Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 647166 |
| ensemblid | ENSG00000226792.8 |
| hgncid | 42693 |
| symbol | C13orf42 |
| name | chromosome 13 open reading frame 42 |
| refseq_nuc | NM_001351589.3 |
| refseq_prot | NP_001338518.1 |
| ensembl_nuc | ENST00000563710.7 |
| ensembl_prot | ENSP00000490517.1 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 51082119 |
| end | 51111274 |
| strand | - |
| ver | v1.2 |
| region | chr13:51082119-51111274 |
| region5000 | chr13:51077119-51116274 |
| regionname0 | C13orf42_chr13_51082119_51111274 |
| regionname5000 | C13orf42_chr13_51077119_51116274 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 325 | 336 | 73 | 64 | 155 | 16 | 26 | 126 | C13orf42_chr13_51077119_51116274 | C13orf42 | MFRKI others(320): Show |
chr13 | 51077119 | 51116274 |
| a0002 | 0/0 | 325 | 107 | 19 | 14 | 50 | 2 | 22 | 33 | C13orf42_chr13_51077119_51116274 | C13orf42 | MFRKI others(320): Show |
chr13 | 51077119 | 51116274 |
| a0003 | 0/0 | 325 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | C13orf42_chr13_51077119_51116274 | C13orf42 | MFRKI others(320): Show |
chr13 | 51077119 | 51116274 |
| a0004 | 0/0 | 325 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | MFRKI others(320): Show |
chr13 | 51077119 | 51116274 |
| a0005 | 0/0 | 325 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | MFRKI others(320): Show |
chr13 | 51077119 | 51116274 |
| a0006 | 0/0 | 325 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | MFRKI others(320): Show |
chr13 | 51077119 | 51116274 |
| a0007 | 0/0 | 325 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | MFRKI others(320): Show |
chr13 | 51077119 | 51116274 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 975 | 335 | 72 | 64 | 155 | 16 | 26 | C13orf42_chr13_51077119_51116274 | C13orf42 | ATGTT others(970): Show |
chr13 | 51077119 | 51116274 | ||
| a0001c0006 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | ATGTT others(970): Show |
chr13 | 51077119 | 51116274 | ||
| a0002c0002 | 0/0 | 975 | 106 | 19 | 13 | 50 | 2 | 22 | C13orf42_chr13_51077119_51116274 | C13orf42 | ATGTT others(970): Show |
chr13 | 51077119 | 51116274 | ||
| a0002c0005 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | ATGTT others(970): Show |
chr13 | 51077119 | 51116274 | ||
| a0003c0003 | 0/0 | 975 | 4 | 0 | 0 | 4 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | ATGTT others(970): Show |
chr13 | 51077119 | 51116274 | ||
| a0004c0004 | 0/0 | 975 | 2 | 0 | 0 | 0 | 0 | 2 | C13orf42_chr13_51077119_51116274 | C13orf42 | ATGTT others(970): Show |
chr13 | 51077119 | 51116274 | ||
| a0005c0007 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | ATGTT others(970): Show |
chr13 | 51077119 | 51116274 | ||
| a0006c0008 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | ATGTT others(970): Show |
chr13 | 51077119 | 51116274 | ||
| a0007c0009 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | ATGTT others(970): Show |
chr13 | 51077119 | 51116274 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3075 | 177 | 34 | 25 | 92 | 8 | 17 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3070): Show |
chr13 | 51077119 | 51116274 |
| a0001c0001t0002 | 0/0 | 3079 | 5 | 4 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3074): Show |
chr13 | 51077119 | 51116274 |
| a0001c0001t0003 | 0/0 | 3075 | 94 | 7 | 12 | 62 | 5 | 8 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3070): Show |
chr13 | 51077119 | 51116274 |
| a0001c0001t0004 | 0/0 | 3075 | 19 | 0 | 17 | 0 | 2 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3070): Show |
chr13 | 51077119 | 51116274 |
| a0001c0001t0005 | 0/0 | 3079 | 11 | 8 | 2 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3074): Show |
chr13 | 51077119 | 51116274 |
| a0001c0001t0006 | 0/0 | 3079 | 11 | 7 | 4 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3074): Show |
chr13 | 51077119 | 51116274 |
| a0001c0001t0007 | 1/0 | 3075 | 5 | 1 | 2 | 0 | 1 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3070): Show |
chr13 | 51077119 | 51116274 |
| a0001c0001t0008 | 0/0 | 3079 | 4 | 4 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3074): Show |
chr13 | 51077119 | 51116274 |
| a0001c0001t0009 | 0/0 | 3075 | 4 | 4 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3070): Show |
chr13 | 51077119 | 51116274 |
| a0001c0001t0010 | 0/0 | 3079 | 3 | 3 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3074): Show |
chr13 | 51077119 | 51116274 |
| a0001c0001t0014 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3070): Show |
chr13 | 51077119 | 51116274 |
| a0001c0001t0015 | 0/0 | 3079 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3074): Show |
chr13 | 51077119 | 51116274 |
| a0001c0006t0013 | 0/0 | 3079 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3074): Show |
chr13 | 51077119 | 51116274 |
| a0002c0002t0002 | 0/0 | 3079 | 103 | 19 | 12 | 49 | 2 | 21 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3074): Show |
chr13 | 51077119 | 51116274 |
| a0002c0002t0012 | 0/0 | 3079 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | ACATC others(3074): Show |
chr13 | 51077119 | 51116274 |
| a0002c0002t0016 | 0/0 | 3079 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3074): Show |
chr13 | 51077119 | 51116274 |
| a0002c0002t0017 | 0/0 | 3079 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3074): Show |
chr13 | 51077119 | 51116274 |
| a0002c0005t0002 | 0/0 | 3079 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3074): Show |
chr13 | 51077119 | 51116274 |
| a0003c0003t0001 | 0/0 | 3075 | 4 | 0 | 0 | 4 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3070): Show |
chr13 | 51077119 | 51116274 |
| a0004c0004t0011 | 0/0 | 3075 | 2 | 0 | 0 | 0 | 0 | 2 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3070): Show |
chr13 | 51077119 | 51116274 |
| a0005c0007t0003 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3070): Show |
chr13 | 51077119 | 51116274 |
| a0006c0008t0001 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3070): Show |
chr13 | 51077119 | 51116274 |
| a0007c0009t0002 | 0/0 | 3079 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | GCATC others(3074): Show |
chr13 | 51077119 | 51116274 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0004 | 0/0 | 11 | 2 | 3 | 4 | 1 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0005 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0008 | 0/0 | 7 | 4 | 0 | 3 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0034 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0035 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0038 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0044 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0053 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0066 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0069 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0070 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0072 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0073 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0074 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0002g0062 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0002 | 0/0 | 16 | 0 | 0 | 15 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0017 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0031 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0033 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0040 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0071 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0004g0006 | 0/0 | 9 | 0 | 9 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0004g0019 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0004g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0005g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0005g0068 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0006g0039 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0006g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0006g0060 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0007g0010 | 1/0 | 5 | 1 | 2 | 0 | 1 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0008g0067 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0009g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0009g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0010g0036 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0014g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0001t0015g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0001c0006t0013g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0001 | 0/0 | 18 | 1 | 0 | 14 | 0 | 3 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0011 | 0/0 | 5 | 2 | 2 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0037 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0046 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0063 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0064 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0016g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0002t0017g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0002c0005t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0003c0003t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0004c0004t0011g0065 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0005c0007t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0006c0008t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| a0007c0009t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | GBR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0146 | EUR | GBR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | FIN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0177 | EUR | FIN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0102 | EUR | FIN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0166 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0225 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00735 | hp2 | a0002 | c0005 | t0002 | g0075 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0152 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01070 | hp2 | a0001 | c0001 | t0014 | g0145 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0224 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0238 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0134 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0047 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0039 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0148 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0222 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01243 | hp2 | a0002 | c0002 | t0016 | g0191 | AMR | PUR | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0019 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0019 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0199 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0043 | EUR | IBS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01516 | hp1 | a0001 | c0001 | t0007 | g0010 | EUR | IBS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0033 | EUR | IBS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0043 | EUR | IBS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0033 | EUR | IBS | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01884 | hp1 | a0005 | c0007 | t0003 | g0247 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0063 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01891 | hp2 | a0006 | c0008 | t0001 | g0093 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0010 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0037 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0085 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0047 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0068 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01981 | hp1 | a0001 | c0001 | t0007 | g0010 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0176 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | KHV | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0188 | EAS | CDX | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CDX | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0060 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0068 