Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7030 |
| ensemblid | ENSG00000068323.17 |
| hgncid | 11752 |
| symbol | TFE3 |
| name | transcription factor binding to IGHM enhancer 3 |
| refseq_nuc | NM_006521.6 |
| refseq_prot | NP_006512.2 |
| ensembl_nuc | ENST00000315869.8 |
| ensembl_prot | ENSP00000314129.7 |
| mane_status | MANE Select |
| chr | chrX |
| start | 49028726 |
| end | 49043357 |
| strand | - |
| ver | v1.2 |
| region | chrX:49028726-49043357 |
| region5000 | chrX:49023726-49048357 |
| regionname0 | TFE3_chrX_49028726_49043357 |
| regionname5000 | TFE3_chrX_49023726_49048357 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 575 | 254 | 73 | 50 | 90 | 9 | 30 | 68 | TFE3_chrX_49023726_49048357 | TFE3 | MSHAA others(570): Show |
chrX | 49023726 | 49048357 |
| a0002 | 0/0 | 575 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | MSHAA others(570): Show |
chrX | 49023726 | 49048357 |
| a0003 | 0/0 | 575 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | MSHAA others(570): Show |
chrX | 49023726 | 49048357 |
| a0004 | 0/0 | 575 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | MSHAA others(570): Show |
chrX | 49023726 | 49048357 |
| a0005 | 0/0 | 575 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | MSHAA others(570): Show |
chrX | 49023726 | 49048357 |
| a0006 | 0/0 | 575 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | MSHAA others(570): Show |
chrX | 49023726 | 49048357 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1725 | 201 | 72 | 29 | 81 | 2 | 16 | TFE3_chrX_49023726_49048357 | TFE3 | ATGTC others(1720): Show |
chrX | 49023726 | 49048357 | ||
| a0001c0002 | 0/1 | 1725 | 53 | 1 | 21 | 9 | 7 | 14 | TFE3_chrX_49023726_49048357 | TFE3 | ATGTC others(1720): Show |
chrX | 49023726 | 49048357 | ||
| a0002c0003 | 0/0 | 1725 | 2 | 2 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | ATGTC others(1720): Show |
chrX | 49023726 | 49048357 | ||
| a0003c0007 | 0/0 | 1725 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | ATGTC others(1720): Show |
chrX | 49023726 | 49048357 | ||
| a0004c0004 | 0/0 | 1725 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | ATGTC others(1720): Show |
chrX | 49023726 | 49048357 | ||
| a0005c0006 | 0/0 | 1725 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | ATGTC others(1720): Show |
chrX | 49023726 | 49048357 | ||
| a0006c0005 | 0/0 | 1725 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | ATGTC others(1720): Show |
chrX | 49023726 | 49048357 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3291 | 141 | 22 | 21 | 80 | 2 | 16 | TFE3_chrX_49023726_49048357 | TFE3 | GCAGT others(3286): Show |
chrX | 49023726 | 49048357 |
| a0001c0001t0002 | 1/0 | 3291 | 56 | 47 | 8 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | GCAGT others(3286): Show |
chrX | 49023726 | 49048357 |
| a0001c0001t0003 | 0/0 | 3291 | 2 | 2 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | GCAGT others(3286): Show |
chrX | 49023726 | 49048357 |
| a0001c0001t0004 | 0/0 | 3291 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | GCAGT others(3286): Show |
chrX | 49023726 | 49048357 |
| a0001c0001t0005 | 0/0 | 3291 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | GCAGT others(3286): Show |
chrX | 49023726 | 49048357 |
| a0001c0002t0001 | 0/1 | 3291 | 53 | 1 | 21 | 9 | 7 | 14 | TFE3_chrX_49023726_49048357 | TFE3 | GCAGT others(3286): Show |
chrX | 49023726 | 49048357 |
| a0002c0003t0001 | 0/0 | 3291 | 2 | 2 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | GCAGT others(3286): Show |
chrX | 49023726 | 49048357 |
| a0003c0007t0001 | 0/0 | 3291 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | GCAGT others(3286): Show |
chrX | 49023726 | 49048357 |
| a0004c0004t0001 | 0/0 | 3291 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | GCAGT others(3286): Show |
chrX | 49023726 | 49048357 |
| a0005c0006t0001 | 0/0 | 3291 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | GCAGT others(3286): Show |
chrX | 49023726 | 49048357 |
| a0006c0005t0002 | 0/0 | 3291 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | GCAGT others(3286): Show |
chrX | 49023726 | 49048357 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 77 | 16 | 12 | 44 | 1 | 4 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0003 | 0/0 | 18 | 0 | 4 | 8 | 0 | 6 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0004 | 1/0 | 9 | 7 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0006 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0002 | 0/0 | 33 | 0 | 16 | 7 | 3 | 7 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0061 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0002c0003t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0003c0007t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0004c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0005c0006t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| a0006c0005t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | GBR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | GBR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0036 | EUR | GBR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0038 | EUR | FIN | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00438 | hp2 | a0003 | c0007 | t0001 | g0051 | EAS | CHS | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00609 | hp1 | a0004 | c0004 | t0001 | g0026 | EAS | CHS | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | CLM | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0014 | EUR | IBS | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0014 | EUR | IBS | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02040 | hp1 | a0005 | c0006 | t0001 | g0050 | EAS | KHV | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | KHV | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CDX | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0011 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0084 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02451 | hp1 | a0006 | c0005 | t0002 | g0077 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | ESN | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ESN | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | MSL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | MSL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | MSL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | MSL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | ESN | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0041 | SAS | STU | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0027 | SAS | BEB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0064 | SAS | BEB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0013 | SAS | BEB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0044 | SAS | STU | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | YRI | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | LWK | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | LWK | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ASW | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | GIH | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | USA | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | USA | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | LWK | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0061 | REF | REF | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0004 | REF | REF | TFE3_chrX_49023726_49048357 | TFE3 | chrX | 49023726 | 49048357 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:49030189 | C | T | 1 | a0003 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.1697G>A | p.Arg566His | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 10/10 | 1828/3291 | 1697/1728 | 566/575 | chrX | 49030189 | |||
| chrX:49030241 | C | T | 1 | a0005 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.1645G>A | p.Asp549Asn | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 10/10 | 1776/3291 | 1645/1728 | 549/575 | chrX | 49030241 | |||
| chrX:49030436 | C | T | 1 | a0002 | 2 | HG02257.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.1450G>A | p.Ala484Thr | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 10/10 | 1581/3291 | 1450/1728 | 484/575 | chrX | 49030436 | |||
| chrX:49034214 | C | T | 1 | a0006 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.923G>A | p.Ser308Asn | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 6/10 | 1054/3291 | 923/1728 | 308/575 | chrX | 49034214 | |||
| chrX:49043201 | C | G | 1 | a0004 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.26G>C | p.Arg9Pro | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/10 | 157/3291 | 26/1728 | 9/575 | chrX | 49043201 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:49030563 | T | C | 1 | a0001c0002 | 52 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(49): Show |
synonymous_variant | LOW | c.1323A>G | p.Val441Val | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 10/10 | 1454/3291 | 1323/1728 | 441/575 | chrX | 49030563 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:49028817 | T | C | 1 | a0001c0001t0005 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1341A>G | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 10/10 | 1341 | chrX | 49028817 | ||||||
| chrX:49028977 | G | A | 1 | a0001c0001t0003 | 2 | HG02622.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1181C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 10/10 | 1181 | chrX | 49028977 | ||||||
| chrX:49029628 | C | A | 1 | a0001c0001t0005 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*530G>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 10/10 | 530 | chrX | 49029628 | ||||||
| chrX:49043305 | C | T | 1 | a0001c0001t0004 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-79G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/10 | 79 | chrX | 49043305 | ||||||
| chrX:49043321 | C | T | 7 | a0001c0001t0001 a0001c0001t0004 a0001c0002t0001 others(4): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
5_prime_UTR_variant | MODIFIER | c.-95G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/10 | 95 | chrX | 49043321 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:49030827 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1285-226G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 9/9 | chrX | 49030827 | |||||||
| chrX:49030973 | T | C | 6 | a0001c0001t0002g0005 a0001c0001t0002g0081 a0001c0001t0002g0087 others(3): Show |
13 | HG01243.hp1 HG01891.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1285-372A>G | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 9/9 | chrX | 49030973 | |||||||
| chrX:49031085 | A | AAAAT | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(67): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1284+308_1284+311d others(6): Show |
TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 9/9 | chrX | 49031085 | |||||||
| chrX:49031085 | A | AAAATAAA others(5): Show |
1 | a0002c0003t0001g0011 | 2 | HG02257.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1284+300_1284+311d others(14): Show |
TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 9/9 | chrX | 49031085 | |||||||
| chrX:49031327 | GCT | G | 8 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0069 others(5): Show |
11 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1284+68_1284+69del others(2): Show |
TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 9/9 | chrX | 49031327 | |||||||
| chrX:49031382 | C | A | 1 | a0002c0003t0001g0011 | 2 | HG02257.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1284+15G>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 9/9 | chrX | 49031382 | |||||||
| chrX:49031897 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1137-353C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 8/9 | chrX | 49031897 | |||||||
| chrX:49032231 | C | CT | 6 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0002g0070 others(3): Show |
8 | HG02055.hp1 HG02145.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1137-688dupA | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 8/9 | chrX | 49032231 | |||||||
| chrX:49032267 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1137-723G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 8/9 | chrX | 49032267 | |||||||
| chrX:49032303 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(69): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1137-759A>G | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 8/9 | chrX | 49032303 | |||||||
| chrX:49032327 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(68): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1137-783G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 8/9 | chrX | 49032327 | |||||||
| chrX:49032328 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(69): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1137-784T>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 8/9 | chrX | 49032328 | |||||||
| chrX:49032623 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(55): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1136+842C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 8/9 | chrX | 49032623 | |||||||
