Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10342 |
| ensemblid | ENSG00000114354.15 |
| hgncid | 11758 |
| symbol | TFG |
| name | trafficking from ER to golgi regulator |
| refseq_nuc | NM_006070.6 |
| refseq_prot | NP_006061.2 |
| ensembl_nuc | ENST00000240851.9 |
| ensembl_prot | ENSP00000240851.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 100709494 |
| end | 100748964 |
| strand | + |
| ver | v1.2 |
| region | chr3:100709494-100748964 |
| region5000 | chr3:100704494-100753964 |
| regionname0 | TFG_chr3_100709494_100748964 |
| regionname5000 | TFG_chr3_100704494_100753964 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 400 | 349 | 87 | 64 | 148 | 16 | 32 | 118 | TFG_chr3_100704494_100753964 | TFG | MNGQL others(395): Show |
chr3 | 100704494 | 100753964 |
| a0002 | 0/0 | 400 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | MNGQL others(395): Show |
chr3 | 100704494 | 100753964 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1200 | 206 | 38 | 42 | 87 | 13 | 25 | TFG_chr3_100704494_100753964 | TFG | ATGAA others(1195): Show |
chr3 | 100704494 | 100753964 | ||
| a0001c0002 | 1/0 | 1200 | 123 | 31 | 21 | 61 | 2 | 7 | TFG_chr3_100704494_100753964 | TFG | ATGAA others(1195): Show |
chr3 | 100704494 | 100753964 | ||
| a0001c0003 | 0/0 | 1200 | 11 | 10 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | ATGAA others(1195): Show |
chr3 | 100704494 | 100753964 | ||
| a0001c0004 | 0/0 | 1200 | 9 | 8 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | ATGAA others(1195): Show |
chr3 | 100704494 | 100753964 | ||
| a0002c0005 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | ATGAA others(1195): Show |
chr3 | 100704494 | 100753964 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1907 | 104 | 11 | 20 | 58 | 6 | 8 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1902): Show |
chr3 | 100704494 | 100753964 |
| a0001c0001t0003 | 0/0 | 1907 | 76 | 21 | 13 | 25 | 6 | 11 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1902): Show |
chr3 | 100704494 | 100753964 |
| a0001c0001t0004 | 0/0 | 1907 | 10 | 0 | 2 | 2 | 1 | 5 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1902): Show |
chr3 | 100704494 | 100753964 |
| a0001c0001t0005 | 0/0 | 1905 | 6 | 0 | 5 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1900): Show |
chr3 | 100704494 | 100753964 |
| a0001c0001t0006 | 0/0 | 1908 | 4 | 3 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1903): Show |
chr3 | 100704494 | 100753964 |
| a0001c0001t0008 | 0/0 | 1907 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1902): Show |
chr3 | 100704494 | 100753964 |
| a0001c0001t0009 | 0/0 | 1907 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1902): Show |
chr3 | 100704494 | 100753964 |
| a0001c0001t0010 | 0/0 | 1907 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1902): Show |
chr3 | 100704494 | 100753964 |
| a0001c0001t0011 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1902): Show |
chr3 | 100704494 | 100753964 |
| a0001c0001t0012 | 0/0 | 1907 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1902): Show |
chr3 | 100704494 | 100753964 |
| a0001c0002t0002 | 1/0 | 1907 | 119 | 30 | 18 | 61 | 2 | 7 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1902): Show |
chr3 | 100704494 | 100753964 |
| a0001c0002t0007 | 0/0 | 1907 | 3 | 0 | 3 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1902): Show |
chr3 | 100704494 | 100753964 |
| a0001c0002t0013 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1902): Show |
chr3 | 100704494 | 100753964 |
| a0001c0003t0001 | 0/0 | 1907 | 11 | 10 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1902): Show |
chr3 | 100704494 | 100753964 |
| a0001c0004t0001 | 0/0 | 1907 | 9 | 8 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1902): Show |
chr3 | 100704494 | 100753964 |
| a0002c0005t0003 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | GTTCT others(1902): Show |
chr3 | 100704494 | 100753964 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 33 | 5 | 4 | 20 | 4 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0004 | 0/0 | 9 | 0 | 0 | 7 | 1 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0004g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0005g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0005g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0006g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0008g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0009g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0010g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0011g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0001t0012g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0002 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0003 | 0/0 | 12 | 2 | 7 | 1 | 2 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0011 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0007g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0007g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0002t0013g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0003t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0003t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0004t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0004t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0004t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0001c0004t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| a0002c0005t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0076 | EUR | GBR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | GBR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0045 | EUR | FIN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0030 | EUR | FIN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0057 | EUR | FIN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0094 | EUR | FIN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0169 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0160 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00735 | hp1 | a0001 | c0004 | t0001 | g0203 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0175 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0171 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01167 | hp2 | a0001 | c0002 | t0007 | g0040 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0089 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0157 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0156 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0039 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0153 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01496 | hp1 | a0001 | c0002 | t0007 | g0003 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0003 | EUR | IBS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0016 | EUR | IBS | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0050 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01928 | hp1 | a0001 | c0001 | t0010 | g0060 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0039 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0201 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0065 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0017 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0145 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0150 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | CDX | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0102 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0174 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0158 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02300 | hp1 | a0001 | c0002 | t0007 | g0003 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0041 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0170 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0041 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02572 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0154 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0029 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0166 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0028 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0054 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0023 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0197 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0071 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0172 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0161 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0167 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0163 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02886 | hp1 | a0001 | c0002 | t0013 | g0055 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0164 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0151 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0059 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03041 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0104 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0152 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0053 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0004 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0148 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0047 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0075 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0198 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0028 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0049 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0155 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0083 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | BEB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0147 | SAS | BEB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0105 | SAS | BEB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | STU | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0096 | SAS | BEB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0182 | AFR | YRI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | YRI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | CHB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | YRI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | YRI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18971 | hp2 | a0001 | c0001 | t0009 | g0129 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18990 | hp2 | a0001 | c0001 | t0012 | g0005 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | LWK | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0168 | AFR | LWK | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0165 | AFR | LWK | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | YRI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0103 | AFR | YRI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | ASW | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0061 | EUR | TSI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0003 | EUR | TSI | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | GIH | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0033 | SAS | GIH | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0082 | AMR | CLM | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02109 | hp1 | a0001 | c0004 | t0001 | g0048 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0162 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0046 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0187 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0052 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | MSL | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | USA | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | USA | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| NA20300 | hp2 | a0002 | c0005 | t0003 | g0015 | AFR | USA | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0139 | REF | REF | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0011 | REF | REF | TFG_chr3_100704494_100753964 | TFG | chr3 | 100704494 | 100753964 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100713753 | G | A | 1 | a0002 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.68G>A | p.Arg23Gln | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/8 | 339/1907 | 68/1203 | 23/400 | chr3 | 100713753 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100732644 | G | A | 2 | a0001c0003 a0001c0004 |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
synonymous_variant | LOW | c.552G>A | p.Ala184Ala | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/8 | 823/1907 | 552/1203 | 184/400 | chr3 | 100732644 | |||
| chr3:100736658 | C | A | 1 | a0001c0004 | 9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
synonymous_variant | LOW | c.663C>A | p.Gly221Gly | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/8 | 934/1907 | 663/1203 | 221/400 | chr3 | 100736658 | |||
| chr3:100748174 | T | C | 4 | a0001c0001 a0001c0003 a0001c0004 others(1): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
synonymous_variant | LOW | c.846T>C | p.Pro282Pro | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 1117/1907 | 846/1203 | 282/400 | chr3 | 100748174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100709512 | A | G | 1 | a0001c0002t0007 | 3 | HG01167.hp2 HG01496.hp1 HG02300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-253A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/8 | 4174 | chr3 | 100709512 | ||||||
