Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23548 |
| ensemblid | ENSG00000113638.14 |
| hgncid | 29959 |
| symbol | TTC33 |
| name | tetratricopeptide repeat domain 33 |
| refseq_nuc | NM_012382.3 |
| refseq_prot | NP_036514.1 |
| ensembl_nuc | ENST00000337702.5 |
| ensembl_prot | ENSP00000338533.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 40711576 |
| end | 40755961 |
| strand | - |
| ver | v1.2 |
| region | chr5:40711576-40755961 |
| region5000 | chr5:40706576-40760961 |
| regionname0 | TTC33_chr5_40711576_40755961 |
| regionname5000 | TTC33_chr5_40706576_40760961 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 262 | 383 | 91 | 78 | 156 | 16 | 40 | 130 | TTC33_chr5_40706576_40760961 | TTC33 | MASFG others(257): Show |
chr5 | 40706576 | 40760961 |
| a0002 | 0/0 | 262 | 10 | 0 | 0 | 10 | 0 | 0 | 4 | TTC33_chr5_40706576_40760961 | TTC33 | MASFG others(257): Show |
chr5 | 40706576 | 40760961 |
| a0003 | 0/0 | 262 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | MASFG others(257): Show |
chr5 | 40706576 | 40760961 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 786 | 383 | 91 | 78 | 156 | 16 | 40 | TTC33_chr5_40706576_40760961 | TTC33 | ATGGC others(781): Show |
chr5 | 40706576 | 40760961 | ||
| a0002c0002 | 0/0 | 786 | 10 | 0 | 0 | 10 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | ATGGC others(781): Show |
chr5 | 40706576 | 40760961 | ||
| a0003c0003 | 0/0 | 786 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | ATGGC others(781): Show |
chr5 | 40706576 | 40760961 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5496 | 91 | 8 | 28 | 36 | 5 | 14 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0002 | 0/0 | 5496 | 83 | 27 | 14 | 34 | 4 | 4 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0003 | 0/1 | 5494 | 49 | 1 | 11 | 33 | 1 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5489): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0004 | 0/0 | 5496 | 45 | 7 | 3 | 26 | 0 | 9 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0005 | 0/0 | 5496 | 20 | 2 | 4 | 11 | 0 | 3 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0006 | 0/0 | 5496 | 19 | 0 | 12 | 0 | 4 | 3 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0007 | 1/0 | 5496 | 10 | 8 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0009 | 0/0 | 5496 | 8 | 8 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0010 | 0/0 | 5496 | 6 | 6 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0011 | 0/0 | 5493 | 4 | 4 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5488): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0012 | 0/0 | 5496 | 4 | 3 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0013 | 0/0 | 5496 | 4 | 3 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0014 | 0/0 | 5496 | 4 | 3 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0015 | 0/0 | 5503 | 3 | 3 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5498): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0016 | 0/0 | 5494 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5489): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0017 | 0/0 | 5496 | 3 | 3 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0018 | 0/0 | 5494 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5489): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0019 | 0/0 | 5496 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0020 | 0/0 | 5494 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5489): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0021 | 0/0 | 5496 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0022 | 0/0 | 5494 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5489): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0023 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0024 | 0/0 | 5494 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5489): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0025 | 0/0 | 5496 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0026 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0027 | 0/0 | 5496 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0028 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0029 | 0/0 | 5496 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0030 | 0/0 | 5496 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0031 | 0/0 | 5496 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0032 | 0/0 | 5496 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0033 | 0/0 | 5496 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0034 | 0/0 | 5494 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5489): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0035 | 0/0 | 5494 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5489): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0036 | 0/0 | 5496 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0037 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0038 | 0/0 | 5496 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0039 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0001c0001t0040 | 0/0 | 5496 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0002c0002t0008 | 0/0 | 5496 | 10 | 0 | 0 | 10 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| a0003c0003t0001 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | GATTT others(5491): Show |
chr5 | 40706576 | 40760961 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 16 | 1 | 7 | 5 | 1 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0017 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0001 | 0/0 | 17 | 0 | 2 | 11 | 1 | 3 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0003 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0009 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0008 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0005g0005 | 0/0 | 8 | 0 | 3 | 4 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0005g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0006g0013 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0006g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0006g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0006g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0006g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0006g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0006g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0006g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0007g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0007g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0007g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0007g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0009g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0009g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0009g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0009g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0010g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0010g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0010g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0010g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0010g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0011g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0011g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0012g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0012g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0012g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0012g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0013g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0013g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0014g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0015g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0015g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0015g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0016g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0016g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0017g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0017g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0017g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0018g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0018g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0018g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0019g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0020g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0021g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0022g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0023g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0024g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0025g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0026g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0027g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0028g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0029g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0030g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0031g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0032g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0033g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0034g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0035g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0036g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0037g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0038g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0039g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0001c0001t0040g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0002c0002t0008g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0002c0002t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0002c0002t0008g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0002c0002t0008g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0002c0002t0008g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0002c0002t0008g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0002c0002t0008g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0002c0002t0008g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| a0003c0003t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0009 | EUR | GBR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0128 | EUR | FIN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | FIN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00408 | hp2 | a0002 | c0002 | t0008 | g0173 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00597 | hp1 | a0002 | c0002 | t0008 | g0016 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0243 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0254 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0041 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0230 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0232 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0263 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01081 | hp2 | a0001 | c0001 | t0027 | g0059 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0233 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01106 | hp1 | a0001 | c0001 | t0013 | g0049 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0252 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01192 | hp1 | a0001 | c0001 | t0012 | g0156 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01192 | hp2 | a0001 | c0001 | t0038 | g0160 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0042 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0042 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0262 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01346 | hp2 | a0001 | c0001 | t0014 | g0010 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01361 | hp2 | a0001 | c0001 | t0007 | g0234 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0239 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0255 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01515 | hp1 | a0001 | c0001 | t0040 | g0257 | EUR | IBS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0019 | EUR | IBS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0040 | EUR | IBS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0135 | EUR | IBS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0040 | EUR | IBS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01884 | hp2 | a0003 | c0003 | t0001 | g0162 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0266 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0258 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02015 | hp1 | a0002 | c0002 | t0008 | g0171 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02040 | hp1 | a0002 | c0002 | t0008 | g0177 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02055 | hp2 | a0001 | c0001 | t0014 | g0010 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02056 | hp1 | a0002 | c0002 | t0008 | g0016 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0212 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02071 | hp2 | a0001 | c0001 | t0030 | g0056 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02080 | hp1 | a0002 | c0002 | t0008 | g0174 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02083 | hp1 | a0001 | c0001 | t0016 | g0020 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0241 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0217 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | CDX | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | CDX | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CDX | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02257 | hp1 | a0001 | c0001 | t0039 | g0143 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0081 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02280 | hp1 | a0001 | c0001 | t0012 | g0170 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02280 | hp2 | a0001 | c0001 | t0015 | g0269 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0039 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02451 | hp2 | a0001 | c0001 | t0010 | g0080 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02572 | hp1 | a0001 | c0001 | t0013 | g0046 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0038 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0215 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0082 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0084 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0260 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02683 | hp2 | a0001 | c0001 | t0021 | g0191 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02717 | hp2 | a0001 | c0001 | t0017 | g0169 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0213 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0242 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0083 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02895 | hp1 | a0001 | c0001 | t0013 | g0047 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02922 | hp2 | a0001 | c0001 | t0017 | g0167 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02965 | hp1 | a0001 | c0001 | t0026 | g0246 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02965 | hp2 | a0001 | c0001 | t0012 | g0157 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02976 | hp1 | a0001 | c0001 | t0011 | g0014 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0265 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0039 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0037 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0014 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0085 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0264 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03225 | hp1 | a0001 | c0001 | t0014 | g0010 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03225 | hp2 | a0001 | c0001 | t0015 | g0270 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0013 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0267 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03486 | hp2 | a0001 | c0001 | t0023 | g0150 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0033 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0033 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0037 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03516 | hp2 | a0001 | c0001 | t0037 | g0051 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0045 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03540 | hp2 | a0001 | c0001 | t0014 | g0010 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03579 | hp2 | a0001 | c0001 | t0017 | g0168 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0226 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03654 | hp2 | a0001 | c0001 | t0024 | g0110 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0041 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03831 | hp1 | a0001 | c0001 | t0025 | g0063 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0008 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0034 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0008 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03942 | hp2 | a0001 | c0001 | t0029 | g0050 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG04184 | hp2 | a0001 | c0001 | t0034 | g0107 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0253 | SAS | STU | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0231 | SAS | STU | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | STU | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0216 | AFR | YRI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0014 | AFR | YRI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0043 | AFR | YRI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18942 | hp2 | a0001 | c0001 | t0033 | g0182 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18946 | hp2 | a0001 | c0001 | t0016 | g0094 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18956 | hp1 | a0001 | c0001 | t0016 | g0020 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18962 | hp2 | a0001 | c0001 | t0035 | g0106 