Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54980 |
| ensemblid | ENSG00000115998.8 |
| hgncid | 26056 |
| symbol | C2orf42 |
| name | chromosome 2 open reading frame 42 |
| refseq_nuc | NM_017880.3 |
| refseq_prot | NP_060350.1 |
| ensembl_nuc | ENST00000264434.7 |
| ensembl_prot | ENSP00000264434.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 70149885 |
| end | 70191019 |
| strand | - |
| ver | v1.2 |
| region | chr2:70149885-70191019 |
| region5000 | chr2:70144885-70196019 |
| regionname0 | C2orf42_chr2_70149885_70191019 |
| regionname5000 | C2orf42_chr2_70144885_70196019 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 574 | 293 | 94 | 43 | 121 | 6 | 27 | 86 | C2orf42_chr2_70144885_70196019 | C2orf42 | MEPNS others(569): Show |
chr2 | 70144885 | 70196019 |
| a0002 | 0/0 | 574 | 35 | 0 | 18 | 14 | 0 | 3 | 9 | C2orf42_chr2_70144885_70196019 | C2orf42 | MEPNS others(569): Show |
chr2 | 70144885 | 70196019 |
| a0003 | 0/0 | 438 | 14 | 1 | 4 | 9 | 0 | 0 | 8 | C2orf42_chr2_70144885_70196019 | C2orf42 | MEPNS others(433): Show |
chr2 | 70144885 | 70196019 |
| a0004 | 0/0 | 574 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | MEPNS others(569): Show |
chr2 | 70144885 | 70196019 |
| a0005 | 0/0 | 438 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | MEPNS others(433): Show |
chr2 | 70144885 | 70196019 |
| a0006 | 0/0 | 574 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | MEPNS others(569): Show |
chr2 | 70144885 | 70196019 |
| a0007 | 0/0 | 574 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | MEPNS others(569): Show |
chr2 | 70144885 | 70196019 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1722 | 276 | 89 | 38 | 115 | 5 | 27 | C2orf42_chr2_70144885_70196019 | C2orf42 | ATGGA others(1717): Show |
chr2 | 70144885 | 70196019 | ||
| a0001c0004 | 0/0 | 1722 | 6 | 1 | 4 | 0 | 1 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | ATGGA others(1717): Show |
chr2 | 70144885 | 70196019 | ||
| a0001c0005 | 0/0 | 1722 | 5 | 4 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | ATGGA others(1717): Show |
chr2 | 70144885 | 70196019 | ||
| a0001c0006 | 0/0 | 1722 | 4 | 0 | 0 | 4 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | ATGGA others(1717): Show |
chr2 | 70144885 | 70196019 | ||
| a0001c0008 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | ATGGA others(1717): Show |
chr2 | 70144885 | 70196019 | ||
| a0001c0011 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | ATGGA others(1717): Show |
chr2 | 70144885 | 70196019 | ||
| a0002c0002 | 0/0 | 1722 | 35 | 0 | 18 | 14 | 0 | 3 | C2orf42_chr2_70144885_70196019 | C2orf42 | ATGGA others(1717): Show |
chr2 | 70144885 | 70196019 | ||
| a0003c0003 | 0/0 | 1723 | 12 | 1 | 2 | 9 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | ATGGA others(1718): Show |
chr2 | 70144885 | 70196019 | ||
| a0003c0007 | 0/0 | 1723 | 2 | 0 | 2 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | ATGGA others(1718): Show |
chr2 | 70144885 | 70196019 | ||
| a0004c0010 | 0/0 | 1722 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | ATGGA others(1717): Show |
chr2 | 70144885 | 70196019 | ||
| a0005c0009 | 0/0 | 1723 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | ATGGA others(1718): Show |
chr2 | 70144885 | 70196019 | ||
| a0006c0013 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | ATGGA others(1717): Show |
chr2 | 70144885 | 70196019 | ||
| a0007c0012 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | ATGGA others(1717): Show |
chr2 | 70144885 | 70196019 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2524 | 273 | 88 | 38 | 114 | 5 | 26 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2519): Show |
chr2 | 70144885 | 70196019 |
| a0001c0001t0002 | 0/0 | 2524 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2519): Show |
chr2 | 70144885 | 70196019 |
| a0001c0001t0003 | 0/0 | 2524 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2519): Show |
chr2 | 70144885 | 70196019 |
| a0001c0001t0004 | 0/0 | 2524 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2519): Show |
chr2 | 70144885 | 70196019 |
| a0001c0004t0001 | 0/0 | 2524 | 6 | 1 | 4 | 0 | 1 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2519): Show |
chr2 | 70144885 | 70196019 |
| a0001c0005t0001 | 0/0 | 2524 | 5 | 4 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2519): Show |
chr2 | 70144885 | 70196019 |
| a0001c0006t0001 | 0/0 | 2524 | 4 | 0 | 0 | 4 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2519): Show |
chr2 | 70144885 | 70196019 |
| a0001c0008t0001 | 0/0 | 2524 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2519): Show |
chr2 | 70144885 | 70196019 |
| a0001c0011t0001 | 0/0 | 2524 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2519): Show |
chr2 | 70144885 | 70196019 |
| a0002c0002t0001 | 0/0 | 2524 | 35 | 0 | 18 | 14 | 0 | 3 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2519): Show |
chr2 | 70144885 | 70196019 |
| a0003c0003t0001 | 0/0 | 2525 | 12 | 1 | 2 | 9 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2520): Show |
chr2 | 70144885 | 70196019 |
| a0003c0007t0001 | 0/0 | 2525 | 2 | 0 | 2 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2520): Show |
chr2 | 70144885 | 70196019 |
| a0004c0010t0001 | 0/0 | 2524 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2519): Show |
chr2 | 70144885 | 70196019 |
| a0005c0009t0001 | 0/0 | 2525 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2520): Show |
chr2 | 70144885 | 70196019 |
| a0006c0013t0001 | 0/0 | 2524 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2519): Show |
chr2 | 70144885 | 70196019 |
| a0007c0012t0001 | 0/0 | 2524 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | AGTTT others(2519): Show |
chr2 | 70144885 | 70196019 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0012 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0020 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0004t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0004t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0004t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0004t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0005t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0005t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0005t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0005t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0005t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0006t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0006t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0006t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0006t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0008t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0001c0011t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0001 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0003c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0003c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0003c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0003c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0003c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0003c0007t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0003c0007t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0004c0010t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0005c0009t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0006c0013t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| a0007c0012t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00280 | hp2 | a0001 | c0004 | t0001 | g0189 | EUR | FIN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00423 | hp1 | a0001 | c0011 | t0001 | g0270 | EAS | CHS | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0200 | EAS | CHS | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | CHS | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00741 | hp1 | a0003 | c0003 | t0001 | g0289 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01069 | hp2 | a0001 | c0004 | t0001 | g0186 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01071 | hp1 | a0001 | c0004 | t0001 | g0217 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01074 | hp1 | a0001 | c0004 | t0001 | g0224 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0077 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01192 | hp2 | a0001 | c0005 | t0001 | g0319 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01257 | hp1 | a0001 | c0004 | t0001 | g0179 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0039 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0051 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0052 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01433 | hp2 | a0003 | c0007 | t0001 | g0226 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01496 | hp2 | a0003 | c0007 | t0001 | g0187 | AMR | CLM | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01943 | hp2 | a0004 | c0010 | t0001 | g0146 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0050 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02071 | hp2 | a0001 | c0008 | t0001 | g0097 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02080 | hp1 | a0005 | c0009 | t0001 | g0035 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CDX | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CDX | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0185 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02523 | hp1 | a0001 | c0006 | t0001 | g0247 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02615 | hp1 | a0001 | c0005 | t0001 | g0175 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02717 | hp2 | a0006 | c0013 | t0001 | g0205 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0140 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03041 | hp2 | a0001 | c0005 | t0001 | g0176 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ESN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03209 | hp1 | a0001 | c0005 | t0001 | g0315 | AFR | MSL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | MSL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0040 | SAS | PJL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | STU | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0031 | SAS | STU | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | STU | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | YRI | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18945 | hp1 | a0001 | c0006 | t0001 | g0239 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18967 | hp1 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18967 | hp2 | a0003 | c0003 | t0001 | g0294 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18968 | hp1 | a0003 | c0003 | t0001 | g0261 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18968 | hp2 | a0003 | c0003 | t0001 | g0203 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18973 | hp1 | a0001 | c0006 | t0001 | g0271 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18985 | hp1 | a0003 | c0003 | t0001 | g0060 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18987 | hp2 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18992 | hp1 | a0003 | c0003 | t0001 | g0016 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18998 | hp2 | a0001 | c0006 | t0001 | g0243 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19010 | hp1 | a0003 | c0003 | t0001 | g0216 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0316 | AFR | LWK | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | LWK | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19063 | hp2 | a0007 | c0012 | t0001 | g0244 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | YRI | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | YRI | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ASW | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | TSI | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | GIH | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | GIH | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG06807 | hp1 | a0001 | c0005 | t0001 | g0310 | AFR | USA | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | USA | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | USA | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | USA | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0020 | REF | REF | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0012 | REF | REF | C2orf42_chr2_70144885_70196019 | C2orf42 | chr2 | 70144885 | 70196019 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:70160750 | C | T | 1 | a0007 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.1391G>A | p.Arg464Gln | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/10 | 1719/2524 | 1391/1725 | 464/574 | chr2 | 70160750 | |||
| chr2:70165549 | G | GT | 2 | a0003 a0005 |
15 | HG00597.hp2 HG00741.hp1 HG01109.hp1 others(12): Show |