| chr3:100709515 | T | G | 1 | a0001c0001t0009 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-250T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/8 | 4171 | chr3 | 100709515 | ||||||
| chr3:100709616 | G | C | 13 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(10): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
5_prime_UTR_variant | MODIFIER | c.-149G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/8 | 4070 | chr3 | 100709616 | ||||||
| chr3:100709629 | C | T | 1 | a0001c0001t0012 | 1 | NA18990.hp2 | 5_prime_UTR_variant | MODIFIER | c.-136C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/8 | 4057 | chr3 | 100709629 | ||||||
| chr3:100709633 | C | G | 1 | a0001c0001t0011 | 1 | HG02572.hp2 | 5_prime_UTR_variant | MODIFIER | c.-132C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/8 | 4053 | chr3 | 100709633 | ||||||
| chr3:100748556 | G | A | 1 | a0001c0002t0013 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 25 | chr3 | 100748556 | ||||||
| chr3:100748640 | A | AT | 1 | a0001c0001t0006 | 4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*115dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 116 | INFO_REALIGN_3_PRIME | chr3 | 100748640 | |||||
| chr3:100748751 | ACT | A | 1 | a0001c0001t0005 | 6 | HG01167.hp1 HG01358.hp1 HG01943.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*221_*222delCT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 221 | chr3 | 100748751 | ||||||
| chr3:100748803 | T | G | 1 | a0001c0001t0008 | 2 | HG02257.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*272T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 272 | chr3 | 100748803 | ||||||
| chr3:100748813 | C | T | 1 | a0001c0001t0010 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*282C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 282 | chr3 | 100748813 | ||||||
| chr3:100748829 | G | A | 1 | a0001c0001t0004 | 10 | HG00099.hp2 HG00438.hp1 HG01257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*298G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 298 | chr3 | 100748829 | ||||||
| chr3:100748832 | A | T | 8 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(5): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*301A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 8/8 | 301 | chr3 | 100748832 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100709743 | G | C | 1 | a0001c0002t0002g0044 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-44+22G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100709743 | |||||||
| chr3:100709784 | C | G | 1 | a0001c0004t0001g0203 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-44+63C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100709784 | |||||||
| chr3:100709785 | G | T | 1 | a0001c0001t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-44+64G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100709785 | |||||||
| chr3:100709800 | T | C | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+79T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100709800 | |||||||
| chr3:100709838 | G | C | 1 | a0001c0001t0003g0030 | 2 | HG00280.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-44+117G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100709838 | |||||||
| chr3:100709846 | T | TGGAGGGA others(10): Show |
3 | a0001c0001t0001g0199 a0001c0001t0003g0200 a0001c0002t0002g0201 |
3 | HG01952.hp1 HG02683.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-44+153_-44+169dup others(17): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100709846 | ||||||
| chr3:100709846 | TGGAGGGA others(10): Show |
T | 1 | a0001c0002t0013g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-44+153_-44+169del others(17): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100709846 | ||||||
| chr3:100709905 | A | C | 1 | a0001c0001t0004g0198 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-44+184A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100709905 | |||||||
| chr3:100710003 | G | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(136): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.-44+282G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710003 | |||||||
| chr3:100710127 | T | C | 1 | a0001c0003t0001g0027 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-44+406T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710127 | |||||||
| chr3:100710185 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-44+464G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710185 | |||||||
| chr3:100710205 | C | T | 1 | a0001c0002t0002g0197 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-44+484C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710205 | |||||||
| chr3:100710266 | C | CT | 13 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(10): Show |
17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-44+548dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100710266 | ||||||
| chr3:100710295 | A | G | 7 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(4): Show |
8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+574A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710295 | |||||||
| chr3:100710334 | A | G | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-44+613A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710334 | |||||||
| chr3:100710352 | A | C | 1 | a0001c0002t0002g0196 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-44+631A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710352 | |||||||
| chr3:100710521 | C | G | 1 | a0001c0001t0003g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-44+800C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710521 | |||||||
| chr3:100710736 | G | A | 1 | a0001c0001t0001g0031 | 2 | NA19064.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-44+1015G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710736 | |||||||
| chr3:100710737 | C | A | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-44+1016C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710737 | |||||||
| chr3:100710864 | G | A | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-44+1143G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710864 | |||||||
| chr3:100710881 | G | A | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+1160G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710881 | |||||||
| chr3:100710915 | G | A | 2 | a0001c0001t0003g0032 a0001c0001t0003g0056 |
3 | HG03654.hp2 HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-44+1194G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100710915 | |||||||
| chr3:100711008 | C | T | 2 | a0001c0001t0005g0039 a0001c0001t0005g0145 |
3 | HG01358.hp1 HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-44+1287C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711008 | |||||||
| chr3:100711051 | C | T | 28 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0024 others(25): Show |
58 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.-44+1330C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711051 | |||||||
| chr3:100711101 | C | G | 2 | a0001c0002t0002g0174 a0001c0002t0002g0175 |
2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-44+1380C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711101 | |||||||
| chr3:100711103 | A | AT | 12 | a0001c0001t0001g0144 a0001c0001t0003g0007 a0001c0001t0003g0142 others(9): Show |
19 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-44+1397dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100711103 | ||||||
| chr3:100711103 | A | ATT | 7 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(4): Show |
8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+1396_-44+1397d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100711103 | ||||||
| chr3:100711103 | AT | A | 62 | a0001c0001t0001g0097 a0001c0001t0003g0004 a0001c0001t0003g0008 others(59): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.-44+1397delT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100711103 | ||||||
| chr3:100711153 | T | G | 24 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0030 others(21): Show |
39 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.-44+1432T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711153 | |||||||
| chr3:100711221 | G | C | 6 | a0001c0004t0001g0013 a0001c0004t0001g0028 a0001c0004t0001g0046 others(3): Show |
9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44+1500G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711221 | |||||||
| chr3:100711234 | C | T | 1 | a0001c0003t0001g0054 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-44+1513C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711234 | |||||||
| chr3:100711257 | G | A | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-44+1536G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711257 | |||||||
| chr3:100711275 | G | T | 1 | a0001c0002t0002g0173 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-44+1554G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711275 | |||||||
| chr3:100711334 | C | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+1613C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711334 | |||||||
| chr3:100711347 | C | T | 1 | a0001c0002t0002g0172 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-44+1626C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711347 | |||||||
| chr3:100711378 | G | A | 3 | a0001c0001t0003g0007 a0001c0001t0003g0142 a0001c0001t0003g0143 |
7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+1657G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711378 | |||||||
| chr3:100711394 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-44+1673C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711394 | |||||||
| chr3:100711492 | T | A | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-44+1771T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711492 | |||||||
| chr3:100711664 | G | A | 6 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0059 others(3): Show |
6 | HG00323.hp1 HG01255.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+1943G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711664 | |||||||
| chr3:100711817 | T | TTA | 6 | a0001c0004t0001g0013 a0001c0004t0001g0028 a0001c0004t0001g0046 others(3): Show |
9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-43-1826_-43-1825i others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711817 | |||||||
| chr3:100711818 | A | C | 6 | a0001c0004t0001g0013 a0001c0004t0001g0028 a0001c0004t0001g0046 others(3): Show |
9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-43-1825A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711818 | |||||||
| chr3:100711821 | T | C | 6 | a0001c0004t0001g0013 a0001c0004t0001g0028 a0001c0004t0001g0046 others(3): Show |
9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-43-1822T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711821 | |||||||
| chr3:100711831 | G | A | 71 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(68): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.-43-1812G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711831 | |||||||
| chr3:100711854 | T | C | 2 | a0001c0002t0002g0044 a0001c0002t0002g0176 |
2 | NA18994.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-43-1789T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711854 | |||||||
| chr3:100711893 | C | A | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-43-1750C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711893 | |||||||
| chr3:100711924 | G | A | 28 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0024 others(25): Show |
58 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.-43-1719G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711924 | |||||||
| chr3:100711967 | C | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-43-1676C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711967 | |||||||
| chr3:100711995 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-43-1648T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100711995 | |||||||
| chr3:100712044 | C | T | 1 | a0001c0001t0004g0096 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-43-1599C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100712044 | |||||||
| chr3:100712171 | T | G | 13 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(10): Show |
17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-43-1472T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100712171 | |||||||
| chr3:100712369 | T | G | 1 | a0001c0001t0003g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-43-1274T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100712369 | |||||||
| chr3:100712662 | G | A | 1 | a0001c0003t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-43-981G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100712662 | |||||||
| chr3:100712762 | A | C | 1 | a0001c0002t0002g0172 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-43-881A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100712762 | |||||||
| chr3:100712804 | TAAATTAG others(74): Show |
T | 1 | a0001c0001t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-43-836_-43-756del others(81): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100712804 | ||||||
