Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 127428 |
| ensemblid | ENSG00000116205.14 |
| hgncid | 26494 |
| symbol | TCEANC2 |
| name | transcription elongation factor A N-terminal and central domain containing 2 |
| refseq_nuc | NM_153035.3 |
| refseq_prot | NP_694580.1 |
| ensembl_nuc | ENST00000234827.6 |
| ensembl_prot | ENSP00000234827.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 54053608 |
| end | 54106082 |
| strand | + |
| ver | v1.2 |
| region | chr1:54053608-54106082 |
| region5000 | chr1:54048608-54111082 |
| regionname0 | TCEANC2_chr1_54053608_54106082 |
| regionname5000 | TCEANC2_chr1_54048608_54111082 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 208 | 349 | 94 | 64 | 155 | 10 | 24 | 121 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | MDKFV others(203): Show |
chr1 | 54048608 | 54111082 |
| a0002 | 0/0 | 208 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | MDKFV others(203): Show |
chr1 | 54048608 | 54111082 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 624 | 344 | 90 | 63 | 155 | 10 | 24 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | ATGGA others(619): Show |
chr1 | 54048608 | 54111082 | ||
| a0001c0003 | 0/0 | 624 | 5 | 4 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | ATGGA others(619): Show |
chr1 | 54048608 | 54111082 | ||
| a0002c0002 | 0/0 | 624 | 5 | 0 | 0 | 5 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | ATGGA others(619): Show |
chr1 | 54048608 | 54111082 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 10429 | 105 | 8 | 22 | 58 | 5 | 11 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10424): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0002 | 0/0 | 10432 | 71 | 5 | 26 | 32 | 3 | 5 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0003 | 0/0 | 10432 | 29 | 0 | 2 | 26 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0004 | 0/0 | 10435 | 25 | 16 | 3 | 5 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10430): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0005 | 0/0 | 10432 | 14 | 0 | 0 | 14 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0006 | 0/0 | 10433 | 10 | 9 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10428): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0007 | 0/0 | 10432 | 9 | 9 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0008 | 0/0 | 10432 | 5 | 5 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0009 | 0/0 | 10432 | 5 | 5 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0010 | 0/0 | 10432 | 4 | 4 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0011 | 1/0 | 10429 | 4 | 0 | 0 | 1 | 2 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10424): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0013 | 0/0 | 10432 | 3 | 3 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0014 | 0/0 | 10432 | 3 | 0 | 0 | 3 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0015 | 0/0 | 10432 | 3 | 0 | 0 | 3 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0016 | 0/0 | 10434 | 3 | 3 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10429): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0017 | 0/0 | 10433 | 3 | 0 | 0 | 3 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10428): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0018 | 0/0 | 10433 | 2 | 0 | 2 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10428): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0019 | 0/0 | 10429 | 2 | 0 | 1 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10424): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0020 | 0/0 | 10432 | 2 | 2 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0021 | 0/0 | 10432 | 2 | 1 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0022 | 0/0 | 10428 | 2 | 2 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10423): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0023 | 0/0 | 10434 | 2 | 2 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10429): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0024 | 0/0 | 10432 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0025 | 0/0 | 10432 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0026 | 0/0 | 10429 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10424): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0027 | 0/0 | 10429 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10424): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0028 | 0/0 | 10429 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10424): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0029 | 0/0 | 10429 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10424): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0030 | 0/0 | 10429 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10424): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0031 | 0/0 | 10432 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0032 | 0/0 | 10428 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10423): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0033 | 0/0 | 10429 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10424): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0034 | 0/0 | 10429 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10424): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0035 | 0/0 | 10433 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10428): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0037 | 0/0 | 10433 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10428): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0039 | 0/0 | 10432 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0040 | 0/0 | 10433 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10428): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0041 | 0/0 | 10432 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0042 | 0/0 | 10433 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10428): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0043 | 0/0 | 10432 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0044 | 0/0 | 10433 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10428): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0045 | 0/0 | 10433 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10428): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0046 | 0/0 | 10435 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10430): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0047 | 0/0 | 10434 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10429): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0048 | 0/0 | 10434 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10429): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0049 | 0/0 | 10433 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10428): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0050 | 0/0 | 10434 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10429): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0051 | 0/0 | 10432 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0052 | 0/0 | 10432 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0053 | 0/0 | 10432 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0054 | 0/0 | 10432 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0055 | 0/0 | 10432 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10427): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0056 | 0/0 | 10436 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10431): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0057 | 0/0 | 10435 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10430): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0058 | 0/0 | 10435 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10430): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0059 | 0/0 | 10435 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10430): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0060 | 0/0 | 10435 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10430): Show |
chr1 | 54048608 | 54111082 |
| a0001c0001t0061 | 0/0 | 10435 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10430): Show |
chr1 | 54048608 | 54111082 |
| a0001c0003t0012 | 0/0 | 10428 | 3 | 2 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10423): Show |
chr1 | 54048608 | 54111082 |
| a0001c0003t0036 | 0/0 | 10429 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10424): Show |
chr1 | 54048608 | 54111082 |
| a0001c0003t0038 | 0/0 | 10428 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10423): Show |
chr1 | 54048608 | 54111082 |
| a0002c0002t0001 | 0/0 | 10429 | 5 | 0 | 0 | 5 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | AGAGG others(10424): Show |
chr1 | 54048608 | 54111082 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 10 | 2 | 3 | 4 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0004 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0002 | 0/0 | 14 | 1 | 3 | 8 | 1 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0006 | 0/0 | 7 | 0 | 4 | 2 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0003g0001 | 0/0 | 14 | 0 | 1 | 13 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0005g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0005g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0006g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0006g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0007g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0007g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0008g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0008g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0008g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0009g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0009g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0009g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0010g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0010g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0010g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0011g0003 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0011g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0011g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0013g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0014g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0014g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0014g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0015g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0015g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0016g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0016g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0017g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0017g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0018g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0019g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0019g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0020g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0021g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0021g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0022g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0022g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0023g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0023g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0024g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0025g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0026g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0027g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0028g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0029g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0030g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0031g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0032g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0033g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0034g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0035g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0037g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0039g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0040g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0041g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0042g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0043g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0044g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0045g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0046g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0047g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0048g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0049g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0050g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0051g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0052g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0053g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0054g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0055g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0056g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0057g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0058g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0059g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0060g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0001t0061g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0003t0012g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0003t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0003t0012g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0003t0036g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0001c0003t0038g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0002c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | GBR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00280 | hp1 | a0001 | c0001 | t0011 | g0003 | EUR | FIN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0025 | EUR | FIN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CHS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00408 | hp2 | a0001 | c0001 | t0014 | g0184 | EAS | CHS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | CHS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00558 | hp2 | a0001 | c0001 | t0043 | g0114 | EAS | CHS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0052 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0176 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00642 | hp2 | a0001 | c0003 | t0012 | g0192 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00735 | hp1 | a0001 | c0001 | t0030 | g0138 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00738 | hp2 | a0001 | c0001 | t0033 | g0139 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01070 | hp2 | a0001 | c0001 | t0024 | g0190 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0061 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01243 | hp2 | a0001 | c0001 | t0021 | g0130 | AMR | PUR | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01256 | hp1 | a0001 | c0001 | t0018 | g0028 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01258 | hp2 | a0001 | c0001 | t0018 | g0028 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0053 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01361 | hp2 | a0001 | c0001 | t0019 | g0076 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01515 | hp2 | a0001 | c0001 | t0011 | g0137 | EUR | IBS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0097 | EUR | IBS | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01884 | hp1 | a0001 | c0001 | t0049 | g0199 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0087 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01891 | hp2 | a0001 | c0001 | t0060 | g0060 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02040 | hp1 | a0001 | c0001 | t0054 | g0001 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02040 | hp2 | a0001 | c0001 | t0040 | g0002 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02055 | hp2 | a0001 | c0001 | t0023 | g0072 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02074 | hp1 | a0001 | c0001 | t0017 | g0213 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0042 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02280 | hp1 | a0001 | c0001 | t0021 | g0182 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02300 | hp1 | a0001 | c0001 | t0041 | g0002 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02451 | hp2 | a0001 | c0001 | t0048 | g0021 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0196 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02572 | hp2 | a0001 | c0001 | t0013 | g0024 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02602 | hp1 | a0001 | c0001 | t0019 | g0075 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02615 | hp1 | a0001 | c0001 | t0055 | g0197 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0042 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0200 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0194 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0055 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02717 | hp1 | a0001 | c0003 | t0038 | g0041 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02809 | hp1 | a0001 | c0001 | t0059 | g0059 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02818 | hp2 | a0001 | c0001 | t0056 | g0009 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0088 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0205 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02896 | hp2 | a0001 | c0001 | t0016 | g0023 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02897 | hp1 | a0001 | c0001 | t0016 | g0023 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0206 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02965 | hp1 | a0001 | c0001 | t0046 | g0021 | AFR | ESN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0090 | AFR | ESN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02970 | hp2 | a0001 | c0001 | t0016 | g0056 | AFR | ESN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0024 | AFR | ESN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0086 | AFR | ESN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03041 | hp1 | a0001 | c0003 | t0036 | g0191 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0198 | AFR | MSL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | MSL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | ESN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03130 | hp2 | a0001 | c0001 | t0058 | g0068 | AFR | ESN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0058 | AFR | ESN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0223 | AFR | ESN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0089 | AFR | ESN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | ESN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03209 | hp1 | a0001 | c0003 | t0012 | g0189 | AFR | MSL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03209 | hp2 | a0001 | c0001 | t0047 | g0070 | AFR | MSL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03239 | hp1 | a0001 | c0001 | t0029 | g0163 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03453 | hp1 | a0001 | c0001 | t0022 | g0166 | AFR | MSL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0040 | AFR | MSL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0195 | AFR | MSL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03490 | hp2 | a0001 | c0001 | t0045 | g0100 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03491 | hp2 | a0001 | c0001 | t0027 | g0008 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03516 | hp1 | a0001 | c0001 | t0039 | g0092 | AFR | ESN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | ESN | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0201 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | GWD | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03579 | hp1 | a0001 | c0003 | t0012 | g0041 | AFR | MSL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03579 | hp2 | a0001 | c0001 | t0020 | g0030 | AFR | MSL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03710 | hp2 | a0001 | c0001 | t0031 | g0180 | SAS | PJL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | BEB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03927 | hp2 | a0001 | c0001 | t0061 | g0067 | SAS | BEB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | STU | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | BEB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | YRI | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0121 | AFR | YRI | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | CHB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | CHB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18906 | hp1 | a0001 | c0001 | t0020 | g0030 | AFR | YRI | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | YRI | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18939 | hp2 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18951 | hp2 | a0001 | c0001 | t0015 | g0037 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18952 | hp2 | a0001 | c0001 | t0057 | g0050 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18972 | hp2 | a0001 | c0001 | t0044 | g0013 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18979 | hp1 | a0001 | c0001 | t0034 | g0126 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18982 | hp1 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18992 | hp1 | a0001 | c0001 | t0014 | g0038 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19001 | hp1 | a0001 | c0001 | t0028 | g0161 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0162 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19011 | hp2 | a0001 | c0001 | t0011 | g0207 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19030 | hp1 | a0001 | c0001 | t0037 | g0047 | AFR | LWK | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19030 | hp2 | a0001 | c0001 | t0050 | g0073 | AFR | LWK | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | LWK | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0135 | AFR | LWK | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19054 | hp1 | a0001 | c0001 | t0014 | g0185 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19060 | hp2 | a0001 | c0001 | t0015 | g0037 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19066 | hp1 | a0001 | c0001 | t0051 | g0001 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19084 | hp2 | a0001 | c0001 | t0025 | g0038 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19088 | hp1 | a0001 | c0001 | t0052 | g0001 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19090 | hp1 | a0001 | c0001 | t0015 | g0172 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19240 | hp1 | a0001 | c0001 | t0042 | g0091 | AFR | YRI | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA19240 | hp2 | a0001 | c0001 | t0032 | g0003 | AFR | YRI | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | ASW | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA20129 | hp2 | a0001 | c0001 | t0023 | g0071 | AFR | ASW | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG01123 | hp2 | a0001 | c0001 | t0026 | g0008 | AMR | CLM | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0040 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02486 | hp2 | a0001 | c0001 | t0022 | g0081 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0119 | AFR | ACB | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03471 | hp1 | a0001 | c0001 | t0053 | g0193 | AFR | MSL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG03471 | hp2 | a0001 | c0001 | t0035 | g0046 | AFR | MSL | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | USA | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0129 | AFR | USA | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0062 | AFR | USA | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | USA | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | LWK | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0128 | REF | REF | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0011 | g0003 | REF | REF | TCEANC2_chr1_54048608_54111082 | TCEANC2 | chr1 | 54048608 | 54111082 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:54088618 | G | A | 1 | a0002 | 5 | NA18940.hp2 NA18959.hp2 NA18982.hp2 others(2): Show |
missense_variant | MODERATE | c.266G>A | p.Arg89His | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/5 | 459/10429 | 266/627 | 89/208 | chr1 | 54088618 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:54088736 | C | T | 1 | a0001c0003 | 5 | HG00642.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
synonymous_variant | LOW | c.384C>T | p.Thr128Thr | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/5 | 577/10429 | 384/627 | 128/208 | chr1 | 54088736 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:54053619 | G | A | 1 | a0001c0001t0024 | 1 | HG01070.hp2 | 5_prime_UTR_variant | MODIFIER | c.-182G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 1/5 | 804 | chr1 | 54053619 | ||||||
| chr1:54053622 | C | T | 7 | a0001c0001t0004 a0001c0001t0056 a0001c0001t0057 others(4): Show |
31 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(28): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-179C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 1/5 | chr1 | 54053622 | |||||||
| chr1:54053734 | G | T | 1 | a0001c0001t0055 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-67G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 1/5 | 689 | chr1 | 54053734 | ||||||
| chr1:54096522 | G | A | 1 | a0001c0001t0025 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*49G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 49 | chr1 | 54096522 | ||||||
| chr1:54096541 | G | T | 1 | a0001c0001t0009 | 5 | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*68G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 68 | chr1 | 54096541 | ||||||
| chr1:54096771 | A | G | 22 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(19): Show |
87 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*298A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 298 | chr1 | 54096771 | ||||||
| chr1:54097277 | G | GT | 2 | a0001c0001t0006 a0001c0001t0045 |
11 | HG00642.hp1 HG02258.hp2 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*811dupT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 812 | INFO_REALIGN_3_PRIME | chr1 | 54097277 | |||||
| chr1:54097293 | T | C | 14 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0023 others(11): Show |
41 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*820T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 820 | chr1 | 54097293 | ||||||
| chr1:54097307 | C | CT | 14 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0023 others(11): Show |
41 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*842dupT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 843 | INFO_REALIGN_3_PRIME | chr1 | 54097307 | |||||
| chr1:54097366 | G | A | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(58): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*893G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 893 | chr1 | 54097366 | ||||||
| chr1:54097479 | G | A | 1 | a0001c0001t0009 | 5 | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1006G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 1006 | chr1 | 54097479 | ||||||
| chr1:54097483 | A | G | 48 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(45): Show |
227 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*1010A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 1010 | chr1 | 54097483 | ||||||
| chr1:54097566 | A | T | 13 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(10): Show |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1093A>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 1093 | chr1 | 54097566 | ||||||
| chr1:54097702 | T | G | 1 | a0001c0001t0051 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1229T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 1229 | chr1 | 54097702 | ||||||
