Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 148534 |
| ensemblid | ENSG00000152078.10 |
| hgncid | 26477 |
| symbol | TLCD4 |
| name | TLC domain containing 4 |
| refseq_nuc | NM_152487.3 |
| refseq_prot | NP_689700.1 |
| ensembl_nuc | ENST00000370203.9 |
| ensembl_prot | ENSP00000359222.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 95117355 |
| end | 95197607 |
| strand | + |
| ver | v1.2 |
| region | chr1:95117355-95197607 |
| region5000 | chr1:95112355-95202607 |
| regionname0 | TLCD4_chr1_95117355_95197607 |
| regionname5000 | TLCD4_chr1_95112355_95202607 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 263 | 377 | 89 | 76 | 170 | 8 | 32 | 136 | TLCD4_chr1_95112355_95202607 | TLCD4 | MEINT others(258): Show |
chr1 | 95112355 | 95202607 |
| a0002 | 0/0 | 263 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | MEINT others(258): Show |
chr1 | 95112355 | 95202607 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 789 | 375 | 89 | 76 | 168 | 8 | 32 | TLCD4_chr1_95112355_95202607 | TLCD4 | ATGGA others(784): Show |
chr1 | 95112355 | 95202607 | ||
| a0001c0003 | 0/0 | 789 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | ATGGA others(784): Show |
chr1 | 95112355 | 95202607 | ||
| a0001c0004 | 0/0 | 789 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | ATGGA others(784): Show |
chr1 | 95112355 | 95202607 | ||
| a0002c0002 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | ATGGA others(784): Show |
chr1 | 95112355 | 95202607 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6803 | 146 | 27 | 20 | 92 | 1 | 6 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6798): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0002 | 0/1 | 6804 | 69 | 13 | 21 | 22 | 2 | 10 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6799): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0003 | 0/0 | 6805 | 30 | 0 | 7 | 23 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0004 | 0/0 | 6805 | 19 | 0 | 0 | 16 | 0 | 3 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0005 | 0/0 | 6805 | 18 | 9 | 5 | 0 | 0 | 4 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0006 | 0/0 | 6805 | 11 | 9 | 2 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0007 | 0/0 | 6805 | 10 | 0 | 3 | 5 | 1 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0008 | 0/0 | 6804 | 11 | 2 | 4 | 0 | 3 | 2 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6799): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0009 | 0/0 | 6805 | 5 | 5 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0010 | 0/0 | 6804 | 4 | 1 | 1 | 0 | 1 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6799): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0011 | 0/0 | 6800 | 4 | 0 | 4 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6795): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0012 | 0/0 | 6803 | 4 | 4 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6798): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0013 | 0/0 | 6805 | 3 | 0 | 1 | 0 | 0 | 2 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0014 | 0/0 | 6804 | 3 | 3 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6799): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0015 | 0/0 | 6803 | 3 | 3 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6798): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0016 | 0/0 | 6805 | 2 | 0 | 2 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0017 | 0/0 | 6804 | 2 | 0 | 0 | 2 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6799): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0018 | 0/0 | 6805 | 2 | 2 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0019 | 0/0 | 6805 | 2 | 0 | 2 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0020 | 0/0 | 6803 | 2 | 2 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6798): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0021 | 0/0 | 6804 | 2 | 0 | 0 | 0 | 0 | 2 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6799): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0022 | 0/0 | 6803 | 2 | 0 | 2 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6798): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0023 | 0/0 | 6805 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0024 | 0/0 | 6805 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0025 | 0/0 | 6805 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0026 | 0/0 | 6805 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0027 | 0/0 | 6805 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0028 | 0/0 | 6805 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0029 | 0/0 | 6804 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6799): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0030 | 0/0 | 6804 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6799): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0031 | 0/0 | 6804 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6799): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0032 | 0/0 | 6803 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6798): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0033 | 0/0 | 6803 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6798): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0034 | 0/0 | 6803 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6798): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0035 | 0/0 | 6803 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6798): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0036 | 0/0 | 6803 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6798): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0037 | 0/0 | 6804 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6799): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0038 | 0/0 | 6803 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6798): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0039 | 0/0 | 6804 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6799): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0040 | 0/0 | 6805 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0041 | 0/0 | 6805 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0042 | 0/0 | 6803 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6798): Show |
chr1 | 95112355 | 95202607 |
| a0001c0001t0043 | 1/0 | 6805 | 1 | 0 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0003t0007 | 0/0 | 6805 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| a0001c0004t0001 | 0/0 | 6803 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6798): Show |
chr1 | 95112355 | 95202607 |
| a0002c0002t0009 | 0/0 | 6805 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | AAGGA others(6800): Show |
chr1 | 95112355 | 95202607 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0006g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0007g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0007g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0007g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0007g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0007g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0008g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0008g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0008g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0008g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0008g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0008g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0008g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0008g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0009g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0010g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0010g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0010g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0011g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0011g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0011g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0011g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0012g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0012g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0012g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0012g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0013g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0013g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0013g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0014g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0014g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0014g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0015g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0015g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0015g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0016g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0016g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0017g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0017g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0018g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0018g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0019g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0019g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0020g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0020g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0021g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0022g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0023g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0024g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0025g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0026g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0027g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0028g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0029g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0030g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0031g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0032g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0033g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0034g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0035g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0036g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0037g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0038g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0039g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0040g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0041g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0042g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0001t0043g0024 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0003t0007g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0001c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| a0002c0002t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | GBR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00099 | hp2 | a0001 | c0001 | t0008 | g0176 | EUR | GBR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00280 | hp1 | a0001 | c0001 | t0010 | g0099 | EUR | FIN | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00280 | hp2 | a0001 | c0001 | t0007 | g0108 | EUR | FIN | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CHS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | CHS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | CHS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | CHS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | CHS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0182 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0244 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00735 | hp2 | a0001 | c0001 | t0022 | g0005 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0195 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0171 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0169 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01074 | hp1 | a0001 | c0001 | t0019 | g0040 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01074 | hp2 | a0001 | c0001 | t0011 | g0276 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01081 | hp2 | a0001 | c0001 | t0022 | g0005 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0124 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01106 | hp1 | a0001 | c0001 | t0019 | g0038 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0247 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01167 | hp1 | a0001 | c0001 | t0011 | g0297 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01169 | hp1 | a0001 | c0001 | t0011 | g0281 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01169 | hp2 | a0001 | c0001 | t0031 | g0212 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01175 | hp1 | a0001 | c0001 | t0008 | g0091 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0140 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0098 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0312 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01256 | hp1 | a0001 | c0001 | t0016 | g0117 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01256 | hp2 | a0001 | c0001 | t0007 | g0156 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01258 | hp1 | a0001 | c0001 | t0016 | g0116 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01346 | hp2 | a0001 | c0001 | t0013 | g0053 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01358 | hp2 | a0001 | c0001 | t0008 | g0301 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01433 | hp1 | a0001 | c0001 | t0011 | g0282 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0170 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01515 | hp1 | a0001 | c0001 | t0008 | g0189 | EUR | IBS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0202 | EUR | IBS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0204 | EUR | IBS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01517 | hp2 | a0001 | c0001 | t0008 | g0186 | EUR | IBS | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0006 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01934 | hp1 | a0001 | c0001 | t0027 | g0037 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01943 | hp1 | a0001 | c0001 | t0008 | g0188 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | KHV | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02074 | hp1 | a0001 | c0001 | t0037 | g0125 | EAS | KHV | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | KHV | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | KHV | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02135 | hp1 | a0001 | c0001 | t0039 | g0033 | EAS | KHV | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | KHV | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0243 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | CDX | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | CDX | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | CDX | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0187 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0305 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02280 | hp1 | a0001 | c0001 | t0012 | g0026 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02451 | hp1 | a0001 | c0001 | t0012 | g0028 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0248 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02572 | hp2 | a0001 | c0001 | t0028 | g0013 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02602 | hp1 | a0001 | c0001 | t0008 | g0181 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0173 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0245 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02622 | hp1 | a0001 | c0001 | t0014 | g0304 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02630 | hp1 | a0001 | c0001 | t0024 | g0311 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02630 | hp2 | a0001 | c0001 | t0020 | g0114 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02647 | hp2 | a0001 | c0001 | t0034 | g0018 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0240 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0103 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0096 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02735 | hp2 | a0001 | c0001 | t0013 | g0107 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0242 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02886 | hp1 | a0001 | c0001 | t0040 | g0027 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0032 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02895 | hp1 | a0001 | c0001 | t0015 | g0109 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0131 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02897 | hp2 | a0001 | c0001 | t0015 | g0110 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0327 | AFR | ESN | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0006 | AFR | ESN | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | ESN | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | ESN | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03098 | hp1 | a0002 | c0002 | t0009 | g0031 | AFR | MSL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | MSL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0214 | AFR | ESN | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03195 | hp2 | a0001 | c0001 | t0015 | g0111 | AFR | ESN | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | MSL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0174 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03453 | hp1 | a0001 | c0001 | t0018 | g0013 | AFR | MSL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03486 | hp1 | a0001 | c0001 | t0018 | g0168 | AFR | MSL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | MSL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03491 | hp2 | a0001 | c0001 | t0021 | g0007 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03492 | hp2 | a0001 | c0001 | t0021 | g0007 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0102 | AFR | ESN | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0310 | AFR | ESN | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03540 | hp2 | a0001 | c0001 | t0014 | g0303 | AFR | GWD | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | MSL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03654 | hp1 | a0001 | c0001 | t0013 | g0106 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0339 | SAS | STU | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03710 | hp2 | a0001 | c0001 | t0008 | g0185 | SAS | PJL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0349 | SAS | BEB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0073 | SAS | BEB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0035 | SAS | STU | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0134 | SAS | STU | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0155 | SAS | BEB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | BEB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG04204 | hp1 | a0001 | c0001 | t0036 | g0341 | SAS | STU | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0137 | SAS | STU | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0334 | SAS | STU | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG04228 | hp2 | a0001 | c0001 | t0010 | g0100 | SAS | STU | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | YRI | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18522 | hp2 | a0001 | c0001 | t0041 | g0022 | AFR | YRI | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | CHB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18612 | hp2 | a0001 | c0001 | t0007 | g0139 | EAS | CHB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | CHB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | YRI | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | YRI | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18948 | hp1 | a0001 | c0001 | t0030 | g0317 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18954 | hp2 | a0001 | c0001 | t0017 | g0319 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18962 | hp2 | a0001 | c0001 | t0033 | g0230 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18965 | hp2 | a0001 | c0004 | t0001 | g0275 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18968 | hp2 | a0001 | c0001 | t0007 | g0315 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18969 | hp1 | a0001 | c0001 | t0026 | g0261 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18987 | hp1 | a0001 | c0001 | t0038 | g0239 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18988 | hp1 | a0001 | c0001 | t0007 | g0149 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18998 | hp1 | a0001 | c0003 | t0007 | g0152 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18999 | hp1 | a0001 | c0001 | t0007 | g0313 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19006 | hp2 | a0001 | c0001 | t0007 | g0314 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0025 | AFR | LWK | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19030 | hp2 | a0001 | c0001 | t0020 | g0113 | AFR | LWK | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | LWK | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0101 | AFR | LWK | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19076 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19080 | hp1 | a0001 | c0001 | t0035 | g0252 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19081 | hp2 | a0001 | c0001 | t0017 | g0268 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19087 | hp2 | a0001 | c0001 | t0025 | g0141 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | YRI | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0029 | AFR | YRI | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | GIH | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0104 | SAS | GIH | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | CLM | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02109 | hp1 | a0001 | c0001 | t0042 | g0023 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02109 | hp2 | a0001 | c0001 | t0029 | g0017 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02486 | hp2 | a0001 | c0001 | t0014 | g0302 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02559 | hp1 | a0001 | c0001 | t0023 | g0318 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0184 | AFR | ACB | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0193 | AFR | MSL | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | USA | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0191 | AFR | USA | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | USA | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | USA | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | LWK | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| NA21309 | hp2 | a0001 | c0001 | t0032 | g0267 | AFR | LWK | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0070 | REF | REF | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0043 | g0024 | REF | REF | TLCD4_chr1_95112355_95202607 | TLCD4 | chr1 | 95112355 | 95202607 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:95150230 | G | A | 1 | a0002 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.268G>A | p.Val90Met | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 4/7 | 542/6805 | 268/792 | 90/263 | chr1 | 95150230 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:95150229 | C | T | 1 | a0001c0004 | 1 | NA18965.hp2 | synonymous_variant | LOW | c.267C>T | p.Asn89Asn | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 4/7 | 541/6805 | 267/792 | 89/263 | chr1 | 95150229 | |||
| chr1:95191595 | C | T | 1 | a0001c0003 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.519C>T | p.Ile173Ile | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 793/6805 | 519/792 | 173/263 | chr1 | 95191595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:95117534 | G | C | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(37): Show |
367 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(364): Show |
5_prime_UTR_variant | MODIFIER | c.-95G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/7 | 26368 | chr1 | 95117534 | ||||||
| chr1:95191880 | C | T | 1 | a0001c0001t0039 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 12 | chr1 | 95191880 | ||||||
| chr1:95192298 | C | CA | 19 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(16): Show |
108 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*444dupA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 445 | INFO_REALIGN_3_PRIME | chr1 | 95192298 | |||||
| chr1:95192403 | A | C | 4 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0019 others(1): Show |
32 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*535A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 535 | chr1 | 95192403 | ||||||