| chr3:100712851 | G | T | 1 | a0001c0001t0003g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-43-792G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100712851 | |||||||
| chr3:100713001 | G | C | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-43-642G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713001 | |||||||
| chr3:100713108 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-43-535G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713108 | |||||||
| chr3:100713140 | T | A | 1 | a0001c0001t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-43-503T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713140 | |||||||
| chr3:100713242 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-43-401C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713242 | |||||||
| chr3:100713329 | A | C | 1 | a0001c0002t0002g0171 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-43-314A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713329 | |||||||
| chr3:100713393 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-43-250G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713393 | |||||||
| chr3:100713449 | A | G | 1 | a0001c0001t0003g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-43-194A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713449 | |||||||
| chr3:100713482 | A | G | 3 | a0001c0001t0003g0007 a0001c0001t0003g0142 a0001c0001t0003g0143 |
7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-161A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713482 | |||||||
| chr3:100713493 | A | C | 1 | a0001c0003t0001g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-43-150A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713493 | |||||||
| chr3:100713554 | G | A | 1 | a0001c0002t0013g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-43-89G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | chr3 | 100713554 | |||||||
| chr3:100713570 | CATCTA | C | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-43-70_-43-66delCT others(3): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 100713570 | ||||||
| chr3:100713902 | C | CCT | 13 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(10): Show |
18 | HG00735.hp1 HG01891.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.184+33_184+34insCT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100713902 | |||||||
| chr3:100713902 | C | CT | 4 | a0001c0001t0001g0202 a0001c0001t0003g0007 a0001c0001t0003g0099 others(1): Show |
8 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+38dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100713902 | ||||||
| chr3:100713907 | T | A | 1 | a0001c0002t0002g0148 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.184+38T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100713907 | |||||||
| chr3:100713907 | T | TA | 4 | a0001c0002t0002g0024 a0001c0002t0002g0044 a0001c0002t0002g0149 others(1): Show |
6 | NA18989.hp2 NA18993.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.184+55dupA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100713907 | ||||||
| chr3:100713907 | TA | T | 12 | a0001c0001t0001g0038 a0001c0001t0001g0140 a0001c0001t0003g0070 others(9): Show |
17 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.184+55delA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100713907 | ||||||
| chr3:100713908 | A | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(115): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.184+39A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100713908 | |||||||
| chr3:100713909 | A | T | 6 | a0001c0001t0001g0038 a0001c0001t0001g0140 a0001c0001t0003g0070 others(3): Show |
7 | HG00323.hp2 HG01168.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.184+40A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100713909 | |||||||
| chr3:100713923 | A | G | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.184+54A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100713923 | |||||||
| chr3:100714131 | C | T | 71 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(68): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.184+262C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714131 | |||||||
| chr3:100714212 | A | G | 1 | a0001c0001t0003g0093 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.184+343A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714212 | |||||||
| chr3:100714374 | G | A | 1 | a0001c0001t0004g0198 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.184+505G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714374 | |||||||
| chr3:100714424 | C | T | 1 | a0001c0002t0002g0169 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.184+555C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714424 | |||||||
| chr3:100714436 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.184+567C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714436 | |||||||
| chr3:100714460 | A | G | 1 | a0001c0002t0002g0193 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.184+591A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714460 | |||||||
| chr3:100714567 | AT | A | 74 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0202 others(71): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.184+706delT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100714567 | ||||||
| chr3:100714585 | A | G | 71 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(68): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.184+716A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714585 | |||||||
| chr3:100714748 | T | C | 25 | a0001c0002t0002g0003 a0001c0002t0002g0023 a0001c0002t0002g0040 others(22): Show |
39 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.184+879T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714748 | |||||||
| chr3:100714953 | T | C | 86 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(83): Show |
121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.184+1084T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100714953 | |||||||
| chr3:100715003 | G | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.184+1134G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715003 | |||||||
| chr3:100715307 | A | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.184+1438A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715307 | |||||||
| chr3:100715379 | G | A | 2 | a0001c0004t0001g0013 a0001c0004t0001g0203 |
4 | HG00735.hp1 HG02615.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+1510G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715379 | |||||||
| chr3:100715498 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(161): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.184+1629G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715498 | |||||||
| chr3:100715662 | T | C | 1 | a0001c0002t0002g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.184+1793T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715662 | |||||||
| chr3:100715674 | A | G | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.184+1805A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715674 | |||||||
| chr3:100715687 | T | G | 2 | a0001c0001t0008g0102 a0001c0001t0008g0103 |
2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.184+1818T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715687 | |||||||
| chr3:100715796 | T | C | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.184+1927T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715796 | |||||||
| chr3:100715933 | T | A | 13 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(10): Show |
17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.184+2064T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715933 | |||||||
| chr3:100715983 | A | G | 1 | a0001c0001t0003g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.184+2114A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100715983 | |||||||
| chr3:100716089 | T | C | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.184+2220T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716089 | |||||||
| chr3:100716101 | A | T | 1 | a0001c0001t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.184+2232A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716101 | |||||||
| chr3:100716128 | A | T | 3 | a0001c0002t0002g0006 a0001c0002t0002g0191 a0001c0002t0002g0192 |
8 | NA18946.hp1 NA18947.hp2 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+2259A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716128 | |||||||
| chr3:100716278 | T | G | 5 | a0001c0002t0002g0006 a0001c0002t0002g0042 a0001c0002t0002g0191 others(2): Show |
11 | NA18946.hp1 NA18947.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.184+2409T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716278 | |||||||
| chr3:100716383 | A | G | 71 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(68): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.184+2514A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716383 | |||||||
| chr3:100716530 | G | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG01928.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.184+2661G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716530 | |||||||
| chr3:100716575 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(121): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.184+2706T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716575 | |||||||
| chr3:100716672 | C | T | 1 | a0001c0001t0001g0021 | 3 | HG01109.hp2 HG02602.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.184+2803C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716672 | |||||||
| chr3:100716739 | T | C | 4 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0002g0179 others(1): Show |
4 | NA18612.hp1 NA18963.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+2870T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716739 | |||||||
| chr3:100716927 | C | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.185-3048C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100716927 | |||||||
| chr3:100717576 | A | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.185-2399A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717576 | |||||||
| chr3:100717579 | GT | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(136): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.185-2381delT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100717579 | ||||||
| chr3:100717579 | GTT | G | 3 | a0001c0001t0003g0007 a0001c0001t0003g0142 a0001c0001t0003g0143 |
7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-2382_185-2381d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100717579 | ||||||
| chr3:100717647 | T | A | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.185-2328T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717647 | |||||||
| chr3:100717651 | T | A | 1 | a0001c0001t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.185-2324T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717651 | |||||||
| chr3:100717687 | T | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(50): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.185-2288T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717687 | |||||||
| chr3:100717694 | A | G | 1 | a0001c0003t0001g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.185-2281A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717694 | |||||||
| chr3:100717781 | G | A | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.185-2194G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717781 | |||||||
| chr3:100717803 | T | A | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.185-2172T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717803 | |||||||
| chr3:100717838 | T | TTGAC | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.185-2135_185-2134i others(6): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100717838 | ||||||
| chr3:100717868 | T | A | 1 | a0001c0001t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.185-2107T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717868 | |||||||
| chr3:100717904 | G | C | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.185-2071G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717904 | |||||||
| chr3:100717981 | G | A | 1 | a0001c0002t0002g0161 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.185-1994G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100717981 | |||||||
| chr3:100718054 | A | G | 1 | a0001c0001t0003g0092 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.185-1921A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718054 | |||||||
| chr3:100718229 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.185-1746T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718229 | |||||||
| chr3:100718275 | CTG | C | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.185-1699_185-1698d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718275 | |||||||
| chr3:100718288 | C | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.185-1687C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718288 | |||||||
| chr3:100718305 | A | G | 4 | a0001c0001t0003g0035 a0001c0001t0003g0089 a0001c0001t0003g0090 others(1): Show |
5 | HG01243.hp1 HG02055.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-1670A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718305 | |||||||