| chr1:54097714 | A | G | 1 | a0001c0001t0022 | 2 | HG02486.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1241A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 1241 | chr1 | 54097714 | ||||||
| chr1:54097849 | G | A | 12 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0023 others(9): Show |
39 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1376G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 1376 | chr1 | 54097849 | ||||||
| chr1:54097869 | C | T | 1 | a0001c0001t0061 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1396C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 1396 | chr1 | 54097869 | ||||||
| chr1:54097882 | T | C | 1 | a0001c0001t0010 | 4 | HG02486.hp1 HG02647.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1409T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 1409 | chr1 | 54097882 | ||||||
| chr1:54098144 | A | T | 1 | a0001c0001t0054 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1671A>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 1671 | chr1 | 54098144 | ||||||
| chr1:54098492 | A | T | 1 | a0001c0001t0009 | 5 | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2019A>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 2019 | chr1 | 54098492 | ||||||
| chr1:54098518 | T | C | 1 | a0001c0001t0056 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2045T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 2045 | chr1 | 54098518 | ||||||
| chr1:54098634 | T | G | 1 | a0001c0001t0057 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2161T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 2161 | chr1 | 54098634 | ||||||
| chr1:54098692 | G | T | 2 | a0001c0001t0005 a0001c0001t0044 |
15 | HG00423.hp1 HG02523.hp1 NA18941.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2219G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 2219 | chr1 | 54098692 | ||||||
| chr1:54098703 | G | T | 1 | a0001c0001t0060 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2230G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 2230 | chr1 | 54098703 | ||||||
| chr1:54098812 | G | A | 5 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0051 others(2): Show |
35 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2339G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 2339 | chr1 | 54098812 | ||||||
| chr1:54098923 | A | C | 1 | a0001c0001t0043 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2450A>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 2450 | chr1 | 54098923 | ||||||
| chr1:54098983 | A | T | 1 | a0001c0001t0042 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2510A>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 2510 | chr1 | 54098983 | ||||||
| chr1:54099048 | C | T | 1 | a0001c0001t0034 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2575C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 2575 | chr1 | 54099048 | ||||||
| chr1:54099259 | G | C | 1 | a0001c0001t0039 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2786G>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 2786 | chr1 | 54099259 | ||||||
| chr1:54099462 | G | A | 1 | a0001c0001t0020 | 2 | HG03579.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2989G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 2989 | chr1 | 54099462 | ||||||
| chr1:54099564 | C | T | 1 | a0001c0001t0033 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3091C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 3091 | chr1 | 54099564 | ||||||
| chr1:54099743 | CA | C | 42 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(39): Show |
219 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*3287delA | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 3287 | INFO_REALIGN_3_PRIME | chr1 | 54099743 | |||||
| chr1:54099915 | G | A | 1 | a0001c0001t0035 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3442G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 3442 | chr1 | 54099915 | ||||||
| chr1:54099977 | A | G | 13 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0023 others(10): Show |
40 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*3504A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 3504 | chr1 | 54099977 | ||||||
| chr1:54100130 | C | T | 1 | a0001c0001t0030 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3657C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 3657 | chr1 | 54100130 | ||||||
| chr1:54100217 | G | A | 1 | a0001c0001t0009 | 5 | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3744G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 3744 | chr1 | 54100217 | ||||||
| chr1:54100254 | A | G | 1 | a0001c0001t0020 | 2 | HG03579.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3781A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 3781 | chr1 | 54100254 | ||||||
| chr1:54100355 | T | A | 2 | a0001c0001t0023 a0001c0001t0047 |
3 | HG02055.hp2 HG03209.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3882T>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 3882 | chr1 | 54100355 | ||||||
| chr1:54100480 | T | A | 1 | a0001c0001t0058 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4007T>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4007 | chr1 | 54100480 | ||||||
| chr1:54100481 | A | C | 1 | a0001c0001t0058 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4008A>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4008 | chr1 | 54100481 | ||||||
| chr1:54100482 | A | T | 1 | a0001c0001t0058 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4009A>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4009 | chr1 | 54100482 | ||||||
| chr1:54100484 | T | C | 4 | a0001c0001t0050 a0001c0003t0012 a0001c0003t0036 others(1): Show |
6 | HG00642.hp2 HG02717.hp1 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4011T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4011 | chr1 | 54100484 | ||||||
| chr1:54100488 | G | T | 1 | a0001c0001t0058 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4015G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4015 | chr1 | 54100488 | ||||||
| chr1:54100517 | G | A | 13 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(10): Show |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*4044G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4044 | chr1 | 54100517 | ||||||
| chr1:54100598 | T | G | 1 | a0001c0001t0021 | 2 | HG01243.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4125T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4125 | chr1 | 54100598 | ||||||
| chr1:54100637 | G | A | 14 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(11): Show |
108 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*4164G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4164 | chr1 | 54100637 | ||||||
| chr1:54100763 | G | A | 4 | a0001c0001t0023 a0001c0001t0046 a0001c0001t0047 others(1): Show |
5 | HG02055.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4290G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4290 | chr1 | 54100763 | ||||||
| chr1:54100875 | T | G | 1 | a0001c0003t0038 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4402T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4402 | chr1 | 54100875 | ||||||
| chr1:54101085 | T | C | 13 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0023 others(10): Show |
40 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4612T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4612 | chr1 | 54101085 | ||||||
| chr1:54101226 | T | C | 2 | a0001c0001t0006 a0001c0001t0045 |
11 | HG00642.hp1 HG02258.hp2 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4753T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4753 | chr1 | 54101226 | ||||||
| chr1:54101228 | G | A | 1 | a0001c0001t0026 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4755G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4755 | chr1 | 54101228 | ||||||
| chr1:54101330 | G | T | 4 | a0001c0001t0023 a0001c0001t0046 a0001c0001t0047 others(1): Show |
5 | HG02055.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4857G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4857 | chr1 | 54101330 | ||||||
| chr1:54101385 | A | G | 1 | a0001c0001t0041 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4912A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 4912 | chr1 | 54101385 | ||||||
| chr1:54101698 | A | G | 7 | a0001c0001t0004 a0001c0001t0056 a0001c0001t0057 others(4): Show |
31 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5225A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 5225 | chr1 | 54101698 | ||||||
| chr1:54101787 | G | A | 2 | a0001c0001t0053 a0001c0001t0055 |
2 | HG02615.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5314G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 5314 | chr1 | 54101787 | ||||||
| chr1:54102087 | C | T | 1 | a0001c0001t0059 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5614C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 5614 | chr1 | 54102087 | ||||||
| chr1:54102145 | C | T | 10 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0010 others(7): Show |
51 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*5672C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 5672 | chr1 | 54102145 | ||||||
| chr1:54102233 | C | T | 1 | a0001c0001t0006 | 10 | HG00642.hp1 HG02258.hp2 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5760C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 5760 | chr1 | 54102233 | ||||||
| chr1:54102764 | G | A | 1 | a0001c0001t0014 | 3 | HG00408.hp2 NA18992.hp1 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6291G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 6291 | chr1 | 54102764 | ||||||
| chr1:54102800 | C | T | 1 | a0001c0001t0061 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6327C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 6327 | chr1 | 54102800 | ||||||
| chr1:54102815 | G | A | 50 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(47): Show |
230 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*6342G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 6342 | chr1 | 54102815 | ||||||
| chr1:54102858 | C | A | 12 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0023 others(9): Show |
39 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*6385C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 6385 | chr1 | 54102858 | ||||||
| chr1:54102872 | T | A | 4 | a0001c0001t0021 a0001c0001t0022 a0001c0001t0035 others(1): Show |
6 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6399T>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 6399 | chr1 | 54102872 | ||||||
| chr1:54103102 | A | G | 1 | a0001c0001t0050 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6629A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 6629 | chr1 | 54103102 | ||||||
| chr1:54103228 | T | C | 1 | a0001c0001t0015 | 3 | NA18951.hp2 NA19060.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6755T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 6755 | chr1 | 54103228 | ||||||
| chr1:54103397 | GGAGA | G | 3 | a0001c0003t0012 a0001c0003t0036 a0001c0003t0038 |
5 | HG00642.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6932_*6935delAGAG | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 6932 | INFO_REALIGN_3_PRIME | chr1 | 54103397 | |||||
| chr1:54103859 | C | CA | 7 | a0001c0001t0004 a0001c0001t0056 a0001c0001t0057 others(4): Show |
31 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*7389dupA | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 7390 | INFO_REALIGN_3_PRIME | chr1 | 54103859 | |||||
| chr1:54103909 | A | G | 8 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0056 others(5): Show |
34 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*7436A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 7436 | chr1 | 54103909 | ||||||
| chr1:54103962 | C | T | 1 | a0001c0001t0029 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7489C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 7489 | chr1 | 54103962 | ||||||
| chr1:54104043 | C | T | 1 | a0001c0001t0046 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7570C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 7570 | chr1 | 54104043 | ||||||
| chr1:54104130 | C | T | 1 | a0001c0001t0028 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7657C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 7657 | chr1 | 54104130 | ||||||
| chr1:54104308 | C | G | 1 | a0001c0001t0019 | 2 | HG01361.hp2 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7835C>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 7835 | chr1 | 54104308 | ||||||
| chr1:54104512 | T | G | 1 | a0001c0001t0052 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8039T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 8039 | chr1 | 54104512 | ||||||
| chr1:54104605 | C | T | 3 | a0001c0001t0008 a0001c0001t0039 a0001c0001t0042 |
7 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8132C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 8132 | chr1 | 54104605 | ||||||
| chr1:54104610 | C | T | 1 | a0001c0001t0027 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8137C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 8137 | chr1 | 54104610 | ||||||
| chr1:54104962 | G | C | 1 | a0001c0001t0021 | 2 | HG01243.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8489G>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 8489 | chr1 | 54104962 | ||||||
| chr1:54105327 | C | G | 1 | a0001c0001t0047 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8854C>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 8854 | chr1 | 54105327 | ||||||
| chr1:54105581 | A | G | 1 | a0001c0001t0028 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9108A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 9108 | chr1 | 54105581 | ||||||
| chr1:54105641 | T | TTTTTC | 14 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0023 others(11): Show |
41 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*9171_*9172insTCTT others(1): Show |
TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 9172 | INFO_REALIGN_3_PRIME | chr1 | 54105641 | |||||