| chr1:95192590 | C | T | 1 | a0001c0001t0021 | 2 | HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*722C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 722 | chr1 | 95192590 | ||||||
| chr1:95192789 | AT | A | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(40): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
3_prime_UTR_variant | MODIFIER | c.*927delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 927 | INFO_REALIGN_3_PRIME | chr1 | 95192789 | |||||
| chr1:95192815 | T | A | 1 | a0001c0001t0022 | 2 | HG00735.hp2 HG01081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*947T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 947 | chr1 | 95192815 | ||||||
| chr1:95192886 | T | G | 1 | a0001c0001t0016 | 2 | HG01256.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1018T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 1018 | chr1 | 95192886 | ||||||
| chr1:95192890 | A | C | 2 | a0001c0001t0018 a0001c0001t0028 |
3 | HG02572.hp2 HG03453.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1022A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 1022 | chr1 | 95192890 | ||||||
| chr1:95192944 | C | T | 16 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(13): Show |
172 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*1076C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 1076 | chr1 | 95192944 | ||||||
| chr1:95193122 | C | G | 1 | a0001c0001t0038 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1254C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 1254 | chr1 | 95193122 | ||||||
| chr1:95193214 | T | C | 21 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(18): Show |
197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1346T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 1346 | chr1 | 95193214 | ||||||
| chr1:95193621 | G | A | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1753G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 1753 | chr1 | 95193621 | ||||||
| chr1:95193636 | G | A | 1 | a0001c0001t0030 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1768G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 1768 | chr1 | 95193636 | ||||||
| chr1:95193996 | C | A | 2 | a0001c0001t0020 a0001c0001t0042 |
3 | HG02109.hp1 HG02630.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2128C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 2128 | chr1 | 95193996 | ||||||
| chr1:95194129 | CCCT | C | 1 | a0001c0001t0011 | 4 | HG01074.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2262_*2264delCCT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 2262 | chr1 | 95194129 | ||||||
| chr1:95194468 | AC | A | 15 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(12): Show |
171 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*2601delC | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 2601 | chr1 | 95194468 | ||||||
| chr1:95195000 | A | G | 4 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0024 others(1): Show |
24 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3132A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 3132 | chr1 | 95195000 | ||||||
| chr1:95195002 | T | G | 1 | a0001c0001t0032 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3134T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 3134 | chr1 | 95195002 | ||||||
| chr1:95195356 | A | G | 1 | a0001c0001t0036 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3488A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 3488 | chr1 | 95195356 | ||||||
| chr1:95195360 | A | G | 1 | a0001c0001t0027 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3492A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 3492 | chr1 | 95195360 | ||||||
| chr1:95195365 | C | G | 5 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0023 others(2): Show |
25 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3497C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 3497 | chr1 | 95195365 | ||||||
| chr1:95195390 | T | C | 1 | a0001c0001t0033 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3522T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 3522 | chr1 | 95195390 | ||||||
| chr1:95195477 | A | G | 1 | a0001c0001t0008 | 11 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3609A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 3609 | chr1 | 95195477 | ||||||
| chr1:95195522 | C | A | 1 | a0001c0001t0034 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3654C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 3654 | chr1 | 95195522 | ||||||
| chr1:95195644 | G | A | 1 | a0001c0001t0008 | 11 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3776G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 3776 | chr1 | 95195644 | ||||||
| chr1:95195737 | T | C | 1 | a0001c0001t0028 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3869T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 3869 | chr1 | 95195737 | ||||||
| chr1:95195984 | A | G | 2 | a0001c0001t0007 a0001c0003t0007 |
11 | HG00280.hp2 HG01099.hp2 HG01255.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4116A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 4116 | chr1 | 95195984 | ||||||
| chr1:95196140 | G | A | 1 | a0001c0001t0011 | 4 | HG01074.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4272G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 4272 | chr1 | 95196140 | ||||||
| chr1:95196272 | A | G | 1 | a0001c0001t0026 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4404A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 4404 | chr1 | 95196272 | ||||||
| chr1:95196379 | T | C | 1 | a0001c0001t0031 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4511T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 4511 | chr1 | 95196379 | ||||||
| chr1:95196616 | A | G | 1 | a0001c0001t0024 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4748A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 4748 | chr1 | 95196616 | ||||||
| chr1:95196646 | A | C | 1 | a0001c0001t0025 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4778A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 4778 | chr1 | 95196646 | ||||||
| chr1:95196702 | C | G | 1 | a0001c0001t0013 | 3 | HG01346.hp2 HG02735.hp2 HG03654.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4834C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 4834 | chr1 | 95196702 | ||||||
| chr1:95196716 | G | A | 1 | a0001c0001t0035 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4848G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 4848 | chr1 | 95196716 | ||||||
| chr1:95196895 | T | C | 1 | a0001c0001t0014 | 3 | HG02486.hp2 HG02622.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5027T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 5027 | chr1 | 95196895 | ||||||
| chr1:95196958 | T | C | 4 | a0001c0001t0003 a0001c0001t0025 a0001c0001t0026 others(1): Show |
33 | HG00558.hp2 HG00621.hp2 HG01081.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*5090T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 5090 | chr1 | 95196958 | ||||||
| chr1:95197102 | G | T | 1 | a0001c0001t0008 | 11 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5234G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 5234 | chr1 | 95197102 | ||||||
| chr1:95197384 | T | C | 1 | a0001c0001t0019 | 2 | HG01074.hp1 HG01106.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5516T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 5516 | chr1 | 95197384 | ||||||
| chr1:95197494 | C | T | 1 | a0001c0001t0015 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5626C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 5626 | chr1 | 95197494 | ||||||
| chr1:95197510 | C | A | 1 | a0001c0001t0010 | 4 | HG00280.hp1 HG01243.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5642C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 7/7 | 5642 | chr1 | 95197510 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:95117838 | A | C | 343 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(340): Show |
367 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.-12+221A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95117838 | |||||||
| chr1:95118108 | C | T | 1 | a0001c0001t0001g0350 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-12+491C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95118108 | |||||||
| chr1:95118216 | T | G | 85 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0051 others(82): Show |
92 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-12+599T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95118216 | |||||||
| chr1:95118401 | C | T | 51 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0306 others(48): Show |
54 | HG01255.hp1 HG01952.hp1 HG01978.hp1 others(51): Show |
intron_variant | MODIFIER | c.-12+784C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95118401 | |||||||
| chr1:95118864 | A | G | 3 | a0001c0001t0007g0108 a0001c0001t0013g0106 a0001c0001t0013g0107 |
3 | HG00280.hp2 HG02735.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-12+1247A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95118864 | |||||||
| chr1:95119108 | C | A | 3 | a0001c0001t0015g0109 a0001c0001t0015g0110 a0001c0001t0015g0111 |
3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+1491C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95119108 | |||||||
| chr1:95119122 | C | G | 1 | a0001c0001t0008g0301 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-12+1505C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95119122 | |||||||
| chr1:95119283 | C | G | 1 | a0001c0001t0002g0349 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-12+1666C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95119283 | |||||||
| chr1:95119325 | C | T | 3 | a0001c0001t0015g0109 a0001c0001t0015g0110 a0001c0001t0015g0111 |
3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+1708C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95119325 | |||||||
| chr1:95119709 | GGCCCAGC others(223): Show |
G | 1 | a0001c0001t0001g0300 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+2095_-12+2324d others(2): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95119709 | ||||||
| chr1:95119991 | A | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(39): Show |
50 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-12+2374A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95119991 | |||||||
| chr1:95120038 | G | C | 3 | a0001c0001t0002g0112 a0001c0001t0020g0113 a0001c0001t0020g0114 |
3 | HG02630.hp2 HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-12+2421G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95120038 | |||||||
| chr1:95120113 | C | A | 3 | a0001c0001t0002g0112 a0001c0001t0020g0113 a0001c0001t0020g0114 |
3 | HG02630.hp2 HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-12+2496C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95120113 | |||||||
| chr1:95120152 | A | G | 1 | a0001c0001t0026g0261 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-12+2535A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95120152 | |||||||
| chr1:95120438 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-12+2821G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95120438 | |||||||
| chr1:95120503 | C | T | 1 | a0001c0001t0003g0105 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-12+2886C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95120503 | |||||||
| chr1:95120545 | A | G | 1 | a0001c0001t0002g0260 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-12+2928A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95120545 | |||||||
| chr1:95120567 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-12+2950G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95120567 | |||||||
| chr1:95120603 | G | A | 58 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(55): Show |
58 | HG00544.hp2 HG00639.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-12+2986G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95120603 | |||||||
| chr1:95120698 | C | T | 7 | a0001c0001t0001g0167 a0001c0001t0005g0169 a0001c0001t0005g0170 others(4): Show |
7 | HG00738.hp2 HG01069.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+3081C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95120698 | |||||||
| chr1:95120767 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(39): Show |
50 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-12+3150C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95120767 | |||||||
| chr1:95120815 | A | G | 41 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0320 others(38): Show |
44 | HG01255.hp1 HG01952.hp1 HG01978.hp1 others(41): Show |
intron_variant | MODIFIER | c.-12+3198A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95120815 | |||||||
| chr1:95120858 | G | A | 3 | a0001c0001t0009g0006 a0001c0001t0009g0032 a0002c0002t0009g0031 |
4 | HG01891.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12+3241G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95120858 | |||||||
| chr1:95121041 | C | T | 3 | a0001c0001t0015g0109 a0001c0001t0015g0110 a0001c0001t0015g0111 |
3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+3424C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95121041 | |||||||
| chr1:95121217 | C | T | 85 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0051 others(82): Show |
92 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-12+3600C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95121217 | |||||||
| chr1:95121361 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-12+3744A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95121361 | |||||||
| chr1:95121447 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0039g0033 |
2 | HG00408.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-12+3830T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95121447 | |||||||
| chr1:95121489 | G | T | 3 | a0001c0001t0015g0109 a0001c0001t0015g0110 a0001c0001t0015g0111 |
3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+3872G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95121489 | |||||||
| chr1:95121619 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0251 others(9): Show |
15 | HG02040.hp2 HG02257.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+4002C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95121619 | |||||||
| chr1:95121632 | G | A | 2 | a0001c0001t0016g0116 a0001c0001t0016g0117 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12+4015G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95121632 | |||||||
| chr1:95121759 | C | T | 2 | a0001c0001t0002g0165 a0001c0001t0002g0166 |
2 | HG00639.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-12+4142C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95121759 | |||||||
| chr1:95122117 | G | T | 1 | a0001c0001t0001g0250 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-12+4500G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95122117 | |||||||
| chr1:95122416 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12+4799G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95122416 | |||||||
| chr1:95122463 | G | C | 50 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(47): Show |
50 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-12+4846G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95122463 | |||||||
| chr1:95122711 | G | A | 1 | a0001c0001t0005g0035 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-12+5094G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95122711 | |||||||
| chr1:95122983 | T | A | 1 | a0001c0001t0008g0176 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-12+5366T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95122983 | |||||||
| chr1:95122983 | T | TA | 9 | a0001c0001t0001g0118 a0001c0001t0001g0177 a0001c0001t0001g0178 others(6): Show |
9 | HG01255.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+5366_-12+5367i others(3): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95122983 | |||||||
| chr1:95122984 | T | A | 100 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(97): Show |
102 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.-12+5367T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95122984 | |||||||
| chr1:95122984 | T | TA | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+5372dupA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95122984 | ||||||
| chr1:95123330 | G | C | 8 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0002g0194 others(5): Show |
9 | HG00738.hp1 HG02486.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+5713G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95123330 | |||||||
| chr1:95123436 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-12+5819A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95123436 | |||||||
| chr1:95123520 | T | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(40): Show |
51 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-12+5903T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95123520 | |||||||
| chr1:95123521 | C | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0162 others(36): Show |
42 | HG01928.hp2 HG01952.hp1 HG01978.hp1 others(39): Show |
intron_variant | MODIFIER | c.-12+5904C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95123521 | |||||||
| chr1:95123547 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0175 a0001c0001t0001g0257 others(2): Show |
5 | HG02647.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+5930A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95123547 | |||||||
| chr1:95123624 | T | C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0119 a0001c0001t0001g0120 others(10): Show |
16 | HG00741.hp2 HG02040.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-12+6007T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95123624 | |||||||
| chr1:95123764 | CAT | C | 8 | a0001c0001t0001g0299 a0001c0001t0002g0172 a0001c0001t0005g0101 others(5): Show |
9 | HG01891.hp2 HG02723.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+6148_-12+6149d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95123764 | |||||||
| chr1:95123795 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0347 a0001c0001t0001g0348 |
5 | NA18957.hp1 NA18960.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+6178A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95123795 | |||||||
| chr1:95123892 | A | T | 1 | a0001c0001t0026g0261 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-12+6275A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95123892 | |||||||
| chr1:95123922 | A | G | 1 | a0001c0001t0002g0249 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-12+6305A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95123922 | |||||||
| chr1:95123995 | T | G | 1 | a0001c0001t0027g0037 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-12+6378T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95123995 | |||||||
| chr1:95124106 | T | C | 1 | a0001c0001t0005g0035 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-12+6489T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95124106 | |||||||
| chr1:95124831 | G | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(40): Show |
51 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-12+7214G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95124831 | |||||||
| chr1:95124843 | A | AT | 69 | a0001c0001t0001g0118 a0001c0001t0001g0146 a0001c0001t0001g0167 others(66): Show |
70 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.-12+7231dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95124843 | ||||||
| chr1:95124865 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12+7248A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95124865 | |||||||
| chr1:95125043 | G | C | 9 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0002g0112 others(6): Show |
9 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12+7426G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95125043 | |||||||
| chr1:95125301 | C | G | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-12+7684C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95125301 | |||||||
| chr1:95125593 | C | A | 1 | a0001c0001t0017g0319 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-12+7976C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95125593 | |||||||
| chr1:95125646 | C | T | 1 | a0001c0001t0002g0316 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-12+8029C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95125646 | |||||||
| chr1:95125908 | T | C | 3 | a0001c0001t0020g0113 a0001c0001t0020g0114 a0001c0001t0042g0023 |
3 | HG02109.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-12+8291T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95125908 | |||||||
| chr1:95125915 | G | T | 15 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 others(12): Show |
15 | HG02080.hp2 HG02155.hp2 HG03688.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+8298G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95125915 | |||||||
| chr1:95125989 | TA | T | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.-12+8384delA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95125989 | ||||||
| chr1:95126128 | T | G | 93 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0049 others(90): Show |
101 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.-12+8511T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95126128 | |||||||
| chr1:95126129 | T | A | 1 | a0001c0001t0012g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12+8512T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95126129 | |||||||
| chr1:95126129 | T | TA | 6 | a0001c0001t0005g0305 a0001c0001t0006g0160 a0001c0001t0006g0161 others(3): Show |
6 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+8525dupA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95126129 | ||||||
| chr1:95126129 | TA | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0258 others(17): Show |
23 | HG01256.hp2 HG01952.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.-12+8525delA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95126129 | ||||||
| chr1:95126192 | T | C | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.-12+8575T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95126192 | |||||||
| chr1:95126196 | G | A | 5 | a0001c0001t0012g0025 a0001c0001t0012g0026 a0001c0001t0012g0028 others(2): Show |
6 | HG00735.hp2 HG01081.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+8579G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95126196 | |||||||
| chr1:95126199 | A | G | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
368 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.-12+8582A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95126199 | |||||||
| chr1:95126418 | ACT | A | 13 | a0001c0001t0001g0183 a0001c0001t0002g0180 a0001c0001t0002g0190 others(10): Show |
13 | HG00099.hp2 HG00639.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12+8804_-12+8805d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95126418 | ||||||
| chr1:95126428 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-12+8811A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95126428 | |||||||
| chr1:95126432 | GA | G | 337 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(334): Show |
360 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.-12+8830delA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95126432 | ||||||
| chr1:95126646 | T | C | 4 | a0001c0001t0005g0305 a0001c0001t0014g0302 a0001c0001t0014g0303 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12+9029T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95126646 | |||||||
| chr1:95126704 | G | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0257 a0001c0001t0034g0018 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-12+9087G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95126704 | |||||||
| chr1:95126758 | C | T | 1 | a0001c0001t0012g0025 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-12+9141C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95126758 | |||||||
| chr1:95126998 | G | A | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
368 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.-12+9381G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95126998 | |||||||
| chr1:95127053 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0021 others(102): Show |
111 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.-12+9436A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95127053 | |||||||
| chr1:95127099 | C | T | 3 | a0001c0001t0020g0113 a0001c0001t0020g0114 a0001c0001t0042g0023 |
3 | HG02109.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-12+9482C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95127099 | |||||||
| chr1:95127119 | T | G | 1 | a0001c0001t0006g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-12+9502T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95127119 | |||||||