frameshift_variant | HIGH | c.1230dupA | p.Arg411fs | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 7/10 | 1558/2524 | 1230/1725 | 410/574 | chr2 | 70165549 | |||
| chr2:70175771 | T | G | 2 | a0002 a0005 |
36 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(33): Show |
missense_variant | MODERATE | c.941A>C | p.Gln314Pro | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/10 | 1269/2524 | 941/1725 | 314/574 | chr2 | 70175771 | |||
| chr2:70179537 | A | G | 1 | a0004 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.929T>C | p.Val310Ala | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/10 | 1257/2524 | 929/1725 | 310/574 | chr2 | 70179537 | |||
| chr2:70179586 | C | A | 1 | a0006 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.880G>T | p.Ala294Ser | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/10 | 1208/2524 | 880/1725 | 294/574 | chr2 | 70179586 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:70150431 | C | T | 1 | a0001c0006 | 4 | HG02523.hp1 NA18945.hp1 NA18973.hp1 others(1): Show |
synonymous_variant | LOW | c.1650G>A | p.Ala550Ala | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 10/10 | 1978/2524 | 1650/1725 | 550/574 | chr2 | 70150431 | |||
| chr2:70150521 | G | A | 2 | a0001c0004 a0003c0007 |
8 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(5): Show |
synonymous_variant | LOW | c.1560C>T | p.Ile520Ile | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 10/10 | 1888/2524 | 1560/1725 | 520/574 | chr2 | 70150521 | |||
| chr2:70169564 | C | T | 1 | a0001c0011 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.1137G>A | p.Gln379Gln | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/10 | 1465/2524 | 1137/1725 | 379/574 | chr2 | 70169564 | |||
| chr2:70181683 | T | C | 1 | a0001c0005 | 5 | HG01192.hp2 HG02615.hp1 HG03041.hp2 others(2): Show |
synonymous_variant | LOW | c.303A>G | p.Thr101Thr | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/10 | 631/2524 | 303/1725 | 101/574 | chr2 | 70181683 | |||
| chr2:70181806 | A | G | 3 | a0001c0008 a0002c0002 a0005c0009 |
37 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(34): Show |
synonymous_variant | LOW | c.180T>C | p.Ser60Ser | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/10 | 508/2524 | 180/1725 | 60/574 | chr2 | 70181806 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:70150323 | T | A | 1 | a0001c0001t0004 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*33A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 10/10 | 33 | chr2 | 70150323 | ||||||
| chr2:70182882 | G | T | 1 | a0001c0001t0003 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-228C>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 2/10 | 897 | chr2 | 70182882 | ||||||
| chr2:70182918 | A | C | 1 | a0001c0001t0002 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-264T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 2/10 | 933 | chr2 | 70182918 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:70150639 | C | G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517-75G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70150639 | |||||||
| chr2:70150776 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0275 |
3 | HG02451.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1517-212G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70150776 | |||||||
| chr2:70150777 | G | A | 11 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1517-213C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70150777 | |||||||
| chr2:70150807 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1517-243C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70150807 | |||||||
| chr2:70150946 | C | T | 31 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0022 others(28): Show |
35 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1517-382G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70150946 | |||||||
| chr2:70151023 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1517-459C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70151023 | |||||||
| chr2:70151122 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1517-558G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70151122 | |||||||
| chr2:70151191 | A | G | 31 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0022 others(28): Show |
35 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1517-627T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70151191 | |||||||
| chr2:70151313 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1517-749C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70151313 | |||||||
| chr2:70151527 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0093 a0001c0001t0001g0301 |
3 | HG02630.hp1 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1517-963C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70151527 | |||||||
| chr2:70151695 | T | G | 6 | a0001c0001t0001g0303 a0001c0001t0001g0306 a0001c0001t0001g0307 others(3): Show |
6 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1517-1131A>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70151695 | |||||||
| chr2:70151716 | T | C | 83 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(80): Show |
85 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1517-1152A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70151716 | |||||||
| chr2:70151731 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1517-1167G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70151731 | |||||||
| chr2:70151778 | TTTTG | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(74): Show |
79 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1517-1218_1517-121 others(8): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70151778 | |||||||
| chr2:70151915 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0109 |
3 | HG01258.hp1 HG01358.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1517-1351A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70151915 | |||||||
| chr2:70151996 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1517-1432G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70151996 | |||||||
| chr2:70152068 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1517-1504G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70152068 | |||||||
| chr2:70152139 | T | A | 4 | a0001c0001t0001g0100 a0001c0001t0001g0124 a0001c0001t0001g0138 others(1): Show |
4 | NA18945.hp2 NA18999.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1517-1575A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70152139 | |||||||
| chr2:70152273 | T | C | 5 | a0001c0001t0001g0156 a0001c0001t0001g0220 a0001c0001t0001g0317 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1517-1709A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70152273 | |||||||
| chr2:70152363 | G | A | 10 | a0001c0001t0001g0048 a0001c0001t0001g0074 a0001c0001t0001g0075 others(7): Show |
10 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1517-1799C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70152363 | |||||||
| chr2:70152578 | T | G | 1 | a0001c0001t0001g0279 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1517-2014A>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70152578 | |||||||
| chr2:70152736 | T | C | 67 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(64): Show |
70 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1517-2172A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70152736 | |||||||
| chr2:70152753 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1517-2189C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70152753 | |||||||
| chr2:70152795 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1517-2231C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70152795 | |||||||
| chr2:70152817 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1517-2253C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70152817 | |||||||
| chr2:70152925 | C | G | 11 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1517-2361G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70152925 | |||||||
| chr2:70152969 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1517-2405C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70152969 | |||||||
| chr2:70152987 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1517-2423G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70152987 | |||||||
| chr2:70153032 | C | CA | 41 | a0001c0001t0001g0029 a0001c0001t0001g0093 a0001c0001t0001g0118 others(38): Show |
45 | HG00609.hp2 HG00621.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1517-2469dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153032 | |||||||
| chr2:70153032 | C | CAA | 9 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(6): Show |
9 | HG01975.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1517-2470_1517-246 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153032 | |||||||
| chr2:70153118 | G | A | 11 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1517-2554C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153118 | |||||||
| chr2:70153152 | A | C | 1 | a0001c0001t0001g0248 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1517-2588T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153152 | |||||||
| chr2:70153211 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1517-2647T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153211 | |||||||
| chr2:70153274 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1517-2710C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153274 | |||||||
| chr2:70153289 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1517-2725G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153289 | |||||||
| chr2:70153365 | C | CT | 46 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0043 others(43): Show |
50 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.1517-2802dupA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153365 | |||||||
| chr2:70153503 | C | T | 42 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(39): Show |
46 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.1517-2939G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153503 | |||||||
| chr2:70153507 | C | T | 1 | a0001c0005t0001g0315 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1517-2943G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153507 | |||||||
| chr2:70153655 | T | G | 2 | a0001c0004t0001g0186 a0001c0004t0001g0217 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1517-3091A>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153655 | |||||||
| chr2:70153672 | A | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0113 a0001c0001t0001g0121 others(2): Show |
5 | HG00558.hp2 HG02015.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1517-3108T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153672 | |||||||
| chr2:70153675 | T | TA | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
139 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.1517-3112dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153675 | |||||||
| chr2:70153675 | T | TAA | 12 | a0001c0001t0001g0155 a0001c0001t0001g0202 a0001c0001t0001g0230 others(9): Show |
12 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1517-3113_1517-311 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153675 | |||||||
| chr2:70153782 | G | A | 7 | a0001c0001t0001g0029 a0001c0001t0001g0093 a0001c0001t0001g0277 others(4): Show |
7 | HG02630.hp1 HG03225.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1517-3218C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153782 | |||||||
| chr2:70153841 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0275 |
3 | HG02451.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1517-3277G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153841 | |||||||
| chr2:70153886 | C | T | 1 | a0001c0001t0001g0320 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1517-3322G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153886 | |||||||
| chr2:70153887 | G | A | 77 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(74): Show |
79 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1517-3323C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153887 | |||||||
| chr2:70153945 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0150 a0004c0010t0001g0146 |
3 | HG00738.hp2 HG01943.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1517-3381G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70153945 | |||||||
| chr2:70154008 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1517-3444C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154008 | |||||||
| chr2:70154068 | C | CAA | 29 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0022 others(26): Show |
33 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1517-3506_1517-350 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154068 | |||||||
| chr2:70154072 | C | A | 32 | a0001c0001t0001g0084 a0002c0002t0001g0001 a0002c0002t0001g0008 others(29): Show |