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18967 | hp2 | a0001 | c0001 | t0031 | g0271 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18977 | hp2 | a0002 | c0002 | t0008 | g0176 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18988 | hp2 | a0001 | c0001 | t0018 | g0098 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18994 | hp1 | a0001 | c0001 | t0020 | g0044 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18995 | hp2 | a0001 | c0001 | t0020 | g0044 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19011 | hp2 | a0001 | c0001 | t0032 | g0178 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19012 | hp1 | a0001 | c0001 | t0019 | g0032 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | LWK | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0256 | AFR | LWK | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0048 | AFR | LWK | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0237 | AFR | LWK | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19059 | hp2 | a0001 | c0001 | t0018 | g0097 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19070 | hp2 | a0001 | c0001 | t0036 | g0227 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19075 | hp1 | a0002 | c0002 | t0008 | g0175 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19077 | hp1 | a0001 | c0001 | t0018 | g0101 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19078 | hp1 | a0002 | c0002 | t0008 | g0016 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19080 | hp2 | a0002 | c0002 | t0008 | g0172 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19088 | hp2 | a0001 | c0001 | t0019 | g0032 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19089 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | YRI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0043 | AFR | YRI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0158 | AFR | ASW | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | ASW | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | TSI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0259 | EUR | TSI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA20805 | hp1 | a0001 | c0001 | t0022 | g0117 | EUR | TSI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0261 | EUR | TSI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | GIH | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | GIH | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0274 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0247 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0248 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0038 | AFR | USA | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | USA | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA21309 | hp1 | a0001 | c0001 | t0015 | g0268 | AFR | LWK | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| NA21309 | hp2 | a0001 | c0001 | t0028 | g0138 | AFR | LWK | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0115 | REF | REF | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0236 | REF | REF | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:40716264 | T | A | 1 | a0003 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.670A>T | p.Thr224Ser | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 809/5497 | 670/789 | 224/262 | chr5 | 40716264 | |||
| chr5:40746814 | A | T | 1 | a0002 | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
missense_variant | MODERATE | c.205T>A | p.Leu69Met | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/5 | 344/5497 | 205/789 | 69/262 | chr5 | 40746814 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:40711586 | T | C | 1 | a0001c0001t0027 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4559A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 4559 | chr5 | 40711586 | ||||||
| chr5:40711671 | G | A | 1 | a0001c0001t0028 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4474C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 4474 | chr5 | 40711671 | ||||||
| chr5:40711865 | C | T | 1 | a0001c0001t0032 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4280G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 4280 | chr5 | 40711865 | ||||||
| chr5:40711893 | T | C | 1 | a0001c0001t0024 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4252A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 4252 | chr5 | 40711893 | ||||||
| chr5:40712142 | A | T | 2 | a0001c0001t0006 a0001c0001t0040 |
20 | HG00733.hp2 HG00741.hp2 HG01074.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4003T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 4003 | chr5 | 40712142 | ||||||
| chr5:40712196 | T | G | 1 | a0001c0001t0033 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3949A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3949 | chr5 | 40712196 | ||||||
| chr5:40712441 | A | G | 2 | a0001c0001t0012 a0001c0001t0023 |
5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3704T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3704 | chr5 | 40712441 | ||||||
| chr5:40712455 | A | T | 1 | a0001c0001t0017 | 3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3690T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3690 | chr5 | 40712455 | ||||||
| chr5:40712465 | C | A | 1 | a0001c0001t0009 | 8 | HG02572.hp2 HG03098.hp2 HG03209.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3680G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3680 | chr5 | 40712465 | ||||||
| chr5:40712646 | C | A | 1 | a0001c0001t0029 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3499G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3499 | chr5 | 40712646 | ||||||
| chr5:40712671 | T | C | 1 | a0001c0001t0013 | 4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3474A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3474 | chr5 | 40712671 | ||||||
| chr5:40712695 | A | C | 20 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(17): Show |
164 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*3450T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3450 | chr5 | 40712695 | ||||||
| chr5:40712821 | C | T | 1 | a0001c0001t0026 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3324G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3324 | chr5 | 40712821 | ||||||
| chr5:40712854 | T | C | 1 | a0001c0001t0030 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3291A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3291 | chr5 | 40712854 | ||||||
| chr5:40712859 | C | G | 1 | a0001c0001t0025 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3286G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3286 | chr5 | 40712859 | ||||||
| chr5:40713334 | T | C | 1 | a0001c0001t0031 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2811A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2811 | chr5 | 40713334 | ||||||
| chr5:40713543 | T | C | 1 | a0001c0001t0005 | 20 | HG00597.hp2 HG00735.hp2 HG01433.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2602A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2602 | chr5 | 40713543 | ||||||
| chr5:40713553 | T | C | 1 | a0001c0001t0016 | 3 | HG02083.hp1 NA18946.hp2 NA18956.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2592A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2592 | chr5 | 40713553 | ||||||
| chr5:40713564 | T | A | 6 | a0001c0001t0001 a0001c0001t0021 a0001c0001t0032 others(3): Show |
96 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2581A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2581 | chr5 | 40713564 | ||||||
| chr5:40713847 | CTA | C | 8 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0018 others(5): Show |
60 | HG00099.hp2 HG00408.hp1 HG01069.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2296_*2297delTA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2296 | chr5 | 40713847 | ||||||
| chr5:40713855 | G | A | 1 | a0001c0001t0019 | 2 | NA19012.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2290C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2290 | chr5 | 40713855 | ||||||
| chr5:40713888 | G | C | 1 | a0001c0001t0034 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2257C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2257 | chr5 | 40713888 | ||||||
| chr5:40713907 | G | A | 1 | a0001c0001t0018 | 3 | NA18988.hp2 NA19059.hp2 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2238C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2238 | chr5 | 40713907 | ||||||
| chr5:40713983 | C | T | 2 | a0001c0001t0012 a0001c0001t0023 |
5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2162G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2162 | chr5 | 40713983 | ||||||
| chr5:40714063 | C | T | 1 | a0001c0001t0022 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2082G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2082 | chr5 | 40714063 | ||||||
| chr5:40714252 | C | A | 1 | a0001c0001t0035 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1893G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1893 | chr5 | 40714252 | ||||||
| chr5:40714507 | CA | C | 2 | a0001c0001t0011 a0001c0001t0015 |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1637delT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1637 | chr5 | 40714507 | ||||||
| chr5:40714579 | C | T | 1 | a0002c0002t0008 | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1566G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1566 | chr5 | 40714579 | ||||||
| chr5:40714635 | C | A | 2 | a0001c0001t0010 a0001c0001t0037 |
7 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1510G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1510 | chr5 | 40714635 | ||||||
| chr5:40714679 | T | C | 1 | a0001c0001t0036 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1466A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1466 | chr5 | 40714679 | ||||||
| chr5:40714776 | C | T | 1 | a0001c0001t0021 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1369G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1369 | chr5 | 40714776 | ||||||
| chr5:40714885 | T | A | 1 | a0001c0001t0037 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1260A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1260 | chr5 | 40714885 | ||||||
| chr5:40714960 | A | G | 1 | a0001c0001t0012 | 4 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1185T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1185 | chr5 | 40714960 | ||||||
| chr5:40715231 | T | G | 1 | a0001c0001t0038 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*914A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 914 | chr5 | 40715231 | ||||||
| chr5:40715327 | T | C | 1 | a0001c0001t0039 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*818A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 818 | chr5 | 40715327 | ||||||
| chr5:40715362 | A | ACCTATCT others(1): Show |
2 | a0001c0001t0011 a0001c0001t0015 |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*775_*782dupCAGATA others(2): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 782 | chr5 | 40715362 | ||||||
| chr5:40715591 | T | C | 1 | a0001c0001t0014 | 4 | HG01346.hp2 HG02055.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*554A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 554 | chr5 | 40715591 | ||||||
| chr5:40716051 | C | A | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
3_prime_UTR_variant | MODIFIER | c.*94G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 94 | chr5 | 40716051 | ||||||
| chr5:40716134 | T | C | 1 | a0001c0001t0040 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 11 | chr5 | 40716134 | ||||||
| chr5:40755838 | T | C | 1 | a0001c0001t0020 | 2 | NA18994.hp1 NA18995.hp2 |
5_prime_UTR_variant | MODIFIER | c.-16A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/5 | 8820 | chr5 | 40755838 | ||||||
| chr5:40755867 | CCACCCCT others(3): Show |
C | 1 | a0001c0001t0011 | 4 | HG02976.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-55_-46delCCCAGGGG others(2): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/5 | 8850 | chr5 | 40755867 | ||||||
| chr5:40755887 | A | G | 1 | a0001c0001t0011 | 4 | HG02976.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-65T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/5 | 8869 | chr5 | 40755887 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:40716531 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.436-33A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40716531 | |||||||
| chr5:40716735 | G | T | 1 | a0001c0001t0004g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.436-237C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40716735 | |||||||
| chr5:40716751 | G | C | 1 | a0001c0001t0010g0085 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.436-253C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40716751 | |||||||
| chr5:40716852 | G | A | 1 | a0001c0001t0009g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.436-354C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40716852 | |||||||
| chr5:40716957 | G | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0161 others(4): Show |
10 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-459C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40716957 | |||||||
| chr5:40717003 | C | T | 119 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0015 others(116): Show |
166 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.436-505G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717003 | |||||||
| chr5:40717041 | C | A | 1 | a0001c0001t0003g0118 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.436-543G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717041 | |||||||
| chr5:40717043 | A | C | 1 | a0001c0001t0003g0118 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.436-545T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717043 | |||||||
| chr5:40717058 | G | C | 1 | a0001c0001t0002g0069 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.436-560C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717058 | |||||||
| chr5:40717143 | C | T | 1 | a0002c0002t0008g0172 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.436-645G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717143 | |||||||
| chr5:40717229 | C | CA | 100 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0031 others(97): Show |
140 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.436-732dupT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717229 | |||||||
| chr5:40717229 | C | CAA | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(79): Show |
128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.436-733_436-732dup others(2): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717229 | |||||||
| chr5:40717229 | C | CAAA | 9 | a0001c0001t0001g0017 a0001c0001t0001g0187 a0001c0001t0001g0188 others(6): Show |
11 | HG00323.hp1 HG01099.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.436-734_436-732dup others(3): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717229 | |||||||
| chr5:40717229 | CA | C | 6 | a0001c0001t0002g0126 a0001c0001t0012g0157 a0001c0001t0013g0046 others(3): Show |
6 | HG01106.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-732delT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717229 | |||||||
| chr5:40717343 | T | C | 1 | a0001c0001t0003g0090 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.436-845A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717343 | |||||||
| chr5:40717376 | A | G | 1 | a0001c0001t0031g0271 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.436-878T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717376 | |||||||
| chr5:40717439 | T | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-941A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717439 | |||||||
| chr5:40717507 | T | A | 5 | a0001c0001t0004g0034 a0001c0001t0004g0230 a0001c0001t0004g0231 others(2): Show |
6 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.436-1009A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717507 | |||||||
| chr5:40717640 | C | T | 2 | a0001c0001t0004g0144 a0001c0001t0004g0145 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.436-1142G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717640 | |||||||
| chr5:40717719 | A | G | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-1221T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717719 | |||||||
| chr5:40717740 | G | A | 13 | a0001c0001t0004g0215 a0001c0001t0005g0005 a0001c0001t0005g0036 others(10): Show |
21 | HG00597.hp2 HG00735.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.436-1242C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717740 | |||||||
| chr5:40717789 | C | A | 1 | a0001c0001t0010g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.436-1291G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717789 | |||||||
| chr5:40717929 | G | T | 107 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0015 others(104): Show |
154 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.436-1431C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717929 | |||||||
| chr5:40717954 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.436-1456G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717954 | |||||||
| chr5:40718045 | A | T | 13 | a0001c0001t0004g0215 a0001c0001t0005g0005 a0001c0001t0005g0036 others(10): Show |
21 | HG00597.hp2 HG00735.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.436-1547T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718045 | |||||||
| chr5:40718057 | C | T | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.436-1559G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718057 | |||||||
| chr5:40718216 | T | C | 4 | a0001c0001t0013g0046 a0001c0001t0013g0047 a0001c0001t0013g0048 others(1): Show |
4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-1718A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718216 | |||||||
| chr5:40718236 | T | C | 1 | a0001c0001t0037g0051 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.436-1738A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718236 | |||||||