| chr3:100718549 | G | GT | 12 | a0001c0002t0002g0012 a0001c0002t0002g0022 a0001c0002t0002g0161 others(9): Show |
17 | HG01099.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.185-1400dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100718549 | ||||||
| chr3:100718549 | GT | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(71): Show |
160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.185-1400delT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100718549 | ||||||
| chr3:100718549 | GTT | G | 7 | a0001c0001t0001g0111 a0001c0001t0003g0067 a0001c0001t0003g0090 others(4): Show |
7 | HG00280.hp1 HG01167.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-1401_185-1400d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100718549 | ||||||
| chr3:100718549 | GTTT | G | 16 | a0001c0001t0001g0110 a0001c0001t0003g0032 a0001c0001t0003g0033 others(13): Show |
19 | HG01106.hp2 HG01243.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.185-1402_185-1400d others(5): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100718549 | ||||||
| chr3:100718549 | GTTTT | G | 59 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0009 others(56): Show |
85 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.185-1403_185-1400d others(6): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100718549 | ||||||
| chr3:100718549 | GTTTTTT | G | 6 | a0001c0001t0003g0007 a0001c0001t0003g0101 a0001c0001t0003g0142 others(3): Show |
12 | HG01975.hp2 HG02258.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.185-1405_185-1400d others(8): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 100718549 | ||||||
| chr3:100718555 | T | G | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.185-1420T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718555 | |||||||
| chr3:100718557 | T | G | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.185-1418T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718557 | |||||||
| chr3:100718600 | T | C | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.185-1375T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718600 | |||||||
| chr3:100718645 | C | A | 1 | a0001c0001t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.185-1330C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718645 | |||||||
| chr3:100718698 | T | C | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.185-1277T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718698 | |||||||
| chr3:100718705 | A | G | 1 | a0001c0001t0009g0129 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.185-1270A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718705 | |||||||
| chr3:100718966 | G | A | 62 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0009 others(59): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.185-1009G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100718966 | |||||||
| chr3:100719048 | A | G | 86 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(83): Show |
121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.185-927A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719048 | |||||||
| chr3:100719082 | G | A | 2 | a0001c0001t0006g0017 a0001c0001t0006g0104 |
4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-893G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719082 | |||||||
| chr3:100719083 | T | G | 2 | a0001c0001t0003g0007 a0001c0001t0003g0143 |
6 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.185-892T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719083 | |||||||
| chr3:100719137 | C | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.185-838C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719137 | |||||||
| chr3:100719177 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.185-798G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719177 | |||||||
| chr3:100719360 | G | A | 1 | a0001c0001t0004g0084 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.185-615G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719360 | |||||||
| chr3:100719410 | A | G | 6 | a0001c0004t0001g0013 a0001c0004t0001g0028 a0001c0004t0001g0046 others(3): Show |
9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.185-565A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719410 | |||||||
| chr3:100719426 | A | G | 1 | a0001c0003t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.185-549A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719426 | |||||||
| chr3:100719515 | G | C | 13 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(10): Show |
17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.185-460G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719515 | |||||||
| chr3:100719523 | A | T | 1 | a0001c0001t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.185-452A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719523 | |||||||
| chr3:100719710 | G | A | 1 | a0001c0001t0005g0145 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.185-265G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719710 | |||||||
| chr3:100719850 | A | C | 1 | a0001c0001t0003g0083 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.185-125A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719850 | |||||||
| chr3:100719940 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(49): Show |
104 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.185-35A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 2/7 | chr3 | 100719940 | |||||||
| chr3:100720280 | TG | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(49): Show |
104 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.268+223delG | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720280 | |||||||
| chr3:100720347 | A | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+289A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720347 | |||||||
| chr3:100720612 | G | A | 13 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(10): Show |
17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.268+554G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720612 | |||||||
| chr3:100720618 | C | T | 1 | a0001c0002t0002g0190 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.268+560C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720618 | |||||||
| chr3:100720628 | C | T | 3 | a0001c0001t0003g0007 a0001c0001t0003g0142 a0001c0001t0003g0143 |
7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.268+570C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720628 | |||||||
| chr3:100720654 | T | G | 1 | a0001c0003t0001g0027 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.268+596T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720654 | |||||||
| chr3:100720814 | C | T | 2 | a0001c0001t0008g0102 a0001c0001t0008g0103 |
2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.268+756C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720814 | |||||||
| chr3:100720885 | T | G | 1 | a0001c0002t0002g0162 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268+827T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720885 | |||||||
| chr3:100720948 | T | A | 1 | a0001c0001t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.268+890T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720948 | |||||||
| chr3:100720950 | A | T | 1 | a0001c0001t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.268+892A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720950 | |||||||
| chr3:100720979 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(135): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.268+921G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100720979 | |||||||
| chr3:100721012 | G | A | 12 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0051 others(9): Show |
16 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.268+954G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721012 | |||||||
| chr3:100721013 | T | A | 1 | a0001c0003t0001g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.268+955T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721013 | |||||||
| chr3:100721211 | C | T | 1 | a0001c0001t0003g0014 | 3 | NA18943.hp2 NA19057.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.268+1153C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721211 | |||||||
| chr3:100721227 | C | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+1169C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721227 | |||||||
| chr3:100721505 | T | C | 1 | a0001c0001t0004g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.268+1447T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721505 | |||||||
| chr3:100721587 | A | G | 2 | a0001c0001t0006g0017 a0001c0001t0006g0104 |
4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+1529A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721587 | |||||||
| chr3:100721826 | A | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+1768A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721826 | |||||||
| chr3:100721980 | A | G | 2 | a0001c0001t0006g0017 a0001c0001t0006g0104 |
4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+1922A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721980 | |||||||
| chr3:100721993 | T | A | 1 | a0001c0002t0002g0164 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.268+1935T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100721993 | |||||||
| chr3:100722107 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.268+2049C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722107 | |||||||
| chr3:100722176 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.268+2118A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722176 | |||||||
| chr3:100722192 | A | G | 28 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0024 others(25): Show |
58 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.268+2134A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722192 | |||||||
| chr3:100722364 | G | A | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.268+2306G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722364 | |||||||
| chr3:100722419 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(120): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.268+2361A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722419 | |||||||
| chr3:100722496 | A | G | 1 | a0001c0001t0003g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.268+2438A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722496 | |||||||
| chr3:100722635 | G | A | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+2577G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722635 | |||||||
| chr3:100722742 | A | C | 1 | a0001c0001t0003g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.268+2684A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722742 | |||||||
| chr3:100722750 | A | G | 1 | a0001c0001t0010g0060 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.268+2692A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722750 | |||||||
| chr3:100722872 | T | C | 26 | a0001c0001t0001g0138 a0001c0002t0002g0003 a0001c0002t0002g0023 others(23): Show |
40 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.268+2814T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100722872 | |||||||
| chr3:100723015 | T | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+2957T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723015 | |||||||
| chr3:100723058 | A | G | 2 | a0001c0001t0003g0009 a0001c0001t0011g0009 |
4 | HG01106.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+3000A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723058 | |||||||
| chr3:100723441 | A | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0134 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.268+3383A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723441 | |||||||
| chr3:100723475 | T | A | 1 | a0001c0001t0003g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.268+3417T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723475 | |||||||
| chr3:100723542 | A | G | 26 | a0001c0001t0001g0138 a0001c0002t0002g0003 a0001c0002t0002g0023 others(23): Show |
40 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.268+3484A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723542 | |||||||
| chr3:100723604 | T | C | 1 | a0001c0003t0001g0027 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.268+3546T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723604 | |||||||
| chr3:100723634 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(49): Show |
104 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.268+3576A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723634 | |||||||
| chr3:100723666 | T | C | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+3608T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723666 | |||||||
| chr3:100723673 | A | G | 2 | a0001c0002t0002g0156 a0001c0002t0002g0157 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.268+3615A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723673 | |||||||
| chr3:100723686 | T | C | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+3628T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723686 | |||||||
| chr3:100723749 | T | G | 3 | a0001c0001t0003g0073 a0001c0001t0003g0085 a0001c0001t0003g0095 |
3 | NA18947.hp1 NA18962.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.268+3691T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723749 | |||||||