| chr1:95127404 | C | A | 1 | a0001c0001t0001g0334 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+9787C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95127404 | |||||||
| chr1:95127726 | C | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0175 a0001c0001t0001g0257 others(2): Show |
5 | HG02647.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+10109C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95127726 | |||||||
| chr1:95127901 | T | G | 72 | a0001c0001t0001g0118 a0001c0001t0001g0146 a0001c0001t0001g0167 others(69): Show |
73 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.-12+10284T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95127901 | |||||||
| chr1:95128219 | T | A | 1 | a0001c0001t0002g0045 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-12+10602T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95128219 | |||||||
| chr1:95128279 | C | G | 78 | a0001c0001t0001g0118 a0001c0001t0001g0146 a0001c0001t0001g0167 others(75): Show |
80 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.-12+10662C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95128279 | |||||||
| chr1:95128399 | G | A | 1 | a0001c0001t0007g0149 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-12+10782G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95128399 | |||||||
| chr1:95128403 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12+10786G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95128403 | |||||||
| chr1:95128667 | A | G | 5 | a0001c0001t0003g0012 a0001c0001t0003g0092 a0001c0001t0003g0093 others(2): Show |
6 | HG00621.hp2 NA18946.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+11050A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95128667 | |||||||
| chr1:95128989 | G | A | 1 | a0001c0001t0017g0319 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-12+11372G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95128989 | |||||||
| chr1:95129018 | A | G | 1 | a0001c0001t0003g0105 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-12+11401A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95129018 | |||||||
| chr1:95129131 | T | C | 85 | a0001c0001t0001g0018 a0001c0001t0001g0118 a0001c0001t0001g0167 others(82): Show |
87 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.-12+11514T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95129131 | |||||||
| chr1:95129141 | A | G | 14 | a0001c0001t0001g0183 a0001c0001t0002g0180 a0001c0001t0002g0190 others(11): Show |
14 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12+11524A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95129141 | |||||||
| chr1:95129165 | A | G | 9 | a0001c0001t0003g0008 a0001c0001t0003g0041 a0001c0001t0003g0042 others(6): Show |
10 | HG01081.hp1 HG01346.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+11548A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95129165 | |||||||
| chr1:95129342 | T | G | 17 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0047 others(14): Show |
19 | HG01099.hp1 HG01109.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.-12+11725T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95129342 | |||||||
| chr1:95129377 | A | G | 1 | a0001c0001t0030g0317 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-12+11760A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95129377 | |||||||
| chr1:95129598 | C | T | 2 | a0001c0001t0004g0142 a0001c0001t0004g0143 |
2 | HG02132.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-12+11981C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95129598 | |||||||
| chr1:95129627 | A | G | 2 | a0001c0001t0016g0116 a0001c0001t0016g0117 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12+12010A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95129627 | |||||||
| chr1:95129650 | G | T | 1 | a0001c0001t0025g0141 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-12+12033G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95129650 | |||||||
| chr1:95129697 | G | A | 3 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0003g0041 |
3 | HG01981.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-12+12080G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95129697 | |||||||
| chr1:95129779 | C | T | 1 | a0001c0001t0002g0260 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-12+12162C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95129779 | |||||||
| chr1:95129930 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-12+12313T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95129930 | |||||||
| chr1:95130082 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-12+12465T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95130082 | |||||||
| chr1:95130162 | A | AT | 16 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0008g0091 others(13): Show |
16 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-12+12554dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95130162 | ||||||
| chr1:95130186 | CTCTGTTG others(24): Show |
C | 71 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0051 others(68): Show |
75 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-12+12573_-12+1260 others(35): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95130186 | ||||||
| chr1:95130215 | C | T | 3 | a0001c0001t0015g0109 a0001c0001t0015g0110 a0001c0001t0015g0111 |
3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+12598C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95130215 | |||||||
| chr1:95130397 | T | C | 16 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0008g0091 others(13): Show |
16 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-12+12780T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95130397 | |||||||
| chr1:95130545 | T | C | 1 | a0001c0001t0001g0323 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-12+12928T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95130545 | |||||||
| chr1:95130555 | G | A | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.-12+12938G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95130555 | |||||||
| chr1:95130673 | T | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-12+13056T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95130673 | |||||||
| chr1:95130739 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-12+13122A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95130739 | |||||||
| chr1:95130741 | T | C | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.-12+13124T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95130741 | |||||||
| chr1:95130917 | T | C | 1 | a0001c0001t0001g0324 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-11-12974T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95130917 | |||||||
| chr1:95130940 | G | T | 70 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0051 others(67): Show |
74 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.-11-12951G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95130940 | |||||||
| chr1:95130999 | C | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(34): Show |
45 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11-12892C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95130999 | |||||||
| chr1:95131127 | A | G | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.-11-12764A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95131127 | |||||||
| chr1:95131568 | A | G | 16 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0008g0091 others(13): Show |
16 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-11-12323A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95131568 | |||||||
| chr1:95131614 | T | A | 1 | a0001c0001t0026g0261 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-11-12277T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95131614 | |||||||
| chr1:95131665 | G | C | 1 | a0001c0001t0002g0048 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-11-12226G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95131665 | |||||||
| chr1:95131857 | A | T | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-11-12034A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95131857 | |||||||
| chr1:95131922 | T | C | 1 | a0001c0001t0002g0180 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-11-11969T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95131922 | |||||||
| chr1:95132019 | T | C | 27 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(24): Show |
27 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.-11-11872T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95132019 | |||||||
| chr1:95132084 | T | C | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.-11-11807T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95132084 | |||||||
| chr1:95132096 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-11-11795C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95132096 | |||||||
| chr1:95132142 | C | A | 4 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | NA18994.hp1 NA19010.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-11749C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95132142 | |||||||
| chr1:95132314 | A | G | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.-11-11577A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95132314 | |||||||
| chr1:95132365 | G | A | 3 | a0001c0001t0009g0006 a0001c0001t0009g0032 a0002c0002t0009g0031 |
4 | HG01891.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-11526G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95132365 | |||||||
| chr1:95132453 | A | T | 27 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(24): Show |
27 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.-11-11438A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95132453 | |||||||
| chr1:95132456 | CA | C | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
302 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.-11-11413delA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95132456 | ||||||
| chr1:95132456 | CAA | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0118 others(44): Show |
50 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.-11-11414_-11-1141 others(6): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95132456 | ||||||
| chr1:95132468 | A | G | 1 | a0001c0001t0001g0346 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-11-11423A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95132468 | |||||||
| chr1:95132630 | T | C | 3 | a0001c0001t0002g0308 a0001c0001t0002g0309 a0001c0001t0002g0310 |
3 | HG02647.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-11-11261T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95132630 | |||||||
| chr1:95132938 | A | G | 31 | a0001c0001t0004g0039 a0001c0001t0004g0079 a0001c0001t0004g0086 others(28): Show |
31 | HG00438.hp2 HG00544.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-11-10953A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95132938 | |||||||
| chr1:95132997 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-11-10894A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95132997 | |||||||
| chr1:95133021 | A | G | 5 | a0001c0001t0001g0270 a0001c0001t0001g0292 a0001c0001t0001g0293 others(2): Show |
5 | HG00438.hp1 NA18959.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-10870A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95133021 | |||||||
| chr1:95133037 | A | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(108): Show |
117 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11-10854A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95133037 | |||||||
| chr1:95133069 | A | C | 1 | a0001c0001t0003g0085 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-11-10822A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95133069 | |||||||
| chr1:95133214 | G | A | 65 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0051 others(62): Show |
68 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-11-10677G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95133214 | |||||||
| chr1:95133383 | A | AT | 13 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0177 others(10): Show |
16 | HG02040.hp2 HG02257.hp1 HG03491.hp1 others(13): Show |
intron_variant | MODIFIER | c.-11-10506dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95133383 | ||||||
| chr1:95133385 | T | TA | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(229): Show |
249 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.-11-10496dupA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95133385 | ||||||
| chr1:95133385 | T | TAA | 29 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(26): Show |
29 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.-11-10497_-11-1049 others(6): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95133385 | ||||||
| chr1:95133404 | A | G | 5 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-10487A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95133404 | |||||||
| chr1:95133511 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-11-10380T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95133511 | |||||||
| chr1:95133690 | T | A | 1 | a0001c0001t0001g0262 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-11-10201T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95133690 | |||||||
| chr1:95133901 | A | T | 1 | a0001c0001t0005g0014 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-11-9990A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95133901 | |||||||
| chr1:95133941 | T | G | 92 | a0001c0001t0001g0167 a0001c0001t0002g0128 a0001c0001t0002g0129 others(89): Show |
98 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.-11-9950T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95133941 | |||||||
| chr1:95134198 | G | A | 60 | a0001c0001t0001g0167 a0001c0001t0002g0128 a0001c0001t0002g0129 others(57): Show |
66 | HG00558.hp2 HG00621.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11-9693G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95134198 | |||||||
| chr1:95134247 | C | T | 7 | a0001c0001t0007g0108 a0001c0001t0007g0156 a0001c0001t0012g0025 others(4): Show |
8 | HG00280.hp2 HG00735.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-9644C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95134247 | |||||||
| chr1:95134408 | G | A | 13 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0008g0091 others(10): Show |
13 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11-9483G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95134408 | |||||||
| chr1:95134462 | C | A | 1 | a0001c0001t0001g0325 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-11-9429C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95134462 | |||||||
| chr1:95134795 | A | T | 4 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0076 others(1): Show |
4 | NA18941.hp1 NA18955.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-9096A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95134795 | |||||||
| chr1:95135214 | T | A | 1 | a0001c0001t0001g0223 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-11-8677T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95135214 | |||||||
| chr1:95135266 | T | C | 28 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-8625T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95135266 | |||||||
| chr1:95135366 | A | G | 1 | a0001c0001t0004g0073 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-11-8525A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95135366 | |||||||
| chr1:95135395 | C | CT | 44 | a0001c0001t0001g0164 a0001c0001t0001g0175 a0001c0001t0001g0218 others(41): Show |
44 | HG00735.hp1 HG01109.hp2 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.-11-8477dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95135395 | ||||||
| chr1:95135459 | TG | T | 5 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-8431delG | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95135459 | |||||||
| chr1:95135466 | A | G | 28 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-8425A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95135466 | |||||||
| chr1:95135483 | G | A | 2 | a0001c0001t0002g0165 a0001c0001t0002g0166 |
2 | HG00639.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-11-8408G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95135483 | |||||||
| chr1:95135515 | G | A | 3 | a0001c0001t0001g0322 a0001c0001t0001g0326 a0001c0001t0002g0327 |
3 | HG02809.hp1 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-11-8376G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95135515 | |||||||
| chr1:95135520 | C | A | 28 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-8371C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95135520 | |||||||
| chr1:95135758 | CAG | C | 28 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-8132_-11-8131d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95135758 | |||||||
| chr1:95135993 | A | C | 2 | a0001c0001t0002g0201 a0001c0001t0002g0209 |
2 | NA18940.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-11-7898A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95135993 | |||||||
| chr1:95136039 | G | GT | 45 | a0001c0001t0001g0115 a0001c0001t0002g0128 a0001c0001t0002g0129 others(42): Show |
50 | HG00558.hp2 HG00621.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.-11-7840dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95136039 | ||||||
| chr1:95136039 | G | GTT | 13 | a0001c0001t0001g0167 a0001c0001t0005g0036 a0001c0001t0005g0101 others(10): Show |
13 | HG00738.hp2 HG01069.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11-7841_-11-7840d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95136039 | ||||||
| chr1:95136051 | T | A | 1 | a0001c0001t0005g0014 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-11-7840T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95136051 | |||||||
| chr1:95136078 | A | G | 1 | a0001c0001t0002g0016 | 2 | HG02004.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-11-7813A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95136078 | |||||||
| chr1:95136137 | C | T | 13 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0008g0091 others(10): Show |
13 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11-7754C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95136137 | |||||||
| chr1:95136244 | G | GT | 11 | a0001c0001t0001g0163 a0001c0001t0001g0290 a0001c0001t0001g0291 others(8): Show |
11 | HG00609.hp1 HG01928.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-7638dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95136244 | ||||||
| chr1:95136252 | T | G | 65 | a0001c0001t0001g0167 a0001c0001t0001g0346 a0001c0001t0002g0128 others(62): Show |
71 | HG00558.hp2 HG00621.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.-11-7639T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95136252 | |||||||
| chr1:95136254 | G | T | 4 | a0001c0001t0002g0034 a0001c0001t0002g0063 a0001c0001t0002g0298 others(1): Show |
4 | HG00408.hp2 HG00609.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-7637G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95136254 | |||||||
| chr1:95136509 | A | G | 1 | a0001c0001t0001g0333 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-11-7382A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95136509 | |||||||
| chr1:95136665 | A | G | 8 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(5): Show |
8 | HG01261.hp2 HG01934.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-7226A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95136665 | |||||||
| chr1:95136732 | G | T | 3 | a0001c0001t0002g0308 a0001c0001t0002g0309 a0001c0001t0002g0310 |
3 | HG02647.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-11-7159G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95136732 | |||||||
| chr1:95137208 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-11-6683A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95137208 | |||||||
| chr1:95137500 | C | G | 13 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0008g0091 others(10): Show |
13 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11-6391C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95137500 | |||||||
| chr1:95137536 | G | A | 12 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0002g0112 others(9): Show |
12 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-6355G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95137536 | |||||||
| chr1:95137556 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0257 a0001c0001t0034g0018 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-11-6335C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95137556 | |||||||
| chr1:95137557 | G | A | 57 | a0001c0001t0001g0167 a0001c0001t0001g0224 a0001c0001t0002g0128 others(54): Show |
63 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.-11-6334G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95137557 | |||||||
| chr1:95137597 | A | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(34): Show |
45 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11-6294A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95137597 | |||||||
| chr1:95137627 | A | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0238 others(11): Show |
17 | NA18612.hp1 NA18944.hp2 NA18949.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11-6264A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95137627 | |||||||
| chr1:95137761 | G | A | 1 | a0001c0001t0002g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-11-6130G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95137761 | |||||||
| chr1:95137770 | G | A | 1 | a0001c0001t0020g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-11-6121G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95137770 | |||||||
| chr1:95137823 | A | C | 3 | a0001c0001t0001g0258 a0001c0001t0001g0332 a0001c0001t0001g0333 |
3 | NA18612.hp1 NA18979.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-11-6068A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95137823 | |||||||
| chr1:95137946 | C | T | 1 | a0001c0001t0005g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-11-5945C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95137946 | |||||||
| chr1:95137982 | C | G | 3 | a0001c0001t0020g0113 a0001c0001t0020g0114 a0001c0001t0042g0023 |
3 | HG02109.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-11-5909C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95137982 | |||||||
| chr1:95138018 | A | G | 4 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0076 others(1): Show |
4 | NA18941.hp1 NA18955.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-5873A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95138018 | |||||||
| chr1:95138054 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(41): Show |
52 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-11-5837G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95138054 | |||||||
| chr1:95138105 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-11-5786T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95138105 | |||||||
| chr1:95138143 | C | G | 1 | a0001c0001t0003g0084 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-11-5748C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95138143 | |||||||
| chr1:95138432 | T | C | 16 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0008g0091 others(13): Show |
16 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-11-5459T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95138432 | |||||||
| chr1:95138529 | C | A | 5 | a0001c0001t0001g0183 a0001c0001t0008g0181 a0001c0001t0008g0182 others(2): Show |
5 | HG00639.hp2 HG01243.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-5362C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95138529 | |||||||
| chr1:95138611 | TTACTGTA others(15): Show |
T | 5 | a0001c0001t0002g0194 a0001c0001t0005g0191 a0001c0001t0005g0192 others(2): Show |
5 | HG00738.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-5263_-11-5242d others(24): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95138611 | ||||||
| chr1:95138626 | C | T | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 |
3 | NA18990.hp1 NA19002.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.-11-5265C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95138626 | |||||||
| chr1:95138814 | G | C | 16 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0008g0091 others(13): Show |
16 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-11-5077G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95138814 | |||||||
| chr1:95138859 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-11-5032A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95138859 | |||||||
| chr1:95138883 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-11-5008G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95138883 | |||||||
| chr1:95139024 | C | CA | 100 | a0001c0001t0001g0167 a0001c0001t0001g0225 a0001c0001t0001g0226 others(97): Show |