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0067 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0219 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0036 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0036 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0241 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0211 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0036 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0151 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0097 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0242 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0237 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0221 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0039 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0147 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0131 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0243 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03017 | hp1 | a0004 | c0004 | t0011 | g0065 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03017 | hp2 | a0002 | c0002 | t0017 | g0189 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0125 | AFR | MSL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0063 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0060 | AFR | MSL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | MSL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | MSL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0154 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0149 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0084 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0064 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0064 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0039 | AFR | ESN | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0123 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | GWD | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0046 | AFR | MSL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0132 | AFR | MSL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0096 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0196 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0182 | SAS | STU | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0200 | SAS | STU | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0011 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0083 | SAS | PJL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0227 | SAS | BEB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0116 | SAS | BEB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | BEB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0143 | SAS | BEB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0217 | SAS | STU | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0082 | SAS | STU | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0024 | SAS | BEB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | STU | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG04199 | hp2 | a0004 | c0004 | t0011 | g0065 | SAS | STU | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0099 | SAS | STU | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0197 | SAS | STU | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0190 | SAS | STU | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | YRI | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | CHB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0215 | AFR | YRI | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0239 | AFR | YRI | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18944 | hp1 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18963 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18975 | hp1 | a0001 | c0001 | t0015 | g0118 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18982 | hp1 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19004 | hp1 | a0002 | c0002 | t0012 | g0001 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | LWK | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0214 | AFR | LWK | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19059 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19076 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19076 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19081 | hp1 | a0007 | c0009 | t0002 | g0194 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | YRI | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0192 | AFR | ASW | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ASW | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0031 | EUR | TSI | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0185 | EUR | TSI | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0081 | SAS | GIH | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | GIH | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0210 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0124 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0220 | AFR | ACB | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0067 | AFR | MSL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG06807 | hp1 | a0001 | c0006 | t0013 | g0246 | AFR | USA | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | USA | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | USA | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | USA | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | LWK | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0044 | REF | REF | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0010 | REF | REF | C13orf42_chr13_51077119_51116274 | C13orf42 | chr13 | 51077119 | 51116274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51084161 | G | A | 2 | a0002 a0007 |
108 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
missense_variant | MODERATE | c.968C>T | p.Thr323Met | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 1033/3075 | 968/978 | 323/325 | chr13 | 51084161 | |||
| chr13:51084182 | C | T | 1 | a0006 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.947G>A | p.Arg316Gln | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 1012/3075 | 947/978 | 316/325 | chr13 | 51084182 | |||
| chr13:51084268 | A | T | 1 | a0004 | 2 | HG03017.hp1 HG04199.hp2 |
missense_variant | MODERATE | c.861T>A | p.Asp287Glu | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 926/3075 | 861/978 | 287/325 | chr13 | 51084268 | |||
| chr13:51085352 | G | C | 1 | a0007 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.770C>G | p.Thr257Ser | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/4 | 835/3075 | 770/978 | 257/325 | chr13 | 51085352 | |||
| chr13:51085361 | G | T | 1 | a0005 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.761C>A | p.Ala254Asp | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/4 | 826/3075 | 761/978 | 254/325 | chr13 | 51085361 | |||
| chr13:51111089 | C | T | 1 | a0003 | 4 | NA18944.hp1 NA18963.hp2 NA18982.hp1 others(1): Show |
missense_variant | MODERATE | c.121G>A | p.Val41Met | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/4 | 186/3075 | 121/978 | 41/325 | chr13 | 51111089 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51084220 | G | A | 3 | a0002c0002 a0002c0005 a0007c0009 |
108 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
synonymous_variant | LOW | c.909C>T | p.Tyr303Tyr | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 974/3075 | 909/978 | 303/325 | chr13 | 51084220 | |||
| chr13:51085468 | C | T | 1 | a0001c0006 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.654G>A | p.Val218Val | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/4 | 719/3075 | 654/978 | 218/325 | chr13 | 51085468 | |||
| chr13:51110973 | A | G | 1 | a0002c0005 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.237T>C | p.Tyr79Tyr | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/4 | 302/3075 | 237/978 | 79/325 | chr13 | 51110973 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51082295 | T | G | 1 | a0001c0001t0004 | 19 | HG00140.hp2 HG00642.hp1 HG01069.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1856A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 1856 | chr13 | 51082295 | ||||||
| chr13:51082391 | T | A | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(19): Show |
446 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(443): Show |
3_prime_UTR_variant | MODIFIER | c.*1760A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 1760 | chr13 | 51082391 | ||||||
| chr13:51082442 | C | G | 1 | a0002c0002t0016 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1709G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 1709 | chr13 | 51082442 | ||||||
| chr13:51082456 | T | G | 1 | a0001c0006t0013 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1695A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 1695 | chr13 | 51082456 | ||||||
| chr13:51082484 | C | G | 1 | a0001c0001t0008 | 4 | HG02451.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1667G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 1667 | chr13 | 51082484 | ||||||
| chr13:51083236 | A | G | 1 | a0001c0001t0010 | 3 | HG02622.hp2 HG02630.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*915T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 915 | chr13 | 51083236 | ||||||
| chr13:51083270 | T | C | 1 | a0001c0001t0014 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*881A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 881 | chr13 | 51083270 | ||||||
| chr13:51083463 | C | A | 1 | a0001c0001t0009 | 4 | HG02615.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*688G>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 688 | chr13 | 51083463 | ||||||
| chr13:51083628 | G | GAGTT | 13 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(10): Show |
144 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*522_*523insAACT | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 522 | chr13 | 51083628 | ||||||
| chr13:51084018 | G | A | 1 | a0001c0001t0006 | 11 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*133C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 133 | chr13 | 51084018 | ||||||
| chr13:51084035 | T | C | 7 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0015 others(4): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*116A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 116 | chr13 | 51084035 | ||||||
| chr13:51084046 | T | G | 7 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0012 others(4): Show |
113 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*105A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 105 | chr13 | 51084046 | ||||||
| chr13:51084090 | G | A | 1 | a0001c0001t0006 | 11 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*61C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 61 | chr13 | 51084090 | ||||||
| chr13:51084098 | C | T | 1 | a0001c0001t0010 | 3 | HG02622.hp2 HG02630.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*53G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 53 | chr13 | 51084098 | ||||||
| chr13:51084129 | A | C | 1 | a0004c0004t0011 | 2 | HG03017.hp1 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*22T>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 4/4 | 22 | chr13 | 51084129 | ||||||
| chr13:51111274 | C | T | 1 | a0002c0002t0012 | 1 | NA19004.hp1 | 5_prime_UTR_variant | MODIFIER | c.-65G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/4 | 65 | chr13 | 51111274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51084328 | A | T | 8 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0060 others(5): Show |
14 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.804-3T>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51084328 | |||||||
| chr13:51084652 | G | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0101 a0001c0001t0001g0105 |
4 | HG00597.hp1 HG02148.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.804-327C>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51084652 | |||||||
| chr13:51084660 | C | A | 3 | a0001c0001t0008g0067 a0001c0001t0008g0214 a0001c0001t0008g0215 |
4 | HG02451.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.804-335G>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51084660 | |||||||