| chr1:54105645 | C | CTTTT | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(32): Show |
187 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*9172_*9173insTTTT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 9173 | chr1 | 54105645 | ||||||
| chr1:54105645 | C | T | 15 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0022 others(12): Show |
43 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*9172C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 9172 | chr1 | 54105645 | ||||||
| chr1:54105957 | A | G | 13 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0023 others(10): Show |
40 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*9484A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 9484 | chr1 | 54105957 | ||||||
| chr1:54105971 | C | G | 7 | a0001c0001t0004 a0001c0001t0056 a0001c0001t0057 others(4): Show |
31 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*9498C>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 5/5 | 9498 | chr1 | 54105971 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:54053960 | C | T | 1 | a0001c0001t0004g0223 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-43+202C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 1/4 | chr1 | 54053960 | |||||||
| chr1:54054058 | A | G | 23 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0214 others(20): Show |
43 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.-43+300A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 1/4 | chr1 | 54054058 | |||||||
| chr1:54054127 | G | A | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.-42-254G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 1/4 | chr1 | 54054127 | |||||||
| chr1:54054150 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-42-231C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 1/4 | chr1 | 54054150 | |||||||
| chr1:54054568 | T | G | 1 | a0001c0001t0002g0074 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.102+44T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54054568 | |||||||
| chr1:54054930 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0019g0075 others(3): Show |
8 | HG00733.hp1 HG01123.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.102+406T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54054930 | |||||||
| chr1:54055223 | C | T | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.102+699C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54055223 | |||||||
| chr1:54055335 | G | C | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.102+811G>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54055335 | |||||||
| chr1:54055557 | A | G | 3 | a0001c0001t0023g0071 a0001c0001t0023g0072 a0001c0001t0047g0070 |
3 | HG02055.hp2 HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.102+1033A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54055557 | |||||||
| chr1:54055906 | C | G | 1 | a0001c0001t0004g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.102+1382C>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54055906 | |||||||
| chr1:54055953 | G | A | 5 | a0001c0001t0023g0071 a0001c0001t0023g0072 a0001c0001t0035g0046 others(2): Show |
5 | HG02055.hp2 HG03209.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+1429G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54055953 | |||||||
| chr1:54056012 | C | T | 1 | a0001c0001t0011g0207 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.102+1488C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056012 | |||||||
| chr1:54056070 | A | G | 2 | a0001c0001t0009g0205 a0001c0001t0009g0206 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.102+1546A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056070 | |||||||
| chr1:54056294 | ATTCTTTT others(3): Show |
A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | NA18954.hp2 NA18960.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.102+1788_102+1797d others(12): Show |
TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54056294 | ||||||
| chr1:54056312 | C | CTT | 29 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(26): Show |
35 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.102+1791_102+1792d others(4): Show |
TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54056312 | ||||||
| chr1:54056312 | C | CTTT | 6 | a0001c0001t0023g0071 a0001c0001t0023g0072 a0001c0001t0035g0046 others(3): Show |
6 | HG02055.hp2 HG03130.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+1790_102+1792d others(5): Show |
TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54056312 | ||||||
| chr1:54056317 | C | T | 35 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(32): Show |
41 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.102+1793C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056317 | |||||||
| chr1:54056391 | C | T | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.102+1867C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056391 | |||||||
| chr1:54056482 | C | T | 1 | a0001c0001t0009g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.102+1958C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056482 | |||||||
| chr1:54056515 | T | C | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.102+1991T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056515 | |||||||
| chr1:54056527 | A | G | 1 | a0001c0001t0010g0200 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.102+2003A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056527 | |||||||
| chr1:54056567 | T | C | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.102+2043T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056567 | |||||||
| chr1:54056607 | G | A | 35 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(32): Show |
41 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.102+2083G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056607 | |||||||
| chr1:54056634 | A | G | 74 | a0001c0001t0001g0010 a0001c0001t0001g0214 a0001c0001t0003g0001 others(71): Show |
103 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.102+2110A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056634 | |||||||
| chr1:54056658 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.102+2134C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056658 | |||||||
| chr1:54056682 | C | T | 30 | a0001c0001t0001g0010 a0001c0001t0001g0214 a0001c0001t0003g0001 others(27): Show |
52 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.102+2158C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056682 | |||||||
| chr1:54056810 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.102+2286G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056810 | |||||||
| chr1:54056933 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.102+2409T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056933 | |||||||
| chr1:54056963 | A | C | 1 | a0001c0001t0002g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.102+2439A>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056963 | |||||||
| chr1:54056972 | C | G | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.102+2448C>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54056972 | |||||||
| chr1:54057157 | A | G | 35 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(32): Show |
41 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.102+2633A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54057157 | |||||||
| chr1:54057166 | G | A | 1 | a0001c0001t0022g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.102+2642G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54057166 | |||||||
| chr1:54057228 | G | GT | 25 | a0001c0001t0001g0039 a0001c0001t0001g0181 a0001c0001t0001g0183 others(22): Show |
35 | HG00408.hp2 HG00642.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.102+2720dupT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54057228 | ||||||
| chr1:54057332 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.102+2808C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54057332 | |||||||
| chr1:54057347 | A | AT | 20 | a0001c0001t0001g0036 a0001c0001t0001g0077 a0001c0001t0001g0165 others(17): Show |
22 | HG01109.hp2 HG01361.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.102+2847dupT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54057347 | ||||||
| chr1:54057347 | A | ATTT | 25 | a0001c0001t0001g0010 a0001c0001t0001g0214 a0001c0001t0003g0001 others(22): Show |
45 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.102+2845_102+2847d others(5): Show |
TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54057347 | ||||||
| chr1:54057347 | AT | A | 67 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0093 others(64): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.102+2847delT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54057347 | ||||||
| chr1:54057617 | C | G | 1 | a0001c0001t0008g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.102+3093C>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54057617 | |||||||
| chr1:54057631 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.102+3107A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54057631 | |||||||
| chr1:54057671 | C | A | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.102+3147C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54057671 | |||||||
| chr1:54057687 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.102+3163T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54057687 | |||||||
| chr1:54058016 | T | C | 38 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0004g0009 others(35): Show |
44 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(41): Show |
intron_variant | MODIFIER | c.102+3492T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54058016 | |||||||
| chr1:54058087 | A | G | 3 | a0001c0001t0023g0071 a0001c0001t0023g0072 a0001c0001t0047g0070 |
3 | HG02055.hp2 HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.102+3563A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54058087 | |||||||
| chr1:54058299 | C | T | 1 | a0001c0001t0029g0163 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.102+3775C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54058299 | |||||||
| chr1:54058863 | G | A | 1 | a0001c0001t0002g0124 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.102+4339G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54058863 | |||||||
| chr1:54058901 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.102+4377C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54058901 | |||||||
| chr1:54058935 | G | A | 2 | a0001c0001t0018g0028 a0001c0001t0031g0180 |
3 | HG01256.hp1 HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.102+4411G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54058935 | |||||||
| chr1:54058956 | C | T | 1 | a0002c0002t0001g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.102+4432C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54058956 | |||||||
| chr1:54059092 | G | A | 1 | a0001c0003t0012g0189 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.102+4568G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54059092 | |||||||
| chr1:54059152 | C | CT | 9 | a0001c0001t0001g0160 a0001c0001t0001g0173 a0001c0001t0002g0188 others(6): Show |
9 | HG01981.hp2 HG02559.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.102+4645dupT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54059152 | ||||||
| chr1:54059152 | CT | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
9 | HG02559.hp1 HG02723.hp2 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.102+4645delT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54059152 | ||||||
| chr1:54059152 | CTTTT | C | 30 | a0001c0001t0001g0010 a0001c0001t0001g0214 a0001c0001t0003g0001 others(27): Show |
52 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.102+4642_102+4645d others(6): Show |
TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54059152 | ||||||
| chr1:54059267 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.102+4743C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54059267 | |||||||
| chr1:54059396 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.102+4872C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54059396 | |||||||
| chr1:54059444 | A | G | 4 | a0001c0001t0004g0058 a0001c0001t0004g0061 a0001c0001t0059g0059 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+4920A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54059444 | |||||||
| chr1:54059477 | C | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0019 a0001c0001t0006g0176 others(1): Show |
12 | HG00642.hp1 HG02258.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.102+4953C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54059477 | |||||||
| chr1:54059822 | G | T | 1 | a0001c0001t0009g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.102+5298G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54059822 | |||||||
| chr1:54059931 | C | A | 1 | a0001c0001t0020g0030 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.102+5407C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54059931 | |||||||
| chr1:54060085 | G | A | 7 | a0001c0001t0009g0086 a0001c0001t0009g0119 a0001c0001t0009g0201 others(4): Show |
8 | HG01884.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.102+5561G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54060085 | |||||||
| chr1:54060134 | G | A | 21 | a0001c0001t0001g0010 a0001c0001t0001g0214 a0001c0001t0003g0001 others(18): Show |
40 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.102+5610G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54060134 | |||||||
| chr1:54060277 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.102+5753C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54060277 | |||||||
| chr1:54060278 | G | A | 30 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(27): Show |
36 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.102+5754G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54060278 | |||||||
