c0002t0004g0011 a0001c0002t0004g0013 others(25): Show |
30 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.218+1106A>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117063579 | |||||||
chr1:117064017 | G | T | 9 | a0001c0002t0043g0192 a0003c0006t0003g0188 a0003c0006t0003g0189 others(6): Show |
9 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+1544G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117064017 | |||||||
chr1:117064199 | C | T | 33 | a0001c0002t0001g0020 a0001c0002t0001g0162 a0001c0002t0001g0163 others(30): Show |
36 | HG00408.hp2 HG00544.hp2 HG01516.hp1 others(33): Show |
intron_variant | MODIFIER | c.218+1726C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117064199 | |||||||
chr1:117064333 | T | C | 262 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(259): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.218+1860T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117064333 | |||||||
chr1:117064469 | A | C | 1 | a0001c0002t0004g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.218+1996A>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117064469 | |||||||
chr1:117064508 | TTTTG | T | 262 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(259): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.218+2055_218+2058d others(6): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117064508 | ||||||
chr1:117064797 | G | T | 1 | a0001c0003t0062g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.218+2324G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117064797 | |||||||
chr1:117064820 | G | GT | 81 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0079 others(78): Show |
84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.218+2359dupT | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117064820 | ||||||
chr1:117064820 | G | GTT | 9 | a0001c0002t0043g0192 a0003c0006t0003g0188 a0003c0006t0003g0189 others(6): Show |
9 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+2358_218+2359d others(4): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117064820 | ||||||
chr1:117064839 | CT | C | 29 | a0001c0002t0003g0193 a0001c0002t0004g0011 a0001c0002t0004g0013 others(26): Show |
31 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.218+2377delT | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117064839 | ||||||
chr1:117065258 | T | C | 2 | a0001c0002t0001g0075 a0001c0002t0001g0076 |
2 | NA19056.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.218+2785T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117065258 | |||||||
chr1:117065293 | T | C | 1 | a0001c0004t0054g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.218+2820T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117065293 | |||||||
chr1:117065348 | T | C | 28 | a0001c0002t0001g0020 a0001c0002t0001g0162 a0001c0002t0001g0163 others(25): Show |
31 | HG00408.hp2 HG00544.hp2 HG01516.hp1 others(28): Show |
intron_variant | MODIFIER | c.218+2875T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117065348 | |||||||
chr1:117065374 | G | A | 42 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0079 others(39): Show |
43 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.218+2901G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117065374 | |||||||
chr1:117065387 | A | G | 1 | a0014c0016t0068g0064 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+2914A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117065387 | |||||||
chr1:117065418 | G | T | 2 | a0002c0001t0002g0029 a0002c0031t0002g0029 |
2 | HG00738.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.218+2945G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117065418 | |||||||
chr1:117065470 | C | T | 4 | a0004c0005t0003g0109 a0004c0005t0003g0110 a0004c0005t0003g0111 others(1): Show |
4 | HG02895.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+2997C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117065470 | |||||||
chr1:117065471 | G | A | 1 | a0001c0003t0024g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.218+2998G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117065471 | |||||||
chr1:117065503 | C | A | 3 | a0003c0008t0014g0116 a0003c0008t0014g0117 a0003c0008t0021g0115 |
3 | HG02723.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.218+3030C>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117065503 | |||||||
chr1:117065522 | C | T | 1 | a0001c0002t0011g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.218+3049C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117065522 | |||||||
chr1:117065553 | C | T | 1 | a0001c0002t0043g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.218+3080C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117065553 | |||||||
chr1:117065720 | A | T | 1 | a0002c0001t0048g0252 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.218+3247A>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117065720 | |||||||
chr1:117065781 | G | GTTA | 252 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(249): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.218+3310_218+3312d others(5): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117065781 | ||||||
chr1:117065824 | G | T | 1 | a0001c0002t0019g0107 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.218+3351G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117065824 | |||||||
chr1:117065825 | G | T | 1 | a0001c0002t0019g0107 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.218+3352G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117065825 | |||||||
chr1:117065988 | C | CT | 81 | a0001c0002t0001g0020 a0001c0002t0001g0097 a0001c0002t0001g0100 others(78): Show |
89 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.218+3544dupT | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117065988 | ||||||
chr1:117065988 | C | CTT | 25 | a0001c0002t0001g0182 a0001c0002t0001g0183 a0001c0002t0008g0106 others(22): Show |
26 | HG00408.hp2 HG00544.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.218+3543_218+3544d others(4): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117065988 | ||||||
chr1:117065988 | C | CTTT | 6 | a0001c0003t0004g0015 a0001c0003t0014g0123 a0001c0003t0024g0114 others(3): Show |
7 | HG01433.hp1 HG02055.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+3542_218+3544d others(5): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117065988 | ||||||
chr1:117065988 | CT | C | 8 | a0001c0002t0001g0075 a0001c0002t0003g0078 a0001c0002t0003g0250 others(5): Show |
8 | HG00323.hp1 HG01361.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+3544delT | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117065988 | ||||||
chr1:117065988 | CTTTTTTT others(3): Show |
C | 1 | a0002c0001t0002g0249 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.218+3535_218+3544d others(12): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117065988 | ||||||
chr1:117065988 | CTTTTTTT others(4): Show |
C | 106 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(103): Show |
140 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.218+3534_218+3544d others(13): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117065988 | ||||||
chr1:117065988 | CTTTTTTT others(5): Show |
C | 1 | a0002c0001t0002g0077 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.218+3533_218+3544d others(14): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117065988 | ||||||
chr1:117066029 | G | T | 1 | a0002c0035t0065g0125 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.218+3556G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117066029 | |||||||
chr1:117066058 | A | G | 1 | a0001c0002t0029g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.218+3585A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117066058 | |||||||
chr1:117066519 | C | T | 2 | a0001c0002t0004g0061 a0006c0009t0004g0065 |
2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.218+4046C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117066519 | |||||||
chr1:117066695 | CT | C | 183 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(180): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.218+4245delT | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117066695 | ||||||
chr1:117066695 | CTT | C | 60 | a0001c0002t0001g0079 a0001c0002t0003g0080 a0001c0002t0043g0192 others(57): Show |
66 | HG00642.hp1 HG01069.hp1 HG01433.hp1 others(63): Show |
intron_variant | MODIFIER | c.218+4244_218+4245d others(4): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117066695 | ||||||
chr1:117066718 | T | A | 5 | a0001c0003t0004g0015 a0001c0003t0004g0118 a0001c0003t0014g0123 others(2): Show |
6 | HG01433.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+4245T>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117066718 | |||||||
chr1:117066893 | G | T | 1 | a0002c0001t0001g0246 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.218+4420G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117066893 | |||||||
chr1:117066923 | A | G | 252 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(249): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.218+4450A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117066923 | |||||||
chr1:117067137 | G | A | 4 | a0004c0005t0003g0109 a0004c0005t0003g0110 a0004c0005t0003g0111 others(1): Show |
4 | HG02895.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+4664G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117067137 | |||||||