| chr5:40718252 | A | G | 1 | a0002c0002t0008g0175 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.436-1754T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718252 | |||||||
| chr5:40718310 | G | T | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-1812C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718310 | |||||||
| chr5:40718367 | C | T | 1 | a0001c0001t0010g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.436-1869G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718367 | |||||||
| chr5:40718480 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.436-1982C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718480 | |||||||
| chr5:40718496 | C | G | 1 | a0001c0001t0023g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.436-1998G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718496 | |||||||
| chr5:40718507 | G | A | 2 | a0001c0001t0018g0098 a0001c0001t0018g0101 |
2 | NA18988.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.436-2009C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718507 | |||||||
| chr5:40718585 | C | T | 6 | a0001c0001t0003g0009 a0001c0001t0003g0108 a0001c0001t0003g0146 others(3): Show |
9 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.436-2087G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718585 | |||||||
| chr5:40718653 | G | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(43): Show |
78 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.436-2155C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718653 | |||||||
| chr5:40718665 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.436-2167C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718665 | |||||||
| chr5:40718682 | G | C | 2 | a0001c0001t0004g0144 a0001c0001t0004g0145 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.436-2184C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718682 | |||||||
| chr5:40718686 | C | T | 117 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0015 others(114): Show |
164 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.436-2188G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718686 | |||||||
| chr5:40718689 | G | A | 3 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0158 |
3 | HG01192.hp1 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.436-2191C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718689 | |||||||
| chr5:40718788 | C | T | 33 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(30): Show |
51 | HG00423.hp1 HG00673.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.436-2290G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718788 | |||||||
| chr5:40718948 | T | C | 1 | a0001c0001t0003g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.436-2450A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718948 | |||||||
| chr5:40718991 | A | G | 7 | a0001c0001t0010g0080 a0001c0001t0010g0081 a0001c0001t0010g0082 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.436-2493T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718991 | |||||||
| chr5:40719045 | A | G | 1 | a0001c0001t0006g0040 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.436-2547T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719045 | |||||||
| chr5:40719139 | C | T | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.436-2641G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719139 | |||||||
| chr5:40719160 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.436-2662A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719160 | |||||||
| chr5:40719340 | C | T | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-2842G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719340 | |||||||
| chr5:40719404 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.436-2906A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719404 | |||||||
| chr5:40719412 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0152 a0001c0001t0001g0153 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-2914G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719412 | |||||||
| chr5:40719441 | T | C | 119 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0015 others(116): Show |
166 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.436-2943A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719441 | |||||||
| chr5:40719442 | C | G | 1 | a0001c0001t0002g0067 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.436-2944G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719442 | |||||||
| chr5:40719582 | C | T | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-3084G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719582 | |||||||
| chr5:40719597 | T | C | 2 | a0001c0001t0002g0074 a0001c0001t0002g0076 |
2 | NA18977.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.436-3099A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719597 | |||||||
| chr5:40719696 | C | G | 6 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(3): Show |
8 | HG00597.hp1 HG02015.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.436-3198G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719696 | |||||||
| chr5:40719848 | T | C | 1 | a0001c0001t0037g0051 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.436-3350A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719848 | |||||||
| chr5:40719999 | C | T | 5 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0158 others(2): Show |
5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.436-3501G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719999 | |||||||
| chr5:40720026 | A | C | 107 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0015 others(104): Show |
154 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.436-3528T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720026 | |||||||
| chr5:40720057 | C | G | 5 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0158 others(2): Show |
5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.436-3559G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720057 | |||||||
| chr5:40720081 | G | C | 1 | a0001c0001t0005g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.436-3583C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720081 | |||||||
| chr5:40720256 | C | T | 1 | a0001c0001t0012g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.436-3758G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720256 | |||||||
| chr5:40720285 | G | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(43): Show |
78 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.436-3787C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720285 | |||||||
| chr5:40720481 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.436-3983A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720481 | |||||||
| chr5:40720514 | C | T | 1 | a0001c0001t0037g0051 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.436-4016G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720514 | |||||||
| chr5:40720576 | A | C | 4 | a0001c0001t0013g0046 a0001c0001t0013g0047 a0001c0001t0013g0048 others(1): Show |
4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-4078T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720576 | |||||||
| chr5:40720593 | A | G | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-4095T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720593 | |||||||
| chr5:40720716 | G | A | 1 | a0001c0001t0023g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.436-4218C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720716 | |||||||
| chr5:40720905 | C | T | 2 | a0001c0001t0004g0144 a0001c0001t0004g0145 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.436-4407G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720905 | |||||||
| chr5:40721140 | G | A | 2 | a0002c0002t0008g0173 a0002c0002t0008g0174 |
2 | HG00408.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.436-4642C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721140 | |||||||
| chr5:40721176 | T | G | 1 | a0001c0001t0003g0092 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.436-4678A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721176 | |||||||
| chr5:40721193 | T | C | 3 | a0001c0001t0002g0126 a0001c0001t0002g0132 a0001c0001t0002g0133 |
3 | HG02809.hp2 HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.436-4695A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721193 | |||||||
| chr5:40721297 | A | G | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-4799T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721297 | |||||||
| chr5:40721331 | C | T | 4 | a0001c0001t0004g0224 a0001c0001t0010g0083 a0001c0001t0010g0084 others(1): Show |
4 | HG02647.hp1 HG02818.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-4833G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721331 | |||||||
| chr5:40721336 | T | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(198): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.436-4838A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721336 | |||||||
| chr5:40721349 | C | T | 4 | a0001c0001t0013g0046 a0001c0001t0013g0047 a0001c0001t0013g0048 others(1): Show |
4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-4851G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721349 | |||||||
| chr5:40721395 | C | A | 1 | a0001c0001t0002g0055 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.436-4897G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721395 | |||||||
| chr5:40721544 | G | A | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-5046C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721544 | |||||||
| chr5:40721560 | A | G | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-5062T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721560 | |||||||
| chr5:40721605 | C | G | 1 | a0001c0001t0026g0246 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.436-5107G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721605 | |||||||
| chr5:40721643 | C | T | 1 | a0001c0001t0004g0231 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.436-5145G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721643 | |||||||
| chr5:40721682 | A | AAAAAC | 43 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0021 others(40): Show |
60 | HG00099.hp2 HG00408.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.436-5189_436-5185d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721682 | |||||||
| chr5:40721821 | C | T | 1 | a0001c0001t0010g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.436-5323G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721821 | |||||||
| chr5:40722160 | G | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(57): Show |
96 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.436-5662C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722160 | |||||||
| chr5:40722243 | T | A | 1 | a0001c0001t0001g0164 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.436-5745A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722243 | |||||||
| chr5:40722282 | T | G | 1 | a0001c0001t0021g0191 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.436-5784A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722282 | |||||||
| chr5:40722321 | C | T | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-5823G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722321 | |||||||
| chr5:40722331 | G | A | 1 | a0001c0001t0035g0106 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.436-5833C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722331 | |||||||
| chr5:40722349 | G | A | 52 | a0001c0001t0002g0007 a0001c0001t0002g0025 a0001c0001t0002g0136 others(49): Show |
75 | HG00099.hp2 HG00408.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.436-5851C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722349 | |||||||
| chr5:40722402 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.436-5904C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722402 | |||||||
| chr5:40722424 | C | T | 1 | a0001c0001t0040g0257 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.435+5921G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722424 | |||||||
| chr5:40722434 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.435+5911G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722434 | |||||||
| chr5:40722438 | C | A | 1 | a0001c0001t0002g0125 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.435+5907G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722438 | |||||||
| chr5:40722486 | G | C | 1 | a0001c0001t0017g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.435+5859C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722486 | |||||||
| chr5:40722557 | G | C | 7 | a0001c0001t0010g0080 a0001c0001t0010g0081 a0001c0001t0010g0082 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.435+5788C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722557 | |||||||
| chr5:40722656 | G | A | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+5689C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722656 | |||||||
| chr5:40722663 | C | T | 39 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(36): Show |
57 | HG00423.hp1 HG00673.hp1 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.435+5682G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722663 | |||||||
| chr5:40722673 | C | T | 7 | a0001c0001t0010g0080 a0001c0001t0010g0081 a0001c0001t0010g0082 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.435+5672G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722673 | |||||||
| chr5:40722674 | C | G | 1 | a0001c0001t0003g0100 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.435+5671G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722674 | |||||||
| chr5:40722708 | G | A | 3 | a0001c0001t0013g0046 a0001c0001t0013g0047 a0001c0001t0013g0049 |
3 | HG01106.hp1 HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.435+5637C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722708 | |||||||
| chr5:40722714 | C | T | 1 | a0001c0001t0004g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.435+5631G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722714 | |||||||
| chr5:40722720 | G | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0015 others(117): Show |
167 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.435+5625C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722720 | |||||||
| chr5:40722747 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0161 others(3): Show |
9 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.435+5598G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722747 | |||||||
| chr5:40722749 | C | T | 1 | a0001c0001t0005g0243 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.435+5596G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722749 | |||||||
| chr5:40722763 | G | A | 2 | a0001c0001t0003g0105 a0001c0001t0003g0112 |
2 | NA18986.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.435+5582C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722763 | |||||||
| chr5:40722812 | A | C | 1 | a0001c0001t0005g0241 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.435+5533T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722812 | |||||||
| chr5:40722822 | C | T | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(176): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.435+5523G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722822 | |||||||
| chr5:40722876 | C | T | 7 | a0001c0001t0004g0144 a0001c0001t0004g0145 a0001c0001t0011g0014 others(4): Show |
9 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.435+5469G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722876 | |||||||
| chr5:40722918 | G | A | 1 | a0001c0001t0012g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.435+5427C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722918 | |||||||
| chr5:40722921 | A | AC | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0200 others(4): Show |
7 | HG01978.hp2 HG02145.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+5423dupG | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722921 | |||||||
| chr5:40722972 | C | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(184): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.435+5373G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722972 | |||||||
| chr5:40723367 | C | T | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+4978G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723367 | |||||||
| chr5:40723443 | A | C | 1 | a0001c0001t0004g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.435+4902T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723443 | |||||||
| chr5:40723445 | T | A | 3 | a0001c0001t0010g0083 a0001c0001t0010g0084 a0001c0001t0010g0085 |
3 | HG02647.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.435+4900A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723445 | |||||||
| chr5:40723510 | A | G | 1 | a0001c0001t0002g0148 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.435+4835T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723510 | |||||||
| chr5:40723512 | TAA | T | 123 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0015 others(120): Show |
169 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.435+4831_435+4832d others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723512 | |||||||
| chr5:40723512 | TAAA | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(64): Show |
103 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.435+4830_435+4832d others(5): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723512 | |||||||
| chr5:40723526 | AAAG | A | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+4816_435+4818d others(5): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723526 | |||||||
| chr5:40723560 | A | G | 1 | a0001c0001t0005g0240 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.435+4785T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723560 | |||||||
| chr5:40723573 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.435+4772G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723573 | |||||||