| chrX:49032663 | A | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(68): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1136+802T>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 8/9 | chrX | 49032663 | |||||||
| chrX:49033044 | G | T | 1 | a0001c0002t0001g0036 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1136+421C>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 8/9 | chrX | 49033044 | |||||||
| chrX:49033247 | G | A | 2 | a0001c0001t0002g0021 a0001c0001t0002g0071 |
3 | HG02622.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1136+218C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 8/9 | chrX | 49033247 | |||||||
| chrX:49033447 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1136+18C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 8/9 | chrX | 49033447 | |||||||
| chrX:49033600 | A | T | 1 | a0006c0005t0002g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1061-60T>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 7/9 | chrX | 49033600 | |||||||
| chrX:49033793 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1004-11C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 6/9 | chrX | 49033793 | |||||||
| chrX:49033821 | G | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0033 others(8): Show |
28 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.1004-39C>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 6/9 | chrX | 49033821 | |||||||
| chrX:49033923 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1004-141C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 6/9 | chrX | 49033923 | |||||||
| chrX:49034018 | C | G | 2 | a0001c0001t0002g0072 a0001c0001t0002g0073 |
2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1003+116G>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 6/9 | chrX | 49034018 | |||||||
| chrX:49034292 | AC | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(68): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.886-42delG | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49034292 | |||||||
| chrX:49034338 | A | T | 1 | a0001c0001t0002g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.886-87T>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49034338 | |||||||
| chrX:49034562 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886-311C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49034562 | |||||||
| chrX:49034954 | G | GT | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.886-704dupA | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49034954 | |||||||
| chrX:49035002 | G | A | 1 | a0001c0002t0001g0054 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.886-751C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035002 | |||||||
| chrX:49035077 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(69): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.886-826T>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035077 | |||||||
| chrX:49035123 | C | A | 1 | a0001c0001t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.886-872G>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035123 | |||||||
| chrX:49035139 | T | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(68): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.886-888A>G | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035139 | |||||||
| chrX:49035217 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.886-966C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035217 | |||||||
| chrX:49035322 | A | AAAATAAA others(5): Show |
55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(52): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.886-1083_886-1072d others(14): Show |
TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035322 | |||||||
| chrX:49035322 | A | AAAATAAA others(9): Show |
14 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0002g0005 others(11): Show |
29 | HG00735.hp1 HG00738.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.886-1087_886-1072d others(18): Show |
TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035322 | |||||||
| chrX:49035322 | A | AAAATAAA others(13): Show |
10 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0070 others(7): Show |
13 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.886-1091_886-1072d others(22): Show |
TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035322 | |||||||
| chrX:49035322 | A | AAAATAAA others(21): Show |
2 | a0001c0001t0002g0069 a0002c0003t0001g0011 |
3 | HG02257.hp1 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.886-1072_886-1071i others(30): Show |
TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035322 | |||||||
| chrX:49035398 | C | CT | 5 | a0001c0001t0002g0023 a0001c0001t0002g0069 a0001c0001t0002g0071 others(2): Show |
6 | HG00741.hp2 HG02559.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.886-1148dupA | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035398 | |||||||
| chrX:49035419 | TTTTTG | T | 3 | a0001c0001t0002g0010 a0001c0001t0002g0083 a0001c0001t0002g0085 |
5 | HG00738.hp1 HG01891.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.886-1173_886-1169d others(7): Show |
TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035419 | |||||||
| chrX:49035420 | TTTTG | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(12): Show |
30 | HG01243.hp1 HG01256.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.886-1173_886-1170d others(6): Show |
TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035420 | |||||||
| chrX:49035421 | TTTG | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(52): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.886-1173_886-1171d others(5): Show |
TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035421 | |||||||
| chrX:49035422 | TTG | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(5): Show |
16 | HG00099.hp2 HG00621.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.886-1173_886-1172d others(4): Show |
TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035422 | |||||||
| chrX:49035588 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.886-1337A>G | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035588 | |||||||
| chrX:49035598 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.886-1347C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035598 | |||||||
| chrX:49035823 | A | G | 1 | a0006c0005t0002g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.886-1572T>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035823 | |||||||