| chr1:54060370 | G | A | 1 | a0001c0001t0003g0212 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.102+5846G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54060370 | |||||||
| chr1:54060404 | C | CA | 10 | a0001c0001t0003g0045 a0001c0001t0003g0210 a0001c0001t0008g0088 others(7): Show |
11 | HG02074.hp1 HG02886.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.102+5895dupA | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54060404 | ||||||
| chr1:54060703 | G | C | 2 | a0001c0001t0022g0081 a0001c0001t0022g0166 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.102+6179G>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54060703 | |||||||
| chr1:54060832 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.102+6308C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54060832 | |||||||
| chr1:54060872 | C | T | 68 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0012 others(65): Show |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.102+6348C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54060872 | |||||||
| chr1:54061091 | A | G | 5 | a0001c0001t0002g0179 a0001c0001t0014g0038 a0001c0001t0014g0184 others(2): Show |
5 | HG00408.hp2 HG02135.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+6567A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54061091 | |||||||
| chr1:54061245 | T | C | 1 | a0001c0001t0007g0194 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.102+6721T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54061245 | |||||||
| chr1:54061320 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.102+6796C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54061320 | |||||||
| chr1:54061338 | G | A | 3 | a0001c0001t0006g0007 a0001c0001t0006g0019 a0001c0001t0006g0176 |
10 | HG00642.hp1 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.102+6814G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54061338 | |||||||
| chr1:54061401 | C | A | 2 | a0001c0001t0021g0130 a0001c0001t0021g0182 |
2 | HG01243.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.102+6877C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54061401 | |||||||
| chr1:54061516 | C | A | 4 | a0001c0001t0021g0130 a0001c0001t0021g0182 a0001c0001t0022g0081 others(1): Show |
4 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+6992C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54061516 | |||||||
| chr1:54061751 | G | GA | 39 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(36): Show |
45 | HG00639.hp1 HG01070.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.103-6993dupA | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54061751 | ||||||
| chr1:54061788 | G | A | 30 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(27): Show |
36 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.103-6968G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54061788 | |||||||
| chr1:54061795 | T | C | 5 | a0001c0001t0023g0071 a0001c0001t0023g0072 a0001c0001t0035g0046 others(2): Show |
5 | HG02055.hp2 HG03209.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-6961T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54061795 | |||||||
| chr1:54061974 | A | G | 8 | a0001c0001t0001g0035 a0001c0001t0001g0080 a0001c0001t0001g0148 others(5): Show |
9 | HG00140.hp2 HG00323.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.103-6782A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54061974 | |||||||
| chr1:54062156 | G | A | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.103-6600G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54062156 | |||||||
| chr1:54062315 | G | A | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.103-6441G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54062315 | |||||||
| chr1:54062415 | T | C | 2 | a0001c0001t0018g0028 a0001c0001t0031g0180 |
3 | HG01256.hp1 HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.103-6341T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54062415 | |||||||
| chr1:54062461 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0214 |
8 | HG01934.hp1 HG02148.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-6295T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54062461 | |||||||
| chr1:54062599 | T | C | 2 | a0001c0001t0021g0130 a0001c0001t0021g0182 |
2 | HG01243.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.103-6157T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54062599 | |||||||
| chr1:54063271 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.103-5485C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54063271 | |||||||
| chr1:54063825 | G | A | 2 | a0001c0001t0022g0081 a0001c0001t0022g0166 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.103-4931G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54063825 | |||||||
| chr1:54063853 | G | A | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.103-4903G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54063853 | |||||||
| chr1:54064159 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.103-4597G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54064159 | |||||||
| chr1:54064324 | G | A | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.103-4432G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54064324 | |||||||
| chr1:54064484 | C | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.103-4272C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54064484 | |||||||
| chr1:54064561 | G | A | 3 | a0001c0001t0023g0071 a0001c0001t0023g0072 a0001c0001t0047g0070 |
3 | HG02055.hp2 HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.103-4195G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54064561 | |||||||
| chr1:54064566 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.103-4190G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54064566 | |||||||
| chr1:54064585 | T | C | 1 | a0001c0001t0006g0176 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.103-4171T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54064585 | |||||||
| chr1:54064692 | C | CT | 23 | a0001c0001t0001g0034 a0001c0001t0001g0123 a0001c0001t0001g0145 others(20): Show |
27 | HG00642.hp2 HG01070.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.103-4041dupT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54064692 | ||||||
| chr1:54064692 | CT | C | 101 | a0001c0001t0001g0082 a0001c0001t0001g0127 a0001c0001t0001g0133 others(98): Show |
159 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.103-4041delT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54064692 | ||||||
| chr1:54064714 | T | G | 1 | a0001c0001t0020g0030 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.103-4042T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54064714 | |||||||
| chr1:54064715 | T | G | 7 | a0001c0001t0006g0007 a0001c0001t0006g0019 a0001c0001t0006g0176 others(4): Show |
14 | HG00642.hp1 HG01070.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.103-4041T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54064715 | |||||||
| chr1:54064853 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.103-3903C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54064853 | |||||||
| chr1:54064889 | G | A | 2 | a0001c0001t0022g0081 a0001c0001t0022g0166 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.103-3867G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54064889 | |||||||
| chr1:54064942 | C | T | 2 | a0001c0001t0035g0046 a0001c0001t0037g0047 |
2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.103-3814C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54064942 | |||||||
| chr1:54064957 | C | A | 2 | a0001c0001t0018g0028 a0001c0001t0031g0180 |
3 | HG01256.hp1 HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.103-3799C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54064957 | |||||||
| chr1:54065029 | A | C | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.103-3727A>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54065029 | |||||||
| chr1:54065038 | G | A | 4 | a0001c0001t0021g0130 a0001c0001t0021g0182 a0001c0001t0022g0081 others(1): Show |
4 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-3718G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54065038 | |||||||
| chr1:54065632 | C | A | 1 | a0001c0001t0002g0118 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.103-3124C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54065632 | |||||||
| chr1:54065651 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.103-3105G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54065651 | |||||||
| chr1:54065716 | A | AAT | 35 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(32): Show |
41 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.103-3026_103-3025d others(4): Show |
TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 54065716 | ||||||
| chr1:54065766 | T | G | 1 | a0001c0001t0002g0115 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.103-2990T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54065766 | |||||||
| chr1:54065931 | G | A | 29 | a0001c0001t0001g0082 a0001c0001t0003g0001 a0001c0001t0003g0044 others(26): Show |
48 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.103-2825G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54065931 | |||||||
| chr1:54066061 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.103-2695C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54066061 | |||||||
| chr1:54066062 | G | A | 3 | a0001c0001t0023g0071 a0001c0001t0023g0072 a0001c0001t0047g0070 |
3 | HG02055.hp2 HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.103-2694G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54066062 | |||||||
| chr1:54066113 | G | A | 1 | a0001c0001t0023g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.103-2643G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54066113 | |||||||
| chr1:54066215 | C | T | 1 | a0001c0001t0024g0190 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.103-2541C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54066215 | |||||||
| chr1:54066448 | C | T | 1 | a0001c0001t0043g0114 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.103-2308C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54066448 | |||||||
| chr1:54066457 | T | C | 2 | a0001c0001t0002g0025 a0001c0001t0002g0152 |
3 | HG00280.hp2 HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.103-2299T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54066457 | |||||||
| chr1:54066633 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.103-2123G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54066633 | |||||||
| chr1:54066634 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.103-2122G>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54066634 | |||||||
| chr1:54066649 | T | C | 33 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(30): Show |
39 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(36): Show |
intron_variant | MODIFIER | c.103-2107T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54066649 | |||||||
| chr1:54066762 | T | C | 33 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(30): Show |
39 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(36): Show |
intron_variant | MODIFIER | c.103-1994T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54066762 | |||||||
| chr1:54066965 | G | A | 20 | a0001c0001t0001g0082 a0001c0001t0003g0001 a0001c0001t0003g0044 others(17): Show |
36 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.103-1791G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54066965 | |||||||
| chr1:54067014 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0144 |
3 | HG01515.hp1 HG02055.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.103-1742A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54067014 | |||||||
| chr1:54067016 | G | A | 2 | a0001c0001t0002g0026 a0001c0001t0002g0095 |
3 | HG00741.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.103-1740G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54067016 | |||||||
| chr1:54067410 | C | T | 1 | a0001c0001t0037g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.103-1346C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54067410 | |||||||
| chr1:54067546 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.103-1210C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54067546 | |||||||
| chr1:54067567 | T | C | 1 | a0001c0001t0037g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.103-1189T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54067567 | |||||||
| chr1:54067619 | G | A | 1 | a0001c0001t0031g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.103-1137G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54067619 | |||||||
| chr1:54067675 | C | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | NA18939.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.103-1081C>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54067675 | |||||||
| chr1:54067765 | T | A | 1 | a0001c0001t0004g0048 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.103-991T>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54067765 | |||||||
| chr1:54067798 | T | C | 1 | a0001c0001t0018g0028 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.103-958T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54067798 | |||||||
| chr1:54067880 | C | T | 1 | a0001c0001t0017g0213 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.103-876C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54067880 | |||||||
| chr1:54068550 | T | C | 29 | a0001c0001t0001g0082 a0001c0001t0003g0001 a0001c0001t0003g0044 others(26): Show |
48 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.103-206T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54068550 | |||||||
| chr1:54068722 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.103-34G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 2/4 | chr1 | 54068722 | |||||||
| chr1:54068935 | A | G | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.244+38A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54068935 | |||||||
| chr1:54069127 | T | C | 1 | a0001c0001t0024g0190 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.244+230T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54069127 | |||||||