| chr5:40723592 | C | T | 1 | a0001c0001t0003g0099 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.435+4753G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723592 | |||||||
| chr5:40723783 | C | T | 3 | a0001c0001t0001g0149 a0001c0001t0001g0186 a0001c0001t0001g0193 |
3 | HG00423.hp2 HG00558.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.435+4562G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723783 | |||||||
| chr5:40723818 | T | C | 1 | a0001c0001t0006g0259 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.435+4527A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723818 | |||||||
| chr5:40723844 | G | A | 16 | a0001c0001t0002g0015 a0001c0001t0002g0023 a0001c0001t0002g0119 others(13): Show |
22 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.435+4501C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723844 | |||||||
| chr5:40723864 | C | CA | 6 | a0001c0001t0002g0140 a0001c0001t0002g0272 a0001c0001t0003g0102 others(3): Show |
6 | HG01167.hp1 HG01358.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+4480dupT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723864 | |||||||
| chr5:40723870 | AAAAC | A | 17 | a0001c0001t0004g0006 a0001c0001t0004g0035 a0001c0001t0004g0218 others(14): Show |
25 | HG00558.hp2 HG02129.hp1 HG02165.hp2 others(22): Show |
intron_variant | MODIFIER | c.435+4471_435+4474d others(6): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723870 | |||||||
| chr5:40724120 | A | C | 5 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0158 others(2): Show |
5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.435+4225T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724120 | |||||||
| chr5:40724304 | G | A | 3 | a0001c0001t0010g0083 a0001c0001t0010g0084 a0001c0001t0010g0085 |
3 | HG02647.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.435+4041C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724304 | |||||||
| chr5:40724451 | G | A | 4 | a0001c0001t0013g0046 a0001c0001t0013g0047 a0001c0001t0013g0048 others(1): Show |
4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+3894C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724451 | |||||||
| chr5:40724655 | C | CA | 5 | a0001c0001t0001g0152 a0001c0001t0003g0072 a0001c0001t0003g0105 others(2): Show |
5 | HG01261.hp1 NA18960.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.435+3689dupT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724655 | |||||||
| chr5:40724659 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.435+3686T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724659 | |||||||
| chr5:40724735 | TACA | T | 4 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0158 others(1): Show |
4 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.435+3607_435+3609d others(5): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724735 | |||||||
| chr5:40724762 | A | G | 1 | a0001c0001t0004g0233 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.435+3583T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724762 | |||||||
| chr5:40724853 | A | AT | 11 | a0001c0001t0002g0062 a0001c0001t0002g0075 a0001c0001t0002g0076 others(8): Show |
11 | HG01261.hp2 HG01433.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.435+3491dupA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724853 | |||||||
| chr5:40724853 | AT | A | 35 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0152 others(32): Show |
48 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.435+3491delA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724853 | |||||||
| chr5:40724853 | ATT | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(41): Show |
76 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.435+3490_435+3491d others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724853 | |||||||
| chr5:40724918 | T | C | 1 | a0001c0001t0002g0065 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.435+3427A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724918 | |||||||
| chr5:40724946 | A | C | 1 | a0001c0001t0035g0106 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.435+3399T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724946 | |||||||
| chr5:40725003 | T | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(43): Show |
78 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.435+3342A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725003 | |||||||
| chr5:40725150 | A | AT | 9 | a0001c0001t0003g0087 a0001c0001t0003g0109 a0001c0001t0004g0144 others(6): Show |
9 | HG02572.hp1 HG02895.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.435+3194dupA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725150 | |||||||
| chr5:40725150 | AT | A | 15 | a0001c0001t0002g0075 a0001c0001t0002g0077 a0001c0001t0004g0222 others(12): Show |
17 | HG01884.hp2 HG02280.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.435+3194delA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725150 | |||||||
| chr5:40725278 | T | C | 2 | a0001c0001t0004g0144 a0001c0001t0004g0145 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.435+3067A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725278 | |||||||
| chr5:40725611 | G | A | 1 | a0001c0001t0035g0106 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.435+2734C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725611 | |||||||
| chr5:40725632 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.435+2713A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725632 | |||||||
| chr5:40725703 | G | A | 1 | a0001c0001t0005g0036 | 2 | NA18989.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.435+2642C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725703 | |||||||
| chr5:40725716 | T | C | 33 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(30): Show |
51 | HG00423.hp1 HG00673.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.435+2629A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725716 | |||||||
| chr5:40725739 | A | G | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.435+2606T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725739 | |||||||
| chr5:40725764 | C | T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG01358.hp1 HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.435+2581G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725764 | |||||||
| chr5:40725784 | C | CT | 38 | a0001c0001t0001g0149 a0001c0001t0001g0181 a0001c0001t0001g0196 others(35): Show |
46 | HG00423.hp2 HG00597.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.435+2560dupA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725784 | |||||||
| chr5:40725784 | CT | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0161 others(12): Show |
18 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.435+2560delA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725784 | |||||||
| chr5:40725843 | T | C | 2 | a0001c0001t0013g0046 a0001c0001t0013g0047 |
2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.435+2502A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725843 | |||||||
| chr5:40725987 | G | A | 6 | a0001c0001t0003g0009 a0001c0001t0003g0108 a0001c0001t0003g0146 others(3): Show |
9 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.435+2358C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725987 | |||||||
| chr5:40726003 | T | A | 1 | a0001c0001t0010g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.435+2342A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726003 | |||||||
| chr5:40726004 | C | T | 1 | a0001c0001t0010g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.435+2341G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726004 | |||||||
| chr5:40726036 | C | T | 96 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0018 others(93): Show |
137 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.435+2309G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726036 | |||||||
| chr5:40726145 | A | T | 180 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(177): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.435+2200T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726145 | |||||||
| chr5:40726160 | TAC | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(184): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.435+2183_435+2184d others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726160 | |||||||
| chr5:40726162 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0179 a0001c0001t0001g0201 others(2): Show |
6 | HG02615.hp2 NA18987.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.435+2183G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726162 | |||||||
| chr5:40726212 | T | TTA | 3 | a0001c0001t0002g0126 a0001c0001t0002g0132 a0001c0001t0002g0133 |
3 | HG02809.hp2 HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.435+2132_435+2133i others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726212 | |||||||
| chr5:40726214 | T | A | 3 | a0001c0001t0002g0126 a0001c0001t0002g0132 a0001c0001t0002g0133 |
3 | HG02809.hp2 HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.435+2131A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726214 | |||||||
| chr5:40726214 | T | TTA | 118 | a0001c0001t0001g0052 a0001c0001t0002g0001 a0001c0001t0002g0007 others(115): Show |
165 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.435+2129_435+2130d others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726214 | |||||||
| chr5:40726394 | A | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(198): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.435+1951T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726394 | |||||||
| chr5:40726550 | C | CA | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(51): Show |
87 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.435+1794dupT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726550 | |||||||
| chr5:40726616 | GA | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(260): Show |
382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.435+1728delT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726616 | |||||||
| chr5:40726699 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(184): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.435+1646G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726699 | |||||||
| chr5:40727081 | T | G | 1 | a0001c0001t0005g0240 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.435+1264A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727081 | |||||||
| chr5:40727255 | T | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+1090A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727255 | |||||||
| chr5:40727385 | T | C | 3 | a0001c0001t0004g0216 a0001c0001t0004g0217 a0001c0001t0026g0246 |
3 | HG02145.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.435+960A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727385 | |||||||
| chr5:40727522 | A | G | 1 | a0002c0002t0008g0175 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.435+823T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727522 | |||||||
| chr5:40727628 | C | T | 4 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(1): Show |
4 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+717G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727628 | |||||||
| chr5:40727672 | C | T | 1 | a0001c0001t0026g0246 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.435+673G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727672 | |||||||
| chr5:40727702 | T | C | 1 | a0001c0001t0002g0066 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.435+643A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727702 | |||||||
| chr5:40727907 | C | A | 1 | a0001c0001t0028g0138 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.435+438G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727907 | |||||||
| chr5:40728134 | A | G | 4 | a0001c0001t0013g0046 a0001c0001t0013g0047 a0001c0001t0013g0048 others(1): Show |
4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+211T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728134 | |||||||
| chr5:40728176 | C | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0161 others(6): Show |
12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.435+169G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728176 | |||||||
| chr5:40728268 | C | T | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.435+77G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728268 | |||||||
| chr5:40728272 | A | C | 1 | a0001c0001t0015g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.435+73T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728272 | |||||||
| chr5:40728281 | C | CAAAAAA | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+58_435+63dupTT others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | |||||||
| chr5:40728281 | C | CAAAAAAA others(3): Show |
6 | a0001c0001t0001g0030 a0001c0001t0001g0161 a0001c0001t0001g0186 others(3): Show |
7 | HG01069.hp1 HG01168.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+54_435+63dupTT others(8): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | |||||||
| chr5:40728281 | C | CAAAAAAA others(4): Show |
58 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(55): Show |
93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.435+53_435+63dupTT others(9): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | |||||||
| chr5:40728281 | C | CAAAAAAA others(5): Show |
64 | a0001c0001t0001g0152 a0001c0001t0001g0166 a0001c0001t0001g0179 others(61): Show |
91 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.435+52_435+63dupTT others(10): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | |||||||
| chr5:40728281 | C | CAAAAAAA others(6): Show |
28 | a0001c0001t0002g0007 a0001c0001t0002g0023 a0001c0001t0002g0061 others(25): Show |
36 | HG00597.hp1 HG01106.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.435+51_435+63dupTT others(11): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | |||||||
| chr5:40728281 | C | CAAAAAAA others(7): Show |
75 | a0001c0001t0001g0052 a0001c0001t0002g0001 a0001c0001t0002g0015 others(72): Show |
115 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.435+50_435+63dupTT others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | |||||||
| chr5:40728281 | C | CAAAAAAA others(8): Show |
20 | a0001c0001t0002g0054 a0001c0001t0002g0067 a0001c0001t0002g0068 others(17): Show |
21 | HG00741.hp1 HG01258.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.435+63_435+64insTT others(13): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | |||||||
| chr5:40728281 | C | CAAAAAAA others(9): Show |
3 | a0001c0001t0003g0113 a0001c0001t0006g0040 a0001c0001t0006g0041 |
5 | HG00741.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.435+63_435+64insTT others(14): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | |||||||
| chr5:40728295 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0004g0238 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.435+49_435+50insCT others(11): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728295 | |||||||
| chr5:40728296 | G | T | 1 | a0001c0001t0023g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.435+49C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728296 | |||||||
| chr5:40728591 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0152 a0001c0001t0001g0153 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-115G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40728591 | |||||||
| chr5:40728612 | C | T | 1 | a0001c0001t0030g0056 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.304-136G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40728612 | |||||||
| chr5:40728677 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.304-201C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40728677 | |||||||
| chr5:40728677 | G | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-201C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40728677 | |||||||
| chr5:40729047 | G | C | 1 | a0001c0001t0012g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.304-571C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729047 | |||||||
| chr5:40729099 | G | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(42): Show |
77 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.304-623C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729099 | |||||||
| chr5:40729140 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(42): Show |
77 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.304-664G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729140 | |||||||
| chr5:40729329 | G | T | 1 | a0001c0001t0010g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.304-853C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729329 | |||||||
| chr5:40729340 | T | G | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-864A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729340 | |||||||
| chr5:40729418 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.303+844G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729418 | |||||||
| chr5:40729440 | T | C | 1 | a0001c0001t0007g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.303+822A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729440 | |||||||
| chr5:40729542 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.303+720C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729542 | |||||||
| chr5:40729648 | C | T | 1 | a0001c0001t0010g0083 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.303+614G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729648 | |||||||
| chr5:40729761 | C | A | 2 | a0002c0002t0008g0173 a0002c0002t0008g0174 |
2 | HG00408.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.303+501G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729761 | |||||||
| chr5:40729872 | T | C | 115 | a0001c0001t0001g0052 a0001c0001t0002g0001 a0001c0001t0002g0007 others(112): Show |
162 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.303+390A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729872 | |||||||
| chr5:40729919 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.303+343C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729919 | |||||||