| chrX:49035826 | C | A | 1 | a0001c0002t0001g0058 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.886-1575G>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035826 | |||||||
| chrX:49035921 | G | A | 1 | a0001c0001t0002g0089 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.886-1670C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035921 | |||||||
| chrX:49035935 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.886-1684G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49035935 | |||||||
| chrX:49036026 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.886-1775G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036026 | |||||||
| chrX:49036184 | T | C | 2 | a0001c0001t0002g0009 a0001c0001t0002g0070 |
4 | HG01081.hp2 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.885+1826A>G | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036184 | |||||||
| chrX:49036196 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(55): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.885+1814C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036196 | |||||||
| chrX:49036206 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(69): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.885+1804T>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036206 | |||||||
| chrX:49036424 | A | AC | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(68): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.885+1585dupG | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036424 | |||||||
| chrX:49036466 | C | CA | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(61): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.885+1543dupT | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036466 | |||||||
| chrX:49036489 | A | T | 1 | a0001c0002t0001g0038 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.885+1521T>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036489 | |||||||
| chrX:49036493 | AAT | A | 16 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0002g0005 others(13): Show |
31 | HG00735.hp1 HG00738.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.885+1515_885+1516d others(4): Show |
TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036493 | |||||||
| chrX:49036494 | AT | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(51): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.885+1515delA | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036494 | |||||||
| chrX:49036495 | T | A | 2 | a0001c0001t0001g0029 a0002c0003t0001g0011 |
3 | HG02257.hp1 HG03516.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.885+1515A>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036495 | |||||||
| chrX:49036498 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.885+1512T>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036498 | |||||||
| chrX:49036499 | T | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.885+1511A>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036499 | |||||||
| chrX:49036503 | T | A | 1 | a0001c0001t0005g0084 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.885+1507A>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036503 | |||||||
| chrX:49036570 | C | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0036 |
5 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.885+1440G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036570 | |||||||
| chrX:49036575 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.885+1435G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036575 | |||||||
| chrX:49036673 | G | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0063 |
7 | HG00408.hp2 HG00544.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.885+1337C>G | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036673 | |||||||
| chrX:49036717 | G | A | 1 | a0001c0001t0001g0007 | 5 | HG00408.hp2 HG00544.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.885+1293C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036717 | |||||||
| chrX:49036734 | G | A | 13 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(10): Show |
27 | HG00735.hp1 HG00738.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.885+1276C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036734 | |||||||
| chrX:49036944 | T | C | 1 | a0001c0001t0004g0025 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.885+1066A>G | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49036944 | |||||||
| chrX:49037029 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(55): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.885+981G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49037029 | |||||||
| chrX:49037055 | G | A | 3 | a0001c0001t0002g0010 a0001c0001t0002g0083 a0001c0001t0005g0084 |
5 | HG00738.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.885+955C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49037055 | |||||||
| chrX:49037514 | C | T | 1 | a0002c0003t0001g0011 | 2 | HG02257.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.885+496G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49037514 | |||||||
| chrX:49037528 | G | A | 1 | a0002c0003t0001g0011 | 2 | HG02257.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.885+482C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49037528 | |||||||
| chrX:49037694 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.885+316C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49037694 | |||||||
| chrX:49037699 | G | GA | 5 | a0001c0001t0001g0029 a0001c0001t0002g0023 a0001c0001t0002g0075 others(2): Show |
6 | HG02559.hp1 HG03209.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.885+310dupT | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49037699 | |||||||
| chrX:49037699 | GA | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0034 others(5): Show |
11 | HG01070.hp1 HG01081.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.885+310delT | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49037699 | |||||||
| chrX:49037857 | T | C | 3 | a0001c0001t0002g0010 a0001c0001t0002g0083 a0001c0001t0005g0084 |
5 | HG00738.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.885+153A>G | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 5/9 | chrX | 49037857 | |||||||
| chrX:49038632 | C | G | 1 | a0001c0001t0001g0032 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.535-190G>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 3/9 | chrX | 49038632 | |||||||