| chr1:54069193 | C | T | 1 | a0001c0001t0004g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.244+296C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54069193 | |||||||
| chr1:54069603 | C | CA | 10 | a0001c0001t0004g0022 a0001c0001t0004g0062 a0001c0001t0005g0096 others(7): Show |
11 | HG01243.hp2 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.244+723dupA | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 54069603 | ||||||
| chr1:54069767 | C | T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0158 |
4 | HG00621.hp1 NA18973.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+870C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54069767 | |||||||
| chr1:54070018 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.244+1121G>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54070018 | |||||||
| chr1:54070302 | T | C | 1 | a0001c0001t0001g0010 | 4 | NA18948.hp1 NA19003.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+1405T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54070302 | |||||||
| chr1:54070337 | A | T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0035 others(21): Show |
38 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.244+1440A>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54070337 | |||||||
| chr1:54070377 | A | G | 2 | a0001c0001t0024g0190 a0001c0001t0050g0073 |
2 | HG01070.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.244+1480A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54070377 | |||||||
| chr1:54070413 | C | T | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.244+1516C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54070413 | |||||||
| chr1:54070466 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0143 |
4 | NA18969.hp1 NA18973.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+1569C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54070466 | |||||||
| chr1:54071077 | C | T | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.244+2180C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54071077 | |||||||
| chr1:54071189 | G | C | 5 | a0001c0001t0009g0086 a0001c0001t0009g0119 a0001c0001t0009g0201 others(2): Show |
5 | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+2292G>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54071189 | |||||||
| chr1:54071351 | G | A | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.244+2454G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54071351 | |||||||
| chr1:54071371 | T | C | 1 | a0001c0001t0011g0137 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.244+2474T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54071371 | |||||||
| chr1:54071478 | A | G | 1 | a0001c0001t0024g0190 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.244+2581A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54071478 | |||||||
| chr1:54071514 | C | G | 1 | a0001c0001t0002g0115 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.244+2617C>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54071514 | |||||||
| chr1:54071904 | C | T | 1 | a0001c0001t0010g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.244+3007C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54071904 | |||||||
| chr1:54072067 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.244+3170T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54072067 | |||||||
| chr1:54072146 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | NA18939.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.244+3249G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54072146 | |||||||
| chr1:54072395 | A | AT | 36 | a0001c0001t0004g0011 a0001c0001t0004g0022 a0001c0001t0004g0048 others(33): Show |
40 | HG00639.hp1 HG01109.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.244+3511dupT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 54072395 | ||||||
| chr1:54072395 | AT | A | 7 | a0001c0001t0010g0040 a0001c0001t0010g0200 a0001c0003t0012g0041 others(4): Show |
8 | HG00642.hp2 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.244+3511delT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 54072395 | ||||||
| chr1:54072408 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.244+3511T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54072408 | |||||||
| chr1:54072457 | C | T | 1 | a0001c0001t0004g0048 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.244+3560C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54072457 | |||||||
| chr1:54072459 | C | T | 1 | a0001c0001t0024g0190 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.244+3562C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54072459 | |||||||
| chr1:54072630 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0031g0180 |
2 | HG03710.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.244+3733C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54072630 | |||||||
| chr1:54072631 | G | A | 1 | a0001c0001t0003g0215 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.244+3734G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54072631 | |||||||
| chr1:54072649 | A | C | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.244+3752A>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54072649 | |||||||
| chr1:54072675 | G | T | 4 | a0001c0001t0016g0023 a0001c0001t0016g0056 a0001c0001t0046g0021 others(1): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+3778G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54072675 | |||||||
| chr1:54072745 | T | G | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.244+3848T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54072745 | |||||||
| chr1:54072956 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.244+4059C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54072956 | |||||||
| chr1:54073026 | C | T | 3 | a0001c0001t0006g0007 a0001c0001t0006g0019 a0001c0001t0006g0176 |
10 | HG00642.hp1 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.244+4129C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54073026 | |||||||
| chr1:54073027 | A | G | 159 | a0001c0001t0001g0082 a0001c0001t0002g0002 a0001c0001t0002g0006 others(156): Show |
231 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.244+4130A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54073027 | |||||||
| chr1:54073430 | C | G | 2 | a0001c0001t0046g0021 a0001c0001t0048g0021 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.244+4533C>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54073430 | |||||||
| chr1:54073609 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.244+4712C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54073609 | |||||||
| chr1:54073666 | C | G | 157 | a0001c0001t0001g0082 a0001c0001t0002g0002 a0001c0001t0002g0006 others(154): Show |
228 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.244+4769C>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54073666 | |||||||
| chr1:54073938 | G | A | 1 | a0001c0001t0002g0099 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.244+5041G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54073938 | |||||||
| chr1:54074054 | C | T | 1 | a0001c0001t0013g0087 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.244+5157C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54074054 | |||||||
| chr1:54074332 | G | T | 1 | a0001c0001t0039g0092 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.244+5435G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54074332 | |||||||
| chr1:54074367 | G | A | 2 | a0001c0001t0018g0028 a0001c0001t0031g0180 |
3 | HG01256.hp1 HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.244+5470G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54074367 | |||||||
| chr1:54074380 | G | A | 1 | a0001c0001t0045g0100 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.244+5483G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54074380 | |||||||
| chr1:54074411 | C | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0019 a0001c0001t0006g0176 others(1): Show |
12 | HG00642.hp1 HG02258.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.244+5514C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54074411 | |||||||
| chr1:54074462 | C | CA | 8 | a0001c0001t0001g0169 a0001c0001t0007g0020 a0001c0001t0007g0042 others(5): Show |
11 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.244+5577dupA | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 54074462 | ||||||
| chr1:54074649 | G | T | 2 | a0001c0001t0021g0130 a0001c0001t0021g0182 |
2 | HG01243.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.244+5752G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54074649 | |||||||
| chr1:54074854 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.244+5957T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54074854 | |||||||
| chr1:54075058 | G | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0019g0075 others(3): Show |
8 | HG00733.hp1 HG01123.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.244+6161G>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54075058 | |||||||
| chr1:54075102 | A | G | 1 | a0001c0001t0004g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.244+6205A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54075102 | |||||||
| chr1:54075198 | C | T | 1 | a0001c0001t0004g0055 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.244+6301C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54075198 | |||||||
| chr1:54075339 | T | TTTTA | 2 | a0001c0001t0018g0028 a0001c0001t0031g0180 |
3 | HG01256.hp1 HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.244+6444_244+6447d others(6): Show |
TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 54075339 | ||||||
| chr1:54075741 | C | T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0158 |
4 | HG00621.hp1 NA18973.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+6844C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54075741 | |||||||
| chr1:54075943 | A | G | 1 | a0001c0001t0005g0112 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.244+7046A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54075943 | |||||||
| chr1:54075991 | G | A | 27 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0045 others(24): Show |
46 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.244+7094G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54075991 | |||||||
| chr1:54076028 | C | CA | 32 | a0001c0001t0002g0116 a0001c0001t0004g0009 a0001c0001t0004g0011 others(29): Show |
38 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.244+7144dupA | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 54076028 | ||||||
| chr1:54076028 | C | CAA | 6 | a0001c0001t0004g0049 a0001c0001t0023g0071 a0001c0001t0023g0072 others(3): Show |
6 | HG02055.hp2 HG03209.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.244+7143_244+7144d others(4): Show |
TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 54076028 | ||||||
| chr1:54076200 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.244+7303G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54076200 | |||||||
| chr1:54076217 | C | T | 1 | a0001c0001t0010g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.244+7320C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54076217 | |||||||
| chr1:54076512 | G | GGCAAAAG others(4): Show |
1 | a0001c0001t0001g0082 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.244+7615_244+7616i others(13): Show |
TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54076512 | |||||||
| chr1:54076648 | G | A | 2 | a0001c0001t0021g0130 a0001c0001t0021g0182 |
2 | HG01243.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.244+7751G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54076648 | |||||||
| chr1:54076689 | G | A | 25 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(22): Show |
30 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.244+7792G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54076689 | |||||||
| chr1:54076716 | A | G | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.244+7819A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54076716 | |||||||
| chr1:54076941 | C | T | 1 | a0001c0001t0003g0210 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.244+8044C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54076941 | |||||||
| chr1:54077000 | A | AAGG | 154 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0012 others(151): Show |
225 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.244+8104_244+8106d others(5): Show |
TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 54077000 | ||||||
| chr1:54077057 | C | T | 3 | a0001c0001t0004g0053 a0001c0001t0046g0021 a0001c0001t0048g0021 |
3 | HG01346.hp1 HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.244+8160C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54077057 | |||||||
| chr1:54077129 | A | G | 80 | a0001c0001t0001g0034 a0001c0001t0001g0094 a0001c0001t0001g0142 others(77): Show |
106 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.244+8232A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54077129 | |||||||
| chr1:54077229 | C | T | 1 | a0001c0001t0013g0024 | 2 | HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.244+8332C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54077229 | |||||||
| chr1:54077246 | G | C | 46 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0016 others(43): Show |
65 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.244+8349G>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54077246 | |||||||
| chr1:54077316 | A | C | 1 | a0001c0001t0001g0033 | 2 | HG01358.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.244+8419A>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54077316 | |||||||
| chr1:54077431 | CA | C | 69 | a0001c0001t0001g0032 a0001c0001t0001g0165 a0001c0001t0002g0002 others(66): Show |
106 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.244+8536delA | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 54077431 | ||||||