| chr5:40729969 | G | A | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.303+293C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729969 | |||||||
| chr5:40729983 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.303+279C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729983 | |||||||
| chr5:40730024 | C | T | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.303+238G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40730024 | |||||||
| chr5:40730435 | T | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-92A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40730435 | |||||||
| chr5:40730572 | T | A | 2 | a0001c0001t0004g0144 a0001c0001t0004g0145 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.222-229A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40730572 | |||||||
| chr5:40730638 | A | G | 6 | a0001c0001t0004g0219 a0001c0001t0004g0220 a0001c0001t0004g0221 others(3): Show |
6 | NA18946.hp1 NA18956.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-295T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40730638 | |||||||
| chr5:40730979 | A | G | 5 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0158 others(2): Show |
5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.222-636T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40730979 | |||||||
| chr5:40731044 | G | A | 10 | a0001c0001t0005g0005 a0001c0001t0005g0036 a0001c0001t0005g0212 others(7): Show |
18 | HG00597.hp2 HG00735.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.222-701C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731044 | |||||||
| chr5:40731052 | T | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(42): Show |
77 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.222-709A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731052 | |||||||
| chr5:40731072 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(59): Show |
98 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.222-729A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731072 | |||||||
| chr5:40731135 | C | G | 1 | a0001c0001t0002g0060 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.222-792G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731135 | |||||||
| chr5:40731234 | A | T | 13 | a0001c0001t0004g0215 a0001c0001t0005g0005 a0001c0001t0005g0036 others(10): Show |
21 | HG00597.hp2 HG00735.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.222-891T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731234 | |||||||
| chr5:40731367 | TAC | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(194): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.222-1026_222-1025d others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731367 | |||||||
| chr5:40731382 | C | A | 1 | a0001c0001t0005g0243 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.222-1039G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731382 | |||||||
| chr5:40731474 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.222-1131C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731474 | |||||||
| chr5:40731647 | G | A | 2 | a0001c0001t0002g0070 a0001c0001t0002g0139 |
2 | HG02886.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.222-1304C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731647 | |||||||
| chr5:40731647 | G | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-1304C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731647 | |||||||
| chr5:40731796 | C | T | 2 | a0001c0001t0004g0144 a0001c0001t0004g0145 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.222-1453G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731796 | |||||||
| chr5:40732029 | T | A | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.222-1686A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732029 | |||||||
| chr5:40732224 | T | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-1881A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732224 | |||||||
| chr5:40732302 | C | G | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.222-1959G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732302 | |||||||
| chr5:40732327 | C | T | 1 | a0001c0001t0038g0160 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.222-1984G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732327 | |||||||
| chr5:40732381 | G | A | 1 | a0001c0001t0004g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.222-2038C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732381 | |||||||
| chr5:40732395 | T | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-2052A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732395 | |||||||
| chr5:40732556 | A | G | 1 | a0002c0002t0008g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.222-2213T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732556 | |||||||
| chr5:40732611 | A | AT | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.222-2269dupA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732611 | |||||||
| chr5:40732733 | C | T | 4 | a0001c0001t0013g0046 a0001c0001t0013g0047 a0001c0001t0013g0048 others(1): Show |
4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-2390G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732733 | |||||||
| chr5:40732739 | G | A | 1 | a0001c0001t0010g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.222-2396C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732739 | |||||||
| chr5:40733101 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0152 a0001c0001t0001g0153 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-2758G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733101 | |||||||
| chr5:40733104 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(59): Show |
98 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.222-2761A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733104 | |||||||
| chr5:40733223 | T | C | 2 | a0001c0001t0010g0080 a0001c0001t0010g0081 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.222-2880A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733223 | |||||||
| chr5:40733458 | G | C | 1 | a0001c0001t0003g0086 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.222-3115C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733458 | |||||||
| chr5:40733475 | A | C | 2 | a0001c0001t0004g0144 a0001c0001t0004g0145 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.222-3132T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733475 | |||||||
| chr5:40733592 | A | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(189): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.222-3249T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733592 | |||||||
| chr5:40733620 | C | T | 1 | a0001c0001t0004g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.222-3277G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733620 | |||||||
| chr5:40733754 | C | T | 2 | a0001c0001t0010g0080 a0001c0001t0010g0081 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.222-3411G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733754 | |||||||
| chr5:40733810 | C | T | 2 | a0001c0001t0009g0037 a0001c0001t0009g0264 |
3 | HG03098.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.222-3467G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733810 | |||||||
| chr5:40733999 | C | T | 1 | a0001c0001t0037g0051 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.222-3656G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733999 | |||||||
| chr5:40734081 | A | C | 4 | a0001c0001t0013g0046 a0001c0001t0013g0047 a0001c0001t0013g0048 others(1): Show |
4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-3738T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734081 | |||||||
| chr5:40734290 | C | G | 3 | a0001c0001t0010g0083 a0001c0001t0010g0084 a0001c0001t0010g0085 |
3 | HG02647.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.222-3947G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734290 | |||||||
| chr5:40734314 | T | TGAACAGA others(1): Show |
108 | a0001c0001t0001g0052 a0001c0001t0002g0001 a0001c0001t0002g0007 others(105): Show |
155 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.222-3972_222-3971i others(10): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734314 | |||||||
| chr5:40734316 | G | GAACAGAC others(1): Show |
108 | a0001c0001t0001g0052 a0001c0001t0002g0001 a0001c0001t0002g0007 others(105): Show |
155 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.222-3974_222-3973i others(10): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734316 | |||||||
| chr5:40734408 | A | G | 1 | a0001c0001t0010g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.222-4065T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734408 | |||||||
| chr5:40734524 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(59): Show |
98 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.222-4181A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734524 | |||||||
| chr5:40734924 | T | C | 3 | a0001c0001t0010g0083 a0001c0001t0010g0084 a0001c0001t0010g0085 |
3 | HG02647.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.222-4581A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734924 | |||||||
| chr5:40734929 | A | G | 1 | a0002c0002t0008g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.222-4586T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734929 | |||||||
| chr5:40735211 | T | C | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.222-4868A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40735211 | |||||||
| chr5:40735241 | G | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-4898C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40735241 | |||||||
| chr5:40735461 | G | C | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.222-5118C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40735461 | |||||||
| chr5:40735737 | G | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-5394C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40735737 | |||||||
| chr5:40735824 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(56): Show |
95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.222-5481C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40735824 | |||||||
| chr5:40735873 | G | T | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.222-5530C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40735873 | |||||||
| chr5:40736065 | A | G | 1 | a0001c0001t0029g0050 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.222-5722T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736065 | |||||||
| chr5:40736187 | C | A | 1 | a0001c0001t0001g0202 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.222-5844G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736187 | |||||||
| chr5:40736189 | G | A | 26 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0033 others(23): Show |
41 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.222-5846C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736189 | |||||||
| chr5:40736209 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG01358.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.222-5866C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736209 | |||||||
| chr5:40736225 | C | A | 1 | a0001c0001t0012g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.222-5882G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736225 | |||||||
| chr5:40736269 | C | T | 1 | a0001c0001t0027g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.222-5926G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736269 | |||||||
| chr5:40736702 | A | G | 2 | a0001c0001t0016g0020 a0001c0001t0016g0094 |
3 | HG02083.hp1 NA18946.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.222-6359T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736702 | |||||||
| chr5:40736759 | T | G | 1 | a0001c0001t0003g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.222-6416A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736759 | |||||||
| chr5:40736802 | C | T | 1 | a0001c0001t0005g0239 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.222-6459G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736802 | |||||||
| chr5:40736885 | ATACTCAC others(11): Show |
A | 1 | a0001c0001t0006g0262 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.222-6560_222-6543d others(20): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736885 | |||||||
| chr5:40737087 | G | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0152 a0001c0001t0001g0153 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-6744C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737087 | |||||||
| chr5:40737098 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(257): Show |
376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.222-6755A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737098 | |||||||
| chr5:40737147 | A | G | 3 | a0001c0001t0004g0220 a0001c0001t0004g0235 a0001c0001t0004g0238 |
3 | NA18956.hp2 NA18957.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.222-6804T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737147 | |||||||
| chr5:40737226 | A | G | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-6883T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737226 | |||||||
| chr5:40737234 | T | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-6891A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737234 | |||||||
| chr5:40737329 | C | T | 2 | a0001c0001t0012g0156 a0001c0001t0012g0157 |
2 | HG01192.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.222-6986G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737329 | |||||||
| chr5:40737522 | C | T | 1 | a0001c0001t0006g0263 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.222-7179G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737522 | |||||||
| chr5:40737600 | A | G | 2 | a0001c0001t0004g0216 a0001c0001t0004g0217 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.222-7257T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737600 | |||||||
| chr5:40737680 | A | G | 1 | a0001c0001t0013g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.222-7337T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737680 | |||||||
| chr5:40737853 | G | C | 4 | a0001c0001t0002g0079 a0001c0001t0002g0120 a0001c0001t0002g0123 others(1): Show |
4 | HG02109.hp1 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-7510C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737853 | |||||||
| chr5:40737921 | G | A | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.222-7578C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737921 | |||||||
| chr5:40738237 | C | A | 1 | a0001c0001t0007g0260 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.222-7894G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738237 | |||||||
| chr5:40738283 | G | A | 1 | a0001c0001t0006g0263 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.222-7940C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738283 | |||||||
| chr5:40738284 | C | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(42): Show |
77 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.222-7941G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738284 | |||||||
| chr5:40738291 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0161 others(6): Show |
12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.222-7948C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738291 | |||||||
| chr5:40738323 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.222-7980C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738323 | |||||||
| chr5:40738378 | G | A | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(198): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.222-8035C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738378 | |||||||
| chr5:40738426 | A | T | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-8083T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738426 | |||||||
| chr5:40738432 | AAATATAA others(90): Show |
A | 1 | a0001c0001t0015g0270 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.222-8186_222-8090d others(99): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738432 | |||||||
| chr5:40738432 | AAATATAA others(100): Show |
A | 4 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(1): Show |
6 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-8196_222-8090d others(2): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738432 | |||||||
| chr5:40738435 | T | C | 1 | a0001c0001t0004g0006 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.222-8092A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738435 | |||||||
| chr5:40738435 | TATAAA | T | 27 | a0001c0001t0001g0017 a0001c0001t0001g0031 a0001c0001t0001g0190 others(24): Show |
30 | HG01099.hp2 HG01123.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.222-8097_222-8093d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738435 | |||||||
| chr5:40738439 | AAATAAAA others(3): Show |
A | 61 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0181 others(58): Show |
81 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.222-8106_222-8097d others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738439 | |||||||
| chr5:40738439 | AAATAAAA others(8): Show |
A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(47): Show |
69 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.222-8111_222-8097d others(17): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738439 | |||||||
| chr5:40738439 | AAATAAAA others(13): Show |
A | 25 | a0001c0001t0001g0004 a0001c0001t0001g0206 a0001c0001t0001g0207 others(22): Show |
27 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.222-8116_222-8097d others(22): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738439 | |||||||
| chr5:40738439 | AAATAAAA others(18): Show |
A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0027 others(23): Show |
36 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.222-8121_222-8097d others(27): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738439 | |||||||
| chr5:40738439 | AAATAAAA others(23): Show |