| chrX:49038929 | C | T | 13 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(10): Show |
27 | HG00735.hp1 HG00738.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.534+178G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 3/9 | chrX | 49038929 | |||||||
| chrX:49039419 | T | G | 7 | a0001c0001t0002g0005 a0001c0001t0002g0081 a0001c0001t0002g0087 others(4): Show |
14 | HG01243.hp1 HG01891.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.231-9A>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 2/9 | chrX | 49039419 | |||||||
| chrX:49039488 | C | T | 1 | a0001c0001t0002g0022 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.231-78G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 2/9 | chrX | 49039488 | |||||||
| chrX:49039536 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.231-126T>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 2/9 | chrX | 49039536 | |||||||
| chrX:49039721 | T | G | 1 | a0001c0001t0001g0019 | 2 | HG01106.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.231-311A>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 2/9 | chrX | 49039721 | |||||||
| chrX:49040096 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.230+359G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 2/9 | chrX | 49040096 | |||||||
| chrX:49040176 | A | T | 1 | a0001c0001t0001g0029 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.230+279T>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 2/9 | chrX | 49040176 | |||||||
| chrX:49040334 | C | CCA | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(67): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.230+120_230+121ins others(2): Show |
TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 2/9 | chrX | 49040334 | |||||||
| chrX:49040649 | G | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(54): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.117-81C>G | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49040649 | |||||||
| chrX:49040652 | A | G | 1 | a0002c0003t0001g0011 | 2 | HG02257.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.117-84T>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49040652 | |||||||
| chrX:49040654 | A | G | 2 | a0001c0001t0002g0010 a0002c0003t0001g0011 |
3 | HG00738.hp1 HG02257.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.117-86T>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49040654 | |||||||
| chrX:49040677 | G | A | 3 | a0001c0001t0002g0010 a0001c0001t0002g0083 a0001c0001t0005g0084 |
5 | HG00738.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.117-109C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49040677 | |||||||
| chrX:49040742 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.117-174G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49040742 | |||||||
| chrX:49040936 | CT | C | 15 | a0001c0001t0001g0020 a0001c0001t0002g0005 a0001c0001t0002g0006 others(12): Show |
31 | HG00735.hp1 HG00738.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.117-369delA | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49040936 | |||||||
| chrX:49041133 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(55): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.117-565C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49041133 | |||||||
| chrX:49041183 | G | A | 1 | a0004c0004t0001g0026 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.117-615C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49041183 | |||||||
| chrX:49041282 | T | TAC | 14 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0002g0005 others(11): Show |
27 | HG00099.hp1 HG00735.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.117-716_117-715dup others(2): Show |
TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49041282 | |||||||
| chrX:49041411 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.117-843A>G | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49041411 | |||||||
| chrX:49041555 | A | G | 1 | a0001c0001t0002g0022 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.117-987T>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49041555 | |||||||
| chrX:49041576 | C | A | 1 | a0001c0001t0003g0024 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.117-1008G>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49041576 | |||||||
| chrX:49041602 | G | A | 1 | a0001c0001t0001g0008 | 3 | NA18986.hp1 NA19075.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.117-1034C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49041602 | |||||||
| chrX:49041632 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.117-1064G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49041632 | |||||||
| chrX:49041743 | C | T | 1 | a0002c0003t0001g0011 | 2 | HG02257.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.117-1175G>A | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49041743 | |||||||
| chrX:49041781 | G | C | 1 | a0001c0001t0001g0068 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.117-1213C>G | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49041781 | |||||||
| chrX:49041973 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(55): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.116+1138C>T | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49041973 | |||||||
| chrX:49042017 | A | AC | 9 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0069 others(6): Show |
12 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.116+1093dupG | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49042017 | |||||||
| chrX:49042017 | AC | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(55): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.116+1093delG | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49042017 | |||||||
| chrX:49042391 | A | G | 1 | a0001c0002t0001g0027 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.116+720T>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49042391 | |||||||
| chrX:49042685 | G | C | 1 | a0001c0001t0002g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.116+426C>G | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49042685 | |||||||
| chrX:49042861 | T | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(55): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.116+250A>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49042861 | |||||||
| chrX:49043046 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(55): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.116+65T>C | TFE3 | ENSG00000068323.17 | transcript | ENST00000315869.8 | protein_coding | 1/9 | chrX | 49043046 |