| chr13:51084662 | G | A | 4 | a0001c0001t0002g0062 a0001c0001t0002g0110 a0001c0001t0002g0173 others(1): Show |
5 | HG00741.hp1 HG02976.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.804-337C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51084662 | |||||||
| chr13:51084776 | C | T | 8 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0060 others(5): Show |
14 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.804-451G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51084776 | |||||||
| chr13:51084878 | G | T | 1 | a0002c0002t0002g0193 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.803+441C>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51084878 | |||||||
| chr13:51084900 | C | T | 4 | a0001c0001t0002g0062 a0001c0001t0002g0110 a0001c0001t0002g0173 others(1): Show |
5 | HG00741.hp1 HG02976.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.803+419G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51084900 | |||||||
| chr13:51085087 | C | G | 1 | a0001c0006t0013g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.803+232G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085087 | |||||||
| chr13:51085113 | G | A | 1 | a0002c0002t0002g0116 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.803+206C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085113 | |||||||
| chr13:51085184 | A | AAT | 13 | a0001c0001t0001g0054 a0001c0001t0001g0212 a0001c0001t0003g0055 others(10): Show |
19 | HG01070.hp2 HG01081.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.803+133_803+134dup others(2): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085184 | |||||||
| chr13:51085184 | A | AATAT | 3 | a0001c0001t0003g0155 a0001c0001t0006g0060 a0005c0007t0003g0247 |
4 | HG01884.hp1 HG02280.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+131_803+134dup others(4): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085184 | |||||||
| chr13:51085184 | A | AATATATA others(1): Show |
4 | a0001c0001t0001g0045 a0001c0001t0001g0128 a0001c0001t0010g0036 others(1): Show |
7 | HG01891.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.803+127_803+134dup others(8): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085184 | |||||||
| chr13:51085184 | A | AATATATA others(5): Show |
1 | a0001c0001t0009g0243 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.803+123_803+134dup others(12): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085184 | |||||||
| chr13:51085184 | A | AATATATA others(25): Show |
1 | a0001c0001t0009g0219 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.803+134_803+135ins others(32): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085184 | |||||||
| chr13:51085184 | A | AATATATA others(27): Show |
1 | a0001c0006t0013g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.803+134_803+135ins others(34): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085184 | |||||||
| chr13:51085184 | A | AATATATA others(37): Show |
1 | a0001c0001t0009g0242 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.803+134_803+135ins others(44): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085184 | |||||||
| chr13:51085184 | A | AATATATA others(39): Show |
1 | a0001c0001t0009g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.803+134_803+135ins others(46): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085184 | |||||||
| chr13:51085184 | AAT | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(69): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.803+133_803+134del others(2): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085184 | |||||||
| chr13:51085184 | AATAT | A | 4 | a0001c0001t0001g0139 a0001c0001t0005g0096 a0002c0002t0002g0150 others(1): Show |
4 | HG00323.hp2 HG02895.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+131_803+134del others(4): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085184 | |||||||
| chr13:51085184 | AATATAT | A | 78 | a0001c0001t0002g0062 a0001c0001t0002g0110 a0001c0001t0002g0173 others(75): Show |
124 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.803+129_803+134del others(6): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085184 | |||||||
| chr13:51085269 | C | T | 1 | a0001c0006t0013g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.803+50G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085269 | |||||||
| chr13:51085311 | G | A | 4 | a0001c0001t0003g0040 a0001c0001t0003g0204 a0001c0001t0003g0248 others(1): Show |
6 | HG01192.hp1 HG02723.hp1 HG03041.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.803+8C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 3/3 | chr13 | 51085311 | |||||||
| chr13:51085589 | G | A | 1 | a0002c0002t0002g0238 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.563-30C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51085589 | |||||||
| chr13:51085603 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.563-44A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51085603 | |||||||
| chr13:51085611 | C | A | 8 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0060 others(5): Show |
14 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.563-52G>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51085611 | |||||||
| chr13:51085834 | G | A | 10 | a0001c0001t0005g0020 a0001c0001t0005g0068 a0001c0001t0005g0096 others(7): Show |
15 | HG01978.hp2 HG02258.hp2 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.563-275C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51085834 | |||||||
| chr13:51085910 | G | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0080 others(6): Show |
17 | HG02074.hp1 HG02074.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.563-351C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51085910 | |||||||
| chr13:51085972 | G | A | 1 | a0002c0002t0002g0195 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.563-413C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51085972 | |||||||
| chr13:51086003 | C | T | 7 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0060 others(4): Show |
11 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.563-444G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086003 | |||||||
| chr13:51086012 | G | A | 5 | a0002c0002t0002g0043 a0002c0002t0002g0083 a0002c0002t0002g0097 others(2): Show |
6 | HG00741.hp2 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.563-453C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086012 | |||||||
| chr13:51086033 | G | A | 1 | a0002c0002t0002g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.563-474C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086033 | |||||||
| chr13:51086163 | C | T | 3 | a0002c0002t0002g0037 a0002c0002t0002g0085 a0002c0002t0002g0199 |
5 | HG01361.hp1 HG01943.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.563-604G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086163 | |||||||
| chr13:51086167 | C | T | 1 | a0001c0001t0010g0036 | 3 | HG02622.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.563-608G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086167 | |||||||
| chr13:51086285 | G | A | 1 | a0001c0001t0003g0136 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.563-726C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086285 | |||||||
| chr13:51086292 | C | T | 2 | a0001c0001t0005g0068 a0001c0001t0005g0096 |
3 | HG01978.hp2 HG02293.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.563-733G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086292 | |||||||
| chr13:51086304 | T | TCAAAAAA others(15): Show |
1 | a0002c0002t0002g0084 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.563-767_563-746dup others(22): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086304 | |||||||
| chr13:51086304 | TCAAAAAA others(15): Show |
T | 1 | a0001c0001t0003g0130 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.563-767_563-746del others(22): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086304 | |||||||
| chr13:51086305 | C | CA | 10 | a0001c0001t0001g0105 a0001c0001t0001g0120 a0001c0001t0006g0039 others(7): Show |
16 | HG00597.hp1 HG01106.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.563-747dupT | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086305 | |||||||
| chr13:51086307 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0175 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.563-758_563-749del others(10): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086307 | |||||||
| chr13:51086317 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.563-758G>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086317 | |||||||
| chr13:51086317 | C | CA | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(21): Show |
52 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.563-759dupT | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086317 | |||||||
| chr13:51086326 | A | AC | 7 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0060 others(4): Show |
11 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.563-768dupG | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086326 | |||||||
| chr13:51086326 | A | C | 1 | a0002c0002t0002g0046 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.563-767T>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086326 | |||||||
| chr13:51086327 | C | CA | 18 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0041 others(15): Show |
26 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.563-769dupT | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086327 | |||||||
| chr13:51086327 | C | CAA | 18 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0028 others(15): Show |
37 | HG00597.hp1 HG01433.hp2 HG01978.hp1 others(34): Show |
intron_variant | MODIFIER | c.563-770_563-769dup others(2): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086327 | |||||||
| chr13:51086338 | A | C | 2 | a0001c0001t0003g0071 a0001c0001t0003g0155 |
3 | NA18964.hp1 NA19057.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.563-779T>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086338 | |||||||
| chr13:51086364 | G | T | 8 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0060 others(5): Show |
14 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.563-805C>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086364 | |||||||
| chr13:51086392 | G | A | 1 | a0001c0006t0013g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.563-833C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086392 | |||||||
| chr13:51086468 | A | G | 1 | a0002c0002t0002g0199 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.563-909T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086468 | |||||||
| chr13:51086491 | AGAGT | A | 4 | a0001c0001t0002g0062 a0001c0001t0002g0110 a0001c0001t0002g0173 others(1): Show |
5 | HG00741.hp1 HG02976.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.563-936_563-933del others(4): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086491 | |||||||
| chr13:51086502 | G | A | 1 | a0001c0001t0005g0020 | 4 | HG02258.hp2 HG02630.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.563-943C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086502 | |||||||
| chr13:51086513 | AGT | A | 10 | a0001c0001t0001g0004 a0001c0001t0006g0039 a0001c0001t0006g0047 others(7): Show |
17 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.563-956_563-955del others(2): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086513 | |||||||
| chr13:51086961 | GAAC | G | 4 | a0001c0001t0009g0219 a0001c0001t0009g0241 a0001c0001t0009g0242 others(1): Show |
4 | HG02615.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.562+964_562+966del others(3): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51086961 | |||||||
| chr13:51087116 | A | G | 8 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0060 others(5): Show |
14 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.562+812T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51087116 | |||||||
| chr13:51087203 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0183 others(2): Show |
9 | HG01109.hp2 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.562+725T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51087203 | |||||||