chr1:117067326 | G | A | 40 | a0001c0003t0004g0018 a0001c0003t0004g0126 a0001c0003t0004g0129 others(37): Show |
45 | HG00642.hp1 HG01496.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.218+4853G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117067326 | |||||||
chr1:117067423 | A | G | 2 | a0002c0001t0005g0033 a0002c0001t0005g0262 |
3 | HG01943.hp2 HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.218+4950A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117067423 | |||||||
chr1:117067448 | C | T | 1 | a0001c0003t0070g0141 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.218+4975C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117067448 | |||||||
chr1:117067498 | C | A | 1 | a0001c0002t0011g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.218+5025C>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117067498 | |||||||
chr1:117067524 | C | CA | 23 | a0001c0002t0001g0081 a0001c0002t0002g0161 a0001c0002t0003g0082 others(20): Show |
29 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.218+5075dupA | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117067524 | ||||||
chr1:117067524 | C | CAA | 7 | a0002c0001t0003g0202 a0002c0001t0005g0030 a0002c0001t0005g0254 others(4): Show |
8 | HG00621.hp2 HG02165.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+5074_218+5075d others(4): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117067524 | ||||||
chr1:117067524 | CA | C | 55 | a0001c0002t0001g0095 a0001c0002t0001g0096 a0001c0002t0002g0071 others(52): Show |
60 | HG00642.hp1 HG01070.hp1 HG01358.hp1 others(57): Show |
intron_variant | MODIFIER | c.218+5075delA | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117067524 | ||||||
chr1:117067823 | A | G | 5 | a0003c0008t0014g0116 a0003c0008t0014g0117 a0003c0008t0021g0115 others(2): Show |
5 | HG02723.hp1 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+5350A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117067823 | |||||||
chr1:117067830 | T | C | 2 | a0002c0001t0001g0113 a0002c0001t0001g0207 |
2 | HG01167.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.218+5357T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117067830 | |||||||
chr1:117067939 | G | T | 1 | a0001c0002t0008g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.218+5466G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117067939 | |||||||
chr1:117067991 | A | G | 252 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(249): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.218+5518A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117067991 | |||||||
chr1:117067999 | G | A | 1 | a0001c0002t0015g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218+5526G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117067999 | |||||||
chr1:117068362 | G | A | 1 | a0001c0002t0002g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.219-5299G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117068362 | |||||||
chr1:117068461 | C | T | 1 | a0001c0002t0010g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.219-5200C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117068461 | |||||||
chr1:117068543 | T | TA | 10 | a0001c0002t0004g0013 a0001c0002t0004g0047 a0001c0002t0004g0061 others(7): Show |
10 | HG01175.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-5104dupA | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117068543 | ||||||
chr1:117068551 | A | G | 5 | a0003c0008t0014g0116 a0003c0008t0014g0117 a0003c0008t0021g0115 others(2): Show |
5 | HG02723.hp1 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-5110A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117068551 | |||||||
chr1:117068821 | C | T | 1 | a0001c0003t0004g0130 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.219-4840C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117068821 | |||||||
chr1:117068968 | T | A | 53 | a0001c0002t0043g0192 a0001c0003t0004g0018 a0001c0003t0004g0126 others(50): Show |
58 | HG00642.hp1 HG01496.hp2 HG01884.hp1 others(55): Show |
intron_variant | MODIFIER | c.219-4693T>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117068968 | |||||||
chr1:117069082 | T | C | 1 | a0012c0030t0020g0208 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.219-4579T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117069082 | |||||||
chr1:117069169 | G | A | 1 | a0002c0001t0002g0209 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.219-4492G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117069169 | |||||||
chr1:117069299 | G | A | 2 | a0008c0011t0011g0040 a0008c0011t0058g0038 |
2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.219-4362G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117069299 | |||||||
chr1:117069352 | G | T | 5 | a0001c0003t0004g0015 a0001c0003t0004g0118 a0001c0003t0014g0123 others(2): Show |
6 | HG01433.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-4309G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117069352 | |||||||
chr1:117069519 | C | T | 30 | a0001c0003t0004g0018 a0001c0003t0004g0126 a0001c0003t0004g0129 others(27): Show |
35 | HG00642.hp1 HG01496.hp2 HG01943.hp1 others(32): Show |
intron_variant | MODIFIER | c.219-4142C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117069519 | |||||||
chr1:117069546 | C | T | 5 | a0001c0003t0004g0015 a0001c0003t0004g0118 a0001c0003t0014g0123 others(2): Show |
6 | HG01433.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-4115C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117069546 | |||||||
chr1:117069676 | A | C | 86 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(83): Show |
113 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.219-3985A>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117069676 | |||||||
chr1:117069701 | G | A | 5 | a0001c0003t0004g0015 a0001c0003t0004g0118 a0001c0003t0014g0123 others(2): Show |
6 | HG01433.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-3960G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117069701 | |||||||
chr1:117069708 | G | A | 50 | a0001c0002t0043g0192 a0001c0003t0004g0018 a0001c0003t0004g0126 others(47): Show |
55 | HG00642.hp1 HG01496.hp2 HG01884.hp1 others(52): Show |
intron_variant | MODIFIER | c.219-3953G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117069708 | |||||||
chr1:117069792 | G | C | 2 | a0002c0001t0001g0113 a0002c0001t0001g0207 |
2 | HG01167.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.219-3869G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117069792 | |||||||
chr1:117069890 | A | G | 5 | a0001c0003t0004g0015 a0001c0003t0004g0118 a0001c0003t0014g0123 others(2): Show |
6 | HG01433.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-3771A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117069890 | |||||||
chr1:117069899 | A | G | 1 | a0006c0009t0072g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.219-3762A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117069899 | |||||||
chr1:117070049 | T | C | 79 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(76): Show |
83 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.219-3612T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117070049 | |||||||
chr1:117070362 | T | C | 1 | a0001c0002t0007g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.219-3299T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117070362 | |||||||
chr1:117070472 | G | C | 1 | a0002c0001t0009g0023 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.219-3189G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117070472 | |||||||
chr1:117070730 | T | A | 2 | a0001c0002t0001g0162 a0001c0002t0027g0180 |
2 | HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.219-2931T>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117070730 | |||||||
chr1:117070852 | G | T | 1 | a0014c0016t0068g0064 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.219-2809G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117070852 | |||||||
chr1:117071214 | T | C | 2 | a0002c0001t0030g0213 a0002c0027t0028g0212 |
2 | HG02886.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.219-2447T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117071214 | |||||||
chr1:117071437 | A | G | 2 | a0007c0012t0003g0093 a0007c0012t0003g0094 |
2 | HG00323.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.219-2224A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117071437 | |||||||
chr1:117071565 | T | A | 40 | a0001c0003t0004g0018 a0001c0003t0004g0126 a0001c0003t0004g0129 others(37): Show |
45 | HG00642.hp1 HG01496.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.219-2096T>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117071565 | |||||||
chr1:117071571 | G | A | 2 | a0002c0001t0030g0213 a0002c0027t0028g0212 |
2 | HG02886.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.219-2090G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117071571 | |||||||
chr1:117071596 | T | C | 1 | a0001c0002t0001g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.219-2065T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117071596 | |||||||
chr1:117071628 | CAA | C | 107 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(104): Show |
141 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.219-2030_219-2029d others(4): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117071628 | ||||||
chr1:117071660 | CAATT | C | 6 | a0001c0002t0004g0056 a0001c0002t0010g0010 a0001c0002t0010g0042 others(3): Show |