| chr3:100723769 | G | A | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+3711G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723769 | |||||||
| chr3:100723814 | A | G | 7 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(4): Show |
8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.268+3756A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723814 | |||||||
| chr3:100723831 | G | GT | 4 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0003g0007 others(1): Show |
8 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+3786dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100723831 | ||||||
| chr3:100723845 | C | G | 6 | a0001c0004t0001g0013 a0001c0004t0001g0028 a0001c0004t0001g0046 others(3): Show |
9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.268+3787C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723845 | |||||||
| chr3:100723881 | G | A | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.268+3823G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723881 | |||||||
| chr3:100723958 | G | T | 2 | a0001c0001t0003g0016 a0001c0001t0003g0082 |
4 | HG01123.hp2 HG01516.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+3900G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723958 | |||||||
| chr3:100723974 | A | T | 1 | a0001c0003t0001g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.268+3916A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100723974 | |||||||
| chr3:100724075 | A | G | 24 | a0001c0001t0001g0138 a0001c0002t0002g0003 a0001c0002t0002g0023 others(21): Show |
38 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.268+4017A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100724075 | |||||||
| chr3:100724264 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(49): Show |
104 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.268+4206G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100724264 | |||||||
| chr3:100724286 | G | T | 1 | a0001c0001t0003g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.268+4228G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100724286 | |||||||
| chr3:100724309 | ATTAG | A | 3 | a0001c0002t0002g0006 a0001c0002t0002g0191 a0001c0002t0002g0192 |
8 | NA18946.hp1 NA18947.hp2 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+4255_268+4258d others(6): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100724309 | ||||||
| chr3:100724482 | G | A | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-4230G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100724482 | |||||||
| chr3:100724664 | T | A | 1 | a0001c0002t0002g0165 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.269-4048T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100724664 | |||||||
| chr3:100724755 | A | G | 1 | a0001c0002t0002g0185 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.269-3957A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100724755 | |||||||
| chr3:100724888 | A | G | 13 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(10): Show |
17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.269-3824A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100724888 | |||||||
| chr3:100725029 | G | C | 3 | a0001c0001t0003g0007 a0001c0001t0003g0142 a0001c0001t0003g0143 |
7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.269-3683G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725029 | |||||||
| chr3:100725060 | C | T | 1 | a0001c0001t0003g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.269-3652C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725060 | |||||||
| chr3:100725061 | G | A | 7 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(4): Show |
8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.269-3651G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725061 | |||||||
| chr3:100725098 | G | T | 63 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0009 others(60): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.269-3614G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725098 | |||||||
| chr3:100725186 | A | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-3526A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725186 | |||||||
| chr3:100725286 | A | G | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.269-3426A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725286 | |||||||
| chr3:100725326 | A | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-3386A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725326 | |||||||
| chr3:100725485 | A | C | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.269-3227A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725485 | |||||||
| chr3:100725622 | C | CA | 14 | a0001c0001t0003g0056 a0001c0001t0003g0072 a0001c0001t0003g0074 others(11): Show |
18 | HG00735.hp2 HG01243.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.269-3067dupA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100725622 | ||||||
| chr3:100725622 | CA | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(73): Show |
142 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.269-3067delA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100725622 | ||||||
| chr3:100725622 | CAA | C | 5 | a0001c0001t0001g0020 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
7 | HG01123.hp1 HG01256.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-3068_269-3067d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100725622 | ||||||
| chr3:100725622 | CAAAA | C | 6 | a0001c0004t0001g0013 a0001c0004t0001g0028 a0001c0004t0001g0046 others(3): Show |
9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.269-3070_269-3067d others(6): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100725622 | ||||||
| chr3:100725622 | CAAAAAA | C | 5 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(2): Show |
6 | HG01891.hp2 HG02615.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-3072_269-3067d others(8): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100725622 | ||||||
| chr3:100725672 | G | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-3040G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725672 | |||||||
| chr3:100725676 | T | TC | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(136): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.269-3034dupC | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100725676 | ||||||
| chr3:100725920 | T | C | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.269-2792T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725920 | |||||||
| chr3:100725923 | G | A | 1 | a0001c0001t0004g0084 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.269-2789G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725923 | |||||||
| chr3:100725928 | A | C | 1 | a0001c0001t0003g0070 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.269-2784A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100725928 | |||||||
| chr3:100726010 | G | C | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-2702G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726010 | |||||||
| chr3:100726118 | G | A | 5 | a0001c0002t0002g0006 a0001c0002t0002g0042 a0001c0002t0002g0191 others(2): Show |
11 | NA18946.hp1 NA18947.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.269-2594G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726118 | |||||||
| chr3:100726223 | G | A | 2 | a0001c0002t0002g0161 a0001c0002t0002g0166 |
2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.269-2489G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726223 | |||||||
| chr3:100726311 | G | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(136): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.269-2401G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726311 | |||||||
| chr3:100726398 | G | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(136): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.269-2314G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726398 | |||||||
| chr3:100726411 | AC | A | 25 | a0001c0002t0002g0003 a0001c0002t0002g0023 a0001c0002t0002g0040 others(22): Show |
39 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.269-2298delC | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100726411 | ||||||
| chr3:100726466 | C | A | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-2246C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726466 | |||||||
| chr3:100726620 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.269-2092C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726620 | |||||||
| chr3:100726684 | A | G | 28 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0024 others(25): Show |
58 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.269-2028A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726684 | |||||||
| chr3:100726773 | A | AT | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-1930dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100726773 | ||||||
| chr3:100726820 | C | T | 2 | a0001c0001t0003g0007 a0001c0001t0003g0143 |
6 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-1892C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726820 | |||||||
| chr3:100726852 | C | T | 7 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(4): Show |
8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.269-1860C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726852 | |||||||
| chr3:100726944 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.269-1768A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100726944 | |||||||
| chr3:100727216 | G | A | 1 | a0001c0002t0002g0177 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.269-1496G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100727216 | |||||||
| chr3:100727340 | C | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0134 a0001c0001t0003g0200 |
3 | HG01891.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.269-1372C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100727340 | |||||||
| chr3:100727542 | C | T | 1 | a0001c0001t0003g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.269-1170C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100727542 | |||||||
| chr3:100727613 | G | A | 1 | a0001c0001t0003g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.269-1099G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100727613 | |||||||
| chr3:100727804 | T | A | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-908T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100727804 | |||||||
| chr3:100728170 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.269-542G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728170 | |||||||
| chr3:100728293 | C | T | 2 | a0001c0001t0010g0060 a0001c0003t0001g0027 |
3 | HG01928.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.269-419C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728293 | |||||||
| chr3:100728321 | T | C | 71 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(68): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.269-391T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728321 | |||||||
| chr3:100728348 | C | T | 1 | a0001c0003t0001g0027 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.269-364C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728348 | |||||||
| chr3:100728364 | ATATT | A | 62 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0009 others(59): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.269-345_269-342del others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100728364 | ||||||
| chr3:100728424 | A | G | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.269-288A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728424 | |||||||
| chr3:100728449 | C | T | 1 | a0001c0001t0003g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.269-263C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728449 | |||||||
| chr3:100728474 | C | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-238C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728474 | |||||||
| chr3:100728526 | C | CT | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.269-179dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 100728526 | ||||||
| chr3:100728571 | T | A | 5 | a0001c0001t0006g0017 a0001c0001t0006g0104 a0001c0001t0008g0102 others(2): Show |
7 | HG00280.hp1 HG01975.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-141T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728571 | |||||||
| chr3:100728572 | T | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(173): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.269-140T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728572 | |||||||
| chr3:100728573 | A | T | 7 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(4): Show |
8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.269-139A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728573 | |||||||
| chr3:100728602 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.269-110T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 3/7 | chr3 | 100728602 | |||||||
| chr3:100728947 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0106 |
2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.415+89G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100728947 | |||||||
| chr3:100729021 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0131 |