A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0187 others(2): Show |
9 | HG01257.hp1 HG01496.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.222-8126_222-8097d others(32): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738439 | |||||||
| chr5:40738444 | A | AAATAC | 11 | a0001c0001t0004g0247 a0001c0001t0004g0248 a0001c0001t0006g0013 others(8): Show |
12 | HG00733.hp2 HG01433.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.222-8106_222-8102d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738444 | |||||||
| chr5:40738444 | A | AAATACAA others(3): Show |
2 | a0001c0001t0006g0253 a0001c0001t0007g0267 |
2 | HG03453.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.222-8111_222-8102d others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738444 | |||||||
| chr5:40738444 | A | C | 9 | a0001c0001t0001g0002 a0001c0001t0002g0001 a0001c0001t0002g0054 others(6): Show |
11 | HG01074.hp2 HG01081.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.222-8101T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738444 | |||||||
| chr5:40738444 | AAATAC | A | 22 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0155 others(19): Show |
26 | HG00735.hp2 HG01074.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.222-8106_222-8102d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738444 | |||||||
| chr5:40738444 | AAATACAA others(3): Show |
A | 7 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0005g0005 others(4): Show |
11 | HG00741.hp2 HG01261.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.222-8111_222-8102d others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738444 | |||||||
| chr5:40738444 | AAATACAA others(13): Show |
A | 4 | a0001c0001t0013g0046 a0001c0001t0013g0047 a0001c0001t0013g0048 others(1): Show |
4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-8121_222-8102d others(22): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738444 | |||||||
| chr5:40738454 | C | A | 2 | a0001c0001t0010g0080 a0001c0001t0010g0081 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.222-8111G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738454 | |||||||
| chr5:40738484 | C | A | 3 | a0001c0001t0012g0157 a0001c0001t0012g0158 a0001c0001t0012g0170 |
3 | HG02280.hp1 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.222-8141G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738484 | |||||||
| chr5:40738489 | C | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0154 |
2 | HG01243.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.222-8146G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738489 | |||||||
| chr5:40738489 | C | CAATAAAA others(3): Show |
1 | a0001c0001t0004g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.222-8147_222-8146i others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738489 | |||||||
| chr5:40738494 | C | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0026 others(11): Show |
16 | HG00099.hp1 HG01167.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.222-8151G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738494 | |||||||
| chr5:40738499 | C | A | 16 | a0001c0001t0001g0011 a0001c0001t0001g0152 a0001c0001t0001g0154 others(13): Show |
17 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.222-8156G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738499 | |||||||
| chr5:40738504 | C | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0152 others(7): Show |
14 | HG00099.hp1 HG01167.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.222-8161G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738504 | |||||||
| chr5:40738509 | A | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0152 a0001c0001t0001g0154 others(9): Show |
15 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.222-8166T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738509 | |||||||
| chr5:40738514 | C | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0152 a0001c0001t0001g0154 others(12): Show |
18 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.222-8171G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738514 | |||||||
| chr5:40738514 | CAATAA | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0161 a0003c0003t0001g0162 |
4 | HG00099.hp1 HG01168.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-8176_222-8172d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738514 | |||||||
| chr5:40738519 | A | AAATAAAA others(3): Show |
6 | a0001c0001t0002g0015 a0001c0001t0002g0023 a0001c0001t0002g0025 others(3): Show |
8 | HG01109.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.222-8186_222-8177d others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738519 | |||||||
| chr5:40738519 | A | C | 16 | a0001c0001t0001g0011 a0001c0001t0001g0152 a0001c0001t0001g0154 others(13): Show |
17 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.222-8176T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738519 | |||||||
| chr5:40738524 | A | C | 11 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0155 others(8): Show |
14 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.222-8181T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738524 | |||||||
| chr5:40738529 | C | A | 16 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0155 others(13): Show |
19 | HG01070.hp1 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.222-8186G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738529 | |||||||
| chr5:40738534 | A | C | 8 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0155 others(5): Show |
11 | HG01070.hp1 HG01071.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.222-8191T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738534 | |||||||
| chr5:40738539 | C | A | 26 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0152 others(23): Show |
32 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.222-8196G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | |||||||
| chr5:40738539 | C | CAATAA | 4 | a0001c0001t0004g0216 a0001c0001t0004g0247 a0001c0001t0004g0248 others(1): Show |
4 | HG02486.hp2 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-8201_222-8197d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | |||||||
| chr5:40738539 | C | CAATAAAA others(3): Show |
5 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(2): Show |
7 | NA18966.hp1 NA18966.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-8206_222-8197d others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | |||||||
| chr5:40738539 | C | CAATAAAA others(8): Show |
14 | a0001c0001t0002g0015 a0001c0001t0002g0119 a0001c0001t0002g0126 others(11): Show |
17 | HG00280.hp1 HG00741.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.222-8197_222-8196i others(17): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | |||||||
| chr5:40738539 | C | CAATAAAA others(13): Show |
65 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0031 others(62): Show |
92 | HG00099.hp2 HG00408.hp1 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.222-8197_222-8196i others(22): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | |||||||
| chr5:40738539 | C | CAATAAAA others(18): Show |
26 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(23): Show |
39 | HG00423.hp1 HG00673.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.222-8197_222-8196i others(27): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | |||||||
| chr5:40738539 | C | CAATAAAA others(23): Show |
7 | a0001c0001t0001g0250 a0001c0001t0002g0001 a0001c0001t0002g0071 others(4): Show |
10 | HG02602.hp1 HG03579.hp1 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.222-8197_222-8196i others(32): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | |||||||
| chr5:40738539 | C | CAATAAAA others(23): Show |
2 | a0001c0001t0001g0052 a0001c0001t0018g0097 |
2 | NA19059.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.222-8197_222-8196i others(32): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | |||||||
| chr5:40738539 | CAATAA | C | 3 | a0001c0001t0004g0033 a0001c0001t0004g0034 a0001c0001t0004g0233 |
5 | HG01099.hp1 HG03017.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.222-8201_222-8197d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | |||||||
| chr5:40738539 | CAATAAAA others(3): Show |
C | 1 | a0001c0001t0026g0246 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.222-8206_222-8197d others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | |||||||
| chr5:40738539 | CAATAAAA others(8): Show |
C | 17 | a0001c0001t0004g0006 a0001c0001t0004g0035 a0001c0001t0004g0218 others(14): Show |
25 | HG00558.hp2 HG02129.hp1 HG02165.hp2 others(22): Show |
intron_variant | MODIFIER | c.222-8211_222-8197d others(17): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | |||||||
| chr5:40738544 | A | C | 4 | a0001c0001t0004g0217 a0001c0001t0004g0230 a0001c0001t0004g0231 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-8201T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738544 | |||||||
| chr5:40738549 | A | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(40): Show |
66 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.222-8206T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738549 | |||||||
| chr5:40738559 | A | T | 1 | a0001c0001t0001g0165 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.222-8216T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738559 | |||||||
| chr5:40738562 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.222-8219A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738562 | |||||||
| chr5:40738564 | A | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0152 others(11): Show |
18 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.222-8221T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738564 | |||||||
| chr5:40738564 | AAAT | A | 2 | a0001c0001t0011g0014 a0001c0001t0011g0045 |
4 | HG02976.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-8224_222-8222d others(5): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738564 | |||||||
| chr5:40738567 | T | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0152 others(16): Show |
23 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.222-8224A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAA others(1): Show |
3 | a0001c0001t0003g0091 a0001c0001t0003g0092 a0001c0001t0003g0093 |
3 | HG01074.hp2 NA18948.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.222-8225_222-8224i others(10): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAA others(8): Show |
2 | a0001c0001t0010g0080 a0001c0001t0010g0081 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.222-8225_222-8224i others(17): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAA others(13): Show |
1 | a0001c0001t0010g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.222-8225_222-8224i others(22): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAA others(6): Show |
3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.222-8225_222-8224i others(15): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAA others(11): Show |
1 | a0001c0001t0002g0121 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.222-8225_222-8224i others(20): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAA others(23): Show |
3 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0030g0056 |
3 | HG02071.hp2 NA18960.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.222-8225_222-8224i others(32): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAA others(33): Show |
1 | a0001c0001t0001g0012 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.222-8225_222-8224i others(42): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAA others(18): Show |
8 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0190 others(5): Show |
8 | HG01175.hp2 HG02683.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.222-8225_222-8224i others(27): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAA others(23): Show |
20 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0030 others(17): Show |
36 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.222-8225_222-8224i others(32): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAA others(28): Show |
6 | a0001c0001t0001g0012 a0001c0001t0001g0180 a0001c0001t0001g0181 others(3): Show |
8 | HG00408.hp2 HG02080.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.222-8225_222-8224i others(37): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAA others(33): Show |
1 | a0001c0001t0001g0183 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.222-8225_222-8224i others(42): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAA others(13): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0002g0077 |
3 | HG00323.hp1 HG02293.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.222-8225_222-8224i others(22): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAA others(18): Show |
2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG01358.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.222-8225_222-8224i others(27): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAA others(8): Show |
3 | a0001c0001t0013g0046 a0001c0001t0013g0047 a0001c0001t0013g0048 |
3 | HG02572.hp1 HG02895.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.222-8225_222-8224i others(17): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAT others(3): Show |
1 | a0001c0001t0013g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.222-8225_222-8224i others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAT others(8): Show |
1 | a0001c0001t0012g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.222-8225_222-8224i others(17): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738567 | T | TAAAATAT others(13): Show |
1 | a0001c0001t0023g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.222-8225_222-8224i others(22): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | |||||||
| chr5:40738569 | T | A | 69 | a0001c0001t0001g0052 a0001c0001t0002g0007 a0001c0001t0002g0015 others(66): Show |
98 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.222-8226A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738569 | |||||||
| chr5:40738572 | A | AAT | 8 | a0001c0001t0002g0121 a0001c0001t0003g0091 a0001c0001t0003g0092 others(5): Show |
8 | HG01074.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.221+8224_221+8225d others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738572 | |||||||
| chr5:40738572 | A | AATAAAAT others(5): Show |
2 | a0001c0001t0010g0083 a0001c0001t0010g0084 |
2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.221+8214_221+8225d others(14): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738572 | |||||||
| chr5:40738572 | A | T | 69 | a0001c0001t0001g0052 a0001c0001t0002g0007 a0001c0001t0002g0015 others(66): Show |
98 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.221+8226T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738572 | |||||||
| chr5:40738669 | T | C | 3 | a0001c0001t0010g0083 a0001c0001t0010g0084 a0001c0001t0010g0085 |
3 | HG02647.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.221+8129A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738669 | |||||||
| chr5:40738838 | T | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(56): Show |
95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.221+7960A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738838 | |||||||
| chr5:40738911 | C | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | NA18983.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.221+7887G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738911 | |||||||
| chr5:40738929 | T | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+7869A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738929 | |||||||
| chr5:40739007 | T | C | 1 | a0002c0002t0008g0174 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.221+7791A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739007 | |||||||
| chr5:40739137 | A | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(198): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.221+7661T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739137 | |||||||
| chr5:40739159 | C | T | 115 | a0001c0001t0001g0052 a0001c0001t0002g0001 a0001c0001t0002g0007 others(112): Show |
162 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.221+7639G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739159 | |||||||
| chr5:40739212 | T | A | 1 | a0002c0002t0008g0174 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.221+7586A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739212 | |||||||
| chr5:40739333 | T | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+7465A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739333 | |||||||
| chr5:40739602 | T | C | 1 | a0001c0001t0004g0233 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.221+7196A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739602 | |||||||
| chr5:40739610 | G | A | 1 | a0001c0001t0006g0252 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.221+7188C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739610 | |||||||
| chr5:40739921 | A | C | 5 | a0001c0001t0001g0026 a0001c0001t0001g0152 a0001c0001t0001g0153 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.221+6877T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739921 | |||||||
| chr5:40739936 | C | CT | 6 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(3): Show |
8 | HG00597.hp1 HG02015.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.221+6861dupA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739936 | |||||||
| chr5:40739943 | T | TA | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+6854_221+6855i others(3): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739943 | |||||||
| chr5:40739944 | T | A | 87 | a0001c0001t0001g0052 a0001c0001t0002g0007 a0001c0001t0002g0025 others(84): Show |
122 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.221+6854A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739944 | |||||||
| chr5:40740152 | T | C | 1 | a0001c0001t0037g0051 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.221+6646A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740152 | |||||||