107 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-11-4847dupA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95139024 | ||||||
| chr1:95139024 | C | CAA | 15 | a0001c0001t0002g0148 a0001c0001t0002g0194 a0001c0001t0002g0310 others(12): Show |
15 | HG01069.hp1 HG01255.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.-11-4848_-11-4847d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95139024 | ||||||
| chr1:95139081 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(41): Show |
52 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-11-4810G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139081 | |||||||
| chr1:95139118 | T | C | 28 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-4773T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139118 | |||||||
| chr1:95139174 | C | CA | 37 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(34): Show |
37 | HG00099.hp2 HG00639.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.-11-4694dupA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95139174 | ||||||
| chr1:95139174 | CA | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
171 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.-11-4694delA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95139174 | ||||||
| chr1:95139214 | C | T | 1 | a0001c0001t0005g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-11-4677C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139214 | |||||||
| chr1:95139279 | C | G | 28 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-4612C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139279 | |||||||
| chr1:95139449 | C | A | 1 | a0001c0001t0002g0123 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-11-4442C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139449 | |||||||
| chr1:95139455 | A | AT | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0021 others(70): Show |
79 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-11-4414dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95139455 | ||||||
| chr1:95139455 | A | ATT | 140 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0052 others(137): Show |
147 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.-11-4415_-11-4414d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95139455 | ||||||
| chr1:95139455 | A | ATTT | 40 | a0001c0001t0002g0016 a0001c0001t0002g0060 a0001c0001t0002g0061 others(37): Show |
42 | HG00735.hp2 HG01081.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.-11-4416_-11-4414d others(5): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95139455 | ||||||
| chr1:95139455 | A | ATTTT | 8 | a0001c0001t0002g0015 a0001c0001t0002g0034 a0001c0001t0002g0047 others(5): Show |
9 | HG00408.hp2 HG01175.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11-4417_-11-4414d others(6): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95139455 | ||||||
| chr1:95139455 | A | ATTTTTTT others(4): Show |
7 | a0001c0001t0008g0176 a0001c0001t0008g0185 a0001c0001t0008g0186 others(4): Show |
7 | HG00099.hp2 HG01517.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-4424_-11-4414d others(13): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95139455 | ||||||
| chr1:95139455 | A | ATTTTTTT others(5): Show |
6 | a0001c0001t0002g0190 a0001c0001t0008g0091 a0001c0001t0008g0181 others(3): Show |
6 | HG00639.hp2 HG01175.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-4425_-11-4414d others(14): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95139455 | ||||||
| chr1:95139455 | A | ATTTTTTT others(6): Show |
3 | a0001c0001t0001g0183 a0001c0001t0008g0184 a0001c0001t0008g0301 |
3 | HG01243.hp2 HG01358.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-11-4426_-11-4414d others(15): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95139455 | ||||||
| chr1:95139455 | AT | A | 8 | a0001c0001t0001g0306 a0001c0001t0002g0112 a0001c0001t0002g0147 others(5): Show |
8 | HG02647.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-4414delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95139455 | ||||||
| chr1:95139455 | ATTTTTTT others(3): Show |
A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(41): Show |
52 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-11-4423_-11-4414d others(12): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95139455 | ||||||
| chr1:95139485 | T | C | 73 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0051 others(70): Show |
77 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.-11-4406T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139485 | |||||||
| chr1:95139488 | C | T | 2 | a0001c0001t0002g0201 a0001c0001t0002g0209 |
2 | NA18940.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-11-4403C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139488 | |||||||
| chr1:95139489 | A | G | 32 | a0001c0001t0004g0039 a0001c0001t0004g0073 a0001c0001t0004g0079 others(29): Show |
32 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11-4402A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139489 | |||||||
| chr1:95139519 | C | T | 28 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-4372C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139519 | |||||||
| chr1:95139534 | C | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0238 others(12): Show |
18 | HG01978.hp1 NA18612.hp1 NA18944.hp2 others(15): Show |
intron_variant | MODIFIER | c.-11-4357C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139534 | |||||||
| chr1:95139542 | T | G | 1 | a0001c0001t0001g0336 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-11-4349T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139542 | |||||||
| chr1:95139565 | T | C | 12 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0002g0112 others(9): Show |
12 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-4326T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139565 | |||||||
| chr1:95139721 | A | G | 1 | a0001c0001t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-11-4170A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139721 | |||||||
| chr1:95139804 | A | G | 60 | a0001c0001t0001g0167 a0001c0001t0002g0128 a0001c0001t0002g0129 others(57): Show |
66 | HG00558.hp2 HG00621.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11-4087A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139804 | |||||||
| chr1:95139808 | C | T | 1 | a0001c0001t0017g0319 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-11-4083C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139808 | |||||||
| chr1:95139890 | T | G | 28 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-4001T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95139890 | |||||||
| chr1:95140000 | A | G | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.-11-3891A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95140000 | |||||||
| chr1:95140054 | C | T | 1 | a0001c0001t0006g0248 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-11-3837C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95140054 | |||||||
| chr1:95140081 | T | C | 1 | a0001c0001t0005g0014 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-11-3810T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95140081 | |||||||
| chr1:95140216 | G | A | 28 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-3675G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95140216 | |||||||
| chr1:95140279 | A | G | 60 | a0001c0001t0001g0167 a0001c0001t0002g0128 a0001c0001t0002g0129 others(57): Show |
66 | HG00558.hp2 HG00621.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11-3612A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95140279 | |||||||
| chr1:95140424 | C | G | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-11-3467C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95140424 | |||||||
| chr1:95140496 | G | A | 28 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-3395G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95140496 | |||||||
| chr1:95140514 | T | G | 28 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-3377T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95140514 | |||||||
| chr1:95140545 | C | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01928.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-11-3346C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95140545 | |||||||
| chr1:95140722 | C | T | 28 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-3169C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95140722 | |||||||
| chr1:95140749 | G | C | 28 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-3142G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95140749 | |||||||
| chr1:95140814 | C | T | 28 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(25): Show |
28 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-3077C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95140814 | |||||||
| chr1:95141278 | ATACAG | A | 12 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0002g0112 others(9): Show |
12 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-2610_-11-2606d others(7): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141278 | ||||||
| chr1:95141283 | G | T | 334 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(331): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.-11-2608G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95141283 | |||||||
| chr1:95141439 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-11-2452C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95141439 | |||||||
| chr1:95141532 | A | T | 13 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0008g0091 others(10): Show |
13 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11-2359A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95141532 | |||||||
| chr1:95141577 | A | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0238 others(12): Show |
18 | HG01978.hp1 NA18612.hp1 NA18944.hp2 others(15): Show |
intron_variant | MODIFIER | c.-11-2314A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95141577 | |||||||
| chr1:95141763 | A | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(34): Show |
45 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11-2128A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95141763 | |||||||
| chr1:95141792 | T | TAC | 23 | a0001c0001t0001g0001 a0001c0001t0001g0119 a0001c0001t0001g0121 others(20): Show |
26 | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.-11-2059_-11-2058d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141792 | ||||||
| chr1:95141792 | T | TACAC | 22 | a0001c0001t0001g0018 a0001c0001t0001g0118 a0001c0001t0001g0175 others(19): Show |
23 | HG00735.hp2 HG01081.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-11-2061_-11-2058d others(6): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141792 | ||||||
| chr1:95141792 | T | TACACAC | 17 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0146 others(14): Show |
17 | HG00544.hp1 HG01257.hp1 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11-2063_-11-2058d others(8): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141792 | ||||||
| chr1:95141792 | T | TACACACA others(1): Show |
26 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0054 others(23): Show |
27 | HG00280.hp1 HG00408.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.-11-2065_-11-2058d others(10): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141792 | ||||||
| chr1:95141792 | T | TACACACA others(3): Show |
18 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0002g0016 others(15): Show |
19 | HG01106.hp2 HG01109.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-11-2067_-11-2058d others(12): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141792 | ||||||
| chr1:95141792 | T | TACACACA others(5): Show |
14 | a0001c0001t0001g0057 a0001c0001t0002g0048 a0001c0001t0002g0055 others(11): Show |
15 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-11-2069_-11-2058d others(14): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141792 | ||||||
| chr1:95141792 | T | TACACACA others(7): Show |
8 | a0001c0001t0001g0115 a0001c0001t0002g0034 a0001c0001t0002g0050 others(5): Show |
8 | HG00408.hp2 HG00741.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-2071_-11-2058d others(16): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141792 | ||||||
| chr1:95141792 | T | TACACACA others(9): Show |
3 | a0001c0001t0002g0069 a0001c0001t0002g0209 a0001c0001t0002g0211 |
3 | HG01261.hp2 HG01433.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.-11-2073_-11-2058d others(18): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141792 | ||||||
| chr1:95141792 | TAC | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(60): Show |
71 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.-11-2059_-11-2058d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141792 | ||||||
| chr1:95141792 | TACAC | T | 24 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0269 others(21): Show |
25 | HG02080.hp2 HG02145.hp2 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.-11-2061_-11-2058d others(6): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141792 | ||||||
| chr1:95141792 | TACACAC | T | 10 | a0001c0001t0001g0274 a0001c0001t0001g0277 a0001c0001t0001g0278 others(7): Show |
10 | HG02280.hp1 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11-2063_-11-2058d others(8): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141792 | ||||||
| chr1:95141792 | TACACACA others(1): Show |
T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0238 others(53): Show |
59 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.-11-2065_-11-2058d others(10): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141792 | ||||||
| chr1:95141792 | TACACACA others(5): Show |
T | 17 | a0001c0001t0001g0183 a0001c0001t0002g0066 a0001c0001t0002g0190 others(14): Show |
17 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-11-2069_-11-2058d others(14): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141792 | ||||||
| chr1:95141833 | A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0159 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-11-2058_-11-2057i others(13): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95141833 | |||||||
| chr1:95141833 | A | ACACACAC others(6): Show |
1 | a0001c0001t0002g0045 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-11-2058_-11-2057i others(15): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95141833 | |||||||
| chr1:95141833 | A | ACACACAC others(10): Show |
1 | a0001c0001t0002g0298 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-11-2058_-11-2057i others(19): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95141833 | |||||||
| chr1:95141834 | A | C | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 |
3 | NA18990.hp1 NA19002.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.-11-2057A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95141834 | |||||||
| chr1:95141861 | CAT | C | 60 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(57): Show |
60 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-11-2027_-11-2026d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95141861 | ||||||
| chr1:95141952 | G | A | 1 | a0001c0001t0008g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-11-1939G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95141952 | |||||||
| chr1:95142130 | C | CT | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
230 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.-11-1744dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95142130 | ||||||
| chr1:95142130 | C | CTT | 122 | a0001c0001t0001g0049 a0001c0001t0001g0115 a0001c0001t0001g0146 others(119): Show |
127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-11-1745_-11-1744d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95142130 | ||||||
| chr1:95142130 | C | CTTT | 8 | a0001c0001t0001g0222 a0001c0001t0003g0041 a0001c0001t0003g0082 others(5): Show |
8 | HG01981.hp2 HG02602.hp1 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11-1746_-11-1744d others(5): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95142130 | ||||||
| chr1:95142200 | A | G | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.-11-1691A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95142200 | |||||||
| chr1:95142291 | CT | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(81): Show |
97 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.-11-1579delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95142291 | ||||||
| chr1:95142291 | CTT | C | 179 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0030 others(176): Show |
185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.-11-1580_-11-1579d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95142291 | ||||||
| chr1:95142291 | CTTT | C | 43 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(40): Show |
48 | HG00558.hp2 HG00621.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.-11-1581_-11-1579d others(5): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95142291 | ||||||
| chr1:95142573 | G | A | 5 | a0001c0001t0012g0025 a0001c0001t0012g0026 a0001c0001t0012g0028 others(2): Show |
6 | HG00735.hp2 HG01081.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-1318G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95142573 | |||||||
| chr1:95142594 | T | C | 1 | a0001c0001t0027g0037 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-11-1297T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95142594 | |||||||
| chr1:95142669 | A | G | 2 | a0001c0001t0002g0017 a0001c0001t0029g0017 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-11-1222A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95142669 | |||||||
| chr1:95142777 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0021 others(55): Show |
64 | HG00741.hp2 HG01928.hp2 HG01978.hp1 others(61): Show |
intron_variant | MODIFIER | c.-11-1114C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95142777 | |||||||
| chr1:95142839 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-11-1052G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95142839 | |||||||
| chr1:95142839 | G | C | 18 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0006g0160 others(15): Show |
18 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-1052G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95142839 | |||||||
| chr1:95142844 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-11-1047C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95142844 | |||||||
| chr1:95142857 | G | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(36): Show |
47 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.-11-1034G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95142857 | |||||||
| chr1:95142875 | G | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
167 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.-11-1016G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95142875 | |||||||
| chr1:95142908 | C | T | 60 | a0001c0001t0001g0183 a0001c0001t0001g0306 a0001c0001t0001g0307 others(57): Show |
60 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-11-983C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95142908 | |||||||
| chr1:95142913 | C | T | 2 | a0001c0001t0002g0308 a0001c0001t0002g0310 |
2 | HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-11-978C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95142913 | |||||||
| chr1:95142970 | C | A | 1 | a0001c0001t0003g0044 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-11-921C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95142970 | |||||||
| chr1:95142978 | A | G | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.-11-913A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95142978 | |||||||
| chr1:95143028 | A | T | 60 | a0001c0001t0001g0167 a0001c0001t0002g0128 a0001c0001t0002g0129 others(57): Show |
66 | HG00558.hp2 HG00621.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11-863A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95143028 | |||||||
| chr1:95143092 | A | C | 60 | a0001c0001t0001g0167 a0001c0001t0002g0128 a0001c0001t0002g0129 others(57): Show |
66 | HG00558.hp2 HG00621.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11-799A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95143092 | |||||||
| chr1:95143099 | C | T | 12 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0002g0112 others(9): Show |
12 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-792C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95143099 | |||||||
| chr1:95143338 | A | T | 54 | a0001c0001t0001g0167 a0001c0001t0002g0128 a0001c0001t0002g0129 others(51): Show |
59 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.-11-553A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95143338 | |||||||
| chr1:95143460 | T | G | 48 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0051 others(45): Show |
49 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.-11-431T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95143460 | |||||||
| chr1:95143465 | CTTGA | C | 12 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0002g0112 others(9): Show |
12 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-422_-11-419del others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 95143465 | ||||||
| chr1:95143861 | A | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0238 others(11): Show |
17 | NA18612.hp1 NA18944.hp2 NA18949.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11-30A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 1/6 | chr1 | 95143861 | |||||||
| chr1:95144424 | C | T | 12 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0002g0112 others(9): Show |
12 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.155+368C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95144424 | |||||||
| chr1:95144595 | G | GT | 16 | a0001c0001t0002g0112 a0001c0001t0002g0147 a0001c0001t0002g0148 others(13): Show |
17 | HG00735.hp2 HG01081.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.155+551dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 95144595 | ||||||
| chr1:95144595 | GT | G | 29 | a0001c0001t0001g0292 a0001c0001t0002g0055 a0001c0001t0003g0095 others(26): Show |
29 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.155+551delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 95144595 | ||||||
| chr1:95144697 | A | G | 13 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0008g0091 others(10): Show |
13 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.155+641A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95144697 | |||||||
| chr1:95145155 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.155+1099C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95145155 | |||||||
| chr1:95145279 | A | G | 4 | a0001c0001t0001g0335 a0001c0001t0001g0343 a0001c0001t0001g0344 others(1): Show |
4 | NA18963.hp1 NA19002.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.155+1223A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95145279 | |||||||
| chr1:95145336 | T | C | 1 | a0001c0001t0001g0337 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.155+1280T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95145336 | |||||||
| chr1:95145497 | C | A | 1 | a0001c0001t0005g0140 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.155+1441C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95145497 | |||||||
| chr1:95145531 | A | G | 1 | a0001c0001t0030g0317 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.155+1475A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95145531 | |||||||
| chr1:95145558 | A | G | 55 | a0001c0001t0001g0183 a0001c0001t0002g0112 a0001c0001t0002g0147 others(52): Show |
55 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.155+1502A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95145558 | |||||||
| chr1:95145645 | G | A | 5 | a0001c0001t0002g0194 a0001c0001t0005g0191 a0001c0001t0005g0192 others(2): Show |
5 | HG00738.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.155+1589G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95145645 | |||||||
| chr1:95145725 | G | C | 1 | a0001c0001t0006g0242 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.155+1669G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95145725 | |||||||
| chr1:95145751 | G | A | 6 | a0001c0001t0012g0025 a0001c0001t0012g0026 a0001c0001t0012g0028 others(3): Show |
7 | HG00735.hp2 HG01081.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+1695G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95145751 | |||||||
| chr1:95145864 | A | G | 55 | a0001c0001t0001g0183 a0001c0001t0002g0112 a0001c0001t0002g0147 others(52): Show |
55 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.155+1808A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95145864 | |||||||
| chr1:95146094 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