3 | NA18971.hp1 NA19001.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.415+163G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729021 | |||||||
| chr3:100729088 | G | A | 3 | a0001c0001t0003g0007 a0001c0001t0003g0142 a0001c0001t0003g0143 |
7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.415+230G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729088 | |||||||
| chr3:100729254 | C | T | 2 | a0001c0001t0008g0102 a0001c0001t0008g0103 |
2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.415+396C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729254 | |||||||
| chr3:100729339 | T | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(161): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.415+481T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729339 | |||||||
| chr3:100729347 | A | T | 7 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(4): Show |
8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+489A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729347 | |||||||
| chr3:100729555 | T | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0001g0136 others(1): Show |
6 | HG01928.hp2 HG01993.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+697T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729555 | |||||||
| chr3:100729582 | CTTA | C | 85 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(82): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.415+733_415+735del others(3): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 100729582 | ||||||
| chr3:100729644 | C | G | 71 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(68): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.415+786C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729644 | |||||||
| chr3:100729653 | T | C | 1 | a0001c0003t0001g0054 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.415+795T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729653 | |||||||
| chr3:100729853 | A | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.415+995A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729853 | |||||||
| chr3:100729865 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(50): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.415+1007A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729865 | |||||||
| chr3:100729920 | G | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(136): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.415+1062G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729920 | |||||||
| chr3:100729928 | A | G | 6 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(3): Show |
7 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.415+1070A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729928 | |||||||
| chr3:100729971 | C | T | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.415+1113C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100729971 | |||||||
| chr3:100730020 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.415+1162G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730020 | |||||||
| chr3:100730181 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.415+1323G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730181 | |||||||
| chr3:100730251 | A | G | 1 | a0001c0002t0002g0168 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.415+1393A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730251 | |||||||
| chr3:100730285 | A | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0134 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.415+1427A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730285 | |||||||
| chr3:100730480 | A | G | 1 | a0001c0001t0004g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.415+1622A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730480 | |||||||
| chr3:100730501 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.415+1643T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730501 | |||||||
| chr3:100730502 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.415+1644A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730502 | |||||||
| chr3:100730657 | C | T | 71 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(68): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.415+1799C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730657 | |||||||
| chr3:100730662 | CAAG | C | 6 | a0001c0004t0001g0013 a0001c0004t0001g0028 a0001c0004t0001g0046 others(3): Show |
9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.415+1807_415+1809d others(5): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 100730662 | ||||||
| chr3:100730819 | T | C | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.416-1689T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730819 | |||||||
| chr3:100730935 | A | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.416-1573A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100730935 | |||||||
| chr3:100731083 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.416-1425G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100731083 | |||||||
| chr3:100731138 | T | C | 3 | a0001c0001t0003g0007 a0001c0001t0003g0142 a0001c0001t0003g0143 |
7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.416-1370T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100731138 | |||||||
| chr3:100731205 | G | T | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.416-1303G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100731205 | |||||||
| chr3:100731536 | C | T | 1 | a0001c0003t0001g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.416-972C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100731536 | |||||||
| chr3:100731667 | G | A | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.416-841G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100731667 | |||||||
| chr3:100731800 | G | A | 2 | a0001c0002t0002g0182 a0001c0002t0002g0187 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.416-708G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100731800 | |||||||
| chr3:100731875 | C | T | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.416-633C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100731875 | |||||||
| chr3:100732112 | C | T | 1 | a0001c0001t0003g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.416-396C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100732112 | |||||||
| chr3:100732155 | C | T | 6 | a0001c0004t0001g0013 a0001c0004t0001g0028 a0001c0004t0001g0046 others(3): Show |
9 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.416-353C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100732155 | |||||||
| chr3:100732184 | C | CA | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.416-317dupA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 100732184 | ||||||
| chr3:100732327 | T | A | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.416-181T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100732327 | |||||||
| chr3:100732399 | A | G | 1 | a0001c0001t0003g0067 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.416-109A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100732399 | |||||||
| chr3:100732499 | T | C | 1 | a0001c0001t0003g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.416-9T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 4/7 | chr3 | 100732499 | |||||||
| chr3:100732722 | G | A | 13 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(10): Show |
17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.580+50G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100732722 | |||||||
| chr3:100732924 | G | A | 3 | a0001c0001t0003g0007 a0001c0001t0003g0142 a0001c0001t0003g0143 |
7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.580+252G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100732924 | |||||||
| chr3:100732936 | T | C | 60 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0014 others(57): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.580+264T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100732936 | |||||||
| chr3:100732998 | A | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.580+326A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100732998 | |||||||
| chr3:100733161 | T | G | 1 | a0001c0001t0003g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.580+489T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733161 | |||||||
| chr3:100733613 | C | G | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.580+941C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733613 | |||||||
| chr3:100733724 | A | G | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.580+1052A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733724 | |||||||
| chr3:100733729 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(50): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.580+1057T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733729 | |||||||
| chr3:100733730 | A | C | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.580+1058A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733730 | |||||||
| chr3:100733740 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.580+1068G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733740 | |||||||
| chr3:100733770 | A | G | 1 | a0001c0002t0002g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.580+1098A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733770 | |||||||
| chr3:100733773 | T | G | 1 | a0001c0003t0001g0027 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.580+1101T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733773 | |||||||
| chr3:100733800 | C | G | 71 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(68): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.580+1128C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733800 | |||||||
| chr3:100733824 | G | C | 71 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(68): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.580+1152G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733824 | |||||||
| chr3:100733965 | T | C | 1 | a0001c0001t0009g0129 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.580+1293T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100733965 | |||||||
| chr3:100734032 | G | C | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.580+1360G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734032 | |||||||
| chr3:100734066 | C | CT | 4 | a0001c0001t0003g0007 a0001c0001t0003g0143 a0001c0002t0002g0150 others(1): Show |
8 | HG02055.hp1 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.580+1404dupT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 100734066 | ||||||
| chr3:100734067 | T | A | 60 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0014 others(57): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.580+1395T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734067 | |||||||
| chr3:100734129 | A | G | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.580+1457A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734129 | |||||||
| chr3:100734177 | T | TA | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.580+1505_580+1506i others(3): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734177 | |||||||
| chr3:100734253 | A | G | 1 | a0001c0002t0002g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.580+1581A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734253 | |||||||
| chr3:100734341 | G | C | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.580+1669G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734341 | |||||||
| chr3:100734347 | T | C | 1 | a0001c0001t0003g0082 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.580+1675T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734347 | |||||||
| chr3:100734401 | G | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.580+1729G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734401 | |||||||
| chr3:100734458 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.580+1786A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734458 | |||||||
| chr3:100734564 | C | A | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.580+1892C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734564 | |||||||
| chr3:100734641 | G | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0063 a0001c0001t0003g0064 others(1): Show |
6 | NA18943.hp2 NA18961.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.581-1935G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734641 | |||||||
| chr3:100734991 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.581-1585A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100734991 | |||||||
| chr3:100735007 | G | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.581-1569G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735007 | |||||||
| chr3:100735015 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(136): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.581-1561T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735015 | |||||||
| chr3:100735022 | T | G | 7 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(4): Show |
8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.581-1554T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735022 | |||||||
| chr3:100735280 | G | A | 3 | a0001c0001t0003g0007 a0001c0001t0003g0142 a0001c0001t0003g0143 |