| chr5:40740601 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.221+6197G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740601 | |||||||
| chr5:40740716 | C | T | 1 | a0001c0001t0002g0148 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.221+6082G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740716 | |||||||
| chr5:40740759 | T | C | 1 | a0001c0001t0002g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.221+6039A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740759 | |||||||
| chr5:40740784 | C | T | 1 | a0001c0001t0002g0053 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.221+6014G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740784 | |||||||
| chr5:40740909 | G | A | 2 | a0001c0001t0006g0042 a0001c0001t0006g0262 |
3 | HG01256.hp2 HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.221+5889C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740909 | |||||||
| chr5:40740997 | A | G | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.221+5801T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740997 | |||||||
| chr5:40740998 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.221+5800C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740998 | |||||||
| chr5:40741021 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(198): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.221+5777G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741021 | |||||||
| chr5:40741406 | C | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(242): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.221+5392G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741406 | |||||||
| chr5:40741522 | T | C | 1 | a0001c0001t0004g0235 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.221+5276A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741522 | |||||||
| chr5:40741595 | C | CCAACTGC others(8): Show |
1 | a0001c0001t0006g0263 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5202_221+5203i others(17): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741595 | |||||||
| chr5:40741596 | A | C | 1 | a0001c0001t0006g0263 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5202T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741596 | |||||||
| chr5:40741603 | A | T | 1 | a0001c0001t0006g0263 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5195T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741603 | |||||||
| chr5:40741609 | C | A | 1 | a0001c0001t0006g0263 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5189G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741609 | |||||||
| chr5:40741614 | C | G | 1 | a0001c0001t0006g0263 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5184G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741614 | |||||||
| chr5:40741618 | A | G | 1 | a0001c0001t0006g0263 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5180T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741618 | |||||||
| chr5:40741620 | G | C | 1 | a0001c0001t0006g0263 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5178C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741620 | |||||||
| chr5:40741620 | G | T | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.221+5178C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741620 | |||||||
| chr5:40741631 | A | T | 2 | a0001c0001t0003g0089 a0001c0001t0003g0090 |
2 | NA18952.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.221+5167T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741631 | |||||||
| chr5:40741648 | T | G | 1 | a0001c0001t0006g0263 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5150A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741648 | |||||||
| chr5:40741661 | T | G | 1 | a0001c0001t0006g0263 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5137A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741661 | |||||||
| chr5:40741702 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0161 others(6): Show |
12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+5096T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741702 | |||||||
| chr5:40741713 | G | A | 1 | a0001c0001t0009g0043 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.221+5085C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741713 | |||||||
| chr5:40741743 | C | A | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+5055G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741743 | |||||||
| chr5:40741890 | G | A | 1 | a0001c0001t0009g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.221+4908C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741890 | |||||||
| chr5:40741904 | G | A | 2 | a0001c0001t0002g0134 a0001c0001t0002g0135 |
2 | HG01123.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.221+4894C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741904 | |||||||
| chr5:40741977 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.221+4821C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741977 | |||||||
| chr5:40742201 | C | T | 1 | a0001c0001t0010g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.221+4597G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742201 | |||||||
| chr5:40742336 | T | C | 5 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0207 others(2): Show |
5 | HG00735.hp1 HG01175.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+4462A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742336 | |||||||
| chr5:40742363 | C | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(56): Show |
95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.221+4435G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742363 | |||||||
| chr5:40742420 | A | G | 1 | a0001c0001t0037g0051 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.221+4378T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742420 | |||||||
| chr5:40742440 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(198): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.221+4358G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742440 | |||||||
| chr5:40742547 | G | GC | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+4250dupG | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742547 | |||||||
| chr5:40742678 | T | A | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+4120A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742678 | |||||||
| chr5:40742759 | G | C | 2 | a0001c0001t0004g0144 a0001c0001t0004g0145 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.221+4039C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742759 | |||||||
| chr5:40742910 | G | A | 1 | a0001c0001t0007g0265 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.221+3888C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742910 | |||||||
| chr5:40742959 | G | A | 120 | a0001c0001t0001g0052 a0001c0001t0002g0001 a0001c0001t0002g0007 others(117): Show |
169 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.221+3839C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742959 | |||||||
| chr5:40742969 | T | C | 1 | a0001c0001t0007g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.221+3829A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742969 | |||||||
| chr5:40742992 | G | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+3806C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742992 | |||||||
| chr5:40743129 | C | A | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+3669G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743129 | |||||||
| chr5:40743229 | A | G | 1 | a0001c0001t0011g0045 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.221+3569T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743229 | |||||||
| chr5:40743237 | T | C | 2 | a0001c0001t0004g0035 a0001c0001t0004g0249 |
3 | NA18954.hp1 NA18968.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.221+3561A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743237 | |||||||
| chr5:40743415 | A | G | 15 | a0001c0001t0002g0015 a0001c0001t0002g0023 a0001c0001t0002g0119 others(12): Show |
18 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.221+3383T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743415 | |||||||
| chr5:40743575 | C | T | 1 | a0001c0001t0004g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.221+3223G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743575 | |||||||
| chr5:40743623 | A | C | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.221+3175T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743623 | |||||||
| chr5:40743852 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(194): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.221+2946A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743852 | |||||||
| chr5:40743870 | T | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(56): Show |
95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.221+2928A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743870 | |||||||
| chr5:40743884 | T | A | 1 | a0001c0001t0004g0238 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.221+2914A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743884 | |||||||
| chr5:40743936 | C | A | 1 | a0001c0001t0004g0238 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.221+2862G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743936 | |||||||
| chr5:40743936 | C | T | 92 | a0001c0001t0001g0052 a0001c0001t0002g0001 a0001c0001t0002g0007 others(89): Show |
133 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.221+2862G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743936 | |||||||
| chr5:40743937 | A | G | 1 | a0001c0001t0004g0238 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.221+2861T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743937 | |||||||
| chr5:40743956 | T | C | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.221+2842A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743956 | |||||||
| chr5:40743972 | T | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0152 a0001c0001t0001g0153 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.221+2826A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743972 | |||||||
| chr5:40744083 | G | A | 3 | a0001c0001t0010g0080 a0001c0001t0010g0081 a0001c0001t0037g0051 |
3 | HG02257.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.221+2715C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40744083 | |||||||
| chr5:40744259 | TAGTTA | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
8 | HG02155.hp2 NA18942.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.221+2534_221+2538d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40744259 | |||||||
| chr5:40744299 | C | T | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.221+2499G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40744299 | |||||||
| chr5:40744487 | G | GT | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
215 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.221+2310dupA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40744487 | |||||||
| chr5:40744487 | G | GTT | 112 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0052 others(109): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.221+2309_221+2310d others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40744487 | |||||||
| chr5:40744487 | G | GTTT | 8 | a0001c0001t0001g0152 a0001c0001t0001g0159 a0001c0001t0002g0120 others(5): Show |
8 | HG00642.hp1 HG01256.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.221+2308_221+2310d others(5): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40744487 | |||||||
| chr5:40744892 | C | A | 4 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0158 others(1): Show |
4 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+1906G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40744892 | |||||||
| chr5:40745105 | G | A | 1 | a0001c0001t0006g0255 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.221+1693C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745105 | |||||||
| chr5:40745231 | C | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(56): Show |
95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.221+1567G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745231 | |||||||
| chr5:40745298 | ATATGT | A | 54 | a0001c0001t0001g0052 a0001c0001t0002g0007 a0001c0001t0002g0025 others(51): Show |
77 | HG00099.hp2 HG00408.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.221+1495_221+1499d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745298 | |||||||
| chr5:40745318 | T | C | 1 | a0001c0001t0002g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.221+1480A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745318 | |||||||
| chr5:40745357 | T | C | 5 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0158 others(2): Show |
5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.221+1441A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745357 | |||||||
| chr5:40745566 | C | A | 1 | a0001c0001t0002g0148 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.221+1232G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745566 | |||||||
| chr5:40745644 | C | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0161 others(6): Show |
12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+1154G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745644 | |||||||
| chr5:40745657 | G | A | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+1141C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745657 | |||||||
| chr5:40745714 | A | C | 4 | a0001c0001t0013g0046 a0001c0001t0013g0047 a0001c0001t0013g0048 others(1): Show |
4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+1084T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745714 | |||||||
| chr5:40745810 | C | G | 4 | a0001c0001t0006g0252 a0001c0001t0006g0253 a0001c0001t0006g0254 others(1): Show |
4 | HG00733.hp2 HG01109.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+988G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745810 | |||||||
| chr5:40745843 | T | C | 1 | a0001c0001t0031g0271 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.221+955A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745843 | |||||||
| chr5:40746001 | TGC | T | 3 | a0001c0001t0015g0268 a0001c0001t0015g0269 a0001c0001t0015g0270 |
3 | HG02280.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.221+795_221+796del others(2): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40746001 | |||||||
| chr5:40746002 | G | A | 189 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(186): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.221+796C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40746002 | |||||||
| chr5:40746005 | T | C | 3 | a0001c0001t0015g0268 a0001c0001t0015g0269 a0001c0001t0015g0270 |
3 | HG02280.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.221+793A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40746005 | |||||||
| chr5:40746066 | T | C | 4 | a0002c0002t0008g0016 a0002c0002t0008g0175 a0002c0002t0008g0176 others(1): Show |
6 | HG00597.hp1 HG02040.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.221+732A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40746066 | |||||||
| chr5:40746213 | A | AAAAGTAA others(58): Show |
1 | a0001c0001t0031g0271 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.221+520_221+584dup others(65): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40746213 | |||||||
| chr5:40746439 | T | C | 1 | a0001c0001t0012g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.221+359A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40746439 | |||||||
| chr5:40746783 | A | T | 108 | a0001c0001t0001g0052 a0001c0001t0002g0001 a0001c0001t0002g0007 others(105): Show |
155 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.221+15T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40746783 | |||||||
| chr5:40747063 | T | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-44A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747063 | |||||||
| chr5:40747169 | T | G | 3 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0158 |
3 | HG01192.hp1 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-1-150A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747169 | |||||||
| chr5:40747354 | G | A | 13 | a0001c0001t0004g0215 a0001c0001t0005g0005 a0001c0001t0005g0036 others(10): Show |
21 | HG00597.hp2 HG00735.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.-1-335C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747354 | |||||||
| chr5:40747442 | A | G | 5 | a0001c0001t0001g0026 a0001c0001t0001g0152 a0001c0001t0001g0153 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-423T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747442 | |||||||
| chr5:40747508 | A | G | 5 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0158 others(2): Show |
5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-489T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747508 | |||||||
| chr5:40747514 | C | A | 1 | a0001c0001t0004g0238 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-1-495G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747514 | |||||||
| chr5:40747594 | A | G | 1 | a0001c0001t0010g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-1-575T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747594 | |||||||
| chr5:40747670 | G | A | 1 | a0001c0001t0002g0076 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-1-651C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747670 | |||||||
| chr5:40747830 | CT | C | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-812delA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747830 | |||||||
| chr5:40747855 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(194): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.-1-836A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747855 | |||||||
| chr5:40747878 | T | G | 1 | a0001c0001t0001g0210 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-1-859A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747878 | |||||||