36 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1517-3508G>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154072 | |||||||
| chr2:70154072 | C | CA | 152 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
157 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1517-3509dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154072 | |||||||
| chr2:70154075 | A | AC | 9 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(6): Show |
9 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1517-3512_1517-351 others(5): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154075 | |||||||
| chr2:70154207 | G | C | 2 | a0001c0001t0001g0281 a0003c0003t0001g0294 |
2 | HG02165.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1517-3643C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154207 | |||||||
| chr2:70154260 | A | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG02818.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1517-3696T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154260 | |||||||
| chr2:70154399 | G | A | 201 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
211 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.1517-3835C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154399 | |||||||
| chr2:70154414 | T | TA | 28 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0072 others(25): Show |
29 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1517-3851dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154414 | |||||||
| chr2:70154414 | T | TAA | 9 | a0001c0001t0001g0106 a0001c0001t0001g0152 a0001c0001t0001g0206 others(6): Show |
9 | HG01891.hp1 HG02293.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1517-3852_1517-385 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154414 | |||||||
| chr2:70154414 | T | TAAAAAAA others(9): Show |
1 | a0001c0001t0001g0320 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1517-3866_1517-385 others(20): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154414 | |||||||
| chr2:70154414 | T | TAAAAAAA others(10): Show |
1 | a0001c0001t0001g0300 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1517-3867_1517-385 others(21): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154414 | |||||||
| chr2:70154414 | T | TAAAAAAA others(13): Show |
1 | a0001c0001t0001g0291 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1517-3870_1517-385 others(24): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154414 | |||||||
| chr2:70154414 | TA | T | 84 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0019 others(81): Show |
86 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1517-3851delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154414 | |||||||
| chr2:70154414 | TAA | T | 54 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(51): Show |
57 | HG00621.hp1 HG00735.hp1 HG01175.hp1 others(54): Show |
intron_variant | MODIFIER | c.1517-3852_1517-385 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154414 | |||||||
| chr2:70154414 | TAAA | T | 36 | a0001c0001t0001g0024 a0001c0001t0001g0044 a0001c0001t0001g0054 others(33): Show |
40 | HG00609.hp2 HG01099.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.1517-3853_1517-385 others(7): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154414 | |||||||
| chr2:70154556 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1517-3992G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154556 | |||||||
| chr2:70154637 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1517-4073T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154637 | |||||||
| chr2:70154687 | A | G | 201 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
211 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.1517-4123T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154687 | |||||||
| chr2:70154696 | C | T | 201 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
211 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.1517-4132G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154696 | |||||||
| chr2:70154703 | C | G | 31 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0022 others(28): Show |
35 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1517-4139G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154703 | |||||||
| chr2:70154742 | A | C | 4 | a0001c0001t0001g0100 a0001c0001t0001g0124 a0001c0001t0001g0138 others(1): Show |
4 | NA18945.hp2 NA18999.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1517-4178T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154742 | |||||||
| chr2:70154745 | T | TTTTTG | 8 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0161 others(5): Show |
9 | HG01243.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1517-4186_1517-418 others(9): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154745 | |||||||
| chr2:70154797 | C | CTAG | 11 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1517-4236_1517-423 others(7): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154797 | |||||||
| chr2:70154859 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1517-4295C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70154859 | |||||||
| chr2:70155324 | A | G | 7 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0181 others(4): Show |
7 | NA18939.hp1 NA18966.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1517-4760T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70155324 | |||||||
| chr2:70155337 | C | A | 5 | a0001c0001t0001g0156 a0001c0001t0001g0220 a0001c0001t0001g0317 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1517-4773G>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70155337 | |||||||
| chr2:70155435 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1517-4871T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70155435 | |||||||
| chr2:70155444 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1517-4880T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70155444 | |||||||
| chr2:70155668 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1516+4957G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70155668 | |||||||
| chr2:70155754 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1516+4871A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70155754 | |||||||
| chr2:70155765 | A | T | 4 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0001g0132 others(1): Show |
4 | NA18979.hp1 NA18980.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1516+4860T>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70155765 | |||||||
| chr2:70155799 | CAAAAAAA others(5): Show |
C | 1 | a0002c0002t0001g0049 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1516+4814_1516+482 others(16): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70155799 | |||||||
| chr2:70155809 | G | A | 11 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+4816C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70155809 | |||||||
| chr2:70155809 | GA | G | 190 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
200 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.1516+4815delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70155809 | |||||||
| chr2:70155810 | A | G | 11 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+4815T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70155810 | |||||||
| chr2:70155987 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1516+4638G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70155987 | |||||||
| chr2:70155996 | A | G | 4 | a0001c0005t0001g0175 a0001c0005t0001g0176 a0001c0005t0001g0315 others(1): Show |
4 | HG01192.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1516+4629T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70155996 | |||||||
| chr2:70156029 | C | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1516+4596G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70156029 | |||||||
| chr2:70156087 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0275 |
3 | HG02451.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1516+4538C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70156087 | |||||||
| chr2:70156118 | G | A | 11 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+4507C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70156118 | |||||||
| chr2:70156266 | T | C | 1 | a0001c0001t0001g0302 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1516+4359A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70156266 | |||||||
| chr2:70156282 | C | G | 11 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+4343G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70156282 | |||||||
| chr2:70156288 | A | C | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1516+4337T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70156288 | |||||||
| chr2:70156440 | A | T | 32 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0022 others(29): Show |
36 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1516+4185T>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70156440 | |||||||
| chr2:70156560 | T | TA | 7 | a0001c0001t0001g0029 a0001c0001t0001g0093 a0001c0001t0001g0277 others(4): Show |
7 | HG02630.hp1 HG03225.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1516+4064dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70156560 | |||||||
| chr2:70156861 | C | CA | 81 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(78): Show |
83 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.1516+3763dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70156861 | |||||||
| chr2:70156992 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1516+3633C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70156992 | |||||||
| chr2:70157012 | ACT | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1516+3611_1516+361 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70157012 | |||||||
| chr2:70157312 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1516+3313C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70157312 | |||||||
| chr2:70157317 | G | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0161 others(5): Show |
9 | HG01243.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1516+3308C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70157317 | |||||||
| chr2:70157399 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1516+3226C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70157399 | |||||||
| chr2:70157419 | C | T | 1 | a0007c0012t0001g0244 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1516+3206G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70157419 | |||||||
| chr2:70157448 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0199 a0001c0001t0001g0201 others(1): Show |
7 | HG00597.hp2 HG02523.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.1516+3177G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70157448 | |||||||
| chr2:70157454 | AAAAC | A | 83 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(80): Show |
85 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1516+3167_1516+317 others(8): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70157454 | |||||||
| chr2:70157751 | C | T | 11 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+2874G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70157751 | |||||||
| chr2:70157755 | C | T | 32 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0022 others(29): Show |
36 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1516+2870G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70157755 | |||||||
| chr2:70157862 | A | C | 11 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+2763T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70157862 | |||||||
| chr2:70157998 | C | T | 5 | a0001c0001t0001g0156 a0001c0001t0001g0220 a0001c0001t0001g0317 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1516+2627G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70157998 | |||||||
| chr2:70157999 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0275 |
3 | HG02451.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1516+2626C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70157999 | |||||||
| chr2:70158001 | C | G | 190 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
199 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.1516+2624G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158001 | |||||||
| chr2:70158113 | T | C | 89 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(86): Show |
91 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1516+2512A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158113 | |||||||
| chr2:70158154 | G | A | 4 | a0001c0001t0001g0277 a0001c0001t0001g0300 a0001c0001t0001g0302 others(1): Show |
4 | HG03486.hp2 NA19240.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1516+2471C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158154 | |||||||