7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.581-1296G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735280 | |||||||
| chr3:100735387 | C | T | 1 | a0001c0003t0001g0027 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.581-1189C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735387 | |||||||
| chr3:100735434 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(49): Show |
104 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.581-1142A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735434 | |||||||
| chr3:100735494 | C | G | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.581-1082C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735494 | |||||||
| chr3:100735541 | T | C | 1 | a0001c0002t0002g0163 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.581-1035T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735541 | |||||||
| chr3:100735712 | T | C | 7 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(4): Show |
8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.581-864T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735712 | |||||||
| chr3:100735787 | A | G | 3 | a0001c0001t0003g0007 a0001c0001t0003g0142 a0001c0001t0003g0143 |
7 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.581-789A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735787 | |||||||
| chr3:100735887 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.581-689C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735887 | |||||||
| chr3:100735902 | G | A | 2 | a0001c0001t0006g0017 a0001c0001t0006g0104 |
4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-674G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100735902 | |||||||
| chr3:100736154 | G | T | 1 | a0001c0003t0001g0027 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.581-422G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100736154 | |||||||
| chr3:100736295 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(50): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.581-281T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100736295 | |||||||
| chr3:100736512 | C | T | 1 | a0001c0002t0002g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.581-64C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 5/7 | chr3 | 100736512 | |||||||
| chr3:100736765 | TG | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(50): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.721+50delG | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100736765 | |||||||
| chr3:100736958 | C | T | 13 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(10): Show |
17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.721+242C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100736958 | |||||||
| chr3:100736985 | G | C | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+269G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100736985 | |||||||
| chr3:100736986 | A | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+270A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100736986 | |||||||
| chr3:100737094 | TA | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+384delA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100737094 | ||||||
| chr3:100737165 | C | A | 1 | a0001c0002t0002g0185 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.721+449C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737165 | |||||||
| chr3:100737218 | G | A | 2 | a0001c0001t0003g0083 a0001c0001t0003g0092 |
2 | HG01346.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.721+502G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737218 | |||||||
| chr3:100737250 | A | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+534A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737250 | |||||||
| chr3:100737383 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.721+667C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737383 | |||||||
| chr3:100737384 | A | G | 1 | a0001c0001t0003g0064 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.721+668A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737384 | |||||||
| chr3:100737562 | G | A | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+846G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737562 | |||||||
| chr3:100737669 | C | T | 1 | a0001c0004t0001g0203 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.721+953C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737669 | |||||||
| chr3:100737735 | A | G | 1 | a0001c0001t0003g0079 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.721+1019A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737735 | |||||||
| chr3:100737740 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.721+1024C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737740 | |||||||
| chr3:100737916 | A | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+1200A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737916 | |||||||
| chr3:100737988 | A | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+1272A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100737988 | |||||||
| chr3:100738085 | CA | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(90): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.721+1382delA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100738085 | ||||||
| chr3:100738085 | CAA | C | 70 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(67): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.721+1381_721+1382d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100738085 | ||||||
| chr3:100738124 | C | T | 1 | a0001c0001t0003g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.721+1408C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738124 | |||||||
| chr3:100738177 | C | T | 1 | a0001c0001t0003g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.721+1461C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738177 | |||||||
| chr3:100738355 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.721+1639G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738355 | |||||||
| chr3:100738556 | A | G | 1 | a0001c0002t0002g0179 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.721+1840A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738556 | |||||||
| chr3:100738763 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.721+2047C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738763 | |||||||
| chr3:100738796 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.721+2080C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738796 | |||||||
| chr3:100738889 | C | T | 1 | a0001c0003t0001g0027 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.721+2173C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738889 | |||||||
| chr3:100738941 | T | C | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.721+2225T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100738941 | |||||||
| chr3:100739053 | G | T | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.721+2337G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739053 | |||||||
| chr3:100739090 | T | G | 1 | a0001c0002t0002g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.721+2374T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739090 | |||||||
| chr3:100739169 | C | T | 2 | a0001c0001t0006g0017 a0001c0001t0006g0104 |
4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.721+2453C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739169 | |||||||
| chr3:100739247 | G | T | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.721+2531G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739247 | |||||||
| chr3:100739259 | T | A | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+2543T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739259 | |||||||
| chr3:100739294 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.721+2578C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739294 | |||||||
| chr3:100739355 | T | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.721+2639T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739355 | |||||||
| chr3:100739416 | G | A | 76 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(73): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.721+2700G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739416 | |||||||
| chr3:100739507 | A | G | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.721+2791A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739507 | |||||||
| chr3:100739786 | A | G | 1 | a0001c0002t0002g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.721+3070A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739786 | |||||||
| chr3:100739807 | C | T | 8 | a0001c0003t0001g0027 a0001c0003t0001g0045 a0001c0004t0001g0013 others(5): Show |
12 | HG00280.hp1 HG00735.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.721+3091C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739807 | |||||||
| chr3:100739914 | A | G | 1 | a0001c0001t0009g0129 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.721+3198A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739914 | |||||||
| chr3:100739922 | G | A | 1 | a0001c0001t0003g0092 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.721+3206G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100739922 | |||||||
| chr3:100740058 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.721+3342C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740058 | |||||||
| chr3:100740061 | T | C | 1 | a0001c0002t0002g0193 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.721+3345T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740061 | |||||||
| chr3:100740152 | A | G | 62 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0009 others(59): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.721+3436A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740152 | |||||||
| chr3:100740252 | C | T | 6 | a0001c0003t0001g0027 a0001c0004t0001g0013 a0001c0004t0001g0028 others(3): Show |
10 | HG00735.hp1 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.721+3536C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740252 | |||||||
| chr3:100740385 | C | T | 4 | a0001c0001t0003g0016 a0001c0001t0003g0059 a0001c0001t0003g0081 others(1): Show |
6 | HG00735.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.721+3669C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740385 | |||||||
| chr3:100740461 | T | A | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.721+3745T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740461 | |||||||
| chr3:100740531 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(50): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.721+3815C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740531 | |||||||
| chr3:100740691 | G | A | 2 | a0001c0001t0003g0009 a0001c0001t0011g0009 |
4 | HG01106.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.721+3975G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740691 | |||||||
| chr3:100740995 | A | G | 6 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(3): Show |
7 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.722-3838A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100740995 | |||||||
| chr3:100741122 | T | G | 24 | a0001c0001t0001g0138 a0001c0002t0002g0003 a0001c0002t0002g0023 others(21): Show |
38 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.722-3711T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741122 | |||||||
| chr3:100741137 | TTTTA | T | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.722-3695_722-3692d others(6): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741137 | |||||||
| chr3:100741196 | G | T | 1 | a0001c0003t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.722-3637G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741196 | |||||||
| chr3:100741257 | G | A | 1 | a0001c0003t0001g0027 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.722-3576G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741257 | |||||||
| chr3:100741426 | T | C | 2 | a0001c0001t0003g0007 a0001c0001t0003g0143 |
6 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.722-3407T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741426 | |||||||
| chr3:100741513 | T | A | 1 | a0001c0001t0004g0075 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.722-3320T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741513 | |||||||
| chr3:100741601 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.722-3232A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741601 | |||||||
| chr3:100741759 | T | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(50): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.722-3074T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741759 | |||||||
| chr3:100741862 | G | A | 1 | a0001c0002t0002g0150 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.722-2971G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741862 | |||||||
| chr3:100741922 | C | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.722-2911C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100741922 | |||||||
| chr3:100742076 | A | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.722-2757A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742076 | |||||||
| chr3:100742155 | G | T | 1 | a0001c0001t0003g0087 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.722-2678G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742155 | |||||||