7 | HG02257.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-1998_219-1995d others(6): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117071660 | ||||||
chr1:117071778 | T | C | 1 | a0002c0001t0037g0199 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.219-1883T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117071778 | |||||||
chr1:117072151 | A | G | 30 | a0001c0003t0004g0018 a0001c0003t0004g0126 a0001c0003t0004g0129 others(27): Show |
35 | HG00642.hp1 HG01496.hp2 HG01943.hp1 others(32): Show |
intron_variant | MODIFIER | c.219-1510A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117072151 | |||||||
chr1:117072422 | C | CT | 91 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(88): Show |
96 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.219-1218dupT | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117072422 | ||||||
chr1:117072422 | C | CTT | 55 | a0001c0002t0001g0183 a0001c0002t0002g0105 a0001c0002t0003g0072 others(52): Show |
60 | HG00544.hp2 HG00642.hp1 HG01123.hp2 others(57): Show |
intron_variant | MODIFIER | c.219-1219_219-1218d others(4): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 117072422 | ||||||
chr1:117072499 | A | G | 1 | a0002c0001t0003g0205 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.219-1162A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117072499 | |||||||
chr1:117072680 | C | T | 1 | a0002c0001t0001g0240 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.219-981C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117072680 | |||||||
chr1:117072700 | G | A | 1 | a0002c0001t0001g0240 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.219-961G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117072700 | |||||||
chr1:117072707 | G | A | 3 | a0009c0023t0001g0187 a0009c0025t0066g0037 a0020c0024t0055g0036 |
3 | HG02055.hp2 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.219-954G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117072707 | |||||||
chr1:117072713 | G | A | 2 | a0002c0001t0003g0214 a0002c0001t0003g0215 |
2 | HG01109.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.219-948G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117072713 | |||||||
chr1:117072774 | C | A | 1 | a0001c0002t0001g0095 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.219-887C>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117072774 | |||||||
chr1:117072893 | G | A | 4 | a0004c0005t0003g0109 a0004c0005t0003g0110 a0004c0005t0003g0111 others(1): Show |
4 | HG02895.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-768G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117072893 | |||||||
chr1:117073118 | T | C | 1 | a0001c0002t0008g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.219-543T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117073118 | |||||||
chr1:117073134 | G | A | 5 | a0001c0003t0004g0015 a0001c0003t0004g0118 a0001c0003t0014g0123 others(2): Show |
6 | HG01433.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-527G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117073134 | |||||||
chr1:117073273 | G | T | 1 | a0002c0001t0001g0239 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.219-388G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117073273 | |||||||
chr1:117073313 | A | G | 252 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(249): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.219-348A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117073313 | |||||||
chr1:117073657 | T | C | 29 | a0001c0002t0001g0020 a0001c0002t0001g0162 a0001c0002t0001g0163 others(26): Show |
32 | HG00408.hp2 HG00544.hp2 HG01516.hp1 others(29): Show |
splice_region_variant&intron_variant | LOW | c.219-4T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 3/22 | chr1 | 117073657 | |||||||
chr1:117074004 | G | T | 1 | a0006c0015t0011g0063 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.285+277G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 4/22 | chr1 | 117074004 | |||||||
chr1:117074026 | A | G | 81 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(78): Show |
85 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.285+299A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 4/22 | chr1 | 117074026 | |||||||
chr1:117074048 | A | G | 89 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(86): Show |
116 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.285+321A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 4/22 | chr1 | 117074048 | |||||||
chr1:117074271 | C | T | 3 | a0002c0001t0002g0005 a0002c0001t0003g0238 a0002c0001t0041g0005 |
5 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+544C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 4/22 | chr1 | 117074271 | |||||||
chr1:117074283 | T | C | 1 | a0001c0004t0015g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.285+556T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 4/22 | chr1 | 117074283 | |||||||
chr1:117074310 | A | G | 1 | a0001c0002t0001g0104 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.286-560A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 4/22 | chr1 | 117074310 | |||||||
chr1:117074460 | T | C | 3 | a0009c0023t0001g0187 a0009c0025t0066g0037 a0020c0024t0055g0036 |
3 | HG02055.hp2 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.286-410T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 4/22 | chr1 | 117074460 | |||||||
chr1:117074472 | G | A | 1 | a0001c0002t0027g0180 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.286-398G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 4/22 | chr1 | 117074472 | |||||||
chr1:117074476 | T | C | 1 | a0002c0001t0003g0214 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.286-394T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 4/22 | chr1 | 117074476 | |||||||
chr1:117074516 | A | G | 1 | a0006c0009t0004g0065 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.286-354A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 4/22 | chr1 | 117074516 | |||||||
chr1:117074702 | ACTAT | A | 16 | a0002c0001t0001g0031 a0002c0001t0001g0253 a0002c0001t0005g0008 others(13): Show |
23 | HG00597.hp2 HG00621.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.286-163_286-160del others(4): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 117074702 | ||||||
chr1:117074814 | CTAG | C | 3 | a0002c0001t0001g0003 a0002c0001t0001g0216 a0002c0001t0005g0254 |
7 | HG01981.hp1 HG02083.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.286-55_286-53delTA others(1): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 4/22 | chr1 | 117074814 | |||||||
chr1:117074843 | T | C | 1 | a0006c0015t0011g0063 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.286-27T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 4/22 | chr1 | 117074843 | |||||||
chr1:117075976 | A | G | 1 | a0001c0002t0004g0059 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1275+117A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 5/22 | chr1 | 117075976 | |||||||
chr1:117076100 | T | C | 279 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(276): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1276-80T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 5/22 | chr1 | 117076100 | |||||||
chr1:117076352 | G | A | 53 | a0001c0002t0043g0192 a0001c0003t0004g0018 a0001c0003t0004g0126 others(50): Show |
58 | HG00642.hp1 HG01496.hp2 HG01884.hp1 others(55): Show |
intron_variant | MODIFIER | c.1390+58G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 6/22 | chr1 | 117076352 | |||||||
chr1:117076584 | G | A | 1 | a0001c0002t0007g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1391-57G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 6/22 | chr1 | 117076584 | |||||||
chr1:117076967 | A | G | 1 | a0001c0002t0008g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1573+144A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 7/22 | chr1 | 117076967 | |||||||
chr1:117077311 | A | G | 1 | a0001c0004t0054g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1573+488A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 7/22 | chr1 | 117077311 | |||||||
chr1:117077314 | G | A | 106 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(103): Show |
140 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1573+491G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 7/22 | chr1 | 117077314 | |||||||
chr1:117077432 | A | G | 4 | a0001c0002t0015g0195 a0001c0002t0067g0039 a0008c0011t0011g0040 others(1): Show |
4 | HG01891.hp2 HG02109.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1574-484A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 7/22 | chr1 | 117077432 | |||||||
chr1:117077490 | G | A | 1 | a0001c0004t0001g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1574-426G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 7/22 | chr1 | 117077490 | |||||||
chr1:117077551 | A | G | 1 | a0001c0002t0008g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1574-365A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 7/22 | chr1 | 117077551 | |||||||
chr1:117077726 | TG | T | 53 | a0001c0002t0043g0192 a0001c0003t0004g0018 a0001c0003t0004g0126 others(50): Show |
58 | HG00642.hp1 HG01496.hp2 HG01884.hp1 others(55): Show |
intron_variant | MODIFIER | c.1574-188delG | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr1 | 117077726 | ||||||
chr1:117077762 | C | G | 17 | a0002c0001t0001g0031 a0002c0001t0001g0253 a0002c0001t0005g0008 others(14): Show |