| chr13:51087265 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.562+663G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51087265 | |||||||
| chr13:51087373 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.562+555T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51087373 | |||||||
| chr13:51087482 | T | C | 7 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0060 others(4): Show |
11 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.562+446A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51087482 | |||||||
| chr13:51087486 | T | G | 1 | a0002c0002t0002g0079 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.562+442A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51087486 | |||||||
| chr13:51087632 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.562+296C>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51087632 | |||||||
| chr13:51087722 | A | G | 8 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0060 others(5): Show |
14 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.562+206T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51087722 | |||||||
| chr13:51087726 | A | T | 1 | a0001c0001t0003g0248 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.562+202T>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51087726 | |||||||
| chr13:51087827 | C | T | 2 | a0001c0001t0005g0068 a0001c0001t0005g0096 |
3 | HG01978.hp2 HG02293.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.562+101G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 2/3 | chr13 | 51087827 | |||||||
| chr13:51088167 | G | A | 8 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0060 others(5): Show |
14 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.415-92C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51088167 | |||||||
| chr13:51088300 | GACA | G | 5 | a0001c0001t0003g0076 a0001c0001t0003g0077 a0001c0001t0003g0102 others(2): Show |
5 | HG00323.hp1 HG00642.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-228_415-226del others(3): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51088300 | |||||||
| chr13:51088662 | A | G | 1 | a0001c0001t0003g0223 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.415-587T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51088662 | |||||||
| chr13:51088740 | A | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0101 a0001c0001t0001g0105 |
4 | HG00597.hp1 HG02148.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-665T>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51088740 | |||||||
| chr13:51088749 | T | G | 1 | a0001c0001t0001g0161 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.415-674A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51088749 | |||||||
| chr13:51088821 | G | C | 2 | a0001c0001t0005g0127 a0001c0001t0005g0131 |
2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.415-746C>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51088821 | |||||||
| chr13:51089115 | G | A | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.415-1040C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51089115 | |||||||
| chr13:51089228 | C | T | 8 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0060 others(5): Show |
14 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.415-1153G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51089228 | |||||||
| chr13:51089286 | G | A | 1 | a0001c0001t0010g0036 | 3 | HG02622.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.415-1211C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51089286 | |||||||
| chr13:51089443 | C | T | 2 | a0001c0001t0001g0025 a0003c0003t0001g0014 |
7 | NA18944.hp1 NA18963.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-1368G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51089443 | |||||||
| chr13:51089719 | T | C | 4 | a0001c0001t0009g0219 a0001c0001t0009g0241 a0001c0001t0009g0242 others(1): Show |
4 | HG02615.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-1644A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51089719 | |||||||
| chr13:51089921 | T | C | 1 | a0005c0007t0003g0247 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.415-1846A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51089921 | |||||||
| chr13:51089922 | G | C | 1 | a0001c0001t0003g0184 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.415-1847C>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51089922 | |||||||
| chr13:51090008 | G | A | 3 | a0001c0001t0005g0020 a0001c0001t0005g0127 a0001c0001t0005g0131 |
6 | HG02258.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-1933C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51090008 | |||||||
| chr13:51090051 | A | G | 3 | a0002c0002t0002g0063 a0002c0002t0002g0132 a0002c0002t0002g0220 |
4 | HG01884.hp2 HG02559.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-1976T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51090051 | |||||||
| chr13:51090173 | A | T | 1 | a0001c0001t0003g0134 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.415-2098T>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51090173 | |||||||
| chr13:51090276 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.415-2201C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51090276 | |||||||
| chr13:51090657 | C | G | 7 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0060 others(4): Show |
11 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-2582G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51090657 | |||||||
| chr13:51090709 | C | T | 9 | a0001c0001t0003g0033 a0001c0001t0003g0091 a0001c0001t0003g0104 others(6): Show |
11 | HG00280.hp2 HG00735.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.415-2634G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51090709 | |||||||
| chr13:51091066 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.415-2991G>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51091066 | |||||||
| chr13:51091149 | G | C | 4 | a0001c0001t0009g0219 a0001c0001t0009g0241 a0001c0001t0009g0242 others(1): Show |
4 | HG02615.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-3074C>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51091149 | |||||||
| chr13:51091192 | A | G | 1 | a0001c0001t0003g0122 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.415-3117T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51091192 | |||||||
| chr13:51091219 | G | A | 1 | a0001c0001t0008g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.415-3144C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51091219 | |||||||
| chr13:51091426 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.415-3351C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51091426 | |||||||
| chr13:51091540 | T | G | 1 | a0002c0002t0002g0198 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.415-3465A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51091540 | |||||||
| chr13:51091574 | G | A | 1 | a0001c0001t0003g0186 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.415-3499C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51091574 | |||||||
| chr13:51091852 | G | C | 4 | a0002c0002t0002g0037 a0002c0002t0002g0064 a0002c0002t0002g0085 others(1): Show |
7 | HG01361.hp1 HG01943.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.415-3777C>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51091852 | |||||||
| chr13:51091892 | C | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0172 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-3817G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51091892 | |||||||
| chr13:51091979 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0245 |
3 | HG02258.hp1 HG02486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.415-3904G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51091979 | |||||||
| chr13:51092091 | C | T | 4 | a0001c0001t0009g0219 a0001c0001t0009g0241 a0001c0001t0009g0242 others(1): Show |
4 | HG02615.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-4016G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51092091 | |||||||
| chr13:51092112 | C | T | 1 | a0002c0002t0002g0238 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.415-4037G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51092112 | |||||||
| chr13:51092151 | T | C | 3 | a0001c0001t0003g0076 a0001c0001t0003g0077 a0001c0001t0003g0102 |
3 | HG00323.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.415-4076A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51092151 | |||||||
| chr13:51092375 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.415-4300C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51092375 | |||||||
| chr13:51092431 | C | T | 1 | a0001c0001t0001g0059 | 2 | NA19059.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.415-4356G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51092431 | |||||||
| chr13:51092432 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0035 a0001c0001t0001g0049 others(5): Show |
18 | HG00621.hp1 HG02004.hp2 NA18943.hp2 others(15): Show |
intron_variant | MODIFIER | c.415-4357C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51092432 | |||||||
| chr13:51092472 | A | G | 8 | a0001c0001t0005g0020 a0001c0001t0005g0068 a0001c0001t0005g0096 others(5): Show |
13 | HG01978.hp2 HG02258.hp2 HG02293.hp1 others(10): Show |
intron_variant | MODIFIER | c.415-4397T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51092472 | |||||||
| chr13:51092957 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.415-4882A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51092957 | |||||||
| chr13:51092994 | C | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0165 |
2 | HG00733.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.415-4919G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51092994 | |||||||
| chr13:51093049 | A | G | 1 | a0002c0002t0002g0213 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.415-4974T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51093049 | |||||||
| chr13:51093269 | T | A | 3 | a0001c0001t0003g0205 a0001c0001t0003g0228 a0001c0001t0003g0234 |
3 | NA18977.hp1 NA18997.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.415-5194A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51093269 | |||||||
| chr13:51093283 | A | G | 1 | a0002c0002t0016g0191 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.415-5208T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51093283 | |||||||
| chr13:51093331 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.415-5256C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51093331 | |||||||
| chr13:51093331 | G | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0094 others(1): Show |
14 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.415-5256C>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51093331 | |||||||
| chr13:51093502 | C | T | 2 | a0002c0002t0002g0147 a0002c0005t0002g0075 |
2 | HG00735.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.415-5427G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51093502 | |||||||
| chr13:51093635 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.415-5560G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51093635 | |||||||
| chr13:51094333 | C | T | 11 | a0001c0001t0002g0062 a0001c0001t0002g0110 a0001c0001t0002g0173 others(8): Show |
16 | HG00741.hp1 HG01106.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.415-6258G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51094333 | |||||||
| chr13:51094366 | A | C | 7 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0060 others(4): Show |
11 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-6291T>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51094366 | |||||||
| chr13:51094402 | T | A | 1 | a0002c0002t0002g0149 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.415-6327A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51094402 | |||||||
| chr13:51094512 | C | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.415-6437G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51094512 | |||||||
| chr13:51094581 | C | T | 1 | a0001c0001t0003g0112 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.415-6506G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51094581 | |||||||