| chr2:70158198 | CA | C | 14 | a0001c0001t0001g0076 a0001c0001t0001g0090 a0001c0001t0001g0128 others(11): Show |
14 | HG01167.hp1 HG01167.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1516+2426delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158198 | |||||||
| chr2:70158271 | C | G | 5 | a0001c0001t0001g0156 a0001c0001t0001g0220 a0001c0001t0001g0317 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1516+2354G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158271 | |||||||
| chr2:70158317 | T | C | 76 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(73): Show |
78 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1516+2308A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158317 | |||||||
| chr2:70158423 | A | ATTAT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0018 others(4): Show |
9 | HG02615.hp2 HG02723.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1516+2198_1516+220 others(8): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158423 | |||||||
| chr2:70158442 | ATTTATTT others(1): Show |
A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(73): Show |
78 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1516+2175_1516+218 others(12): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158442 | |||||||
| chr2:70158450 | G | A | 12 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1516+2175C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158450 | |||||||
| chr2:70158456 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1516+2169A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158456 | |||||||
| chr2:70158493 | A | G | 43 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(40): Show |
47 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.1516+2132T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158493 | |||||||
| chr2:70158513 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1516+2112C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158513 | |||||||
| chr2:70158518 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0275 |
3 | HG02451.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1516+2107G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158518 | |||||||
| chr2:70158666 | C | T | 88 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(85): Show |
90 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1516+1959G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158666 | |||||||
| chr2:70158900 | C | CT | 70 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(67): Show |
73 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1516+1724dupA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158900 | |||||||
| chr2:70158900 | CT | C | 105 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(102): Show |
111 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.1516+1724delA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158900 | |||||||
| chr2:70158968 | G | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1516+1657C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158968 | |||||||
| chr2:70158980 | C | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0059 others(48): Show |
53 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1516+1645G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70158980 | |||||||
| chr2:70159036 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1516+1589G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159036 | |||||||
| chr2:70159118 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1516+1507G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159118 | |||||||
| chr2:70159188 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1516+1437G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159188 | |||||||
| chr2:70159311 | G | A | 32 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0022 others(29): Show |
36 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1516+1314C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159311 | |||||||
| chr2:70159326 | A | G | 91 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(88): Show |
93 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1516+1299T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159326 | |||||||
| chr2:70159347 | G | A | 67 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(64): Show |
70 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1516+1278C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159347 | |||||||
| chr2:70159394 | C | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0213 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1516+1231G>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159394 | |||||||
| chr2:70159417 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0275 |
3 | HG02451.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1516+1208C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159417 | |||||||
| chr2:70159498 | G | C | 5 | a0001c0001t0001g0156 a0001c0001t0001g0220 a0001c0001t0001g0317 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1516+1127C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159498 | |||||||
| chr2:70159578 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0063 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1516+1047C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159578 | |||||||
| chr2:70159591 | C | CA | 33 | a0001c0001t0001g0159 a0001c0001t0001g0225 a0002c0002t0001g0001 others(30): Show |
37 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.1516+1033dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159591 | |||||||
| chr2:70159591 | CA | C | 89 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(86): Show |
91 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1516+1033delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159591 | |||||||
| chr2:70159620 | A | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1516+1005T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159620 | |||||||
| chr2:70159691 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0210 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1516+934C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159691 | |||||||
| chr2:70159698 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1516+927A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159698 | |||||||
| chr2:70159703 | A | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(77): Show |
82 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.1516+922T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159703 | |||||||
| chr2:70159860 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1516+765C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70159860 | |||||||
| chr2:70160062 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1516+563C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70160062 | |||||||
| chr2:70160133 | C | CT | 83 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(80): Show |
85 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1516+491dupA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70160133 | |||||||
| chr2:70160133 | CT | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0135 others(9): Show |
13 | HG01243.hp1 HG01261.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1516+491delA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70160133 | |||||||
| chr2:70160209 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1516+416C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70160209 | |||||||
| chr2:70160289 | G | A | 2 | a0001c0001t0001g0280 a0003c0003t0001g0289 |
2 | HG00741.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1516+336C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 9/9 | chr2 | 70160289 | |||||||
| chr2:70160814 | A | C | 1 | a0001c0001t0001g0288 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1354-27T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70160814 | |||||||
| chr2:70160822 | G | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0142 |
2 | HG01243.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1354-35C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70160822 | |||||||
| chr2:70161400 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0197 |
2 | NA18979.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1354-613G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70161400 | |||||||
| chr2:70161539 | C | T | 123 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(120): Show |
129 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.1354-752G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70161539 | |||||||
| chr2:70161701 | G | A | 5 | a0001c0001t0001g0156 a0001c0001t0001g0220 a0001c0001t0001g0317 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1354-914C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70161701 | |||||||
| chr2:70161840 | C | CA | 34 | a0001c0001t0001g0139 a0001c0001t0001g0165 a0001c0001t0001g0215 others(31): Show |
38 | HG00609.hp2 HG00735.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1354-1054dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70161840 | |||||||
| chr2:70161840 | CA | C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(79): Show |
84 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1354-1054delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70161840 | |||||||
| chr2:70161872 | C | T | 1 | a0001c0001t0001g0311 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1354-1085G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70161872 | |||||||
| chr2:70162081 | A | G | 91 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(88): Show |
93 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1354-1294T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70162081 | |||||||
| chr2:70162143 | C | CT | 3 | a0001c0001t0001g0072 a0001c0001t0001g0256 a0001c0001t0001g0295 |
3 | HG02132.hp1 HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1354-1357dupA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70162143 | |||||||
| chr2:70162200 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-1413C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70162200 | |||||||
| chr2:70162302 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0275 |
3 | HG02451.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1354-1515G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70162302 | |||||||
| chr2:70162329 | CTTTCTTT others(1): Show |
C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1354-1550_1354-154 others(12): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70162329 | |||||||
| chr2:70162333 | CTTTT | C | 88 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(85): Show |
90 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1354-1550_1354-154 others(8): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70162333 | |||||||
| chr2:70162570 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1354-1783C>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70162570 | |||||||
| chr2:70162589 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1354-1802T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70162589 | |||||||
| chr2:70162622 | A | G | 1 | a0003c0003t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1354-1835T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70162622 | |||||||
| chr2:70162712 | A | G | 1 | a0003c0003t0001g0148 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1354-1925T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70162712 | |||||||
| chr2:70162768 | A | G | 91 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(88): Show |
93 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1354-1981T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70162768 | |||||||
| chr2:70162953 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1353+2139G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70162953 | |||||||
| chr2:70163029 | G | A | 91 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(88): Show |
93 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1353+2063C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70163029 | |||||||
| chr2:70163164 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1353+1928C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70163164 | |||||||
| chr2:70163185 | T | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0003c0003t0001g0148 |
3 | NA18979.hp1 NA18987.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1353+1907A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70163185 | |||||||
| chr2:70163283 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1353+1809G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70163283 | |||||||
| chr2:70163338 | G | A | 32 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0022 others(29): Show |
36 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1353+1754C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70163338 | |||||||