| chr1:54077478 | A | G | 1 | a0001c0001t0018g0028 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.244+8581A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54077478 | |||||||
| chr1:54077647 | T | G | 1 | a0001c0001t0030g0138 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.244+8750T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54077647 | |||||||
| chr1:54077743 | C | G | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.244+8846C>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54077743 | |||||||
| chr1:54078028 | T | C | 1 | a0001c0001t0016g0023 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.244+9131T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54078028 | |||||||
| chr1:54078115 | A | G | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.244+9218A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54078115 | |||||||
| chr1:54078264 | C | T | 3 | a0001c0001t0023g0071 a0001c0001t0023g0072 a0001c0001t0047g0070 |
3 | HG02055.hp2 HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.244+9367C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54078264 | |||||||
| chr1:54078755 | T | C | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-9842T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54078755 | |||||||
| chr1:54078760 | G | A | 7 | a0001c0001t0005g0005 a0001c0001t0005g0013 a0001c0001t0005g0096 others(4): Show |
15 | HG00423.hp1 HG02523.hp1 NA18941.hp1 others(12): Show |
intron_variant | MODIFIER | c.245-9837G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54078760 | |||||||
| chr1:54078842 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.245-9755G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54078842 | |||||||
| chr1:54078921 | G | A | 3 | a0001c0001t0023g0071 a0001c0001t0023g0072 a0001c0001t0047g0070 |
3 | HG02055.hp2 HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.245-9676G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54078921 | |||||||
| chr1:54078921 | G | T | 1 | a0001c0001t0004g0064 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.245-9676G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54078921 | |||||||
| chr1:54078966 | C | T | 1 | a0001c0001t0019g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.245-9631C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54078966 | |||||||
| chr1:54079058 | C | T | 1 | a0001c0001t0010g0200 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.245-9539C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54079058 | |||||||
| chr1:54079227 | C | T | 2 | a0001c0001t0022g0081 a0001c0001t0022g0166 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.245-9370C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54079227 | |||||||
| chr1:54079249 | A | G | 2 | a0001c0001t0008g0090 a0001c0001t0039g0092 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.245-9348A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54079249 | |||||||
| chr1:54079392 | G | A | 1 | a0001c0001t0013g0024 | 2 | HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.245-9205G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54079392 | |||||||
| chr1:54079942 | T | A | 1 | a0001c0001t0002g0124 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.245-8655T>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54079942 | |||||||
| chr1:54080146 | C | CT | 6 | a0001c0001t0001g0017 a0001c0001t0001g0125 a0001c0001t0002g0157 others(3): Show |
8 | HG00609.hp1 HG04115.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.245-8434dupT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 54080146 | ||||||
| chr1:54080216 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.245-8381G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54080216 | |||||||
| chr1:54080682 | C | G | 1 | a0001c0001t0021g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.245-7915C>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54080682 | |||||||
| chr1:54080776 | G | A | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.245-7821G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54080776 | |||||||
| chr1:54081276 | C | A | 1 | a0001c0001t0004g0065 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.245-7321C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54081276 | |||||||
| chr1:54081331 | C | T | 2 | a0001c0001t0021g0130 a0001c0001t0021g0182 |
2 | HG01243.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.245-7266C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54081331 | |||||||
| chr1:54081381 | A | T | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-7216A>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54081381 | |||||||
| chr1:54081469 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.245-7128A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54081469 | |||||||
| chr1:54081618 | T | C | 1 | a0001c0003t0012g0189 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.245-6979T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54081618 | |||||||
| chr1:54081620 | G | A | 2 | a0001c0001t0006g0007 a0001c0001t0006g0176 |
7 | HG00642.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-6977G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54081620 | |||||||
| chr1:54081651 | C | T | 1 | a0001c0001t0024g0190 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.245-6946C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54081651 | |||||||
| chr1:54081678 | AGTC | A | 66 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0012 others(63): Show |
102 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.245-6918_245-6916d others(5): Show |
TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54081678 | |||||||
| chr1:54081715 | C | T | 1 | a0001c0001t0017g0213 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.245-6882C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54081715 | |||||||
| chr1:54081786 | C | G | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.245-6811C>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54081786 | |||||||
| chr1:54081806 | A | G | 3 | a0001c0001t0023g0071 a0001c0001t0023g0072 a0001c0001t0047g0070 |
3 | HG02055.hp2 HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.245-6791A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54081806 | |||||||
| chr1:54081849 | G | A | 1 | a0001c0001t0035g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.245-6748G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54081849 | |||||||
| chr1:54082261 | T | G | 4 | a0001c0001t0021g0130 a0001c0001t0021g0182 a0001c0001t0022g0081 others(1): Show |
4 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-6336T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54082261 | |||||||
| chr1:54082280 | A | G | 26 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(23): Show |
31 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.245-6317A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54082280 | |||||||
| chr1:54082339 | G | T | 2 | a0001c0001t0018g0028 a0001c0001t0031g0180 |
3 | HG01256.hp1 HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.245-6258G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54082339 | |||||||
| chr1:54082396 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0142 |
2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.245-6201T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54082396 | |||||||
| chr1:54082978 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.245-5619C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54082978 | |||||||
| chr1:54083010 | C | T | 1 | a0001c0001t0004g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.245-5587C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54083010 | |||||||
| chr1:54083125 | T | C | 6 | a0001c0001t0001g0149 a0001c0001t0006g0007 a0001c0001t0006g0019 others(3): Show |
14 | HG00642.hp1 HG02258.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.245-5472T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54083125 | |||||||
| chr1:54083186 | G | A | 5 | a0001c0001t0002g0027 a0001c0001t0002g0101 a0001c0001t0002g0104 others(2): Show |
6 | HG01071.hp1 HG01255.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-5411G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54083186 | |||||||
| chr1:54083232 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.245-5365A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54083232 | |||||||
| chr1:54083346 | C | A | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.245-5251C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54083346 | |||||||
| chr1:54083583 | A | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0019 a0001c0001t0006g0176 others(1): Show |
11 | HG00642.hp1 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.245-5014A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54083583 | |||||||
| chr1:54083588 | T | A | 1 | a0001c0001t0002g0105 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.245-5009T>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54083588 | |||||||
| chr1:54083615 | T | G | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-4982T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54083615 | |||||||
| chr1:54083618 | G | A | 2 | a0001c0001t0019g0075 a0001c0001t0019g0076 |
2 | HG01361.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.245-4979G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54083618 | |||||||
| chr1:54083643 | G | A | 1 | a0001c0001t0003g0216 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.245-4954G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54083643 | |||||||
| chr1:54083706 | A | G | 1 | a0001c0001t0007g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.245-4891A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54083706 | |||||||
| chr1:54083754 | A | G | 3 | a0001c0001t0023g0071 a0001c0001t0023g0072 a0001c0001t0047g0070 |
3 | HG02055.hp2 HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.245-4843A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54083754 | |||||||
| chr1:54083952 | A | T | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.245-4645A>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54083952 | |||||||
| chr1:54084020 | GT | G | 74 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0012 others(71): Show |
112 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.245-4565delT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 54084020 | ||||||
| chr1:54084039 | G | A | 28 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0045 others(25): Show |
47 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.245-4558G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54084039 | |||||||
| chr1:54084169 | T | C | 1 | a0001c0001t0002g0084 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.245-4428T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54084169 | |||||||
| chr1:54084209 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.245-4388C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54084209 | |||||||
| chr1:54084283 | G | A | 1 | a0001c0001t0004g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.245-4314G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54084283 | |||||||
| chr1:54084505 | C | T | 5 | a0001c0003t0012g0041 a0001c0003t0012g0189 a0001c0003t0012g0192 others(2): Show |
5 | HG00642.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-4092C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54084505 | |||||||
| chr1:54084537 | A | G | 5 | a0001c0001t0023g0071 a0001c0001t0023g0072 a0001c0001t0035g0046 others(2): Show |
5 | HG02055.hp2 HG03209.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-4060A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54084537 | |||||||
| chr1:54084632 | C | T | 1 | a0001c0001t0002g0109 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.245-3965C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54084632 | |||||||
| chr1:54084766 | C | T | 1 | a0001c0001t0059g0059 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245-3831C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54084766 | |||||||
| chr1:54084807 | T | C | 7 | a0001c0001t0008g0088 a0001c0001t0008g0089 a0001c0001t0008g0090 others(4): Show |
7 | HG02886.hp2 HG02970.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-3790T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54084807 | |||||||
| chr1:54084922 | C | A | 2 | a0001c0001t0018g0028 a0001c0001t0031g0180 |
3 | HG01256.hp1 HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.245-3675C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54084922 | |||||||
| chr1:54085209 | A | G | 5 | a0001c0003t0012g0041 a0001c0003t0012g0189 a0001c0003t0012g0192 others(2): Show |
5 | HG00642.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-3388A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54085209 | |||||||
| chr1:54085276 | T | A | 1 | a0001c0001t0003g0215 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.245-3321T>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54085276 | |||||||
| chr1:54085416 | G | T | 5 | a0001c0001t0009g0086 a0001c0001t0009g0119 a0001c0001t0009g0201 others(2): Show |
5 | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-3181G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54085416 | |||||||
| chr1:54085472 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.245-3125C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54085472 | |||||||
| chr1:54085999 | G | A | 1 | a0001c0001t0031g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.245-2598G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54085999 | |||||||
| chr1:54086018 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.245-2579G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54086018 | |||||||
| chr1:54086125 | T | C | 1 | a0001c0001t0002g0115 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.245-2472T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54086125 | |||||||
| chr1:54086158 | T | A | 2 | a0001c0001t0018g0028 a0001c0001t0031g0180 |
3 | HG01256.hp1 HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.245-2439T>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54086158 | |||||||