| chr13:51094952 | T | C | 11 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0060 others(8): Show |
15 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.415-6877A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51094952 | |||||||
| chr13:51095021 | A | T | 3 | a0001c0001t0008g0067 a0001c0001t0008g0214 a0001c0001t0008g0215 |
4 | HG02451.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-6946T>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095021 | |||||||
| chr13:51095120 | C | T | 5 | a0002c0002t0002g0147 a0002c0002t0002g0148 a0002c0002t0002g0149 others(2): Show |
5 | HG00639.hp1 HG00735.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-7045G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095120 | |||||||
| chr13:51095312 | C | CTGT | 133 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0021 others(130): Show |
216 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.415-7240_415-7238d others(5): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095312 | |||||||
| chr13:51095394 | T | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7319A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095394 | |||||||
| chr13:51095397 | C | T | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7322G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095397 | |||||||
| chr13:51095398 | A | T | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7323T>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095398 | |||||||
| chr13:51095399 | G | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7324C>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095399 | |||||||
| chr13:51095404 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7329A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095404 | |||||||
| chr13:51095406 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7331A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095406 | |||||||
| chr13:51095415 | A | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7340T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095415 | |||||||
| chr13:51095417 | A | T | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7342T>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095417 | |||||||
| chr13:51095418 | T | C | 2 | a0001c0001t0003g0229 a0001c0001t0010g0036 |
4 | HG02622.hp2 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-7343A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095418 | |||||||
| chr13:51095430 | C | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7355G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095430 | |||||||
| chr13:51095446 | T | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7371A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095446 | |||||||
| chr13:51095449 | T | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7374A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095449 | |||||||
| chr13:51095450 | C | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7375G>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095450 | |||||||
| chr13:51095456 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7381A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095456 | |||||||
| chr13:51095457 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7382A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095457 | |||||||
| chr13:51095461 | G | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7386C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095461 | |||||||
| chr13:51095462 | C | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7387G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095462 | |||||||
| chr13:51095463 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7388A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095463 | |||||||
| chr13:51095464 | A | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7389T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095464 | |||||||
| chr13:51095469 | T | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7394A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095469 | |||||||
| chr13:51095482 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7407A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095482 | |||||||
| chr13:51095483 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7408A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095483 | |||||||
| chr13:51095484 | G | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7409C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095484 | |||||||
| chr13:51095485 | A | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7410T>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095485 | |||||||
| chr13:51095490 | G | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7415C>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095490 | |||||||
| chr13:51095495 | A | T | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7420T>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095495 | |||||||
| chr13:51095496 | T | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7421A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095496 | |||||||
| chr13:51095499 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7424A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095499 | |||||||
| chr13:51095500 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7425A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095500 | |||||||
| chr13:51095502 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7427A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095502 | |||||||
| chr13:51095503 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7428A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095503 | |||||||
| chr13:51095504 | G | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7429C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095504 | |||||||
| chr13:51095505 | G | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7430C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095505 | |||||||
| chr13:51095507 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7432A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095507 | |||||||
| chr13:51095512 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7437A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095512 | |||||||
| chr13:51095514 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7439A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095514 | |||||||
| chr13:51095515 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7440A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095515 | |||||||
| chr13:51095516 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7441A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095516 | |||||||
| chr13:51095517 | T | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7442A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095517 | |||||||
| chr13:51095518 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7443A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095518 | |||||||
| chr13:51095523 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7448A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095523 | |||||||
| chr13:51095526 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7451A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095526 | |||||||
| chr13:51095527 | T | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7452A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095527 | |||||||
| chr13:51095528 | A | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7453T>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095528 | |||||||
| chr13:51095530 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7455A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095530 | |||||||
| chr13:51095531 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7456A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095531 | |||||||
| chr13:51095533 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7458A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095533 | |||||||
| chr13:51095534 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7459A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095534 | |||||||
| chr13:51095538 | T | G | 10 | a0001c0001t0005g0020 a0001c0001t0005g0068 a0001c0001t0005g0096 others(7): Show |
15 | HG01978.hp2 HG02258.hp2 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.415-7463A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095538 | |||||||
| chr13:51095547 | T | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7472A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095547 | |||||||
| chr13:51095550 | C | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7475G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095550 | |||||||
| chr13:51095551 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7476A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095551 | |||||||
| chr13:51095552 | A | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7477T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095552 | |||||||
| chr13:51095557 | T | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7482A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095557 | |||||||
| chr13:51095558 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7483A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095558 | |||||||
| chr13:51095560 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7485A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095560 | |||||||
| chr13:51095561 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7486A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095561 | |||||||
| chr13:51095562 | T | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7487A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095562 | |||||||
| chr13:51095563 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7488A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095563 | |||||||
| chr13:51095564 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7489A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095564 | |||||||
| chr13:51095568 | T | A | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7493A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095568 | |||||||
| chr13:51095569 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7494A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095569 | |||||||
| chr13:51095572 | T | C | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7497A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095572 | |||||||
| chr13:51095573 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7498A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095573 | |||||||
| chr13:51095574 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7499A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095574 | |||||||
| chr13:51095575 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7500A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095575 | |||||||
| chr13:51095578 | T | G | 1 | a0001c0001t0003g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.415-7503A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095578 | |||||||
| chr13:51095610 | A | T | 10 | a0001c0001t0005g0020 a0001c0001t0005g0068 a0001c0001t0005g0096 others(7): Show |
15 | HG01978.hp2 HG02258.hp2 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.415-7535T>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095610 | |||||||
| chr13:51095703 | G | T | 1 | a0001c0001t0003g0111 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.415-7628C>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095703 | |||||||
| chr13:51095722 | C | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(39): Show |
87 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.415-7647G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51095722 | |||||||
| chr13:51096048 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0172 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-7973C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51096048 | |||||||
| chr13:51096140 | A | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0183 others(2): Show |
9 | HG01109.hp2 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-8065T>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51096140 | |||||||