| chr2:70163373 | T | C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0213 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1353+1719A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70163373 | |||||||
| chr2:70163793 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1353+1299A>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70163793 | |||||||
| chr2:70163804 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1353+1288G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70163804 | |||||||
| chr2:70163919 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1353+1173G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70163919 | |||||||
| chr2:70164005 | A | AT | 8 | a0001c0001t0001g0048 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG01109.hp1 HG01169.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1353+1086_1353+108 others(5): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70164005 | |||||||
| chr2:70164006 | A | T | 86 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(83): Show |
88 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.1353+1086T>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70164006 | |||||||
| chr2:70164006 | AT | A | 36 | a0001c0001t0001g0045 a0001c0001t0001g0157 a0001c0001t0001g0183 others(33): Show |
40 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1353+1085delA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70164006 | |||||||
| chr2:70164209 | G | A | 45 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0059 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1353+883C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70164209 | |||||||
| chr2:70164301 | C | CA | 5 | a0001c0001t0001g0057 a0001c0001t0001g0153 a0001c0001t0001g0157 others(2): Show |
5 | HG02056.hp1 HG02165.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+790dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70164301 | |||||||
| chr2:70164331 | CA | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0138 others(2): Show |
5 | HG02451.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1353+760delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70164331 | |||||||
| chr2:70164389 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1353+703C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70164389 | |||||||
| chr2:70164394 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1353+698G>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70164394 | |||||||
| chr2:70164403 | T | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1353+689A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70164403 | |||||||
| chr2:70164524 | C | T | 2 | a0001c0001t0001g0251 a0006c0013t0001g0205 |
2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1353+568G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70164524 | |||||||
| chr2:70164555 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1353+537G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70164555 | |||||||
| chr2:70164926 | T | C | 4 | a0001c0001t0001g0303 a0001c0001t0001g0306 a0001c0001t0001g0307 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1353+166A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70164926 | |||||||
| chr2:70165071 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1353+21C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70165071 | |||||||
| chr2:70165081 | T | A | 1 | a0001c0001t0003g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1353+11A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 8/9 | chr2 | 70165081 | |||||||
| chr2:70165247 | G | A | 89 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(86): Show |
91 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1253-55C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 7/9 | chr2 | 70165247 | |||||||
| chr2:70165491 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1252+37C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 7/9 | chr2 | 70165491 | |||||||
| chr2:70165665 | T | A | 1 | a0001c0001t0001g0190 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1145-30A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70165665 | |||||||
| chr2:70165668 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1145-33T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70165668 | |||||||
| chr2:70165669 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1145-34C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70165669 | |||||||
| chr2:70165688 | G | C | 89 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(86): Show |
91 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1145-53C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70165688 | |||||||
| chr2:70165899 | T | A | 32 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0022 others(29): Show |
36 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1145-264A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70165899 | |||||||
| chr2:70165969 | C | T | 66 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(63): Show |
69 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1145-334G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70165969 | |||||||
| chr2:70165976 | T | C | 66 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(63): Show |
69 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1145-341A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70165976 | |||||||
| chr2:70165977 | G | A | 66 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(63): Show |
69 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1145-342C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70165977 | |||||||
| chr2:70165984 | G | A | 66 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(63): Show |
69 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1145-349C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70165984 | |||||||
| chr2:70165995 | A | G | 66 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(63): Show |
69 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1145-360T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70165995 | |||||||
| chr2:70165997 | C | T | 66 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(63): Show |
69 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1145-362G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70165997 | |||||||
| chr2:70166001 | C | A | 66 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(63): Show |
69 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1145-366G>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166001 | |||||||
| chr2:70166092 | T | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0182 |
2 | NA18966.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1145-457A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166092 | |||||||
| chr2:70166277 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1145-642G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166277 | |||||||
| chr2:70166310 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1145-675G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166310 | |||||||
| chr2:70166333 | A | G | 3 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0142 |
3 | HG01243.hp2 HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1145-698T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166333 | |||||||
| chr2:70166392 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-757C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166392 | |||||||
| chr2:70166503 | T | TA | 23 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0066 others(20): Show |
23 | HG01109.hp2 HG01192.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1145-869dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166503 | |||||||
| chr2:70166503 | T | TAA | 12 | a0001c0001t0001g0087 a0001c0001t0001g0102 a0001c0001t0001g0105 others(9): Show |
12 | HG02074.hp2 HG02083.hp1 NA18951.hp2 others(9): Show |
intron_variant | MODIFIER | c.1145-870_1145-869d others(4): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166503 | |||||||
| chr2:70166503 | TA | T | 16 | a0001c0001t0001g0021 a0001c0001t0001g0080 a0001c0001t0001g0084 others(13): Show |
16 | HG00738.hp2 HG01069.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1145-869delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166503 | |||||||
| chr2:70166503 | TAA | T | 29 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0022 others(26): Show |
33 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1145-870_1145-869d others(4): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166503 | |||||||
| chr2:70166515 | A | AG | 4 | a0001c0001t0001g0277 a0001c0001t0001g0300 a0001c0001t0001g0302 others(1): Show |
4 | HG03486.hp2 NA19240.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-881_1145-880i others(3): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166515 | |||||||
| chr2:70166515 | A | G | 7 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1145-880T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166515 | |||||||
| chr2:70166613 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1145-978A>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166613 | |||||||
| chr2:70166659 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1145-1024C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166659 | |||||||
| chr2:70166791 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0071 |
4 | HG01884.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-1156G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166791 | |||||||
| chr2:70166837 | C | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-1202G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166837 | |||||||
| chr2:70166854 | C | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(74): Show |
79 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1145-1219G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166854 | |||||||
| chr2:70166951 | T | G | 1 | a0001c0001t0001g0017 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1145-1316A>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166951 | |||||||
| chr2:70166963 | G | T | 88 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(85): Show |
90 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1145-1328C>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70166963 | |||||||
| chr2:70167003 | CTT | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0055 others(1): Show |
4 | HG02451.hp2 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145-1370_1145-136 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70167003 | |||||||
| chr2:70167087 | A | G | 127 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(124): Show |
133 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.1145-1452T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70167087 | |||||||
| chr2:70167336 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0055 others(1): Show |
4 | HG02451.hp2 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145-1701G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70167336 | |||||||
| chr2:70167357 | C | CA | 14 | a0002c0002t0001g0008 a0002c0002t0001g0022 a0002c0002t0001g0023 others(11): Show |
15 | HG01257.hp2 HG01258.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1145-1723dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70167357 | |||||||
| chr2:70167465 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-1830C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70167465 | |||||||
| chr2:70167468 | T | C | 91 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(88): Show |
93 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1145-1833A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70167468 | |||||||
| chr2:70167648 | C | T | 32 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0022 others(29): Show |
36 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1144+1909G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70167648 | |||||||
| chr2:70167690 | G | C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0213 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1144+1867C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70167690 | |||||||
| chr2:70167884 | G | A | 66 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(63): Show |
69 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1144+1673C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70167884 | |||||||
| chr2:70167945 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1144+1612A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70167945 | |||||||
| chr2:70167961 | G | A | 1 | a0002c0002t0001g0030 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1144+1596C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70167961 | |||||||
| chr2:70168053 | T | C | 127 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(124): Show |