24 | HG00597.hp2 HG00621.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1574-154C>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 7/22 | chr1 | 117077762 | |||||||
chr1:117077783 | A | G | 1 | a0006c0009t0072g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1574-133A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 7/22 | chr1 | 117077783 | |||||||
chr1:117078457 | G | C | 1 | a0001c0003t0023g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1701+414G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 8/22 | chr1 | 117078457 | |||||||
chr1:117078484 | C | T | 1 | a0001c0002t0001g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1701+441C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 8/22 | chr1 | 117078484 | |||||||
chr1:117078551 | G | A | 3 | a0009c0023t0001g0187 a0009c0025t0066g0037 a0020c0024t0055g0036 |
3 | HG02055.hp2 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1701+508G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 8/22 | chr1 | 117078551 | |||||||
chr1:117078565 | G | T | 1 | a0008c0011t0011g0040 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1701+522G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 8/22 | chr1 | 117078565 | |||||||
chr1:117078659 | T | G | 46 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0079 others(43): Show |
47 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.1701+616T>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 8/22 | chr1 | 117078659 | |||||||
chr1:117078812 | G | A | 1 | a0001c0003t0006g0132 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1702-756G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 8/22 | chr1 | 117078812 | |||||||
chr1:117079019 | C | G | 79 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(76): Show |
83 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1702-549C>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 8/22 | chr1 | 117079019 | |||||||
chr1:117079066 | C | T | 1 | a0002c0001t0012g0237 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1702-502C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 8/22 | chr1 | 117079066 | |||||||
chr1:117079206 | C | T | 1 | a0002c0001t0012g0257 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1702-362C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 8/22 | chr1 | 117079206 | |||||||
chr1:117079223 | G | A | 8 | a0001c0003t0004g0134 a0001c0003t0004g0144 a0001c0003t0004g0145 others(5): Show |
8 | HG00642.hp1 HG01496.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1702-345G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 8/22 | chr1 | 117079223 | |||||||
chr1:117079325 | G | C | 42 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0079 others(39): Show |
43 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1702-243G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 8/22 | chr1 | 117079325 | |||||||
chr1:117079522 | T | G | 1 | a0001c0002t0002g0165 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1702-46T>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 8/22 | chr1 | 117079522 | |||||||
chr1:117079664 | A | G | 111 | a0001c0002t0004g0011 a0001c0002t0004g0052 a0001c0002t0004g0053 others(108): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1783+15A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117079664 | |||||||
chr1:117080007 | T | C | 2 | a0001c0002t0003g0263 a0001c0002t0008g0264 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1783+358T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117080007 | |||||||
chr1:117080008 | C | CT | 7 | a0001c0002t0002g0105 a0001c0002t0003g0263 a0001c0002t0007g0035 others(4): Show |
7 | HG01978.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1783+377dupT | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr1 | 117080008 | ||||||
chr1:117080029 | G | C | 1 | a0001c0003t0023g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1783+380G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117080029 | |||||||
chr1:117080142 | TG | T | 3 | a0001c0002t0003g0263 a0001c0002t0007g0035 a0001c0002t0008g0264 |
3 | HG02818.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1783+496delG | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr1 | 117080142 | ||||||
chr1:117080262 | T | C | 1 | a0014c0016t0068g0064 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1783+613T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117080262 | |||||||
chr1:117080408 | G | C | 260 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(257): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1783+759G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117080408 | |||||||
chr1:117080446 | A | T | 6 | a0004c0005t0003g0109 a0004c0005t0003g0110 a0004c0005t0003g0111 others(3): Show |
6 | HG02622.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1783+797A>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117080446 | |||||||
chr1:117080470 | G | T | 1 | a0002c0001t0033g0236 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1783+821G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117080470 | |||||||
chr1:117080651 | C | T | 1 | a0006c0009t0072g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1783+1002C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117080651 | |||||||
chr1:117080795 | G | C | 1 | a0001c0002t0001g0104 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1784-1033G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117080795 | |||||||
chr1:117080806 | C | T | 1 | a0001c0002t0011g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1784-1022C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117080806 | |||||||
chr1:117080814 | C | G | 1 | a0001c0002t0004g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1784-1014C>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117080814 | |||||||
chr1:117080933 | T | C | 1 | a0001c0002t0035g0083 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1784-895T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117080933 | |||||||
chr1:117081108 | T | C | 1 | a0001c0002t0067g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1784-720T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117081108 | |||||||
chr1:117081116 | C | G | 1 | a0002c0001t0001g0235 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1784-712C>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117081116 | |||||||
chr1:117081354 | C | T | 1 | a0001c0003t0070g0141 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1784-474C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117081354 | |||||||
chr1:117081670 | G | C | 50 | a0001c0002t0043g0192 a0001c0003t0004g0018 a0001c0003t0004g0126 others(47): Show |
55 | HG00642.hp1 HG01496.hp2 HG01884.hp1 others(52): Show |
intron_variant | MODIFIER | c.1784-158G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117081670 | |||||||
chr1:117081710 | C | T | 1 | a0002c0001t0005g0256 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1784-118C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 9/22 | chr1 | 117081710 | |||||||
chr1:117081985 | G | A | 1 | a0002c0001t0001g0219 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1903+38G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117081985 | |||||||
chr1:117082236 | CAG | C | 106 | a0001c0004t0054g0034 a0002c0001t0001g0001 a0002c0001t0001g0002 others(103): Show |
140 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1903+290_1903+291d others(4): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117082236 | |||||||
chr1:117082599 | C | G | 3 | a0009c0023t0001g0187 a0009c0025t0066g0037 a0020c0024t0055g0036 |
3 | HG02055.hp2 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1903+652C>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117082599 | |||||||
chr1:117082734 | T | C | 2 | a0002c0001t0002g0249 a0002c0001t0040g0220 |
2 | HG00639.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1903+787T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117082734 | |||||||
chr1:117082744 | A | G | 7 | a0001c0002t0004g0056 a0001c0002t0007g0057 a0001c0002t0010g0010 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1903+797A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117082744 | |||||||
chr1:117082772 | T | C | 111 | a0001c0003t0007g0014 a0001c0003t0007g0120 a0001c0003t0011g0121 others(108): Show |
145 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1903+825T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117082772 | |||||||
chr1:117082913 | T | C | 2 | a0008c0011t0011g0040 a0008c0011t0058g0038 |
2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1903+966T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117082913 | |||||||
chr1:117083025 | A | C | 1 | a0002c0001t0012g0237 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1904-993A>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117083025 | |||||||
chr1:117083058 | C | T | 1 | a0002c0001t0005g0032 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1904-960C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117083058 | |||||||
chr1:117083059 | G | A | 1 | a0001c0002t0001g0097 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1904-959G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117083059 | |||||||
chr1:117083241 | C | CA | 22 | a0001c0002t0001g0075 a0001c0002t0002g0105 a0001c0002t0004g0047 others(19): Show |
22 | HG00735.hp1 HG01106.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1904-755dupA | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr1 | 117083241 | ||||||