| chr13:51096165 | T | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0042 others(6): Show |
17 | HG00597.hp1 HG01978.hp1 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.415-8090A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51096165 | |||||||
| chr13:51096327 | A | G | 2 | a0002c0002t0002g0179 a0002c0002t0002g0187 |
2 | NA18967.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.415-8252T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51096327 | |||||||
| chr13:51096333 | C | G | 4 | a0001c0001t0003g0040 a0001c0001t0003g0204 a0001c0001t0003g0248 others(1): Show |
6 | HG01192.hp1 HG02723.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-8258G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51096333 | |||||||
| chr13:51096351 | G | A | 3 | a0001c0001t0005g0020 a0001c0001t0005g0127 a0001c0001t0005g0131 |
6 | HG02258.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-8276C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51096351 | |||||||
| chr13:51096491 | T | C | 1 | a0002c0002t0002g0238 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.415-8416A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51096491 | |||||||
| chr13:51096658 | C | T | 3 | a0001c0001t0005g0020 a0001c0001t0005g0127 a0001c0001t0005g0131 |
6 | HG02258.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-8583G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51096658 | |||||||
| chr13:51096750 | C | T | 2 | a0001c0001t0002g0173 a0001c0001t0005g0125 |
2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415-8675G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51096750 | |||||||
| chr13:51096862 | A | G | 5 | a0001c0001t0005g0125 a0001c0001t0005g0126 a0001c0001t0008g0067 others(2): Show |
6 | HG02451.hp2 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-8787T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51096862 | |||||||
| chr13:51096969 | G | A | 1 | a0001c0001t0003g0230 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.415-8894C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51096969 | |||||||
| chr13:51097023 | G | T | 1 | a0001c0001t0006g0047 | 2 | HG01106.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.415-8948C>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51097023 | |||||||
| chr13:51097047 | C | T | 1 | a0001c0001t0010g0036 | 3 | HG02622.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.415-8972G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51097047 | |||||||
| chr13:51097068 | T | G | 1 | a0001c0001t0010g0036 | 3 | HG02622.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.415-8993A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51097068 | |||||||
| chr13:51097166 | C | G | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(62): Show |
127 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.415-9091G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51097166 | |||||||
| chr13:51097276 | A | G | 2 | a0001c0001t0005g0125 a0001c0001t0005g0126 |
2 | HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.415-9201T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51097276 | |||||||
| chr13:51097323 | G | A | 1 | a0002c0002t0002g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.415-9248C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51097323 | |||||||
| chr13:51097656 | C | T | 65 | a0001c0001t0001g0137 a0002c0002t0002g0001 a0002c0002t0002g0011 others(62): Show |
105 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.415-9581G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51097656 | |||||||
| chr13:51097745 | T | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.415-9670A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51097745 | |||||||
| chr13:51097748 | A | AT | 5 | a0002c0002t0002g0063 a0002c0002t0002g0132 a0002c0002t0002g0192 others(2): Show |
6 | HG01243.hp2 HG01884.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-9674dupA | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51097748 | |||||||
| chr13:51097811 | G | T | 1 | a0002c0002t0002g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.415-9736C>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51097811 | |||||||
| chr13:51098332 | C | A | 65 | a0001c0001t0001g0137 a0002c0002t0002g0001 a0002c0002t0002g0011 others(62): Show |
105 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.415-10257G>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51098332 | |||||||
| chr13:51098596 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0218 |
3 | HG02055.hp2 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.415-10521G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51098596 | |||||||
| chr13:51098747 | A | G | 1 | a0001c0001t0003g0048 | 2 | NA18945.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.415-10672T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51098747 | |||||||
| chr13:51098773 | C | T | 1 | a0002c0002t0002g0188 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.415-10698G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51098773 | |||||||
| chr13:51098834 | G | GTGCCTGA others(100): Show |
1 | a0001c0001t0010g0036 | 3 | HG02622.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.415-10760_415-1075 others(111): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51098834 | |||||||
| chr13:51098871 | C | T | 1 | a0001c0001t0010g0036 | 3 | HG02622.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.415-10796G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51098871 | |||||||
| chr13:51098970 | G | A | 1 | a0002c0002t0002g0200 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.415-10895C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51098970 | |||||||
| chr13:51099097 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.415-11022A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51099097 | |||||||
| chr13:51099269 | G | A | 5 | a0001c0001t0005g0020 a0001c0001t0005g0068 a0001c0001t0005g0096 others(2): Show |
9 | HG01978.hp2 HG02258.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-11194C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51099269 | |||||||
| chr13:51099473 | C | T | 1 | a0002c0002t0002g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.414+11323G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51099473 | |||||||
| chr13:51099486 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.414+11310T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51099486 | |||||||
| chr13:51099570 | C | CAG | 1 | a0001c0001t0010g0036 | 3 | HG02622.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.414+11224_414+1122 others(6): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51099570 | |||||||
| chr13:51099576 | G | A | 1 | a0002c0002t0002g0117 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.414+11220C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51099576 | |||||||
| chr13:51099705 | G | A | 1 | a0001c0001t0001g0057 | 2 | NA18942.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.414+11091C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51099705 | |||||||
| chr13:51099841 | C | T | 1 | a0001c0001t0003g0226 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.414+10955G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51099841 | |||||||
| chr13:51099952 | G | T | 4 | a0002c0002t0002g0016 a0002c0002t0002g0114 a0002c0002t0002g0179 others(1): Show |
7 | HG00558.hp2 HG00597.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+10844C>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51099952 | |||||||
| chr13:51100092 | C | T | 9 | a0001c0001t0001g0045 a0001c0001t0001g0128 a0001c0001t0006g0039 others(6): Show |
13 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.414+10704G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51100092 | |||||||
| chr13:51100093 | G | T | 3 | a0001c0001t0008g0067 a0001c0001t0008g0214 a0001c0001t0008g0215 |
4 | HG02451.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+10703C>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51100093 | |||||||
| chr13:51100120 | CCTA | C | 10 | a0001c0001t0005g0020 a0001c0001t0005g0068 a0001c0001t0005g0096 others(7): Show |
15 | HG01978.hp2 HG02258.hp2 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.414+10673_414+1067 others(7): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51100120 | |||||||
| chr13:51100171 | T | A | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.414+10625A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51100171 | |||||||
| chr13:51100268 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.414+10528G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51100268 | |||||||
| chr13:51100273 | G | A | 6 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0123 others(3): Show |
9 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+10523C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51100273 | |||||||
| chr13:51100330 | C | T | 1 | a0001c0001t0006g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.414+10466G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51100330 | |||||||
| chr13:51100359 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.414+10437G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51100359 | |||||||
| chr13:51100495 | G | A | 63 | a0001c0001t0010g0036 a0002c0002t0002g0001 a0002c0002t0002g0013 others(60): Show |
101 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.414+10301C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51100495 | |||||||
| chr13:51100544 | C | T | 1 | a0002c0002t0002g0079 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.414+10252G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51100544 | |||||||
| chr13:51100816 | T | G | 6 | a0001c0001t0006g0039 a0001c0001t0006g0047 a0001c0001t0006g0123 others(3): Show |
9 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+9980A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51100816 | |||||||
| chr13:51100890 | G | A | 1 | a0001c0001t0010g0036 | 3 | HG02622.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.414+9906C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51100890 | |||||||
| chr13:51100956 | A | C | 1 | a0001c0001t0010g0036 | 3 | HG02622.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.414+9840T>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51100956 | |||||||
| chr13:51101116 | A | C | 1 | a0001c0001t0010g0036 | 3 | HG02622.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.414+9680T>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101116 | |||||||
| chr13:51101142 | T | C | 1 | a0002c0002t0002g0201 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.414+9654A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101142 | |||||||
| chr13:51101341 | A | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0218 |
3 | HG02055.hp2 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.414+9455T>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101341 | |||||||
| chr13:51101344 | C | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0025 others(28): Show |
58 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.414+9452G>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101344 | |||||||
| chr13:51101373 | T | C | 4 | a0001c0001t0003g0040 a0001c0001t0003g0204 a0001c0001t0003g0248 others(1): Show |
6 | HG01192.hp1 HG02723.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+9423A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101373 | |||||||
| chr13:51101407 | T | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0164 |
3 | NA18981.hp2 NA19002.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.414+9389A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101407 | |||||||
| chr13:51101413 | G | A | 107 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(104): Show |
204 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.414+9383C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101413 | |||||||
| chr13:51101528 | G | C | 7 | a0001c0001t0005g0020 a0001c0001t0005g0096 a0001c0001t0005g0125 others(4): Show |
10 | HG01884.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+9268C>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101528 | |||||||