133 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.1144+1504A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168053 | |||||||
| chr2:70168157 | C | G | 91 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(88): Show |
93 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1144+1400G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168157 | |||||||
| chr2:70168213 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+1344C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168213 | |||||||
| chr2:70168256 | A | C | 91 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(88): Show |
93 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1144+1301T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168256 | |||||||
| chr2:70168290 | CT | C | 97 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(94): Show |
99 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.1144+1266delA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168290 | |||||||
| chr2:70168401 | C | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0161 others(5): Show |
9 | HG01243.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1144+1156G>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168401 | |||||||
| chr2:70168413 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1144+1144C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168413 | |||||||
| chr2:70168433 | A | G | 91 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(88): Show |
93 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1144+1124T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168433 | |||||||
| chr2:70168436 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1144+1121G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168436 | |||||||
| chr2:70168646 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1144+911C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168646 | |||||||
| chr2:70168674 | C | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0219 |
2 | NA18977.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1144+883G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168674 | |||||||
| chr2:70168720 | C | CT | 66 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(63): Show |
69 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1144+836dupA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168720 | |||||||
| chr2:70168720 | CT | C | 6 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1144+836delA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168720 | |||||||
| chr2:70168838 | A | G | 1 | a0003c0003t0001g0261 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1144+719T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168838 | |||||||
| chr2:70168840 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0055 others(1): Show |
4 | HG02451.hp2 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144+717C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168840 | |||||||
| chr2:70168880 | T | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0199 a0001c0001t0001g0201 others(1): Show |
7 | HG00597.hp2 HG02523.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144+677A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168880 | |||||||
| chr2:70168924 | A | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+633T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70168924 | |||||||
| chr2:70169172 | T | C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0150 a0004c0010t0001g0146 |
3 | HG00738.hp2 HG01943.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1144+385A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70169172 | |||||||
| chr2:70169247 | C | CCA | 15 | a0001c0001t0001g0009 a0001c0001t0001g0100 a0001c0001t0001g0124 others(12): Show |
16 | HG00738.hp2 HG01943.hp2 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.1144+308_1144+309d others(4): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70169247 | |||||||
| chr2:70169247 | C | CCACA | 5 | a0001c0001t0001g0191 a0001c0001t0001g0204 a0001c0001t0001g0227 others(2): Show |
5 | HG00621.hp1 NA18940.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144+306_1144+309d others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70169247 | |||||||
| chr2:70169247 | C | CCACACAC others(3): Show |
3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0275 |
3 | HG02451.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1144+300_1144+309d others(12): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70169247 | |||||||
| chr2:70169247 | CCA | C | 140 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(137): Show |
147 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.1144+308_1144+309d others(4): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70169247 | |||||||
| chr2:70169247 | CCACA | C | 7 | a0001c0001t0001g0116 a0001c0001t0001g0132 a0001c0001t0001g0152 others(4): Show |
7 | HG00280.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144+306_1144+309d others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70169247 | |||||||
| chr2:70169247 | CCACACA | C | 9 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0161 others(6): Show |
10 | HG01243.hp1 HG01346.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1144+304_1144+309d others(8): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70169247 | |||||||
| chr2:70169247 | CCACACAC others(1): Show |
C | 7 | a0001c0001t0001g0069 a0001c0001t0001g0115 a0001c0001t0001g0156 others(4): Show |
7 | HG01496.hp1 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144+302_1144+309d others(10): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70169247 | |||||||
| chr2:70169251 | A | C | 31 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0022 others(28): Show |
35 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1144+306T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70169251 | |||||||
| chr2:70169458 | T | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+99A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 6/9 | chr2 | 70169458 | |||||||
| chr2:70169672 | A | G | 4 | a0001c0001t0001g0277 a0001c0001t0001g0300 a0001c0001t0001g0302 others(1): Show |
4 | HG03486.hp2 NA19240.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-11T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70169672 | |||||||
| chr2:70170024 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0093 a0001c0001t0001g0301 |
3 | HG02630.hp1 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1040-363C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170024 | |||||||
| chr2:70170041 | G | A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(73): Show |
78 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1040-380C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170041 | |||||||
| chr2:70170050 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1040-389G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170050 | |||||||
| chr2:70170060 | G | C | 1 | a0001c0001t0001g0173 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1040-399C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170060 | |||||||
| chr2:70170181 | G | GA | 71 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(68): Show |
74 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1040-521dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170181 | |||||||
| chr2:70170181 | GA | G | 91 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0021 others(88): Show |
93 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1040-521delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170181 | |||||||
| chr2:70170183 | A | G | 1 | a0007c0012t0001g0244 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1040-522T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170183 | |||||||
| chr2:70170218 | A | T | 1 | a0001c0001t0001g0295 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1040-557T>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170218 | |||||||
| chr2:70170254 | AT | A | 82 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0044 others(79): Show |
84 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1040-594delA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170254 | |||||||
| chr2:70170286 | G | A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(73): Show |
78 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1040-625C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170286 | |||||||
| chr2:70170394 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1040-733C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170394 | |||||||
| chr2:70170565 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1040-904G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170565 | |||||||
| chr2:70170746 | TA | T | 128 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(125): Show |
134 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.1040-1086delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170746 | |||||||
| chr2:70170766 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0055 others(1): Show |
4 | HG02451.hp2 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1040-1105C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170766 | |||||||
| chr2:70170803 | A | C | 1 | a0001c0001t0001g0287 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1040-1142T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170803 | |||||||
| chr2:70170882 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1040-1221C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170882 | |||||||
| chr2:70170905 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1040-1244C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170905 | |||||||
| chr2:70170912 | G | A | 90 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(87): Show |
92 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1040-1251C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170912 | |||||||
| chr2:70170986 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1040-1325C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70170986 | |||||||
| chr2:70171046 | C | T | 2 | a0001c0001t0001g0309 a0003c0003t0001g0316 |
2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1040-1385G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70171046 | |||||||
| chr2:70171114 | C | CA | 90 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(87): Show |
92 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1040-1454dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70171114 | |||||||
| chr2:70171215 | G | A | 33 | a0001c0001t0001g0057 a0002c0002t0001g0001 a0002c0002t0001g0008 others(30): Show |
37 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.1040-1554C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70171215 | |||||||
| chr2:70171305 | A | G | 8 | a0001c0001t0001g0017 a0001c0001t0001g0305 a0001c0001t0001g0308 others(5): Show |
8 | HG01192.hp2 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1040-1644T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70171305 | |||||||
| chr2:70171455 | A | G | 91 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(88): Show |
93 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1040-1794T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70171455 | |||||||
| chr2:70171464 | C | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG02818.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1040-1803G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70171464 | |||||||
| chr2:70171535 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0070 a0001c0001t0001g0071 |
5 | HG01884.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1040-1874C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70171535 | |||||||
| chr2:70171545 | C | CG | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0275 |
3 | HG02451.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1040-1885_1040-188 others(5): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70171545 | |||||||
| chr2:70171546 | T | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0275 |
3 | HG02451.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1040-1885A>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70171546 | |||||||
| chr2:70171580 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1040-1919T>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70171580 | |||||||
| chr2:70171791 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1040-2130A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70171791 | |||||||
| chr2:70171994 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1040-2333C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70171994 | |||||||
| chr2:70172117 | G | A | 90 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(87): Show |
92 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1040-2456C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70172117 | |||||||