chr1:117083241 | CA | C | 8 | a0001c0002t0002g0070 a0001c0002t0003g0080 a0001c0004t0001g0179 others(5): Show |
8 | HG02895.hp2 HG02922.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1904-755delA | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr1 | 117083241 | ||||||
chr1:117083301 | G | A | 5 | a0001c0002t0003g0193 a0001c0002t0004g0050 a0001c0002t0007g0049 others(2): Show |
5 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1904-717G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117083301 | |||||||
chr1:117083341 | T | C | 246 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(243): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1904-677T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117083341 | |||||||
chr1:117083385 | A | G | 46 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0079 others(43): Show |
47 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.1904-633A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117083385 | |||||||
chr1:117083400 | C | T | 1 | a0002c0001t0005g0258 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1904-618C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117083400 | |||||||
chr1:117083641 | G | A | 251 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(248): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1904-377G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117083641 | |||||||
chr1:117083736 | A | C | 6 | a0004c0005t0003g0109 a0004c0005t0003g0110 a0004c0005t0003g0111 others(3): Show |
6 | HG02622.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1904-282A>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117083736 | |||||||
chr1:117083753 | A | C | 1 | a0004c0005t0007g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1904-265A>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117083753 | |||||||
chr1:117083801 | G | C | 1 | a0001c0003t0007g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1904-217G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117083801 | |||||||
chr1:117083883 | AG | A | 4 | a0004c0005t0003g0109 a0004c0005t0003g0110 a0004c0005t0003g0111 others(1): Show |
4 | HG02895.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1904-133delG | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr1 | 117083883 | ||||||
chr1:117084011 | T | C | 1 | a0006c0015t0011g0063 | 1 | HG03486.hp1 | splice_region_variant&intron_variant | LOW | c.1904-7T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 10/22 | chr1 | 117084011 | |||||||
chr1:117084304 | G | A | 5 | a0002c0001t0001g0247 a0002c0001t0009g0004 a0002c0001t0009g0023 others(2): Show |
8 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.2054+136G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117084304 | |||||||
chr1:117084305 | T | C | 1 | a0001c0004t0054g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2054+137T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117084305 | |||||||
chr1:117084414 | A | G | 2 | a0002c0001t0003g0214 a0002c0001t0003g0215 |
2 | HG01109.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.2054+246A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117084414 | |||||||
chr1:117084430 | A | G | 252 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(249): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.2054+262A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117084430 | |||||||
chr1:117084673 | G | C | 3 | a0001c0004t0001g0167 a0001c0004t0001g0179 a0001c0004t0001g0181 |
3 | HG02145.hp1 HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2054+505G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117084673 | |||||||
chr1:117084679 | C | T | 2 | a0001c0002t0004g0061 a0006c0009t0004g0065 |
2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2054+511C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117084679 | |||||||
chr1:117084702 | C | T | 3 | a0009c0023t0001g0187 a0009c0025t0066g0037 a0020c0024t0055g0036 |
3 | HG02055.hp2 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2054+534C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117084702 | |||||||
chr1:117084806 | C | T | 1 | a0001c0002t0011g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2054+638C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117084806 | |||||||
chr1:117084858 | C | A | 42 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0079 others(39): Show |
43 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2054+690C>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117084858 | |||||||
chr1:117084912 | A | G | 1 | a0001c0002t0008g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2054+744A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117084912 | |||||||
chr1:117085153 | G | A | 1 | a0001c0018t0001g0168 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2054+985G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117085153 | |||||||
chr1:117085245 | C | T | 1 | a0001c0002t0050g0178 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2054+1077C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117085245 | |||||||
chr1:117085344 | A | G | 30 | a0001c0002t0001g0020 a0001c0002t0001g0104 a0001c0002t0001g0162 others(27): Show |
33 | HG00408.hp2 HG00544.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.2055-1073A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117085344 | |||||||
chr1:117085435 | G | C | 252 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(249): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.2055-982G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117085435 | |||||||
chr1:117085529 | G | A | 1 | a0002c0035t0065g0125 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2055-888G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117085529 | |||||||
chr1:117085998 | G | A | 17 | a0002c0001t0001g0031 a0002c0001t0001g0253 a0002c0001t0005g0008 others(14): Show |
24 | HG00597.hp2 HG00621.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2055-419G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117085998 | |||||||
chr1:117086177 | T | C | 2 | a0003c0010t0052g0266 a0003c0010t0064g0045 |
2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2055-240T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117086177 | |||||||
chr1:117086247 | A | ATG | 39 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0079 others(36): Show |
40 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.2055-147_2055-146d others(4): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr1 | 117086247 | ||||||
chr1:117086247 | A | ATGTG | 4 | a0001c0002t0004g0013 a0001c0002t0004g0051 a0010c0021t0060g0013 others(1): Show |
4 | HG01243.hp1 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2055-149_2055-146d others(6): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr1 | 117086247 | ||||||
chr1:117086247 | ATG | A | 104 | a0001c0002t0001g0020 a0001c0002t0001g0162 a0001c0002t0001g0163 others(101): Show |
113 | HG00408.hp2 HG00544.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.2055-147_2055-146d others(4): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr1 | 117086247 | ||||||
chr1:117086270 | TGC | T | 3 | a0001c0002t0015g0195 a0008c0011t0011g0040 a0008c0011t0058g0038 |
3 | HG01891.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2055-145_2055-144d others(4): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr1 | 117086270 | ||||||
chr1:117086273 | G | A | 1 | a0001c0003t0004g0131 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2055-144G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 11/22 | chr1 | 117086273 | |||||||
chr1:117086546 | A | T | 1 | a0001c0002t0008g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2160+24A>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117086546 | |||||||
chr1:117086681 | C | T | 1 | a0001c0002t0011g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2160+159C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117086681 | |||||||
chr1:117086793 | C | T | 1 | a0009c0023t0001g0187 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2160+271C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117086793 | |||||||
chr1:117086900 | G | A | 35 | a0001c0003t0004g0018 a0001c0003t0004g0126 a0001c0003t0004g0129 others(32): Show |
40 | HG00642.hp1 HG01496.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.2160+378G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117086900 | |||||||
chr1:117086946 | GA | G | 30 | a0001c0002t0001g0020 a0001c0002t0001g0104 a0001c0002t0001g0162 others(27): Show |
33 | HG00408.hp2 HG00544.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.2160+435delA | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr1 | 117086946 | ||||||
chr1:117087038 | G | A | 35 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0079 others(32): Show |
35 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2160+516G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117087038 | |||||||
chr1:117087134 | C | T | 1 | a0001c0002t0008g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2160+612C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117087134 | |||||||
chr1:117087212 | T | C | 1 | a0001c0002t0008g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2160+690T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117087212 | |||||||
chr1:117087329 | G | T | 1 | a0009c0023t0001g0187 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2160+807G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117087329 | |||||||