| chr13:51101531 | T | C | 7 | a0001c0001t0002g0062 a0001c0001t0002g0110 a0001c0001t0002g0173 others(4): Show |
9 | HG00741.hp1 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+9265A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101531 | |||||||
| chr13:51101604 | T | C | 12 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0041 others(9): Show |
20 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.414+9192A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101604 | |||||||
| chr13:51101615 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0172 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+9181T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101615 | |||||||
| chr13:51101656 | G | A | 5 | a0002c0002t0002g0013 a0002c0002t0002g0211 a0002c0002t0002g0237 others(2): Show |
9 | HG01074.hp2 HG01891.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.414+9140C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101656 | |||||||
| chr13:51101722 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.414+9074C>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101722 | |||||||
| chr13:51101785 | C | T | 1 | a0005c0007t0003g0247 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.414+9011G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101785 | |||||||
| chr13:51101816 | T | C | 1 | a0001c0001t0003g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.414+8980A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51101816 | |||||||
| chr13:51102011 | G | C | 7 | a0001c0001t0001g0070 a0001c0001t0001g0218 a0001c0001t0001g0240 others(4): Show |
11 | HG02055.hp2 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+8785C>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51102011 | |||||||
| chr13:51102146 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG00280.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.414+8650G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51102146 | |||||||
| chr13:51102288 | C | G | 1 | a0002c0002t0002g0182 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.414+8508G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51102288 | |||||||
| chr13:51102375 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.414+8421A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51102375 | |||||||
| chr13:51102526 | C | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(39): Show |
80 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.414+8270G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51102526 | |||||||
| chr13:51102559 | G | A | 7 | a0001c0001t0001g0074 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
8 | HG02258.hp1 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.414+8237C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51102559 | |||||||
| chr13:51102629 | A | T | 7 | a0001c0001t0001g0074 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
8 | HG02258.hp1 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.414+8167T>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51102629 | |||||||
| chr13:51102832 | T | C | 191 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(188): Show |
342 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.414+7964A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51102832 | |||||||
| chr13:51102844 | G | A | 2 | a0001c0001t0008g0214 a0001c0001t0008g0215 |
2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.414+7952C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51102844 | |||||||
| chr13:51103007 | G | T | 7 | a0001c0001t0001g0074 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
8 | HG02258.hp1 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.414+7789C>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51103007 | |||||||
| chr13:51103061 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.414+7735A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51103061 | |||||||
| chr13:51103111 | G | A | 2 | a0002c0002t0002g0170 a0002c0002t0002g0171 |
2 | NA18969.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.414+7685C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51103111 | |||||||
| chr13:51103431 | A | G | 55 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0070 others(52): Show |
104 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.414+7365T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51103431 | |||||||
| chr13:51103432 | G | A | 46 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0070 others(43): Show |
91 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.414+7364C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51103432 | |||||||
| chr13:51103483 | A | T | 1 | a0001c0001t0001g0142 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.414+7313T>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51103483 | |||||||
| chr13:51103657 | C | T | 1 | a0001c0001t0002g0110 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.414+7139G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51103657 | |||||||
| chr13:51103675 | C | T | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0003g0030 others(3): Show |
13 | HG00639.hp2 HG00673.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.414+7121G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51103675 | |||||||
| chr13:51103691 | ACT | A | 46 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0070 others(43): Show |
91 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.414+7103_414+7104d others(4): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51103691 | |||||||
| chr13:51103798 | A | G | 235 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(232): Show |
420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
intron_variant | MODIFIER | c.414+6998T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51103798 | |||||||
| chr13:51103901 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.414+6895C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51103901 | |||||||
| chr13:51103926 | T | G | 1 | a0001c0001t0001g0052 | 2 | NA18941.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.414+6870A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51103926 | |||||||
| chr13:51103927 | G | A | 1 | a0001c0001t0003g0234 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.414+6869C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51103927 | |||||||
| chr13:51104173 | A | G | 1 | a0002c0002t0002g0179 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+6623T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51104173 | |||||||
| chr13:51104250 | C | T | 233 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
418 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(415): Show |
intron_variant | MODIFIER | c.414+6546G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51104250 | |||||||
| chr13:51104280 | T | C | 1 | a0001c0001t0001g0069 | 2 | NA18979.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.414+6516A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51104280 | |||||||
| chr13:51104428 | C | T | 39 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0070 others(36): Show |
78 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.414+6368G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51104428 | |||||||
| chr13:51104462 | A | G | 39 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0070 others(36): Show |
78 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.414+6334T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51104462 | |||||||
| chr13:51104487 | G | A | 1 | a0002c0002t0002g0099 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.414+6309C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51104487 | |||||||
| chr13:51104774 | TA | T | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(173): Show |
326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.414+6021delT | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51104774 | |||||||
| chr13:51104774 | TAA | T | 9 | a0001c0001t0001g0070 a0001c0001t0001g0141 a0001c0001t0001g0174 others(6): Show |
10 | HG00280.hp2 HG01074.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.414+6020_414+6021d others(4): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51104774 | |||||||
| chr13:51104858 | G | A | 12 | a0001c0001t0001g0049 a0001c0001t0002g0110 a0001c0001t0003g0007 others(9): Show |
24 | HG00544.hp1 HG00621.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.414+5938C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51104858 | |||||||
| chr13:51104897 | G | A | 46 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0070 others(43): Show |
86 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.414+5899C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51104897 | |||||||
| chr13:51104901 | C | T | 9 | a0001c0001t0001g0128 a0001c0001t0001g0172 a0001c0001t0001g0240 others(6): Show |
12 | HG02109.hp2 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.414+5895G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51104901 | |||||||
| chr13:51104908 | A | G | 46 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0070 others(43): Show |
86 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.414+5888T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51104908 | |||||||
| chr13:51104953 | G | A | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0003g0030 others(3): Show |
13 | HG00639.hp2 HG00673.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.414+5843C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51104953 | |||||||
| chr13:51105037 | A | C | 1 | a0002c0002t0002g0176 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.414+5759T>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105037 | |||||||
| chr13:51105119 | TG | T | 46 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0070 others(43): Show |
86 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.414+5676delC | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105119 | |||||||
| chr13:51105277 | C | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0041 |
5 | HG00280.hp1 HG01256.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+5519G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105277 | |||||||
| chr13:51105439 | A | G | 16 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(13): Show |
35 | HG00408.hp2 HG00733.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.414+5357T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105439 | |||||||
| chr13:51105460 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.414+5336T>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105460 | |||||||
| chr13:51105461 | T | G | 1 | a0001c0001t0001g0100 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.414+5335A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105461 | |||||||
| chr13:51105606 | C | T | 233 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
418 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(415): Show |
intron_variant | MODIFIER | c.414+5190G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105606 | |||||||
| chr13:51105690 | T | A | 1 | a0002c0002t0002g0239 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414+5106A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105690 | |||||||
| chr13:51105693 | A | G | 2 | a0001c0001t0003g0076 a0001c0001t0003g0077 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.414+5103T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105693 | |||||||
| chr13:51105732 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.414+5064A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105732 | |||||||
| chr13:51105836 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.414+4960C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105836 | |||||||
| chr13:51105860 | T | C | 187 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(184): Show |
338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.414+4936A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105860 | |||||||
| chr13:51105862 | G | A | 6 | a0001c0001t0001g0074 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
7 | HG02258.hp1 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+4934C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105862 | |||||||