| chr2:70172223 | C | CA | 14 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0126 others(11): Show |
14 | HG01243.hp1 HG01361.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1040-2563dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70172223 | |||||||
| chr2:70172223 | CA | C | 32 | a0001c0001t0001g0057 a0001c0001t0001g0134 a0002c0002t0001g0001 others(29): Show |
36 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1040-2563delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70172223 | |||||||
| chr2:70172238 | A | AG | 12 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1040-2578_1040-257 others(5): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70172238 | |||||||
| chr2:70172238 | A | G | 78 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(75): Show |
80 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.1040-2577T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70172238 | |||||||
| chr2:70172286 | C | A | 1 | a0001c0001t0001g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1040-2625G>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70172286 | |||||||
| chr2:70172407 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1040-2746C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70172407 | |||||||
| chr2:70172534 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1040-2873A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70172534 | |||||||
| chr2:70172931 | G | C | 76 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(73): Show |
78 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1039+2742C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70172931 | |||||||
| chr2:70172938 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1039+2735C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70172938 | |||||||
| chr2:70173114 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1039+2559C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173114 | |||||||
| chr2:70173267 | C | CT | 31 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0044 others(28): Show |
32 | HG00735.hp1 HG01175.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1039+2405dupA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173267 | |||||||
| chr2:70173267 | C | CTT | 27 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0001c0001t0001g0074 others(24): Show |
27 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1039+2404_1039+240 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173267 | |||||||
| chr2:70173267 | CT | C | 8 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0168 others(5): Show |
8 | HG02273.hp2 HG02683.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039+2405delA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173267 | |||||||
| chr2:70173267 | CTTTTTTT others(5): Show |
C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0059 a0001c0001t0001g0073 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1039+2394_1039+240 others(16): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173267 | |||||||
| chr2:70173296 | C | T | 87 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(84): Show |
89 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.1039+2377G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173296 | |||||||
| chr2:70173364 | T | A | 75 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(72): Show |
77 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.1039+2309A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173364 | |||||||
| chr2:70173509 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0276 a0001c0001t0001g0298 |
4 | HG02109.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039+2164A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173509 | |||||||
| chr2:70173571 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1039+2102C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173571 | |||||||
| chr2:70173802 | G | GT | 8 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0161 others(5): Show |
9 | HG01243.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039+1870dupA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173802 | |||||||
| chr2:70173803 | T | G | 1 | a0001c0001t0001g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1039+1870A>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173803 | |||||||
| chr2:70173812 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1039+1861C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173812 | |||||||
| chr2:70173869 | C | T | 87 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(84): Show |
89 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.1039+1804G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173869 | |||||||
| chr2:70173976 | A | G | 66 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(63): Show |
69 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1039+1697T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173976 | |||||||
| chr2:70173983 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1039+1690G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70173983 | |||||||
| chr2:70174099 | G | T | 1 | a0001c0001t0001g0230 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1039+1574C>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70174099 | |||||||
| chr2:70174123 | C | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0275 |
3 | HG02451.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1039+1550G>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70174123 | |||||||
| chr2:70174222 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1039+1451G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70174222 | |||||||
| chr2:70174356 | G | A | 203 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
213 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.1039+1317C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70174356 | |||||||
| chr2:70174578 | G | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0142 |
3 | HG01243.hp2 HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1039+1095C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70174578 | |||||||
| chr2:70174628 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0093 a0001c0001t0001g0301 |
3 | HG02630.hp1 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1039+1045A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70174628 | |||||||
| chr2:70174733 | C | T | 76 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(73): Show |
78 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1039+940G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70174733 | |||||||
| chr2:70174836 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1039+837T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70174836 | |||||||
| chr2:70175048 | T | A | 93 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(90): Show |
95 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1039+625A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70175048 | |||||||
| chr2:70175219 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1039+454G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70175219 | |||||||
| chr2:70175369 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0275 |
3 | HG02451.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1039+304G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70175369 | |||||||
| chr2:70175385 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1039+288G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70175385 | |||||||
| chr2:70175471 | T | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0159 |
2 | HG00738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1039+202A>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70175471 | |||||||
| chr2:70175505 | T | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0275 |
3 | HG02451.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1039+168A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70175505 | |||||||
| chr2:70175657 | G | C | 32 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0022 others(29): Show |
36 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1039+16C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 5/9 | chr2 | 70175657 | |||||||
| chr2:70176029 | T | C | 4 | a0001c0001t0001g0281 a0001c0001t0001g0287 a0001c0001t0001g0288 others(1): Show |
4 | HG00673.hp1 HG02015.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.935-252A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70176029 | |||||||
| chr2:70176148 | T | C | 1 | a0002c0002t0001g0032 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.935-371A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70176148 | |||||||
| chr2:70176227 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.935-450A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70176227 | |||||||
| chr2:70176275 | T | C | 69 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(66): Show |
72 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.935-498A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70176275 | |||||||
| chr2:70176279 | C | T | 2 | a0001c0001t0001g0281 a0003c0003t0001g0294 |
2 | HG02165.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.935-502G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70176279 | |||||||
| chr2:70176333 | A | T | 190 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
199 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.935-556T>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70176333 | |||||||
| chr2:70176416 | A | C | 1 | a0001c0001t0001g0275 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.935-639T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70176416 | |||||||
| chr2:70176418 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.935-641G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70176418 | |||||||
| chr2:70176501 | CA | C | 32 | a0001c0001t0001g0113 a0002c0002t0001g0001 a0002c0002t0001g0008 others(29): Show |
36 | HG00558.hp2 HG00609.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.935-725delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70176501 | |||||||
| chr2:70176636 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.935-859C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70176636 | |||||||
| chr2:70176926 | C | T | 1 | a0001c0006t0001g0247 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.935-1149G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70176926 | |||||||
| chr2:70177043 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.935-1266C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70177043 | |||||||
| chr2:70177097 | C | A | 10 | a0001c0001t0001g0048 a0001c0001t0001g0074 a0001c0001t0001g0075 others(7): Show |
10 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.935-1320G>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70177097 | |||||||
| chr2:70177173 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.935-1396C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70177173 | |||||||
| chr2:70177227 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.935-1450C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70177227 | |||||||
| chr2:70177260 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.935-1483G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70177260 | |||||||
| chr2:70177279 | G | GA | 69 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(66): Show |
72 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.935-1503dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70177279 | |||||||
| chr2:70177617 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.935-1840C>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70177617 | |||||||
| chr2:70177668 | T | G | 5 | a0001c0001t0001g0156 a0001c0001t0001g0220 a0001c0001t0001g0317 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.934+1864A>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70177668 | |||||||
| chr2:70177823 | G | A | 121 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0029 others(118): Show |
127 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.934+1709C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70177823 | |||||||
| chr2:70177901 | A | C | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.934+1631T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70177901 | |||||||
| chr2:70177943 | G | A | 35 | a0001c0001t0001g0057 a0001c0001t0001g0305 a0001c0001t0001g0308 others(32): Show |
39 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.934+1589C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70177943 | |||||||
| chr2:70177990 | T | A | 69 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(66): Show |
72 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.934+1542A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70177990 | |||||||
| chr2:70178181 | T | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.934+1351A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70178181 | |||||||