172 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.155+2038A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95146094 | |||||||
| chr1:95146161 | A | G | 60 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(57): Show |
66 | HG00558.hp2 HG00621.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.155+2105A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95146161 | |||||||
| chr1:95146202 | T | C | 55 | a0001c0001t0001g0183 a0001c0001t0002g0112 a0001c0001t0002g0147 others(52): Show |
55 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.155+2146T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95146202 | |||||||
| chr1:95146211 | C | T | 2 | a0001c0001t0016g0116 a0001c0001t0016g0117 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.155+2155C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95146211 | |||||||
| chr1:95146349 | T | C | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.155+2293T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95146349 | |||||||
| chr1:95146354 | G | A | 3 | a0001c0001t0020g0113 a0001c0001t0020g0114 a0001c0001t0042g0023 |
3 | HG02109.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.155+2298G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95146354 | |||||||
| chr1:95146466 | G | T | 13 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0008g0091 others(10): Show |
13 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.156-2236G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95146466 | |||||||
| chr1:95146476 | A | G | 2 | a0001c0001t0007g0108 a0001c0001t0007g0156 |
2 | HG00280.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.156-2226A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95146476 | |||||||
| chr1:95146489 | C | A | 1 | a0001c0001t0001g0250 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.156-2213C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95146489 | |||||||
| chr1:95146659 | A | C | 60 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(57): Show |
66 | HG00558.hp2 HG00621.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.156-2043A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95146659 | |||||||
| chr1:95146690 | G | A | 15 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0006g0160 others(12): Show |
15 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.156-2012G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95146690 | |||||||
| chr1:95146766 | A | G | 1 | a0001c0001t0005g0014 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.156-1936A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95146766 | |||||||
| chr1:95146881 | A | G | 3 | a0001c0001t0020g0113 a0001c0001t0020g0114 a0001c0001t0042g0023 |
3 | HG02109.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.156-1821A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95146881 | |||||||
| chr1:95147017 | TAG | T | 15 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0006g0160 others(12): Show |
15 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.156-1680_156-1679d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 95147017 | ||||||
| chr1:95147076 | A | ATT | 11 | a0001c0001t0002g0194 a0001c0001t0003g0093 a0001c0001t0003g0105 others(8): Show |
12 | HG00738.hp1 HG01496.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.156-1612_156-1611d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 95147076 | ||||||
| chr1:95147076 | A | ATTT | 47 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(44): Show |
52 | HG00558.hp2 HG00738.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.156-1613_156-1611d others(5): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 95147076 | ||||||
| chr1:95147184 | G | A | 4 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0002g0204 others(1): Show |
4 | HG01099.hp1 HG01109.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.156-1518G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95147184 | |||||||
| chr1:95147331 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.156-1371C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95147331 | |||||||
| chr1:95147370 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.156-1332G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95147370 | |||||||
| chr1:95147762 | T | TGAAAA | 55 | a0001c0001t0001g0183 a0001c0001t0002g0112 a0001c0001t0002g0147 others(52): Show |
55 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.156-937_156-936ins others(5): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 95147762 | ||||||
| chr1:95147943 | T | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(44): Show |
55 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.156-759T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95147943 | |||||||
| chr1:95148121 | T | C | 1 | a0001c0001t0002g0308 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.156-581T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95148121 | |||||||
| chr1:95148157 | A | G | 1 | a0001c0001t0004g0073 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.156-545A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95148157 | |||||||
| chr1:95148163 | A | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0119 others(13): Show |
19 | HG00741.hp2 HG02040.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.156-539A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95148163 | |||||||
| chr1:95148239 | GT | G | 4 | a0001c0001t0002g0034 a0001c0001t0002g0063 a0001c0001t0002g0298 others(1): Show |
4 | HG00408.hp2 HG00609.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-459delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 95148239 | ||||||
| chr1:95148380 | G | T | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.156-322G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95148380 | |||||||
| chr1:95148469 | C | T | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.156-233C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95148469 | |||||||
| chr1:95148576 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.156-126G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95148576 | |||||||
| chr1:95148589 | C | A | 1 | a0001c0001t0001g0334 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.156-113C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95148589 | |||||||
| chr1:95148607 | C | T | 5 | a0001c0001t0002g0194 a0001c0001t0005g0191 a0001c0001t0005g0192 others(2): Show |
5 | HG00738.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-95C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95148607 | |||||||
| chr1:95148659 | G | A | 55 | a0001c0001t0001g0183 a0001c0001t0002g0112 a0001c0001t0002g0147 others(52): Show |
55 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.156-43G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 2/6 | chr1 | 95148659 | |||||||
| chr1:95148878 | A | G | 2 | a0001c0001t0004g0132 a0001c0001t0004g0135 |
2 | HG00544.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.245+87A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 3/6 | chr1 | 95148878 | |||||||
| chr1:95149010 | A | C | 55 | a0001c0001t0001g0183 a0001c0001t0002g0112 a0001c0001t0002g0147 others(52): Show |
55 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.245+219A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 3/6 | chr1 | 95149010 | |||||||
| chr1:95149120 | T | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0162 others(36): Show |
42 | HG01928.hp2 HG01978.hp1 HG02080.hp2 others(39): Show |
intron_variant | MODIFIER | c.245+329T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 3/6 | chr1 | 95149120 | |||||||
| chr1:95149121 | A | G | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.245+330A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 3/6 | chr1 | 95149121 | |||||||
| chr1:95149282 | T | C | 55 | a0001c0001t0001g0183 a0001c0001t0002g0112 a0001c0001t0002g0147 others(52): Show |
55 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.245+491T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 3/6 | chr1 | 95149282 | |||||||
| chr1:95149596 | C | G | 1 | a0001c0001t0001g0342 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.246-612C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 3/6 | chr1 | 95149596 | |||||||
| chr1:95149683 | G | A | 53 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(50): Show |
59 | HG00558.hp2 HG00621.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.246-525G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 3/6 | chr1 | 95149683 | |||||||
| chr1:95149931 | T | G | 13 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0006g0214 others(10): Show |
13 | HG00735.hp1 HG01109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.246-277T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 3/6 | chr1 | 95149931 | |||||||
| chr1:95149984 | A | C | 2 | a0001c0001t0002g0308 a0001c0001t0002g0310 |
2 | HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.246-224A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 3/6 | chr1 | 95149984 | |||||||
| chr1:95149998 | G | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(44): Show |
55 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.246-210G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 3/6 | chr1 | 95149998 | |||||||
| chr1:95150119 | T | A | 1 | a0001c0001t0001g0255 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.246-89T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 3/6 | chr1 | 95150119 | |||||||
| chr1:95150122 | T | C | 55 | a0001c0001t0001g0183 a0001c0001t0002g0112 a0001c0001t0002g0147 others(52): Show |
55 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.246-86T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 3/6 | chr1 | 95150122 | |||||||
| chr1:95150192 | C | CT | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0021 others(55): Show |
64 | HG00741.hp2 HG01928.hp2 HG01978.hp1 others(61): Show |
splice_region_variant&intron_variant | LOW | c.246-4dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 95150192 | ||||||
| chr1:95150332 | T | C | 55 | a0001c0001t0001g0183 a0001c0001t0002g0112 a0001c0001t0002g0147 others(52): Show |
55 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.304+66T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 4/6 | chr1 | 95150332 | |||||||
| chr1:95150354 | T | C | 1 | a0001c0001t0005g0195 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.304+88T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 4/6 | chr1 | 95150354 | |||||||
| chr1:95150553 | G | A | 27 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(24): Show |
32 | HG00558.hp2 HG00621.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.304+287G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 4/6 | chr1 | 95150553 | |||||||
| chr1:95150578 | A | G | 55 | a0001c0001t0001g0183 a0001c0001t0002g0112 a0001c0001t0002g0147 others(52): Show |
55 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.304+312A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 4/6 | chr1 | 95150578 | |||||||
| chr1:95150610 | T | G | 1 | a0001c0001t0001g0338 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.304+344T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 4/6 | chr1 | 95150610 | |||||||
| chr1:95150757 | A | G | 16 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0241 others(13): Show |
16 | HG00735.hp1 HG01109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.304+491A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 4/6 | chr1 | 95150757 | |||||||
| chr1:95150768 | AT | A | 53 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(50): Show |
59 | HG00558.hp2 HG00621.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.304+508delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 95150768 | ||||||
| chr1:95150812 | C | T | 3 | a0001c0001t0020g0113 a0001c0001t0020g0114 a0001c0001t0042g0023 |
3 | HG02109.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.305-513C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 4/6 | chr1 | 95150812 | |||||||
| chr1:95151132 | G | C | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.305-193G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 4/6 | chr1 | 95151132 | |||||||
| chr1:95151596 | T | C | 1 | a0001c0001t0001g0338 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.399+177T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95151596 | |||||||
| chr1:95151650 | C | A | 53 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(50): Show |
59 | HG00558.hp2 HG00621.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.399+231C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95151650 | |||||||
| chr1:95151953 | A | G | 1 | a0001c0001t0001g0332 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.399+534A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95151953 | |||||||
| chr1:95151975 | C | A | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.399+556C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95151975 | |||||||
| chr1:95152016 | A | G | 55 | a0001c0001t0001g0183 a0001c0001t0002g0112 a0001c0001t0002g0147 others(52): Show |
55 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.399+597A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95152016 | |||||||
| chr1:95152041 | A | G | 1 | a0001c0001t0003g0081 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.399+622A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95152041 | |||||||
| chr1:95152070 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.399+651A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95152070 | |||||||
| chr1:95152164 | A | G | 1 | a0001c0001t0007g0134 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.399+745A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95152164 | |||||||
| chr1:95152170 | A | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0061 |
2 | HG00741.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.399+751A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95152170 | |||||||
| chr1:95152291 | C | G | 1 | a0001c0001t0007g0134 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.399+872C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95152291 | |||||||
| chr1:95152364 | T | C | 1 | a0001c0001t0021g0007 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.399+945T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95152364 | |||||||
| chr1:95152954 | T | A | 55 | a0001c0001t0001g0183 a0001c0001t0002g0112 a0001c0001t0002g0147 others(52): Show |
55 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.399+1535T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95152954 | |||||||
| chr1:95153033 | GC | G | 55 | a0001c0001t0001g0183 a0001c0001t0002g0112 a0001c0001t0002g0147 others(52): Show |
55 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.399+1615delC | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95153033 | |||||||
| chr1:95153044 | C | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0167 a0001c0001t0001g0175 others(6): Show |
9 | HG02109.hp2 HG02647.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.399+1625C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95153044 | |||||||
| chr1:95153139 | G | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0119 others(13): Show |
19 | HG00741.hp2 HG02040.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.399+1720G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95153139 | |||||||
| chr1:95153220 | G | A | 1 | a0001c0001t0005g0014 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.399+1801G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95153220 | |||||||
| chr1:95153812 | T | G | 134 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0051 others(131): Show |
138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.399+2393T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95153812 | |||||||
| chr1:95153865 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.399+2446G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95153865 | |||||||
| chr1:95153993 | A | C | 83 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(80): Show |
89 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.399+2574A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95153993 | |||||||
| chr1:95154110 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.399+2691T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95154110 | |||||||
| chr1:95154187 | G | A | 93 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0051 others(90): Show |
95 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.399+2768G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95154187 | |||||||
| chr1:95154248 | C | T | 11 | a0001c0001t0001g0183 a0001c0001t0002g0190 a0001c0001t0008g0091 others(8): Show |
11 | HG00280.hp1 HG00639.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.399+2829C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95154248 | |||||||
| chr1:95154307 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
284 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.399+2888G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95154307 | |||||||
| chr1:95154730 | G | C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0030 others(48): Show |
55 | HG00735.hp2 HG01081.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.399+3311G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95154730 | |||||||
| chr1:95154839 | G | T | 5 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+3420G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95154839 | |||||||
| chr1:95154862 | A | G | 45 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0002g0034 others(42): Show |
46 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.399+3443A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95154862 | |||||||
| chr1:95155015 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
183 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.399+3596T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95155015 | |||||||
| chr1:95155448 | G | A | 1 | a0001c0001t0003g0084 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.399+4029G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95155448 | |||||||
| chr1:95155677 | C | G | 1 | a0001c0001t0012g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.399+4258C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95155677 | |||||||
| chr1:95155750 | GT | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.399+4347delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95155750 | ||||||
| chr1:95155750 | GTT | G | 84 | a0001c0001t0001g0289 a0001c0001t0001g0335 a0001c0001t0002g0015 others(81): Show |
87 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.399+4346_399+4347d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95155750 | ||||||
| chr1:95155853 | G | A | 5 | a0001c0001t0002g0194 a0001c0001t0005g0191 a0001c0001t0005g0192 others(2): Show |
5 | HG00738.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+4434G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95155853 | |||||||
| chr1:95155896 | A | C | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.399+4477A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95155896 | |||||||
| chr1:95155981 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.399+4562G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95155981 | |||||||
| chr1:95155986 | T | C | 1 | a0001c0001t0040g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.399+4567T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95155986 | |||||||
| chr1:95156188 | AATT | A | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(73): Show |
79 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.399+4770_399+4772d others(5): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95156188 | |||||||
| chr1:95156228 | C | T | 2 | a0001c0001t0006g0160 a0001c0001t0006g0161 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.399+4809C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95156228 | |||||||
| chr1:95156301 | G | C | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.399+4882G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95156301 | |||||||
| chr1:95156366 | ATGGGATT others(87): Show |
A | 2 | a0001c0001t0005g0173 a0001c0001t0005g0174 |
2 | HG02602.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.399+4950_399+5043d others(96): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95156366 | ||||||
| chr1:95156500 | G | T | 3 | a0001c0001t0002g0017 a0001c0001t0002g0316 a0001c0001t0029g0017 |
3 | HG02109.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.399+5081G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95156500 | |||||||
| chr1:95156785 | C | T | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.399+5366C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95156785 | |||||||
| chr1:95156971 | C | T | 14 | a0001c0001t0006g0160 a0001c0001t0006g0161 a0001c0001t0008g0091 others(11): Show |
14 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.399+5552C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95156971 | |||||||
| chr1:95157234 | A | T | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(73): Show |
79 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.399+5815A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95157234 | |||||||
| chr1:95157373 | A | G | 2 | a0001c0001t0002g0308 a0001c0001t0002g0310 |
2 | HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.399+5954A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95157373 | |||||||
| chr1:95157516 | A | G | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.399+6097A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95157516 | |||||||
| chr1:95157793 | G | A | 1 | a0001c0001t0002g0150 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.399+6374G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95157793 | |||||||
| chr1:95157846 | T | C | 2 | a0001c0001t0004g0151 a0001c0001t0004g0154 |
2 | NA19080.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.399+6427T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95157846 | |||||||
| chr1:95157922 | G | A | 1 | a0001c0001t0026g0261 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.399+6503G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95157922 | |||||||
| chr1:95158083 | T | C | 1 | a0001c0001t0004g0143 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.399+6664T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95158083 | |||||||
| chr1:95158151 | T | A | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.399+6732T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95158151 | |||||||
| chr1:95158188 | C | CT | 121 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(118): Show |
128 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.399+6786dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95158188 | ||||||
| chr1:95158188 | C | CTT | 8 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0052 others(5): Show |
8 | HG01109.hp2 HG02148.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.399+6785_399+6786d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95158188 | ||||||
| chr1:95158188 | CT | C | 11 | a0001c0001t0002g0069 a0001c0001t0002g0147 a0001c0001t0002g0148 others(8): Show |
11 | HG00099.hp2 HG01261.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.399+6786delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95158188 | ||||||
| chr1:95158188 | CTT | C | 83 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(80): Show |
86 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.399+6785_399+6786d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95158188 | ||||||
| chr1:95158260 | T | G | 1 | a0001c0001t0005g0014 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.399+6841T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95158260 | |||||||
| chr1:95158291 | G | A | 1 | a0001c0001t0002g0309 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.399+6872G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95158291 | |||||||
| chr1:95158294 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.399+6875C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95158294 | |||||||
| chr1:95158400 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
182 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.399+6981C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95158400 | |||||||
| chr1:95158494 | C | CATTT | 57 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(54): Show |
59 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.399+7096_399+7099d others(6): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95158494 | ||||||
| chr1:95158494 | CATTTATT others(1): Show |
C | 36 | a0001c0001t0002g0034 a0001c0001t0002g0045 a0001c0001t0002g0048 others(33): Show |
37 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.399+7092_399+7099d others(10): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95158494 | ||||||
| chr1:95158615 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