| chr13:51105873 | G | A | 2 | a0001c0001t0003g0102 a0002c0002t0002g0043 |
3 | HG00323.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.414+4923C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105873 | |||||||
| chr13:51105891 | C | G | 1 | a0001c0001t0003g0031 | 3 | HG01070.hp1 HG01071.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.414+4905G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105891 | |||||||
| chr13:51105925 | T | G | 46 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0070 others(43): Show |
91 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.414+4871A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105925 | |||||||
| chr13:51105971 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0003g0104 |
2 | HG03490.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.414+4825C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51105971 | |||||||
| chr13:51106324 | C | T | 8 | a0001c0001t0001g0074 a0001c0001t0001g0240 a0001c0001t0001g0244 others(5): Show |
12 | HG02258.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.414+4472G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51106324 | |||||||
| chr13:51106345 | T | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0023 others(42): Show |
79 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.414+4451A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51106345 | |||||||
| chr13:51106386 | TAC | T | 39 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0070 others(36): Show |
78 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.414+4408_414+4409d others(4): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51106386 | |||||||
| chr13:51106404 | C | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0028 others(14): Show |
35 | HG00741.hp1 HG01243.hp1 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.414+4392G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51106404 | |||||||
| chr13:51106418 | C | A | 1 | a0001c0006t0013g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.414+4378G>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51106418 | |||||||
| chr13:51106489 | C | T | 3 | a0001c0001t0003g0071 a0001c0001t0003g0223 a0001c0001t0003g0235 |
4 | NA18939.hp1 NA18953.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+4307G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51106489 | |||||||
| chr13:51106532 | G | A | 1 | a0002c0002t0002g0213 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.414+4264C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51106532 | |||||||
| chr13:51106594 | G | A | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0003g0030 others(3): Show |
13 | HG00639.hp2 HG00673.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.414+4202C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51106594 | |||||||
| chr13:51106797 | T | C | 2 | a0001c0001t0008g0214 a0001c0001t0008g0215 |
2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.414+3999A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51106797 | |||||||
| chr13:51106871 | A | G | 9 | a0001c0001t0001g0128 a0001c0001t0001g0172 a0001c0001t0001g0240 others(6): Show |
12 | HG02109.hp2 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.414+3925T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51106871 | |||||||
| chr13:51106915 | C | T | 57 | a0001c0001t0001g0038 a0001c0001t0001g0066 a0001c0001t0001g0069 others(54): Show |
95 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.414+3881G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51106915 | |||||||
| chr13:51107054 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0218 others(5): Show |
14 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.414+3742C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51107054 | |||||||
| chr13:51107171 | C | G | 63 | a0001c0001t0001g0038 a0001c0001t0001g0053 a0001c0001t0001g0054 others(60): Show |
108 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.414+3625G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51107171 | |||||||
| chr13:51107311 | T | C | 1 | a0002c0002t0002g0216 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.414+3485A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51107311 | |||||||
| chr13:51107315 | A | T | 1 | a0001c0001t0001g0073 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.414+3481T>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51107315 | |||||||
| chr13:51107486 | A | G | 1 | a0001c0001t0003g0129 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.414+3310T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51107486 | |||||||
| chr13:51107561 | G | A | 23 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0070 others(20): Show |
43 | HG00544.hp1 HG00621.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.414+3235C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51107561 | |||||||
| chr13:51107639 | T | C | 1 | a0001c0006t0013g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.414+3157A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51107639 | |||||||
| chr13:51107804 | G | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0028 others(14): Show |
35 | HG00741.hp1 HG01243.hp1 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.414+2992C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51107804 | |||||||
| chr13:51107804 | G | C | 2 | a0001c0001t0001g0105 a0001c0001t0003g0106 |
2 | HG00597.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.414+2992C>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51107804 | |||||||
| chr13:51107812 | G | A | 22 | a0001c0001t0001g0049 a0001c0001t0001g0074 a0001c0001t0001g0244 others(19): Show |
37 | HG00544.hp1 HG00621.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.414+2984C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51107812 | |||||||
| chr13:51107878 | C | T | 119 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(116): Show |
206 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(203): Show |
intron_variant | MODIFIER | c.414+2918G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51107878 | |||||||
| chr13:51107966 | T | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0023 others(42): Show |
79 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.414+2830A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51107966 | |||||||
| chr13:51108024 | C | G | 9 | a0001c0001t0001g0074 a0001c0001t0001g0240 a0001c0001t0001g0244 others(6): Show |
13 | HG02258.hp1 HG02258.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.414+2772G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51108024 | |||||||
| chr13:51108453 | C | A | 1 | a0001c0001t0003g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.414+2343G>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51108453 | |||||||
| chr13:51108527 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.414+2269G>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51108527 | |||||||
| chr13:51108667 | T | G | 39 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0070 others(36): Show |
78 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.414+2129A>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51108667 | |||||||
| chr13:51108716 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0005g0020 |
5 | HG02258.hp2 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+2080G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51108716 | |||||||
| chr13:51108801 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0052 |
5 | HG00423.hp1 NA18747.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+1995G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51108801 | |||||||
| chr13:51108815 | C | T | 7 | a0001c0001t0001g0074 a0001c0001t0001g0240 a0001c0001t0001g0244 others(4): Show |
11 | HG02258.hp1 HG02258.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+1981G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51108815 | |||||||
| chr13:51109208 | T | A | 1 | a0002c0002t0002g0107 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.414+1588A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51109208 | |||||||
| chr13:51109252 | T | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.414+1544A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51109252 | |||||||
| chr13:51109371 | G | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0028 others(14): Show |
35 | HG00741.hp1 HG01243.hp1 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.414+1425C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51109371 | |||||||
| chr13:51109390 | G | A | 56 | a0001c0001t0001g0038 a0001c0001t0001g0066 a0001c0001t0001g0069 others(53): Show |
94 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.414+1406C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51109390 | |||||||
| chr13:51109428 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0051 others(8): Show |
23 | HG02040.hp2 HG02071.hp1 HG02080.hp1 others(20): Show |
intron_variant | MODIFIER | c.414+1368G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51109428 | |||||||
| chr13:51109533 | G | A | 1 | a0001c0001t0003g0217 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.414+1263C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51109533 | |||||||
| chr13:51109599 | T | A | 10 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0240 others(7): Show |
15 | HG02258.hp1 HG02258.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.414+1197A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51109599 | |||||||
| chr13:51109599 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.414+1197A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51109599 | |||||||
| chr13:51109663 | A | T | 9 | a0001c0001t0001g0074 a0001c0001t0001g0240 a0001c0001t0001g0244 others(6): Show |
13 | HG02258.hp1 HG02258.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.414+1133T>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51109663 | |||||||
| chr13:51109706 | A | G | 10 | a0001c0001t0001g0049 a0001c0001t0002g0110 a0001c0001t0003g0007 others(7): Show |
22 | HG00544.hp1 HG00621.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.414+1090T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51109706 | |||||||
| chr13:51109805 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.414+991G>A | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51109805 | |||||||
| chr13:51110042 | GCC | G | 9 | a0001c0001t0001g0074 a0001c0001t0001g0240 a0001c0001t0001g0244 others(6): Show |
13 | HG02258.hp1 HG02258.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.414+752_414+753del others(2): Show |
C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51110042 | |||||||
| chr13:51110057 | C | G | 1 | a0001c0001t0001g0045 | 2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.414+739G>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51110057 | |||||||
| chr13:51110117 | T | C | 1 | a0001c0001t0001g0073 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.414+679A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51110117 | |||||||
| chr13:51110163 | C | A | 1 | a0001c0001t0003g0235 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.414+633G>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51110163 | |||||||
| chr13:51110192 | G | A | 38 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0074 others(35): Show |
69 | HG00408.hp2 HG00733.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.414+604C>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51110192 | |||||||
| chr13:51110429 | T | A | 1 | a0001c0001t0001g0044 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.414+367A>T | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51110429 | |||||||
| chr13:51110609 | A | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0023 others(42): Show |
79 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.414+187T>C | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51110609 | |||||||
| chr13:51110739 | T | C | 21 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(18): Show |
33 | HG00140.hp1 HG01074.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.414+57A>G | C13orf42 | ENSG00000226792.8 | transcript | ENST00000563710.7 | protein_coding | 1/3 | chr13 | 51110739 |