| chr1:54086202 | G | T | 156 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0012 others(153): Show |
227 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.245-2395G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54086202 | |||||||
| chr1:54086243 | G | T | 1 | a0001c0001t0037g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.245-2354G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54086243 | |||||||
| chr1:54086552 | A | T | 1 | a0001c0001t0002g0115 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.245-2045A>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54086552 | |||||||
| chr1:54086565 | A | G | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.245-2032A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54086565 | |||||||
| chr1:54086814 | G | A | 1 | a0001c0001t0033g0139 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.245-1783G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54086814 | |||||||
| chr1:54087059 | A | G | 1 | a0001c0001t0008g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.245-1538A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54087059 | |||||||
| chr1:54087062 | G | A | 1 | a0001c0001t0002g0106 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.245-1535G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54087062 | |||||||
| chr1:54087238 | G | A | 68 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0012 others(65): Show |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.245-1359G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54087238 | |||||||
| chr1:54087357 | T | C | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.245-1240T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54087357 | |||||||
| chr1:54087444 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.245-1153A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54087444 | |||||||
| chr1:54087534 | T | C | 156 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0012 others(153): Show |
227 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.245-1063T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54087534 | |||||||
| chr1:54087603 | C | T | 1 | a0001c0001t0004g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.245-994C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54087603 | |||||||
| chr1:54087935 | G | A | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.245-662G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54087935 | |||||||
| chr1:54088490 | G | T | 2 | a0001c0001t0046g0021 a0001c0001t0048g0021 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.245-107G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 3/4 | chr1 | 54088490 | |||||||
| chr1:54088810 | C | T | 1 | a0001c0001t0049g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.438+20C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54088810 | |||||||
| chr1:54088873 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0183 |
3 | NA18939.hp1 NA19000.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.438+83C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54088873 | |||||||
| chr1:54088967 | A | G | 1 | a0001c0001t0002g0109 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.438+177A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54088967 | |||||||
| chr1:54089137 | G | A | 1 | a0001c0001t0004g0054 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.438+347G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54089137 | |||||||
| chr1:54089491 | C | T | 5 | a0001c0001t0023g0071 a0001c0001t0023g0072 a0001c0001t0035g0046 others(2): Show |
5 | HG02055.hp2 HG03209.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.438+701C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54089491 | |||||||
| chr1:54089522 | A | G | 2 | a0001c0001t0021g0130 a0001c0001t0021g0182 |
2 | HG01243.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.438+732A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54089522 | |||||||
| chr1:54089732 | T | A | 156 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0012 others(153): Show |
227 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.438+942T>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54089732 | |||||||
| chr1:54090069 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.438+1279G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54090069 | |||||||
| chr1:54090471 | C | A | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.438+1681C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54090471 | |||||||
| chr1:54091016 | T | A | 1 | a0001c0001t0001g0141 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.438+2226T>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54091016 | |||||||
| chr1:54091111 | T | A | 2 | a0001c0001t0022g0081 a0001c0001t0022g0166 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.438+2321T>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54091111 | |||||||
| chr1:54091150 | C | CA | 76 | a0001c0001t0001g0202 a0001c0001t0002g0002 a0001c0001t0002g0006 others(73): Show |
114 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.438+2374dupA | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 54091150 | ||||||
| chr1:54091290 | T | A | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.438+2500T>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54091290 | |||||||
| chr1:54091296 | A | C | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.438+2506A>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54091296 | |||||||
| chr1:54091298 | T | G | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.438+2508T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54091298 | |||||||
| chr1:54091587 | G | A | 1 | a0001c0001t0003g0210 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.438+2797G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54091587 | |||||||
| chr1:54091590 | C | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0019 a0001c0001t0006g0176 others(1): Show |
12 | HG00642.hp1 HG02258.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.438+2800C>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54091590 | |||||||
| chr1:54091617 | C | T | 70 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0012 others(67): Show |
107 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.438+2827C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54091617 | |||||||
| chr1:54091857 | A | G | 1 | a0001c0001t0003g0217 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.438+3067A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54091857 | |||||||
| chr1:54091928 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.438+3138T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54091928 | |||||||
| chr1:54092045 | A | G | 1 | a0001c0001t0020g0030 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.438+3255A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54092045 | |||||||
| chr1:54092369 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0127 a0001c0001t0001g0131 others(2): Show |
7 | HG00738.hp1 HG01074.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.438+3579G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54092369 | |||||||
| chr1:54092428 | T | C | 157 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0012 others(154): Show |
229 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.438+3638T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54092428 | |||||||
| chr1:54092429 | G | A | 1 | a0001c0001t0050g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.438+3639G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54092429 | |||||||
| chr1:54092491 | T | C | 2 | a0001c0001t0016g0023 a0001c0001t0016g0056 |
3 | HG02896.hp2 HG02897.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.438+3701T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54092491 | |||||||
| chr1:54092603 | T | G | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.439-3682T>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54092603 | |||||||
| chr1:54092624 | C | T | 1 | a0001c0003t0012g0192 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.439-3661C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54092624 | |||||||
| chr1:54092749 | C | CT | 3 | a0001c0001t0010g0040 a0001c0001t0010g0135 a0001c0001t0010g0200 |
4 | HG02486.hp1 HG02647.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.439-3535dupT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 54092749 | ||||||
| chr1:54092813 | A | G | 1 | a0001c0001t0035g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.439-3472A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54092813 | |||||||
| chr1:54092873 | T | TAGAC | 36 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(33): Show |
42 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.439-3410_439-3409i others(6): Show |
TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 54092873 | ||||||
| chr1:54093146 | A | G | 30 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(27): Show |
36 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.439-3139A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54093146 | |||||||
| chr1:54093195 | T | A | 5 | a0001c0001t0009g0086 a0001c0001t0009g0119 a0001c0001t0009g0201 others(2): Show |
5 | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.439-3090T>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54093195 | |||||||
| chr1:54093285 | G | T | 2 | a0001c0001t0018g0028 a0001c0001t0031g0180 |
3 | HG01256.hp1 HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.439-3000G>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54093285 | |||||||
| chr1:54093406 | C | T | 2 | a0001c0001t0046g0021 a0001c0001t0048g0021 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.439-2879C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54093406 | |||||||
| chr1:54093410 | A | C | 41 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0022 others(38): Show |
55 | HG00639.hp1 HG00642.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.439-2875A>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54093410 | |||||||
| chr1:54093733 | CT | C | 73 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0012 others(70): Show |
111 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.439-2536delT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 54093733 | ||||||
| chr1:54093733 | CTT | C | 30 | a0001c0001t0004g0009 a0001c0001t0004g0022 a0001c0001t0004g0048 others(27): Show |
34 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.439-2537_439-2536d others(4): Show |
TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 54093733 | ||||||
| chr1:54094121 | T | C | 9 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0095 others(6): Show |
11 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.439-2164T>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54094121 | |||||||
| chr1:54094165 | C | G | 2 | a0001c0001t0013g0024 a0001c0001t0013g0087 |
3 | HG01884.hp2 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.439-2120C>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54094165 | |||||||
| chr1:54094266 | A | G | 1 | a0001c0001t0004g0052 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.439-2019A>G | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54094266 | |||||||
| chr1:54094301 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.439-1984C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54094301 | |||||||
| chr1:54094999 | G | A | 68 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0012 others(65): Show |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.439-1286G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54094999 | |||||||
| chr1:54095389 | C | T | 2 | a0001c0001t0013g0024 a0001c0001t0013g0087 |
3 | HG01884.hp2 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.439-896C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54095389 | |||||||
| chr1:54095599 | C | T | 1 | a0001c0001t0002g0107 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.439-686C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54095599 | |||||||
| chr1:54095617 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0142 |
2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.439-668C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54095617 | |||||||
| chr1:54095639 | G | A | 1 | a0001c0001t0005g0162 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.439-646G>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54095639 | |||||||
| chr1:54095693 | G | GA | 5 | a0001c0001t0009g0086 a0001c0001t0009g0119 a0001c0001t0009g0201 others(2): Show |
5 | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.439-589dupA | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 54095693 | ||||||
| chr1:54095816 | A | AT | 5 | a0001c0001t0023g0071 a0001c0001t0023g0072 a0001c0001t0046g0021 others(2): Show |
5 | HG02055.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-468dupT | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 54095816 | ||||||
| chr1:54095940 | C | CA | 4 | a0001c0001t0002g0026 a0001c0001t0002g0095 a0001c0001t0002g0099 others(1): Show |
5 | HG00735.hp2 HG00741.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-336dupA | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 54095940 | ||||||
| chr1:54095976 | T | A | 2 | a0001c0001t0002g0098 a0001c0001t0002g0155 |
2 | HG00639.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.439-309T>A | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54095976 | |||||||
| chr1:54096107 | G | C | 5 | a0001c0001t0009g0086 a0001c0001t0009g0119 a0001c0001t0009g0201 others(2): Show |
5 | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.439-178G>C | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54096107 | |||||||
| chr1:54096243 | C | T | 156 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0012 others(153): Show |
227 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.439-42C>T | TCEANC2 | ENSG00000116205.14 | transcript | ENST00000234827.6 | protein_coding | 4/4 | chr1 | 54096243 |