182 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.399+7196C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95158615 | |||||||
| chr1:95158665 | C | A | 1 | a0001c0001t0001g0271 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.399+7246C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95158665 | |||||||
| chr1:95158723 | C | T | 5 | a0001c0001t0002g0194 a0001c0001t0005g0191 a0001c0001t0005g0192 others(2): Show |
5 | HG00738.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+7304C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95158723 | |||||||
| chr1:95158777 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(207): Show |
220 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.399+7358C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95158777 | |||||||
| chr1:95158911 | C | T | 1 | a0001c0001t0005g0014 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.399+7492C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95158911 | |||||||
| chr1:95158938 | T | C | 47 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(44): Show |
52 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.399+7519T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95158938 | |||||||
| chr1:95158976 | G | A | 1 | a0001c0001t0020g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.399+7557G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95158976 | |||||||
| chr1:95159006 | C | G | 1 | a0001c0001t0002g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.399+7587C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159006 | |||||||
| chr1:95159125 | T | C | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.399+7706T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159125 | |||||||
| chr1:95159150 | C | G | 31 | a0001c0001t0001g0018 a0001c0001t0001g0115 a0001c0001t0001g0146 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.399+7731C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159150 | |||||||
| chr1:95159193 | C | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0167 a0001c0001t0001g0175 others(3): Show |
6 | HG02647.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.399+7774C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159193 | |||||||
| chr1:95159279 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.399+7860C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159279 | |||||||
| chr1:95159282 | G | A | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(73): Show |
79 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.399+7863G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159282 | |||||||
| chr1:95159284 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.399+7865C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159284 | |||||||
| chr1:95159286 | G | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.399+7867G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159286 | |||||||
| chr1:95159349 | T | A | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.399+7930T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159349 | |||||||
| chr1:95159481 | T | C | 32 | a0001c0001t0004g0039 a0001c0001t0004g0073 a0001c0001t0004g0079 others(29): Show |
32 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.399+8062T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159481 | |||||||
| chr1:95159517 | G | A | 51 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0030 others(48): Show |
55 | HG00735.hp2 HG01081.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.399+8098G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159517 | |||||||
| chr1:95159597 | T | C | 1 | a0001c0001t0007g0314 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.399+8178T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159597 | |||||||
| chr1:95159645 | C | T | 90 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(87): Show |
93 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.399+8226C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159645 | |||||||
| chr1:95159778 | C | T | 3 | a0001c0001t0002g0017 a0001c0001t0002g0316 a0001c0001t0029g0017 |
3 | HG02109.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.399+8359C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159778 | |||||||
| chr1:95159893 | G | A | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(73): Show |
79 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.399+8474G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159893 | |||||||
| chr1:95159904 | T | C | 1 | a0001c0001t0003g0084 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.399+8485T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159904 | |||||||
| chr1:95159986 | C | T | 8 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.399+8567C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95159986 | |||||||
| chr1:95160003 | C | T | 1 | a0001c0001t0005g0169 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.399+8584C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95160003 | |||||||
| chr1:95160231 | A | C | 14 | a0001c0001t0006g0160 a0001c0001t0006g0161 a0001c0001t0008g0091 others(11): Show |
14 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.399+8812A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95160231 | |||||||
| chr1:95160278 | T | G | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.399+8859T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95160278 | |||||||
| chr1:95160368 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.399+8949C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95160368 | |||||||
| chr1:95160491 | G | C | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.399+9072G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95160491 | |||||||
| chr1:95160629 | C | T | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.399+9210C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95160629 | |||||||
| chr1:95160658 | T | C | 1 | a0001c0001t0002g0205 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.399+9239T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95160658 | |||||||
| chr1:95160705 | C | T | 1 | a0001c0001t0005g0173 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.399+9286C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95160705 | |||||||
| chr1:95160730 | G | A | 86 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(83): Show |
92 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.399+9311G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95160730 | |||||||
| chr1:95160926 | G | C | 4 | a0001c0001t0002g0130 a0001c0001t0002g0206 a0001c0001t0002g0207 others(1): Show |
4 | NA18990.hp1 NA19002.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+9507G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95160926 | |||||||
| chr1:95160938 | A | T | 85 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(82): Show |
91 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.399+9519A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95160938 | |||||||
| chr1:95160953 | C | T | 14 | a0001c0001t0006g0160 a0001c0001t0006g0161 a0001c0001t0008g0091 others(11): Show |
14 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.399+9534C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95160953 | |||||||
| chr1:95161091 | T | C | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG00741.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.399+9672T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95161091 | |||||||
| chr1:95161146 | A | G | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.399+9727A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95161146 | |||||||
| chr1:95161328 | G | T | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.399+9909G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95161328 | |||||||
| chr1:95161357 | T | G | 85 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(82): Show |
91 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.399+9938T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95161357 | |||||||
| chr1:95161364 | T | G | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.399+9945T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95161364 | |||||||
| chr1:95161595 | G | A | 2 | a0001c0001t0001g0266 a0001c0001t0032g0267 |
2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.399+10176G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95161595 | |||||||
| chr1:95161621 | T | C | 1 | a0001c0001t0026g0261 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.399+10202T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95161621 | |||||||
| chr1:95161743 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
182 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.399+10324C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95161743 | |||||||
| chr1:95161794 | C | G | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.399+10375C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95161794 | |||||||
| chr1:95161966 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.399+10547A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95161966 | |||||||
| chr1:95161995 | G | C | 1 | a0001c0001t0020g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.399+10576G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95161995 | |||||||
| chr1:95162035 | A | C | 1 | a0001c0001t0024g0311 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.399+10616A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162035 | |||||||
| chr1:95162115 | A | G | 2 | a0001c0001t0002g0050 a0001c0001t0002g0072 |
2 | NA18966.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.399+10696A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162115 | |||||||
| chr1:95162156 | A | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0021 others(68): Show |
78 | HG00735.hp2 HG00741.hp2 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.399+10737A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162156 | |||||||
| chr1:95162217 | A | G | 3 | a0001c0001t0002g0017 a0001c0001t0002g0316 a0001c0001t0029g0017 |
3 | HG02109.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.399+10798A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162217 | |||||||
| chr1:95162239 | C | G | 8 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.399+10820C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162239 | |||||||
| chr1:95162258 | G | T | 2 | a0001c0001t0001g0237 a0001c0001t0004g0153 |
2 | HG02129.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.399+10839G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162258 | |||||||
| chr1:95162312 | T | TAGGATTG others(19): Show |
1 | a0001c0001t0017g0268 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.399+10894_399+1091 others(30): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95162312 | ||||||
| chr1:95162349 | G | A | 32 | a0001c0001t0004g0039 a0001c0001t0004g0073 a0001c0001t0004g0079 others(29): Show |
32 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.399+10930G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162349 | |||||||
| chr1:95162351 | TC | T | 65 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(62): Show |
68 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.399+10933delC | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162351 | |||||||
| chr1:95162368 | A | T | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.399+10949A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162368 | |||||||
| chr1:95162388 | T | G | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.399+10969T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162388 | |||||||
| chr1:95162409 | T | C | 1 | a0001c0003t0007g0152 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.399+10990T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162409 | |||||||
| chr1:95162456 | A | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(29): Show |
40 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.399+11037A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162456 | |||||||
| chr1:95162588 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.399+11169T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162588 | |||||||
| chr1:95162685 | AAGGC | A | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.400-11126_400-1112 others(8): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95162685 | ||||||
| chr1:95162710 | G | C | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.400-11106G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162710 | |||||||
| chr1:95162752 | C | T | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.400-11064C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162752 | |||||||
| chr1:95162762 | G | A | 2 | a0001c0001t0016g0116 a0001c0001t0016g0117 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.400-11054G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162762 | |||||||
| chr1:95162762 | G | C | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.400-11054G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162762 | |||||||
| chr1:95162806 | C | G | 32 | a0001c0001t0004g0039 a0001c0001t0004g0073 a0001c0001t0004g0079 others(29): Show |
32 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.400-11010C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162806 | |||||||
| chr1:95162841 | C | G | 3 | a0001c0001t0002g0017 a0001c0001t0002g0316 a0001c0001t0029g0017 |
3 | HG02109.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.400-10975C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162841 | |||||||
| chr1:95162887 | G | T | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(73): Show |
79 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.400-10929G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162887 | |||||||
| chr1:95162940 | T | C | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.400-10876T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162940 | |||||||
| chr1:95162979 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0273 a0001c0001t0001g0285 others(3): Show |
9 | HG00609.hp1 HG02056.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-10837C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95162979 | |||||||
| chr1:95163192 | C | T | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.400-10624C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95163192 | |||||||
| chr1:95163193 | G | A | 85 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(82): Show |
91 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-10623G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95163193 | |||||||
| chr1:95163201 | C | G | 1 | a0001c0001t0002g0201 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.400-10615C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95163201 | |||||||
| chr1:95163259 | T | G | 1 | a0001c0001t0002g0309 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.400-10557T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95163259 | |||||||
| chr1:95163327 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.400-10489C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95163327 | |||||||
| chr1:95163423 | C | CT | 79 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(76): Show |
82 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.400-10387dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95163423 | ||||||
| chr1:95163473 | A | C | 1 | a0001c0001t0002g0059 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.400-10343A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95163473 | |||||||
| chr1:95163692 | A | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.400-10124A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95163692 | |||||||
| chr1:95163788 | A | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0199 |
3 | HG01123.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.400-10028A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95163788 | |||||||
| chr1:95163946 | G | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.400-9870G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95163946 | |||||||
| chr1:95163975 | G | A | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.400-9841G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95163975 | |||||||
| chr1:95164138 | G | T | 3 | a0001c0001t0002g0129 a0001c0001t0002g0150 a0001c0001t0037g0125 |
3 | HG02074.hp1 NA18945.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.400-9678G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95164138 | |||||||
| chr1:95164155 | C | G | 1 | a0001c0001t0010g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.400-9661C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95164155 | |||||||
| chr1:95164302 | G | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(36): Show |
47 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.400-9514G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95164302 | |||||||
| chr1:95164440 | G | A | 4 | a0001c0001t0003g0012 a0001c0001t0003g0092 a0001c0001t0003g0093 others(1): Show |
5 | NA18946.hp1 NA18954.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.400-9376G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95164440 | |||||||
| chr1:95164442 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.400-9374G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95164442 | |||||||
| chr1:95164465 | C | T | 1 | a0001c0001t0007g0108 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.400-9351C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95164465 | |||||||
| chr1:95164483 | A | G | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.400-9333A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95164483 | |||||||
| chr1:95164592 | T | G | 6 | a0001c0001t0005g0169 a0001c0001t0005g0170 a0001c0001t0005g0171 others(3): Show |
6 | HG00738.hp2 HG01069.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.400-9224T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95164592 | |||||||
| chr1:95164614 | G | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(193): Show |
206 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.400-9202G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95164614 | |||||||
| chr1:95164686 | TA | T | 3 | a0001c0001t0002g0308 a0001c0001t0002g0309 a0001c0001t0002g0310 |
3 | HG02647.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.400-9129delA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95164686 | |||||||
| chr1:95164696 | A | C | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.400-9120A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95164696 | |||||||
| chr1:95164905 | A | C | 85 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(82): Show |
91 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-8911A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95164905 | |||||||
| chr1:95164984 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.400-8832A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95164984 | |||||||
| chr1:95165065 | T | A | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.400-8751T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165065 | |||||||
| chr1:95165102 | T | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(44): Show |
55 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.400-8714T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165102 | |||||||
| chr1:95165191 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.400-8625A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165191 | |||||||
| chr1:95165208 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.400-8608C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165208 | |||||||
| chr1:95165428 | A | G | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.400-8388A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165428 | |||||||
| chr1:95165451 | ATG | A | 3 | a0001c0001t0001g0262 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | HG02258.hp1 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.400-8349_400-8348d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95165451 | ||||||
| chr1:95165466 | T | G | 89 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(86): Show |
92 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.400-8350T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165466 | |||||||
| chr1:95165466 | TG | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
168 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.400-8349delG | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165466 | |||||||
| chr1:95165467 | G | T | 104 | a0001c0001t0001g0052 a0001c0001t0001g0115 a0001c0001t0001g0157 others(101): Show |
107 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.400-8349G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165467 | |||||||
| chr1:95165484 | A | G | 6 | a0001c0001t0001g0215 a0001c0001t0001g0219 a0001c0001t0001g0220 others(3): Show |
6 | NA18941.hp2 NA18994.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.400-8332A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165484 | |||||||
| chr1:95165496 | G | A | 3 | a0001c0001t0004g0039 a0001c0001t0019g0038 a0001c0001t0019g0040 |
3 | HG01074.hp1 HG01106.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.400-8320G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165496 | |||||||
| chr1:95165523 | T | TG | 3 | a0001c0001t0002g0017 a0001c0001t0002g0316 a0001c0001t0029g0017 |
3 | HG02109.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.400-8291dupG | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95165523 | ||||||
| chr1:95165608 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.400-8208G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165608 | |||||||
| chr1:95165656 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.400-8160G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165656 | |||||||
| chr1:95165689 | G | C | 93 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.400-8127G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165689 | |||||||
| chr1:95165758 | G | A | 14 | a0001c0001t0006g0160 a0001c0001t0006g0161 a0001c0001t0008g0091 others(11): Show |
14 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.400-8058G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165758 | |||||||
| chr1:95165758 | G | T | 1 | a0001c0001t0002g0190 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.400-8058G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95165758 | |||||||
| chr1:95166441 | C | T | 4 | a0001c0001t0002g0130 a0001c0001t0002g0206 a0001c0001t0002g0207 others(1): Show |
4 | NA18990.hp1 NA19002.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-7375C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95166441 | |||||||
| chr1:95166775 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0316 a0001c0001t0029g0017 |
3 | HG02109.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.400-7041G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95166775 | |||||||
| chr1:95166878 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.400-6938G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95166878 | |||||||
| chr1:95166908 | T | A | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.400-6908T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95166908 | |||||||
| chr1:95166972 | C | T | 3 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0005g0131 |
3 | HG02895.hp2 NA18963.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.400-6844C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95166972 | |||||||
| chr1:95167081 | T | G | 5 | a0001c0001t0002g0194 a0001c0001t0005g0191 a0001c0001t0005g0192 others(2): Show |
5 | HG00738.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.400-6735T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95167081 | |||||||
| chr1:95167439 | T | C | 2 | a0001c0001t0001g0227 a0001c0001t0038g0239 |
2 | NA18942.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.400-6377T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95167439 | |||||||
| chr1:95167446 | T | C | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.400-6370T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95167446 | |||||||
| chr1:95167521 | G | A | 1 | a0001c0001t0005g0192 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.400-6295G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95167521 | |||||||
| chr1:95167597 | G | A | 21 | a0001c0001t0001g0018 a0001c0001t0001g0167 a0001c0001t0001g0175 others(18): Show |
21 | HG00735.hp1 HG01109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.400-6219G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95167597 | |||||||
| chr1:95167601 | G | C | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.400-6215G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95167601 | |||||||
| chr1:95167631 | C | T | 65 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(62): Show |