| chr5:40747897 | A | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(189): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.-1-878T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747897 | |||||||
| chr5:40748070 | G | A | 3 | a0001c0001t0005g0036 a0001c0001t0005g0244 a0001c0001t0005g0245 |
4 | NA18989.hp2 NA18998.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-1051C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748070 | |||||||
| chr5:40748107 | G | A | 1 | a0001c0001t0004g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-1-1088C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748107 | |||||||
| chr5:40748166 | G | A | 120 | a0001c0001t0001g0052 a0001c0001t0002g0001 a0001c0001t0002g0007 others(117): Show |
167 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.-1-1147C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748166 | |||||||
| chr5:40748252 | A | G | 5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(2): Show |
8 | HG03017.hp1 HG03490.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-1233T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748252 | |||||||
| chr5:40748266 | G | A | 11 | a0001c0001t0005g0005 a0001c0001t0005g0036 a0001c0001t0005g0212 others(8): Show |
19 | HG00597.hp2 HG00735.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-1247C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748266 | |||||||
| chr5:40748575 | T | C | 1 | a0001c0001t0002g0073 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-1-1556A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748575 | |||||||
| chr5:40748628 | C | T | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-1609G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748628 | |||||||
| chr5:40748866 | G | A | 120 | a0001c0001t0001g0052 a0001c0001t0002g0001 a0001c0001t0002g0007 others(117): Show |
167 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.-1-1847C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748866 | |||||||
| chr5:40748873 | G | A | 2 | a0001c0001t0010g0080 a0001c0001t0010g0081 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-1-1854C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748873 | |||||||
| chr5:40748960 | T | C | 1 | a0001c0001t0023g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-1-1941A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748960 | |||||||
| chr5:40749050 | C | T | 3 | a0001c0001t0017g0167 a0001c0001t0017g0168 a0001c0001t0017g0169 |
3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-1-2031G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40749050 | |||||||
| chr5:40749113 | A | C | 1 | a0001c0001t0003g0087 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-1-2094T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40749113 | |||||||
| chr5:40749429 | TC | T | 5 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0158 others(2): Show |
5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-2411delG | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40749429 | |||||||
| chr5:40749547 | G | A | 1 | a0001c0001t0003g0116 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-1-2528C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40749547 | |||||||
| chr5:40749599 | T | C | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-2580A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40749599 | |||||||
| chr5:40749681 | G | C | 6 | a0001c0001t0002g0079 a0001c0001t0002g0120 a0001c0001t0002g0121 others(3): Show |
6 | HG02109.hp1 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-2662C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40749681 | |||||||
| chr5:40749731 | A | G | 1 | a0001c0001t0013g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-1-2712T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40749731 | |||||||
| chr5:40750020 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(191): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-1-3001T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750020 | |||||||
| chr5:40750084 | T | C | 1 | a0001c0001t0022g0117 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-1-3065A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750084 | |||||||
| chr5:40750087 | C | CA | 11 | a0001c0001t0004g0216 a0001c0001t0004g0217 a0001c0001t0004g0247 others(8): Show |
11 | HG01192.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-3069dupT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750087 | |||||||
| chr5:40750087 | CA | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(178): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-1-3069delT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750087 | |||||||
| chr5:40750087 | CAA | C | 7 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0011g0014 others(4): Show |
9 | HG01258.hp2 HG02280.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-3070_-1-3069del others(2): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750087 | |||||||
| chr5:40750143 | C | T | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-3124G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750143 | |||||||
| chr5:40750174 | C | G | 1 | a0001c0001t0003g0118 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-1-3155G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750174 | |||||||
| chr5:40750323 | A | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(198): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.-1-3304T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750323 | |||||||
| chr5:40750360 | A | C | 2 | a0001c0001t0004g0216 a0001c0001t0004g0217 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-1-3341T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750360 | |||||||
| chr5:40750386 | T | C | 2 | a0001c0001t0004g0144 a0001c0001t0004g0145 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1-3367A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750386 | |||||||
| chr5:40750419 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-3400C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750419 | |||||||
| chr5:40750421 | G | A | 1 | a0001c0001t0003g0086 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-1-3402C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750421 | |||||||
| chr5:40750438 | G | C | 1 | a0001c0001t0022g0117 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-1-3419C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750438 | |||||||
| chr5:40750540 | T | A | 1 | a0001c0001t0001g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1-3521A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750540 | |||||||
| chr5:40750767 | T | A | 1 | a0001c0001t0002g0142 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-1-3748A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750767 | |||||||
| chr5:40751165 | G | A | 5 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0158 others(2): Show |
5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-4146C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751165 | |||||||
| chr5:40751235 | GA | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0161 others(6): Show |
12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-4217delT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751235 | |||||||
| chr5:40751241 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0161 others(6): Show |
12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-4222T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751241 | |||||||
| chr5:40751516 | T | C | 1 | a0001c0001t0004g0251 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-2+4308A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751516 | |||||||
| chr5:40751632 | T | C | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+4192A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751632 | |||||||
| chr5:40751650 | C | T | 1 | a0001c0001t0004g0219 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-2+4174G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751650 | |||||||
| chr5:40751730 | G | A | 28 | a0001c0001t0003g0022 a0001c0001t0003g0118 a0001c0001t0006g0013 others(25): Show |
39 | HG00733.hp2 HG00741.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-2+4094C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751730 | |||||||
| chr5:40751768 | C | T | 6 | a0001c0001t0002g0079 a0001c0001t0002g0120 a0001c0001t0002g0121 others(3): Show |
6 | HG02109.hp1 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+4056G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751768 | |||||||
| chr5:40751818 | G | T | 1 | a0001c0001t0002g0119 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-2+4006C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751818 | |||||||
| chr5:40751838 | T | C | 1 | a0001c0001t0020g0044 | 2 | NA18994.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-2+3986A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751838 | |||||||
| chr5:40751961 | GA | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(194): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.-2+3862delT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751961 | |||||||
| chr5:40752067 | C | T | 5 | a0001c0001t0012g0156 a0001c0001t0012g0157 a0001c0001t0012g0158 others(2): Show |
5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+3757G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752067 | |||||||
| chr5:40752156 | A | G | 5 | a0001c0001t0001g0026 a0001c0001t0001g0152 a0001c0001t0001g0153 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+3668T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752156 | |||||||
| chr5:40752198 | G | T | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2+3626C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752198 | |||||||
| chr5:40752434 | A | G | 115 | a0001c0001t0001g0052 a0001c0001t0002g0001 a0001c0001t0002g0007 others(112): Show |
162 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.-2+3390T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752434 | |||||||
| chr5:40752572 | G | A | 1 | a0001c0001t0010g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-2+3252C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752572 | |||||||
| chr5:40752590 | T | C | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+3234A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752590 | |||||||
| chr5:40752663 | T | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(197): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.-2+3161A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752663 | |||||||
| chr5:40752707 | A | G | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+3117T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752707 | |||||||
| chr5:40752732 | C | A | 1 | a0001c0001t0002g0077 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-2+3092G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752732 | |||||||
| chr5:40752792 | T | C | 1 | a0001c0001t0012g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2+3032A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752792 | |||||||
| chr5:40752859 | C | T | 1 | a0001c0001t0003g0086 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-2+2965G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752859 | |||||||
| chr5:40752876 | G | A | 3 | a0001c0001t0010g0083 a0001c0001t0010g0084 a0001c0001t0010g0085 |
3 | HG02647.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-2+2948C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752876 | |||||||
| chr5:40753139 | C | T | 1 | a0001c0001t0004g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-2+2685G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753139 | |||||||
| chr5:40753149 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-2+2675C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753149 | |||||||
| chr5:40753193 | C | G | 1 | a0001c0001t0031g0271 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-2+2631G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753193 | |||||||
| chr5:40753315 | G | A | 8 | a0002c0002t0008g0016 a0002c0002t0008g0171 a0002c0002t0008g0172 others(5): Show |
10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+2509C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753315 | |||||||
| chr5:40753372 | A | AAAAG | 45 | a0001c0001t0001g0052 a0001c0001t0003g0003 a0001c0001t0003g0009 others(42): Show |
61 | HG00099.hp2 HG00408.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.-2+2448_-2+2451dup others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753372 | |||||||
| chr5:40753509 | T | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(41): Show |
76 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.-2+2315A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753509 | |||||||
| chr5:40753775 | G | A | 34 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(31): Show |
52 | HG00423.hp1 HG00673.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.-2+2049C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753775 | |||||||
| chr5:40753883 | C | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(197): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.-2+1941G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753883 | |||||||
| chr5:40753917 | G | A | 1 | a0001c0001t0023g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-2+1907C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753917 | |||||||
| chr5:40753919 | A | T | 1 | a0001c0001t0023g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-2+1905T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753919 | |||||||
| chr5:40753929 | A | C | 8 | a0001c0001t0002g0079 a0001c0001t0010g0080 a0001c0001t0010g0081 others(5): Show |
8 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+1895T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753929 | |||||||
| chr5:40754119 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(41): Show |
76 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.-2+1705C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754119 | |||||||
| chr5:40754127 | A | G | 34 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(31): Show |
52 | HG00423.hp1 HG00673.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.-2+1697T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754127 | |||||||
| chr5:40754190 | C | T | 1 | a0001c0001t0005g0213 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-2+1634G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754190 | |||||||
| chr5:40754298 | GAGACAAA others(14): Show |
G | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2+1505_-2+1525del others(21): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754298 | |||||||
| chr5:40754585 | A | AAGGCCTG others(11): Show |
1 | a0001c0001t0001g0052 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-2+1238_-2+1239ins others(18): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754585 | |||||||
| chr5:40754593 | A | C | 1 | a0001c0001t0001g0052 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-2+1231T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754593 | |||||||
| chr5:40754602 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-2+1222A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754602 | |||||||
| chr5:40754614 | G | T | 1 | a0001c0001t0001g0052 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-2+1210C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754614 | |||||||
| chr5:40754778 | C | G | 4 | a0001c0001t0013g0046 a0001c0001t0013g0047 a0001c0001t0013g0048 others(1): Show |
4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+1046G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754778 | |||||||
| chr5:40754797 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-2+1027G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754797 | |||||||
| chr5:40754919 | T | C | 2 | a0001c0001t0003g0146 a0001c0001t0003g0147 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-2+905A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754919 | |||||||
| chr5:40755014 | A | G | 1 | a0001c0001t0005g0212 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-2+810T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755014 | |||||||
| chr5:40755108 | T | C | 1 | a0001c0001t0007g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-2+716A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755108 | |||||||
| chr5:40755178 | G | T | 199 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(196): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-2+646C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755178 | |||||||
| chr5:40755412 | T | C | 5 | a0001c0001t0011g0014 a0001c0001t0011g0045 a0001c0001t0015g0268 others(2): Show |
7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2+412A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755412 | |||||||
| chr5:40755450 | G | T | 1 | a0001c0001t0037g0051 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-2+374C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755450 | |||||||
| chr5:40755466 | C | T | 116 | a0001c0001t0001g0052 a0001c0001t0002g0001 a0001c0001t0002g0007 others(113): Show |
163 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.-2+358G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755466 | |||||||
| chr5:40755532 | AG | A | 3 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0031g0271 |
3 | NA18967.hp2 NA18968.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-2+291delC | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755532 | |||||||
| chr5:40755724 | C | T | 1 | a0001c0001t0029g0050 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-2+100G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755724 | |||||||
| chr5:40755753 | A | C | 4 | a0001c0001t0013g0046 a0001c0001t0013g0047 a0001c0001t0013g0048 others(1): Show |
4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+71T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755753 | |||||||
| chr5:40755782 | C | A | 1 | a0001c0001t0007g0274 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2+42G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755782 |