| chr3:100742178 | G | A | 2 | a0001c0001t0006g0017 a0001c0001t0006g0104 |
4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-2655G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742178 | |||||||
| chr3:100742262 | T | C | 2 | a0001c0001t0008g0102 a0001c0001t0008g0103 |
2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.722-2571T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742262 | |||||||
| chr3:100742271 | G | A | 1 | a0001c0002t0002g0152 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.722-2562G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742271 | |||||||
| chr3:100742273 | A | G | 2 | a0001c0001t0006g0017 a0001c0001t0006g0104 |
4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-2560A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742273 | |||||||
| chr3:100742532 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.722-2301T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742532 | |||||||
| chr3:100742598 | T | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(121): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.722-2235T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742598 | |||||||
| chr3:100742620 | A | G | 1 | a0001c0003t0001g0027 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.722-2213A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742620 | |||||||
| chr3:100742693 | T | C | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.722-2140T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100742693 | |||||||
| chr3:100742789 | CTG | C | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.722-2040_722-2039d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100742789 | ||||||
| chr3:100742890 | C | CA | 69 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0009 others(66): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.722-1932dupA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100742890 | ||||||
| chr3:100742890 | CA | C | 15 | a0001c0001t0001g0109 a0001c0003t0001g0027 a0001c0003t0001g0029 others(12): Show |
20 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.722-1932delA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100742890 | ||||||
| chr3:100743040 | GT | G | 2 | a0001c0002t0002g0022 a0001c0002t0002g0162 |
4 | HG02257.hp1 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-1791delT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100743040 | ||||||
| chr3:100743064 | A | G | 4 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0144 others(1): Show |
4 | NA18951.hp1 NA18997.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.722-1769A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743064 | |||||||
| chr3:100743249 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.722-1584C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743249 | |||||||
| chr3:100743398 | C | T | 2 | a0001c0001t0006g0017 a0001c0001t0006g0104 |
4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-1435C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743398 | |||||||
| chr3:100743418 | C | T | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.722-1415C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743418 | |||||||
| chr3:100743657 | C | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.722-1176C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743657 | |||||||
| chr3:100743683 | A | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(136): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.722-1150A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743683 | |||||||
| chr3:100743694 | G | A | 2 | a0001c0001t0008g0102 a0001c0001t0008g0103 |
2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.722-1139G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743694 | |||||||
| chr3:100743731 | C | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.722-1102C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100743731 | |||||||
| chr3:100743803 | C | CTT | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.722-1020_722-1019d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100743803 | ||||||
| chr3:100744029 | A | G | 2 | a0001c0001t0008g0102 a0001c0001t0008g0103 |
2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.722-804A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744029 | |||||||
| chr3:100744036 | T | G | 1 | a0001c0001t0003g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.722-797T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744036 | |||||||
| chr3:100744043 | G | GA | 7 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(4): Show |
8 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.722-786dupA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100744043 | ||||||
| chr3:100744141 | A | G | 2 | a0001c0001t0003g0007 a0001c0001t0003g0143 |
6 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.722-692A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744141 | |||||||
| chr3:100744334 | C | G | 1 | a0001c0002t0002g0184 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.722-499C>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744334 | |||||||
| chr3:100744424 | A | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(50): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.722-409A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744424 | |||||||
| chr3:100744514 | A | G | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.722-319A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744514 | |||||||
| chr3:100744548 | G | T | 2 | a0001c0004t0001g0046 a0001c0004t0001g0047 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.722-285G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744548 | |||||||
| chr3:100744776 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.722-57C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744776 | |||||||
| chr3:100744806 | C | CGT | 2 | a0001c0002t0002g0025 a0001c0002t0002g0188 |
4 | HG02083.hp1 HG02135.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-27_722-26insGT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744806 | |||||||
| chr3:100744807 | T | G | 28 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0024 others(25): Show |
58 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.722-26T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744807 | |||||||
| chr3:100744807 | T | TTG | 2 | a0001c0001t0006g0017 a0001c0001t0006g0104 |
4 | HG01975.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.722-8_722-7dupGT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 100744807 | ||||||
| chr3:100744825 | G | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
splice_region_variant&intron_variant | LOW | c.722-8G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 6/7 | chr3 | 100744825 | |||||||
| chr3:100744990 | T | C | 1 | a0001c0003t0001g0027 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.820+59T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100744990 | |||||||
| chr3:100745012 | TTGTAG | T | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.820+83_820+87delGT others(3): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 100745012 | ||||||
| chr3:100745031 | T | C | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.820+100T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745031 | |||||||
| chr3:100745036 | A | T | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.820+105A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745036 | |||||||
| chr3:100745075 | A | C | 1 | a0001c0002t0002g0183 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.820+144A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745075 | |||||||
| chr3:100745140 | T | C | 71 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(68): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.820+209T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745140 | |||||||
| chr3:100745165 | T | C | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.820+234T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745165 | |||||||
| chr3:100745179 | GTT | G | 71 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(68): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.820+252_820+253del others(2): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 100745179 | ||||||
| chr3:100745390 | T | A | 1 | a0001c0001t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.820+459T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745390 | |||||||
| chr3:100745609 | T | G | 1 | a0001c0003t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.820+678T>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745609 | |||||||
| chr3:100745694 | A | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.820+763A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745694 | |||||||
| chr3:100745710 | A | G | 1 | a0001c0001t0005g0065 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.820+779A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745710 | |||||||
| chr3:100745721 | T | C | 1 | a0001c0001t0003g0034 | 2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.820+790T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745721 | |||||||
| chr3:100745878 | G | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.820+947G>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745878 | |||||||
| chr3:100745920 | C | A | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.820+989C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100745920 | |||||||
| chr3:100746086 | C | A | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.820+1155C>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746086 | |||||||
| chr3:100746391 | A | G | 24 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0030 others(21): Show |
39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.820+1460A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746391 | |||||||
| chr3:100746432 | C | T | 20 | a0001c0001t0003g0008 a0001c0001t0003g0057 a0001c0001t0003g0073 others(17): Show |
22 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.820+1501C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746432 | |||||||
| chr3:100746510 | A | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.820+1579A>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746510 | |||||||
| chr3:100746618 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.821-1531T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746618 | |||||||
| chr3:100746618 | TAC | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.821-1519_821-1518d others(4): Show |
TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 100746618 | ||||||
| chr3:100746753 | TA | T | 15 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0045 others(12): Show |
20 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.821-1387delA | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 100746753 | ||||||
| chr3:100746765 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(121): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.821-1384A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746765 | |||||||
| chr3:100746917 | G | A | 1 | a0001c0003t0001g0027 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.821-1232G>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746917 | |||||||
| chr3:100746922 | A | G | 2 | a0001c0001t0003g0074 a0001c0001t0003g0077 |
2 | NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.821-1227A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746922 | |||||||
| chr3:100746984 | C | T | 14 | a0001c0003t0001g0027 a0001c0003t0001g0029 a0001c0003t0001g0049 others(11): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.821-1165C>T | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100746984 | |||||||
| chr3:100747134 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.821-1015G>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100747134 | |||||||
| chr3:100747342 | CT | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(51): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.821-796delT | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 100747342 | ||||||
| chr3:100747499 | T | A | 1 | a0001c0001t0004g0075 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.821-650T>A | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100747499 | |||||||
| chr3:100747577 | A | C | 3 | a0001c0002t0002g0153 a0001c0002t0002g0156 a0001c0002t0002g0157 |
3 | HG01256.hp2 HG01258.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.821-572A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100747577 | |||||||
| chr3:100747685 | T | C | 1 | a0001c0002t0002g0168 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.821-464T>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100747685 | |||||||
| chr3:100747727 | A | C | 13 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(10): Show |
17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.821-422A>C | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100747727 | |||||||
| chr3:100747864 | A | G | 13 | a0001c0003t0001g0029 a0001c0003t0001g0049 a0001c0003t0001g0050 others(10): Show |
17 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.821-285A>G | TFG | ENSG00000114354.15 | transcript | ENST00000240851.9 | protein_coding | 7/7 | chr3 | 100747864 |