68 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.400-6185C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95167631 | |||||||
| chr1:95167689 | C | G | 1 | a0001c0001t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.400-6127C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95167689 | |||||||
| chr1:95167770 | T | G | 2 | a0001c0001t0001g0266 a0001c0001t0032g0267 |
2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.400-6046T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95167770 | |||||||
| chr1:95167973 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0238 others(11): Show |
17 | HG01978.hp1 NA18612.hp1 NA18944.hp2 others(14): Show |
intron_variant | MODIFIER | c.400-5843C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95167973 | |||||||
| chr1:95167987 | A | AC | 6 | a0001c0001t0001g0295 a0001c0001t0001g0330 a0001c0001t0001g0335 others(3): Show |
6 | HG02109.hp1 NA18954.hp2 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.400-5824dupC | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95167987 | ||||||
| chr1:95168166 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.400-5650A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95168166 | |||||||
| chr1:95168421 | G | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.400-5395G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95168421 | |||||||
| chr1:95168554 | CT | C | 14 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0129 others(11): Show |
15 | HG00558.hp2 HG00621.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.400-5233delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95168554 | ||||||
| chr1:95168554 | CTT | C | 68 | a0001c0001t0002g0016 a0001c0001t0002g0047 a0001c0001t0002g0050 others(65): Show |
74 | HG00280.hp1 HG00738.hp2 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.400-5234_400-5233d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95168554 | ||||||
| chr1:95168554 | CTTT | C | 77 | a0001c0001t0002g0034 a0001c0001t0002g0045 a0001c0001t0002g0048 others(74): Show |
79 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.400-5235_400-5233d others(5): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95168554 | ||||||
| chr1:95168554 | CTTTT | C | 22 | a0001c0001t0001g0052 a0001c0001t0001g0146 a0001c0001t0001g0157 others(19): Show |
22 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.400-5236_400-5233d others(6): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95168554 | ||||||
| chr1:95168554 | CTTTTT | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
169 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(166): Show |
intron_variant | MODIFIER | c.400-5237_400-5233d others(7): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95168554 | ||||||
| chr1:95168554 | CTTTTTT | C | 6 | a0001c0001t0001g0227 a0001c0001t0001g0241 a0001c0001t0001g0285 others(3): Show |
6 | HG00099.hp2 HG01943.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.400-5238_400-5233d others(8): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95168554 | ||||||
| chr1:95168554 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01928.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.400-5245_400-5233d others(15): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95168554 | ||||||
| chr1:95168554 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0004g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.400-5250_400-5233d others(20): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95168554 | ||||||
| chr1:95168591 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.400-5225G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95168591 | |||||||
| chr1:95168913 | C | A | 1 | a0001c0001t0001g0283 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.400-4903C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95168913 | |||||||
| chr1:95169045 | C | T | 85 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(82): Show |
91 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-4771C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95169045 | |||||||
| chr1:95169046 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.400-4770A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95169046 | |||||||
| chr1:95169178 | C | A | 1 | a0001c0001t0020g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.400-4638C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95169178 | |||||||
| chr1:95169610 | G | A | 2 | a0001c0001t0001g0336 a0001c0001t0001g0346 |
2 | NA18970.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.400-4206G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95169610 | |||||||
| chr1:95169635 | AT | A | 341 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(338): Show |
365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.400-4171delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95169635 | ||||||
| chr1:95169649 | T | C | 1 | a0001c0003t0007g0152 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.400-4167T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95169649 | |||||||
| chr1:95169700 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.400-4116C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95169700 | |||||||
| chr1:95170192 | G | T | 1 | a0001c0001t0005g0014 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.400-3624G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95170192 | |||||||
| chr1:95170257 | A | G | 1 | a0001c0001t0007g0108 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.400-3559A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95170257 | |||||||
| chr1:95170284 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0167 a0001c0001t0001g0175 others(3): Show |
6 | HG02647.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-3532A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95170284 | |||||||
| chr1:95170330 | C | CT | 160 | a0001c0001t0001g0270 a0001c0001t0002g0015 a0001c0001t0002g0016 others(157): Show |
169 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.400-3468dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95170330 | ||||||
| chr1:95170430 | C | T | 84 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(81): Show |
90 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.400-3386C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95170430 | |||||||
| chr1:95170572 | G | A | 1 | a0001c0001t0001g0343 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.400-3244G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95170572 | |||||||
| chr1:95170917 | A | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(44): Show |
55 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.400-2899A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95170917 | |||||||
| chr1:95170931 | AAAAG | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0119 others(13): Show |
19 | HG00741.hp2 HG02040.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.400-2884_400-2881d others(6): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95170931 | |||||||
| chr1:95171050 | TC | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(116): Show |
126 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.400-2758delC | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95171050 | ||||||
| chr1:95171058 | C | T | 2 | a0001c0001t0007g0108 a0001c0001t0007g0156 |
2 | HG00280.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.400-2758C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95171058 | |||||||
| chr1:95171059 | T | C | 4 | a0001c0001t0008g0091 a0001c0001t0008g0182 a0001c0001t0008g0184 others(1): Show |
4 | HG00639.hp2 HG01175.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-2757T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95171059 | |||||||
| chr1:95171239 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.400-2577A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95171239 | |||||||
| chr1:95171309 | G | A | 1 | a0001c0001t0021g0007 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.400-2507G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95171309 | |||||||
| chr1:95171375 | C | T | 2 | a0001c0001t0006g0160 a0001c0001t0006g0161 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.400-2441C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95171375 | |||||||
| chr1:95171376 | G | T | 85 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(82): Show |
91 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-2440G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95171376 | |||||||
| chr1:95171569 | T | G | 2 | a0001c0001t0001g0266 a0001c0001t0032g0267 |
2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.400-2247T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95171569 | |||||||
| chr1:95171573 | AATGAGAA others(5): Show |
A | 2 | a0001c0001t0001g0336 a0001c0001t0001g0346 |
2 | NA18970.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.400-2238_400-2227d others(14): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95171573 | ||||||
| chr1:95171763 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
182 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.400-2053G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95171763 | |||||||
| chr1:95171833 | T | C | 1 | a0001c0001t0003g0042 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.400-1983T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95171833 | |||||||
| chr1:95171984 | G | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(44): Show |
55 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.400-1832G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95171984 | |||||||
| chr1:95172319 | T | G | 1 | a0001c0001t0001g0325 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.400-1497T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95172319 | |||||||
| chr1:95172476 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.400-1340A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95172476 | |||||||
| chr1:95172516 | A | G | 2 | a0001c0001t0002g0205 a0001c0001t0007g0315 |
2 | HG02165.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.400-1300A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95172516 | |||||||
| chr1:95172563 | C | T | 2 | a0001c0001t0002g0112 a0001c0001t0002g0327 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.400-1253C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95172563 | |||||||
| chr1:95172698 | A | G | 1 | a0001c0001t0006g0245 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.400-1118A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95172698 | |||||||
| chr1:95172911 | TTAG | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0167 a0001c0001t0001g0257 others(1): Show |
4 | HG02647.hp2 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-901_400-899del others(3): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95172911 | ||||||
| chr1:95173110 | C | T | 2 | a0001c0001t0006g0160 a0001c0001t0006g0161 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.400-706C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95173110 | |||||||
| chr1:95173111 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.400-705A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95173111 | |||||||
| chr1:95173178 | G | C | 1 | a0001c0001t0020g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.400-638G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95173178 | |||||||
| chr1:95173314 | C | CT | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(117): Show |
127 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(124): Show |
intron_variant | MODIFIER | c.400-489dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 95173314 | ||||||
| chr1:95173352 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.400-464C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95173352 | |||||||
| chr1:95173376 | C | T | 2 | a0001c0001t0006g0160 a0001c0001t0006g0161 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.400-440C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95173376 | |||||||
| chr1:95173639 | G | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
182 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.400-177G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95173639 | |||||||
| chr1:95173723 | A | T | 1 | a0001c0001t0001g0333 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.400-93A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 5/6 | chr1 | 95173723 | |||||||
| chr1:95174302 | G | A | 32 | a0001c0001t0004g0039 a0001c0001t0004g0073 a0001c0001t0004g0079 others(29): Show |
32 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.473+413G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95174302 | |||||||
| chr1:95174350 | A | G | 1 | a0001c0001t0012g0029 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.473+461A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95174350 | |||||||
| chr1:95174471 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0316 a0001c0001t0029g0017 |
3 | HG02109.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.473+582G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95174471 | |||||||
| chr1:95174507 | CA | C | 104 | a0001c0001t0001g0115 a0001c0001t0001g0175 a0001c0001t0001g0200 others(101): Show |
107 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.473+637delA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95174507 | ||||||
| chr1:95174523 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.473+634A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95174523 | |||||||
| chr1:95174530 | A | G | 4 | a0001c0001t0001g0164 a0001c0001t0001g0292 a0001c0001t0001g0325 others(1): Show |
4 | HG01978.hp1 HG02145.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.473+641A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95174530 | |||||||
| chr1:95174531 | AAAG | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
178 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.473+645_473+647del others(3): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95174531 | ||||||
| chr1:95174534 | G | A | 4 | a0001c0001t0001g0164 a0001c0001t0001g0292 a0001c0001t0001g0325 others(1): Show |
4 | HG01978.hp1 HG02145.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.473+645G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95174534 | |||||||
| chr1:95174535 | A | T | 3 | a0001c0001t0020g0113 a0001c0001t0020g0114 a0001c0001t0042g0023 |
3 | HG02109.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.473+646A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95174535 | |||||||
| chr1:95174602 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.473+713T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95174602 | |||||||
| chr1:95174640 | C | G | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(73): Show |
79 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.473+751C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95174640 | |||||||
| chr1:95174693 | T | C | 1 | a0001c0001t0003g0044 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.473+804T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95174693 | |||||||
| chr1:95174723 | A | G | 1 | a0001c0001t0012g0029 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.473+834A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95174723 | |||||||
| chr1:95174832 | A | G | 8 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.473+943A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95174832 | |||||||
| chr1:95175012 | T | G | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.473+1123T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95175012 | |||||||
| chr1:95175068 | G | T | 1 | a0001c0001t0003g0011 | 2 | NA19074.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.473+1179G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95175068 | |||||||
| chr1:95175174 | ACT | A | 2 | a0001c0001t0009g0006 a0002c0002t0009g0031 |
3 | HG01891.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.473+1288_473+1289d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95175174 | ||||||
| chr1:95175290 | T | A | 1 | a0001c0001t0001g0333 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.473+1401T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95175290 | |||||||
| chr1:95175447 | T | C | 47 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(44): Show |
52 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.473+1558T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95175447 | |||||||
| chr1:95175832 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.473+1943G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95175832 | |||||||
| chr1:95175841 | T | A | 1 | a0001c0001t0040g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.473+1952T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95175841 | |||||||
| chr1:95175956 | TG | T | 85 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(82): Show |
91 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.473+2068delG | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95175956 | |||||||
| chr1:95175976 | A | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0119 others(12): Show |
18 | HG00741.hp2 HG02040.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.473+2087A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95175976 | |||||||
| chr1:95176083 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.473+2194C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95176083 | |||||||
| chr1:95176198 | C | CT | 12 | a0001c0001t0001g0283 a0001c0001t0008g0091 a0001c0001t0008g0176 others(9): Show |
12 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.473+2322dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95176198 | ||||||
| chr1:95176216 | C | A | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(73): Show |
79 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.473+2327C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95176216 | |||||||
| chr1:95176346 | C | T | 15 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0011 others(12): Show |
19 | HG00558.hp2 HG00621.hp2 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.473+2457C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95176346 | |||||||
| chr1:95176347 | A | G | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
368 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.473+2458A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95176347 | |||||||
| chr1:95176372 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0316 a0001c0001t0029g0017 |
3 | HG02109.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.473+2483G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95176372 | |||||||
| chr1:95176667 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.473+2778A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95176667 | |||||||
| chr1:95176697 | T | G | 85 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(82): Show |
91 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.473+2808T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95176697 | |||||||
| chr1:95176749 | A | G | 1 | a0001c0001t0002g0123 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.473+2860A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95176749 | |||||||
| chr1:95177005 | C | G | 1 | a0001c0001t0005g0014 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.473+3116C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95177005 | |||||||
| chr1:95177006 | T | C | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.473+3117T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95177006 | |||||||
| chr1:95177148 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.473+3259G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95177148 | |||||||
| chr1:95177165 | T | A | 1 | a0001c0001t0003g0011 | 2 | NA19074.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.473+3276T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95177165 | |||||||
| chr1:95177316 | CG | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0167 a0001c0001t0001g0257 others(2): Show |
5 | HG02647.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+3431delG | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95177316 | ||||||
| chr1:95177350 | T | C | 1 | a0001c0001t0013g0053 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.473+3461T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95177350 | |||||||
| chr1:95177361 | G | A | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.473+3472G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95177361 | |||||||
| chr1:95177505 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0223 a0001c0001t0001g0234 |
3 | NA18941.hp2 NA19007.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.473+3616G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95177505 | |||||||
| chr1:95177668 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
182 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.473+3779T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95177668 | |||||||
| chr1:95177881 | G | A | 3 | a0001c0001t0020g0113 a0001c0001t0020g0114 a0001c0001t0042g0023 |
3 | HG02109.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.473+3992G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95177881 | |||||||
| chr1:95177935 | C | CT | 6 | a0001c0001t0001g0225 a0001c0001t0001g0237 a0001c0001t0020g0113 others(3): Show |
6 | HG02109.hp1 HG02129.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+4061dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95177935 | ||||||
| chr1:95177940 | T | C | 1 | a0001c0001t0001g0340 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.473+4051T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95177940 | |||||||
| chr1:95177951 | G | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0346 |
2 | NA18993.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.473+4062G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95177951 | |||||||
| chr1:95177951 | GT | G | 85 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(82): Show |
91 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.473+4071delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95177951 | ||||||
| chr1:95177952 | T | G | 1 | a0001c0001t0004g0086 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.473+4063T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95177952 | |||||||
| chr1:95178012 | G | A | 1 | a0001c0001t0017g0319 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.473+4123G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95178012 | |||||||
| chr1:95178242 | C | T | 1 | a0001c0001t0005g0014 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.473+4353C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95178242 | |||||||
| chr1:95178243 | G | A | 2 | a0001c0001t0006g0160 a0001c0001t0006g0161 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.473+4354G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95178243 | |||||||
| chr1:95178362 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0032g0267 |
2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.473+4473C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95178362 | |||||||
| chr1:95178391 | C | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
182 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.473+4502C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95178391 | |||||||
| chr1:95178458 | T | A | 1 | a0001c0001t0001g0274 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473+4569T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95178458 | |||||||
| chr1:95178464 | C | T | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.473+4575C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95178464 | |||||||
| chr1:95178552 | C | A | 1 | a0001c0001t0001g0224 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.473+4663C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95178552 | |||||||
| chr1:95178555 | G | T | 3 | a0001c0001t0002g0045 a0001c0001t0002g0048 a0001c0001t0002g0060 |
3 | NA18953.hp2 NA19064.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.473+4666G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95178555 | |||||||
| chr1:95178556 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.473+4667C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95178556 | |||||||
| chr1:95178563 | C | CT | 6 | a0001c0001t0002g0017 a0001c0001t0002g0316 a0001c0001t0004g0079 others(3): Show |
6 | HG02109.hp2 HG03209.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+4697dupT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95178563 | ||||||
| chr1:95178563 | C | CTTT | 8 | a0001c0001t0001g0078 a0001c0001t0001g0197 a0001c0001t0001g0224 others(5): Show |
8 | HG01975.hp2 HG02451.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.473+4695_473+4697d others(5): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95178563 | ||||||
| chr1:95178563 | C | CTTTT | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(101): Show |