chr1:117087332 | G | A | 1 | a0008c0011t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2160+810G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117087332 | |||||||
chr1:117087512 | C | T | 121 | a0001c0002t0002g0012 a0001c0002t0002g0085 a0001c0002t0002g0086 others(118): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2160+990C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117087512 | |||||||
chr1:117087544 | C | T | 2 | a0001c0002t0003g0177 a0001c0002t0034g0176 |
2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2160+1022C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117087544 | |||||||
chr1:117087631 | G | A | 1 | a0002c0001t0005g0032 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2160+1109G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117087631 | |||||||
chr1:117087644 | T | A | 1 | a0001c0002t0015g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2160+1122T>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117087644 | |||||||
chr1:117087657 | C | T | 50 | a0001c0002t0027g0180 a0001c0002t0051g0073 a0002c0001t0001g0001 others(47): Show |
70 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.2160+1135C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117087657 | |||||||
chr1:117087684 | T | C | 1 | a0001c0003t0022g0147 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2161-1117T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117087684 | |||||||
chr1:117087743 | C | T | 1 | a0001c0002t0011g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2161-1058C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117087743 | |||||||
chr1:117087839 | C | T | 4 | a0001c0003t0006g0006 a0001c0003t0006g0140 a0001c0003t0006g0150 others(1): Show |
6 | NA18747.hp2 NA18941.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.2161-962C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117087839 | |||||||
chr1:117087911 | T | C | 35 | a0001c0003t0004g0018 a0001c0003t0004g0126 a0001c0003t0004g0129 others(32): Show |
40 | HG00642.hp1 HG01496.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.2161-890T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117087911 | |||||||
chr1:117088253 | G | C | 253 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(250): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.2161-548G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117088253 | |||||||
chr1:117088311 | G | T | 1 | a0001c0003t0004g0126 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2161-490G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117088311 | |||||||
chr1:117088320 | G | A | 1 | a0001c0003t0024g0122 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2161-481G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117088320 | |||||||
chr1:117088332 | T | G | 1 | a0001c0002t0002g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2161-469T>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117088332 | |||||||
chr1:117088454 | G | A | 1 | a0001c0002t0004g0050 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2161-347G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117088454 | |||||||
chr1:117088462 | C | T | 3 | a0009c0023t0001g0187 a0009c0025t0066g0037 a0020c0024t0055g0036 |
3 | HG02055.hp2 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2161-339C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117088462 | |||||||
chr1:117088488 | G | T | 29 | a0001c0002t0001g0020 a0001c0002t0001g0162 a0001c0002t0001g0163 others(26): Show |
32 | HG00408.hp2 HG00544.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.2161-313G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117088488 | |||||||
chr1:117088494 | G | A | 1 | a0001c0002t0002g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2161-307G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117088494 | |||||||
chr1:117088550 | G | A | 4 | a0001c0002t0003g0263 a0001c0002t0007g0035 a0001c0002t0008g0194 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2161-251G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117088550 | |||||||
chr1:117088598 | G | T | 1 | a0002c0035t0065g0125 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2161-203G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117088598 | |||||||
chr1:117088769 | T | C | 250 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(247): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.2161-32T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 12/22 | chr1 | 117088769 | |||||||
chr1:117089085 | GT | G | 4 | a0001c0002t0003g0193 a0001c0002t0007g0049 a0001c0002t0007g0055 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2342+106delT | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089085 | ||||||
chr1:117089099 | A | G | 1 | a0001c0002t0011g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2342+117A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | chr1 | 117089099 | |||||||
chr1:117089132 | ATATT | A | 4 | a0001c0002t0003g0263 a0001c0002t0007g0035 a0001c0002t0008g0194 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2342+154_2342+157d others(6): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089132 | ||||||
chr1:117089220 | TATATATG others(4): Show |
T | 1 | a0006c0009t0072g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2342+261_2342+271d others(13): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089220 | ||||||
chr1:117089248 | T | C | 1 | a0001c0002t0018g0084 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2342+266T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | chr1 | 117089248 | |||||||
chr1:117089260 | C | CTA | 20 | a0001c0002t0004g0013 a0001c0002t0004g0050 a0001c0002t0004g0051 others(17): Show |
22 | HG01243.hp1 HG01257.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.2342+294_2342+295d others(4): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATA | 3 | a0001c0002t0003g0175 a0001c0002t0003g0263 a0004c0005t0008g0108 |
3 | HG02056.hp2 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2342+290_2342+295d others(8): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATAT others(3): Show |
3 | a0001c0002t0004g0061 a0001c0002t0011g0043 a0001c0002t0015g0195 |
3 | HG02809.hp2 NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2342+286_2342+295d others(12): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATAT others(5): Show |
9 | a0001c0002t0001g0079 a0001c0002t0001g0089 a0001c0002t0001g0090 others(6): Show |
9 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.2342+284_2342+295d others(14): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATAT others(7): Show |
10 | a0001c0002t0001g0081 a0001c0002t0001g0100 a0001c0002t0001g0163 others(7): Show |
11 | HG02109.hp1 HG02559.hp2 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.2342+282_2342+295d others(16): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATAT others(9): Show |
5 | a0001c0002t0001g0097 a0001c0002t0001g0162 a0001c0002t0003g0072 others(2): Show |
5 | HG00438.hp2 HG01358.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.2342+280_2342+295d others(18): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATAT others(11): Show |
10 | a0001c0002t0001g0182 a0001c0002t0001g0186 a0001c0002t0008g0169 others(7): Show |
10 | HG00408.hp2 HG01891.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.2342+295_2342+296i others(20): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATAT others(13): Show |
7 | a0001c0002t0001g0020 a0001c0002t0001g0183 a0001c0002t0003g0088 others(4): Show |
8 | HG00544.hp2 HG00733.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.2342+295_2342+296i others(22): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATAT others(15): Show |
2 | a0001c0002t0003g0019 a0007c0012t0003g0093 |
3 | HG00323.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2342+295_2342+296i others(24): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATAT others(17): Show |
5 | a0001c0002t0003g0098 a0001c0002t0003g0250 a0001c0002t0007g0035 others(2): Show |
5 | HG01361.hp2 HG02109.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2342+295_2342+296i others(26): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATAT others(19): Show |
5 | a0001c0002t0001g0104 a0001c0002t0002g0087 a0001c0002t0003g0078 others(2): Show |
5 | HG00741.hp2 HG01243.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.2342+295_2342+296i others(28): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATAT others(21): Show |
5 | a0001c0002t0001g0095 a0001c0002t0002g0071 a0001c0002t0008g0106 others(2): Show |
5 | HG02145.hp1 HG02738.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.2342+295_2342+296i others(30): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATAT others(23): Show |
2 | a0001c0002t0002g0069 a0001c0004t0001g0167 |
2 | HG01081.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2342+295_2342+296i others(32): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATAT others(25): Show |
4 | a0001c0002t0002g0068 a0001c0002t0002g0070 a0001c0002t0003g0082 others(1): Show |
4 | HG01123.hp2 HG03098.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2342+295_2342+296i others(34): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATAT others(29): Show |
1 | a0001c0002t0003g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2342+295_2342+296i others(38): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | C | CTATATAT others(31): Show |
3 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0003g0080 |