112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.473+4694_473+4697d others(6): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95178563 | ||||||
| chr1:95178563 | C | CTTTTT | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(52): Show |
61 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.473+4693_473+4697d others(7): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95178563 | ||||||
| chr1:95178563 | C | CTTTTTT | 10 | a0001c0001t0001g0020 a0001c0001t0001g0122 a0001c0001t0001g0178 others(7): Show |
11 | HG00741.hp2 HG01123.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.473+4692_473+4697d others(8): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95178563 | ||||||
| chr1:95178563 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0335 a0001c0001t0001g0343 a0001c0001t0001g0344 others(1): Show |
4 | NA18963.hp1 NA19002.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+4687_473+4697d others(13): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95178563 | ||||||
| chr1:95178563 | CT | C | 90 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(87): Show |
93 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.473+4697delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95178563 | ||||||
| chr1:95178646 | T | C | 5 | a0001c0001t0002g0194 a0001c0001t0005g0191 a0001c0001t0005g0192 others(2): Show |
5 | HG00738.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+4757T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95178646 | |||||||
| chr1:95178706 | G | A | 3 | a0001c0001t0020g0113 a0001c0001t0020g0114 a0001c0001t0042g0023 |
3 | HG02109.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.473+4817G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95178706 | |||||||
| chr1:95178729 | C | A | 1 | a0001c0001t0001g0274 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473+4840C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95178729 | |||||||
| chr1:95178819 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.473+4930C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95178819 | |||||||
| chr1:95179096 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.473+5207A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95179096 | |||||||
| chr1:95179183 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.473+5294A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95179183 | |||||||
| chr1:95179403 | C | T | 6 | a0001c0001t0002g0034 a0001c0001t0002g0059 a0001c0001t0002g0061 others(3): Show |
6 | HG00408.hp2 HG00609.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+5514C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95179403 | |||||||
| chr1:95179445 | A | G | 1 | a0001c0001t0007g0149 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.473+5556A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95179445 | |||||||
| chr1:95179693 | C | T | 1 | a0001c0001t0040g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.473+5804C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95179693 | |||||||
| chr1:95180640 | C | T | 3 | a0001c0001t0002g0017 a0001c0001t0002g0316 a0001c0001t0029g0017 |
3 | HG02109.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.473+6751C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95180640 | |||||||
| chr1:95180645 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0119 a0001c0001t0001g0120 others(9): Show |
15 | HG00741.hp2 HG02040.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.473+6756G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95180645 | |||||||
| chr1:95180766 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.473+6877C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95180766 | |||||||
| chr1:95180789 | A | G | 1 | a0001c0001t0005g0036 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.473+6900A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95180789 | |||||||
| chr1:95180830 | C | T | 14 | a0001c0001t0006g0160 a0001c0001t0006g0161 a0001c0001t0008g0091 others(11): Show |
14 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.473+6941C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95180830 | |||||||
| chr1:95181128 | A | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0051 others(8): Show |
11 | HG01167.hp2 HG01243.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.473+7239A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95181128 | |||||||
| chr1:95181202 | CA | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
188 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.473+7324delA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95181202 | ||||||
| chr1:95181202 | CAA | C | 9 | a0001c0001t0001g0241 a0001c0001t0001g0262 a0001c0001t0001g0263 others(6): Show |
9 | HG01891.hp1 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.473+7323_473+7324d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95181202 | ||||||
| chr1:95181480 | T | C | 1 | a0001c0001t0004g0088 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.473+7591T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95181480 | |||||||
| chr1:95181575 | G | A | 1 | a0001c0001t0003g0144 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.473+7686G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95181575 | |||||||
| chr1:95181575 | G | GTTTATTT others(1): Show |
39 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0010 others(36): Show |
42 | HG00621.hp2 HG01081.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.473+7690_473+7691i others(10): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95181575 | ||||||
| chr1:95181575 | G | GTTTATTT others(5): Show |
18 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0080 others(15): Show |
21 | HG00544.hp2 HG00558.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.473+7690_473+7691i others(14): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95181575 | ||||||
| chr1:95181575 | G | GTTTATTT others(9): Show |
26 | a0001c0001t0004g0039 a0001c0001t0004g0073 a0001c0001t0004g0079 others(23): Show |
26 | HG00280.hp2 HG00438.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.473+7690_473+7691i others(18): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95181575 | ||||||
| chr1:95181575 | G | GTTTATTT others(13): Show |
2 | a0001c0001t0004g0087 a0001c0001t0007g0313 |
2 | NA18939.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.473+7690_473+7691i others(22): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95181575 | ||||||
| chr1:95181580 | A | ATTAT | 5 | a0001c0001t0001g0251 a0001c0001t0001g0254 a0001c0001t0001g0274 others(2): Show |
5 | HG03654.hp2 NA18998.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+7714_473+7717d others(6): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95181580 | ||||||
| chr1:95181580 | A | T | 90 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(87): Show |
96 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.473+7691A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95181580 | |||||||
| chr1:95181595 | ATTTATTT others(5): Show |
A | 3 | a0001c0001t0020g0113 a0001c0001t0020g0114 a0001c0001t0042g0023 |
3 | HG02109.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.473+7710_473+7721d others(14): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95181595 | ||||||
| chr1:95181603 | A | T | 5 | a0001c0001t0002g0172 a0001c0001t0009g0006 a0001c0001t0009g0032 others(2): Show |
6 | HG01891.hp2 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+7714A>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95181603 | |||||||
| chr1:95181607 | T | A | 341 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(338): Show |
365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.473+7718T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95181607 | |||||||
| chr1:95181627 | C | T | 1 | a0001c0001t0031g0212 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.473+7738C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95181627 | |||||||
| chr1:95181768 | T | C | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.473+7879T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95181768 | |||||||
| chr1:95181780 | C | T | 1 | a0001c0001t0018g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.473+7891C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95181780 | |||||||
| chr1:95182034 | A | C | 2 | a0001c0001t0001g0274 a0001c0001t0001g0278 |
2 | NA18998.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.473+8145A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95182034 | |||||||
| chr1:95182523 | G | C | 3 | a0001c0001t0006g0243 a0001c0001t0006g0244 a0001c0001t0006g0246 |
3 | HG00735.hp1 HG02145.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.473+8634G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95182523 | |||||||
| chr1:95182800 | C | T | 10 | a0001c0001t0002g0112 a0001c0001t0002g0147 a0001c0001t0002g0148 others(7): Show |
10 | HG02486.hp2 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.474-8750C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95182800 | |||||||
| chr1:95182891 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.474-8659C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95182891 | |||||||
| chr1:95183166 | C | T | 2 | a0001c0001t0002g0165 a0001c0001t0002g0166 |
2 | HG00639.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.474-8384C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95183166 | |||||||
| chr1:95183250 | A | G | 3 | a0001c0001t0010g0096 a0001c0001t0010g0098 a0001c0001t0010g0099 |
3 | HG00280.hp1 HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.474-8300A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95183250 | |||||||
| chr1:95183276 | C | T | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.474-8274C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95183276 | |||||||
| chr1:95183297 | C | T | 10 | a0001c0001t0005g0036 a0001c0001t0005g0101 a0001c0001t0005g0131 others(7): Show |
10 | HG00738.hp2 HG01069.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.474-8253C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95183297 | |||||||
| chr1:95183357 | A | G | 2 | a0001c0001t0004g0132 a0001c0001t0004g0135 |
2 | HG00544.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.474-8193A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95183357 | |||||||
| chr1:95183374 | G | C | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.474-8176G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95183374 | |||||||
| chr1:95183424 | CAG | C | 75 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(72): Show |
78 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.474-8123_474-8122d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95183424 | ||||||
| chr1:95183586 | C | T | 86 | a0001c0001t0002g0194 a0001c0001t0003g0008 a0001c0001t0003g0009 others(83): Show |
92 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.474-7964C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95183586 | |||||||
| chr1:95183668 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0238 a0001c0001t0001g0329 others(4): Show |
9 | NA18949.hp2 NA18957.hp1 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-7882C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95183668 | |||||||
| chr1:95183816 | G | A | 65 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(62): Show |
68 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.474-7734G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95183816 | |||||||
| chr1:95183836 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.474-7714A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95183836 | |||||||
| chr1:95184004 | C | T | 2 | a0001c0001t0019g0038 a0001c0001t0019g0040 |
2 | HG01074.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.474-7546C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95184004 | |||||||
| chr1:95184019 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
171 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.474-7531G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95184019 | |||||||
| chr1:95184020 | T | A | 2 | a0001c0001t0002g0112 a0001c0001t0002g0327 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.474-7530T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95184020 | |||||||
| chr1:95184285 | A | G | 2 | a0001c0001t0002g0339 a0001c0001t0024g0311 |
2 | HG02630.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.474-7265A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95184285 | |||||||
| chr1:95184352 | CT | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(311): Show |
338 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(335): Show |
intron_variant | MODIFIER | c.474-7187delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95184352 | ||||||
| chr1:95184352 | CTT | C | 6 | a0001c0001t0003g0042 a0001c0001t0005g0035 a0001c0001t0005g0104 others(3): Show |
6 | HG01346.hp1 HG01346.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-7188_474-7187d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95184352 | ||||||
| chr1:95184423 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.474-7127A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95184423 | |||||||
| chr1:95184515 | A | G | 2 | a0001c0001t0006g0160 a0001c0001t0006g0161 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.474-7035A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95184515 | |||||||
| chr1:95184684 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
171 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.474-6866C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95184684 | |||||||
| chr1:95185022 | CT | C | 9 | a0001c0001t0001g0197 a0001c0001t0001g0228 a0001c0001t0001g0229 others(6): Show |
9 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-6517delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95185022 | ||||||
| chr1:95185043 | T | A | 14 | a0001c0001t0006g0160 a0001c0001t0006g0161 a0001c0001t0006g0214 others(11): Show |
14 | HG00735.hp1 HG01109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.474-6507T>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95185043 | |||||||
| chr1:95185240 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
172 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.474-6310G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95185240 | |||||||
| chr1:95185447 | G | A | 1 | a0001c0001t0001g0346 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.474-6103G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95185447 | |||||||
| chr1:95185561 | G | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0119 others(11): Show |
17 | HG00741.hp2 HG02040.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.474-5989G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95185561 | |||||||
| chr1:95185582 | T | G | 1 | a0001c0001t0005g0140 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.474-5968T>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95185582 | |||||||
| chr1:95185702 | C | T | 48 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(45): Show |
53 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.474-5848C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95185702 | |||||||
| chr1:95185865 | A | C | 7 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 others(4): Show |
7 | HG01261.hp2 HG01934.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-5685A>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95185865 | |||||||
| chr1:95186081 | A | G | 5 | a0001c0001t0002g0194 a0001c0001t0005g0191 a0001c0001t0005g0192 others(2): Show |
5 | HG00738.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-5469A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95186081 | |||||||
| chr1:95186227 | G | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.474-5323G>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95186227 | |||||||
| chr1:95186248 | C | A | 1 | a0001c0001t0006g0242 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.474-5302C>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95186248 | |||||||
| chr1:95186718 | G | A | 1 | a0001c0001t0018g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.474-4832G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95186718 | |||||||
| chr1:95186744 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.474-4806A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95186744 | |||||||
| chr1:95186806 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.474-4744A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95186806 | |||||||
| chr1:95186911 | CT | C | 12 | a0001c0001t0006g0160 a0001c0001t0006g0161 a0001c0001t0006g0214 others(9): Show |
12 | HG00735.hp1 HG01109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.474-4634delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95186911 | ||||||
| chr1:95187405 | G | A | 48 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(45): Show |
53 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.474-4145G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95187405 | |||||||
| chr1:95187475 | G | T | 31 | a0001c0001t0001g0018 a0001c0001t0001g0115 a0001c0001t0001g0167 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.474-4075G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95187475 | |||||||
| chr1:95187682 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0119 others(10): Show |
16 | HG00741.hp2 HG02040.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.474-3868C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95187682 | |||||||
| chr1:95187756 | A | G | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.474-3794A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95187756 | |||||||
| chr1:95187873 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474-3677C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95187873 | |||||||
| chr1:95187932 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.474-3618C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95187932 | |||||||
| chr1:95188154 | G | A | 7 | a0001c0001t0008g0091 a0001c0001t0008g0182 a0001c0001t0008g0184 others(4): Show |
7 | HG00639.hp2 HG01175.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.474-3396G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95188154 | |||||||
| chr1:95188159 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.474-3391G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95188159 | |||||||
| chr1:95188214 | C | T | 13 | a0001c0001t0006g0160 a0001c0001t0006g0161 a0001c0001t0006g0214 others(10): Show |
13 | HG00735.hp1 HG01109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.474-3336C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95188214 | |||||||
| chr1:95188260 | C | G | 1 | a0001c0001t0015g0111 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.474-3290C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95188260 | |||||||
| chr1:95188260 | C | T | 1 | a0001c0001t0023g0318 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.474-3290C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95188260 | |||||||
| chr1:95188266 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.474-3284T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95188266 | |||||||
| chr1:95188281 | G | T | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.474-3269G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95188281 | |||||||
| chr1:95188304 | C | T | 1 | a0001c0001t0039g0033 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.474-3246C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95188304 | |||||||
| chr1:95188389 | G | GA | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(146): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.474-3141dupA | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95188389 | ||||||
| chr1:95188389 | G | GAA | 88 | a0001c0001t0001g0158 a0001c0001t0001g0270 a0001c0001t0001g0288 others(85): Show |
91 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.474-3142_474-3141d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95188389 | ||||||
| chr1:95188766 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.474-2784C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95188766 | |||||||
| chr1:95188794 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.474-2756T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95188794 | |||||||
| chr1:95188878 | C | T | 36 | a0001c0001t0001g0018 a0001c0001t0001g0115 a0001c0001t0001g0167 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.474-2672C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95188878 | |||||||
| chr1:95189357 | C | G | 1 | a0001c0001t0001g0224 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.474-2193C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95189357 | |||||||
| chr1:95189471 | C | G | 2 | a0001c0001t0016g0116 a0001c0001t0016g0117 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.474-2079C>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95189471 | |||||||
| chr1:95189647 | C | T | 2 | a0001c0001t0004g0151 a0001c0001t0004g0154 |
2 | NA19080.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.474-1903C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95189647 | |||||||
| chr1:95190096 | CT | C | 188 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(185): Show |
197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.474-1440delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95190096 | ||||||
| chr1:95190096 | CTT | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
172 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.474-1441_474-1440d others(4): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95190096 | ||||||
| chr1:95190318 | GTTTCT | G | 74 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(71): Show |
77 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.474-1208_474-1204d others(7): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95190318 | ||||||
| chr1:95190318 | GTTTCTTT others(3): Show |
G | 2 | a0001c0001t0002g0058 a0001c0001t0009g0102 |
2 | HG02300.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.474-1213_474-1204d others(12): Show |
TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95190318 | ||||||
| chr1:95190342 | CT | C | 5 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-1202delT | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 95190342 | ||||||
| chr1:95190369 | C | T | 1 | a0001c0001t0032g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.474-1181C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95190369 | |||||||
| chr1:95190400 | G | A | 2 | a0001c0001t0005g0173 a0001c0001t0005g0174 |
2 | HG02602.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.474-1150G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95190400 | |||||||
| chr1:95190571 | C | T | 25 | a0001c0001t0006g0160 a0001c0001t0006g0161 a0001c0001t0006g0214 others(22): Show |
25 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.474-979C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95190571 | |||||||
| chr1:95190609 | G | A | 75 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0034 others(72): Show |
78 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.474-941G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95190609 | |||||||
| chr1:95190609 | G | T | 4 | a0001c0001t0004g0132 a0001c0001t0004g0133 a0001c0001t0004g0135 others(1): Show |
4 | HG00544.hp2 NA18955.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-941G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95190609 | |||||||
| chr1:95190952 | G | A | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.474-598G>A | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95190952 | |||||||
| chr1:95190990 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
171 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.474-560T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95190990 | |||||||
| chr1:95191063 | G | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(104): Show |
114 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.474-487G>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95191063 | |||||||
| chr1:95191086 | A | G | 3 | a0001c0001t0002g0017 a0001c0001t0002g0316 a0001c0001t0029g0017 |
3 | HG02109.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.474-464A>G | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95191086 | |||||||
| chr1:95191306 | T | C | 3 | a0001c0001t0002g0017 a0001c0001t0002g0316 a0001c0001t0029g0017 |
3 | HG02109.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.474-244T>C | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95191306 | |||||||
| chr1:95191361 | C | T | 3 | a0001c0001t0020g0113 a0001c0001t0020g0114 a0001c0001t0042g0023 |
3 | HG02109.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.474-189C>T | TLCD4 | ENSG00000152078.10 | transcript | ENST00000370203.9 | protein_coding | 6/6 | chr1 | 95191361 |