3 | HG03710.hp2 NA19056.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.2342+295_2342+296i others(40): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089260 | CTA | C | 124 | a0001c0002t0002g0012 a0001c0002t0002g0085 a0001c0002t0002g0086 others(121): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.2342+294_2342+295d others(4): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089260 | ||||||
chr1:117089694 | G | GA | 5 | a0001c0003t0006g0152 a0001c0003t0011g0151 a0005c0014t0007g0154 others(2): Show |
5 | HG01884.hp1 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2343-354dupA | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 117089694 | ||||||
chr1:117089739 | T | A | 2 | a0001c0002t0001g0075 a0001c0002t0001g0076 |
2 | NA19056.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.2343-316T>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | chr1 | 117089739 | |||||||
chr1:117089823 | G | A | 4 | a0001c0003t0006g0006 a0001c0003t0006g0140 a0001c0003t0006g0150 others(1): Show |
6 | NA18747.hp2 NA18941.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.2343-232G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | chr1 | 117089823 | |||||||
chr1:117089910 | G | A | 7 | a0002c0001t0005g0008 a0002c0001t0005g0024 a0002c0001t0005g0032 others(4): Show |
11 | HG01106.hp2 HG01358.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.2343-145G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 13/22 | chr1 | 117089910 | |||||||
chr1:117090335 | G | A | 3 | a0001c0002t0011g0043 a0004c0005t0007g0041 a0014c0016t0068g0064 |
3 | HG02622.hp1 HG02647.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2496+127G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 14/22 | chr1 | 117090335 | |||||||
chr1:117090744 | T | C | 36 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0079 others(33): Show |
36 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2588+121T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 15/22 | chr1 | 117090744 | |||||||
chr1:117090750 | C | CT | 19 | a0002c0001t0001g0031 a0002c0001t0005g0008 a0002c0001t0005g0009 others(16): Show |
27 | HG00597.hp2 HG00621.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.2588+138dupT | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr1 | 117090750 | ||||||
chr1:117090854 | T | C | 2 | a0002c0001t0002g0225 a0002c0001t0003g0205 |
2 | HG00639.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2588+231T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 15/22 | chr1 | 117090854 | |||||||
chr1:117090883 | A | G | 51 | a0001c0002t0043g0192 a0001c0003t0004g0018 a0001c0003t0004g0126 others(48): Show |
56 | HG00642.hp1 HG01496.hp2 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.2588+260A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 15/22 | chr1 | 117090883 | |||||||
chr1:117090957 | A | G | 3 | a0001c0003t0014g0123 a0001c0003t0024g0114 a0001c0003t0024g0122 |
3 | HG01433.hp1 HG02717.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2588+334A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 15/22 | chr1 | 117090957 | |||||||
chr1:117090983 | T | C | 250 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(247): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.2589-345T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 15/22 | chr1 | 117090983 | |||||||
chr1:117091186 | A | G | 7 | a0001c0002t0011g0043 a0004c0005t0003g0109 a0004c0005t0003g0110 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2589-142A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 15/22 | chr1 | 117091186 | |||||||
chr1:117091260 | G | T | 1 | a0001c0003t0062g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2589-68G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 15/22 | chr1 | 117091260 | |||||||
chr1:117091296 | C | T | 3 | a0001c0002t0003g0082 a0001c0002t0003g0099 a0001c0002t0035g0083 |
3 | HG00741.hp2 HG01123.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2589-32C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 15/22 | chr1 | 117091296 | |||||||
chr1:117091611 | C | T | 1 | a0009c0023t0001g0187 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2671+201C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 16/22 | chr1 | 117091611 | |||||||
chr1:117091669 | A | G | 1 | a0001c0002t0007g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2672-148A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 16/22 | chr1 | 117091669 | |||||||
chr1:117092586 | T | C | 3 | a0001c0003t0014g0123 a0001c0003t0024g0114 a0001c0003t0024g0122 |
3 | HG01433.hp1 HG02717.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2806-145T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 17/22 | chr1 | 117092586 | |||||||
chr1:117093064 | T | G | 3 | a0001c0003t0014g0123 a0001c0003t0024g0114 a0001c0003t0024g0122 |
3 | HG01433.hp1 HG02717.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2976+163T>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117093064 | |||||||
chr1:117093283 | C | T | 37 | a0001c0002t0043g0192 a0001c0003t0004g0018 a0001c0003t0004g0134 others(34): Show |
42 | HG00642.hp1 HG01496.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.2976+382C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117093283 | |||||||
chr1:117093340 | T | C | 1 | a0001c0002t0003g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2976+439T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117093340 | |||||||
chr1:117093378 | G | T | 1 | a0002c0028t0032g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2976+477G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117093378 | |||||||
chr1:117093871 | G | A | 69 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(66): Show |
72 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2976+970G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117093871 | |||||||
chr1:117094073 | G | C | 241 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0076 others(238): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.2976+1172G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117094073 | |||||||
chr1:117094301 | A | G | 5 | a0001c0002t0007g0035 a0001c0002t0011g0043 a0001c0003t0014g0123 others(2): Show |
5 | HG01433.hp1 HG02717.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2977-1008A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117094301 | |||||||
chr1:117094476 | C | T | 1 | a0001c0002t0001g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2977-833C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117094476 | |||||||
chr1:117094500 | A | C | 9 | a0001c0002t0008g0194 a0001c0003t0007g0014 a0001c0003t0007g0120 others(6): Show |
9 | HG02280.hp1 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2977-809A>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117094500 | |||||||
chr1:117094538 | C | T | 9 | a0001c0003t0004g0134 a0001c0003t0004g0144 a0001c0003t0006g0152 others(6): Show |
9 | HG00642.hp1 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2977-771C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117094538 | |||||||
chr1:117094703 | C | T | 1 | a0003c0006t0045g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2977-606C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117094703 | |||||||
chr1:117094788 | C | T | 12 | a0001c0002t0003g0177 a0001c0002t0008g0169 a0001c0002t0034g0176 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2977-521C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117094788 | |||||||
chr1:117094862 | A | G | 1 | a0001c0002t0035g0083 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2977-447A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117094862 | |||||||
chr1:117094874 | G | A | 23 | a0001c0002t0003g0193 a0001c0002t0004g0011 a0001c0002t0004g0013 others(20): Show |
26 | HG00323.hp1 HG00741.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.2977-435G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117094874 | |||||||
chr1:117094918 | G | C | 1 | a0001c0002t0063g0062 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2977-391G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117094918 | |||||||
chr1:117094936 | G | A | 4 | a0001c0003t0011g0151 a0001c0004t0054g0034 a0009c0023t0001g0187 others(1): Show |
4 | HG02055.hp2 HG02559.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2977-373G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117094936 | |||||||
chr1:117095012 | A | G | 213 | a0001c0002t0001g0020 a0001c0002t0001g0075 a0001c0002t0001g0079 others(210): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.2977-297A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117095012 | |||||||
chr1:117095023 | C | T | 1 | a0004c0005t0007g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2977-286C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 18/22 | chr1 | 117095023 | |||||||
chr1:117095383 | C | T | 2 | a0001c0004t0054g0034 a0009c0023t0001g0187 |
2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.3035+16C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 19/22 | chr1 | 117095383 | |||||||
chr1:117095586 | T | TAAAAGTA others(299): Show |
1 | a0001c0003t0011g0151 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3035+233_3035+234i others(308): Show |
TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr1 | 117095586 | ||||||
chr1:117095648 | C | T | 193 | a0001c0002t0001g0092 a0001c0002t0001g0182 a0001c0002t0002g0012 others(190): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.3035+281C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 19/22 | chr1 | 117095648 | |||||||
chr1:117095755 | C | G | 1 | a0004c0005t0003g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3035+388C>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 19/22 | chr1 | 117095755 | |||||||
chr1:117096028 | G | C | 1 | a0001c0002t0067g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3036-121G>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 19/22 | chr1 | 117096028 | |||||||
chr1:117096074 | G | A | 17 | a0001c0002t0027g0180 a0002c0001t0005g0008 a0002c0001t0005g0009 others(14): Show |
25 | HG00597.hp2 HG00621.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.3036-75G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 19/22 | chr1 | 117096074 | |||||||
chr1:117096339 | C | T | 1 | a0002c0001t0003g0230 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3186+40C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 20/22 | chr1 | 117096339 | |||||||
chr1:117096350 | A | G | 2 | a0016c0020t0056g0112 a0020c0024t0055g0036 |
2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3186+51A>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 20/22 | chr1 | 117096350 | |||||||
chr1:117096446 | T | TG | 4 | a0001c0002t0015g0195 a0001c0002t0067g0039 a0001c0004t0015g0164 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3186+149dupG | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 117096446 | ||||||
chr1:117097206 | TA | T | 77 | a0001c0002t0003g0067 a0001c0002t0003g0072 a0001c0002t0003g0078 others(74): Show |
85 | HG00597.hp2 HG00621.hp2 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.3187-134delA | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 117097206 | ||||||
chr1:117097445 | G | A | 1 | a0001c0003t0024g0122 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3269+12G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/22 | chr1 | 117097445 | |||||||
chr1:117097497 | G | A | 2 | a0001c0002t0015g0195 a0001c0004t0015g0164 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3269+64G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/22 | chr1 | 117097497 | |||||||
chr1:117097518 | T | C | 1 | a0001c0003t0011g0151 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3269+85T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/22 | chr1 | 117097518 | |||||||
chr1:117097689 | C | T | 1 | a0002c0028t0032g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3269+256C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/22 | chr1 | 117097689 | |||||||
chr1:117097906 | G | T | 2 | a0016c0020t0056g0112 a0020c0024t0055g0036 |
2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3269+473G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/22 | chr1 | 117097906 | |||||||
chr1:117098124 | G | A | 14 | a0001c0002t0029g0074 a0001c0002t0050g0178 a0001c0003t0011g0121 others(11): Show |
14 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.3269+691G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/22 | chr1 | 117098124 | |||||||
chr1:117098188 | CT | C | 94 | a0001c0002t0003g0019 a0001c0002t0003g0067 a0001c0002t0003g0072 others(91): Show |
103 | HG00597.hp2 HG00621.hp2 HG00733.hp1 others(100): Show |
intron_variant | MODIFIER | c.3270-631delT | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr1 | 117098188 | ||||||
chr1:117098379 | G | T | 1 | a0002c0027t0028g0212 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3270-454G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/22 | chr1 | 117098379 | |||||||
chr1:117098425 | G | A | 5 | a0001c0002t0043g0192 a0001c0003t0011g0151 a0009c0025t0066g0037 others(2): Show |
5 | HG02258.hp1 HG02723.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3270-408G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/22 | chr1 | 117098425 | |||||||
chr1:117098469 | C | T | 1 | a0001c0003t0062g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3270-364C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/22 | chr1 | 117098469 | |||||||
chr1:117098609 | C | T | 1 | a0002c0001t0001g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3270-224C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/22 | chr1 | 117098609 | |||||||
chr1:117098724 | A | C | 2 | a0002c0001t0005g0223 a0002c0001t0005g0224 |
2 | HG03834.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.3270-109A>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/22 | chr1 | 117098724 | |||||||
chr1:117098770 | C | T | 2 | a0002c0001t0002g0222 a0002c0001t0002g0233 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3270-63C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/22 | chr1 | 117098770 | |||||||
chr1:117098786 | C | G | 4 | a0001c0002t0015g0195 a0001c0004t0015g0164 a0001c0004t0054g0034 others(1): Show |
4 | HG02559.hp2 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3270-47C>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 21/22 | chr1 | 117098786 | |||||||
chr1:117099046 | G | A | 18 | a0001c0002t0027g0180 a0001c0002t0035g0083 a0002c0001t0005g0008 others(15): Show |
26 | HG00597.hp2 HG00621.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.3344+139G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117099046 | |||||||
chr1:117099204 | G | T | 40 | a0001c0002t0003g0019 a0001c0002t0003g0067 a0001c0002t0003g0072 others(37): Show |
41 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.3344+297G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117099204 | |||||||
chr1:117099243 | C | T | 59 | a0001c0002t0003g0019 a0001c0002t0003g0067 a0001c0002t0003g0072 others(56): Show |
60 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.3344+336C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117099243 | |||||||
chr1:117099310 | T | C | 1 | a0001c0003t0004g0018 | 2 | HG02698.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3344+403T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117099310 | |||||||
chr1:117099372 | C | T | 1 | a0002c0001t0001g0229 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3344+465C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117099372 | |||||||
chr1:117099509 | G | A | 12 | a0001c0002t0003g0263 a0001c0002t0007g0057 a0001c0003t0007g0014 others(9): Show |
12 | HG02280.hp1 HG02622.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.3344+602G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117099509 | |||||||
chr1:117099703 | T | G | 2 | a0001c0002t0003g0098 a0002c0001t0003g0205 |
2 | HG03490.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3344+796T>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117099703 | |||||||
chr1:117099975 | C | T | 1 | a0001c0002t0002g0161 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3344+1068C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117099975 | |||||||
chr1:117100224 | T | C | 5 | a0001c0002t0027g0180 a0002c0001t0005g0009 a0002c0001t0005g0033 others(2): Show |
8 | HG00597.hp2 HG01943.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.3345-1156T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117100224 | |||||||
chr1:117100306 | T | A | 1 | a0001c0003t0011g0151 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3345-1074T>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117100306 | |||||||
chr1:117100373 | C | G | 117 | a0001c0002t0001g0079 a0001c0002t0001g0090 a0001c0002t0001g0096 others(114): Show |
130 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.3345-1007C>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117100373 | |||||||
chr1:117100412 | C | T | 1 | a0002c0001t0001g0232 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3345-968C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117100412 | |||||||
chr1:117100440 | G | T | 2 | a0016c0020t0056g0112 a0020c0024t0055g0036 |
2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3345-940G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117100440 | |||||||
chr1:117100644 | C | G | 1 | a0001c0003t0011g0151 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3345-736C>G | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117100644 | |||||||
chr1:117100783 | G | A | 1 | a0001c0002t0002g0087 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3345-597G>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117100783 | |||||||
chr1:117100860 | T | C | 130 | a0001c0002t0003g0019 a0001c0002t0003g0067 a0001c0002t0003g0072 others(127): Show |
146 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(143): Show |
intron_variant | MODIFIER | c.3345-520T>C | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117100860 | |||||||
chr1:117100950 | C | A | 2 | a0001c0002t0011g0043 a0008c0011t0011g0040 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3345-430C>A | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117100950 | |||||||
chr1:117100980 | C | T | 12 | a0001c0002t0003g0263 a0001c0002t0007g0057 a0001c0003t0007g0014 others(9): Show |
12 | HG02280.hp1 HG02622.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.3345-400C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117100980 | |||||||
chr1:117101040 | C | T | 1 | a0006c0009t0072g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3345-340C>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117101040 | |||||||
chr1:117101108 | G | T | 3 | a0004c0005t0003g0111 a0005c0014t0007g0154 a0005c0014t0007g0155 |
3 | HG02895.hp2 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3345-272G>T | TTF2 | ENSG00000116830.12 | transcript | ENST00000369466.9 | protein_coding | 22/22 | chr1 | 117101108 |