| chr2:70178296 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.934+1236A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70178296 | |||||||
| chr2:70178424 | T | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0169 a0001c0001t0001g0177 |
3 | NA18942.hp2 NA19001.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.934+1108A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70178424 | |||||||
| chr2:70178435 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.934+1097G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70178435 | |||||||
| chr2:70178499 | C | T | 7 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0181 others(4): Show |
7 | NA18939.hp1 NA18966.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.934+1033G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70178499 | |||||||
| chr2:70178634 | T | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.934+898A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70178634 | |||||||
| chr2:70179052 | T | A | 1 | a0001c0001t0001g0017 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.934+480A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70179052 | |||||||
| chr2:70179069 | T | C | 1 | a0003c0003t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.934+463A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70179069 | |||||||
| chr2:70179125 | T | TTTAAGGG others(10): Show |
1 | a0001c0001t0001g0045 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.934+390_934+406dup others(17): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70179125 | |||||||
| chr2:70179274 | CAT | C | 77 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0048 others(74): Show |
79 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.934+256_934+257del others(2): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70179274 | |||||||
| chr2:70179278 | A | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
6 | HG02451.hp1 HG02615.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.934+254T>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70179278 | |||||||
| chr2:70179476 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.934+56G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 4/9 | chr2 | 70179476 | |||||||
| chr2:70179729 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.824-87A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70179729 | |||||||
| chr2:70179784 | A | T | 203 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
213 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.824-142T>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70179784 | |||||||
| chr2:70179901 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.824-259A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70179901 | |||||||
| chr2:70179917 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.824-275G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70179917 | |||||||
| chr2:70179955 | A | C | 1 | a0001c0001t0001g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.824-313T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70179955 | |||||||
| chr2:70179972 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.824-330T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70179972 | |||||||
| chr2:70179991 | T | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0014 others(75): Show |
82 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.824-349A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70179991 | |||||||
| chr2:70180014 | G | A | 5 | a0001c0001t0001g0156 a0001c0001t0001g0220 a0001c0001t0001g0317 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-372C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180014 | |||||||
| chr2:70180025 | C | T | 33 | a0001c0001t0001g0057 a0002c0002t0001g0001 a0002c0002t0001g0008 others(30): Show |
37 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.824-383G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180025 | |||||||
| chr2:70180030 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.824-388C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180030 | |||||||
| chr2:70180073 | C | G | 46 | a0001c0001t0001g0006 a0001c0001t0001g0059 a0001c0001t0001g0073 others(43): Show |
48 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.824-431G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180073 | |||||||
| chr2:70180494 | G | A | 1 | a0002c0002t0001g0034 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.823+669C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180494 | |||||||
| chr2:70180548 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0229 |
2 | NA19087.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.823+615G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180548 | |||||||
| chr2:70180607 | C | CA | 135 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(132): Show |
142 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.823+555dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180607 | |||||||
| chr2:70180607 | C | CAA | 23 | a0001c0001t0001g0005 a0001c0001t0001g0070 a0001c0001t0001g0071 others(20): Show |
25 | HG00438.hp1 HG00621.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.823+554_823+555dup others(2): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180607 | |||||||
| chr2:70180607 | C | CAAA | 52 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(49): Show |
53 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.823+553_823+555dup others(3): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180607 | |||||||
| chr2:70180607 | C | CAAAA | 8 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0197 others(5): Show |
8 | HG01433.hp2 HG02258.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+552_823+555dup others(4): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180607 | |||||||
| chr2:70180607 | CA | C | 6 | a0001c0001t0001g0087 a0001c0001t0001g0112 a0001c0001t0001g0161 others(3): Show |
6 | HG02280.hp2 HG02622.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+555delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180607 | |||||||
| chr2:70180722 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.823+441G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180722 | |||||||
| chr2:70180734 | G | A | 1 | a0002c0002t0001g0033 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.823+429C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180734 | |||||||
| chr2:70180735 | C | T | 1 | a0002c0002t0001g0033 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.823+428G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180735 | |||||||
| chr2:70180913 | G | C | 1 | a0001c0001t0001g0105 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.823+250C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70180913 | |||||||
| chr2:70181000 | CA | C | 19 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(16): Show |
20 | HG00423.hp2 HG00741.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.823+162delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70181000 | |||||||
| chr2:70181000 | CAA | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
190 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.823+161_823+162del others(2): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70181000 | |||||||
| chr2:70181000 | CAAA | C | 104 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(101): Show |
113 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.823+160_823+162del others(3): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70181000 | |||||||
| chr2:70181000 | CAAAA | C | 9 | a0001c0001t0001g0045 a0001c0001t0001g0220 a0001c0001t0001g0223 others(6): Show |
9 | HG01257.hp1 HG02293.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+159_823+162del others(4): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70181000 | |||||||
| chr2:70181000 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0233 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.823+147_823+162del others(16): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 3/9 | chr2 | 70181000 | |||||||
| chr2:70182101 | C | T | 5 | a0001c0001t0001g0156 a0001c0001t0001g0220 a0001c0001t0001g0317 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-104G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 2/9 | chr2 | 70182101 | |||||||
| chr2:70182122 | C | T | 11 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0062 others(8): Show |
11 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12-125G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 2/9 | chr2 | 70182122 | |||||||
| chr2:70182163 | G | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0275 |
3 | HG02451.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-12-166C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 2/9 | chr2 | 70182163 | |||||||
| chr2:70182319 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-12-322G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 2/9 | chr2 | 70182319 | |||||||
| chr2:70182492 | T | A | 1 | a0001c0008t0001g0097 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-13+175A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 2/9 | chr2 | 70182492 | |||||||
| chr2:70182965 | G | A | 16 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(13): Show |
16 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-281-30C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70182965 | |||||||
| chr2:70183152 | T | C | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0044 others(32): Show |
37 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.-281-217A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70183152 | |||||||
| chr2:70183395 | C | G | 27 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0111 others(24): Show |
29 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.-281-460G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70183395 | |||||||
| chr2:70183439 | T | A | 1 | a0001c0001t0003g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-281-504A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70183439 | |||||||
| chr2:70183539 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-281-604G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70183539 | |||||||
| chr2:70183619 | C | T | 5 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0320 others(2): Show |
5 | HG01192.hp2 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-281-684G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70183619 | |||||||
| chr2:70183620 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-281-685C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70183620 | |||||||
| chr2:70183712 | G | A | 14 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0308 others(11): Show |
14 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-281-777C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70183712 | |||||||
| chr2:70183725 | T | G | 4 | a0001c0001t0001g0093 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02630.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-281-790A>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70183725 | |||||||
| chr2:70183729 | T | TA | 227 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(224): Show |
241 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.-281-795dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70183729 | |||||||
| chr2:70183738 | A | AC | 5 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0320 others(2): Show |
5 | HG01192.hp2 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-281-804_-281-803i others(3): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70183738 | |||||||
| chr2:70183829 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-281-894T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70183829 | |||||||
| chr2:70184131 | C | T | 9 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0308 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-281-1196G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184131 | |||||||
| chr2:70184200 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0267 |
2 | HG02040.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.-281-1265A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184200 | |||||||
| chr2:70184213 | G | GACT | 243 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
257 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(254): Show |
intron_variant | MODIFIER | c.-281-1279_-281-127 others(7): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184213 | |||||||
| chr2:70184309 | C | T | 5 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0320 others(2): Show |
5 | HG01192.hp2 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-281-1374G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184309 | |||||||
| chr2:70184479 | A | AT | 20 | a0001c0001t0001g0088 a0001c0001t0001g0092 a0001c0001t0001g0101 others(17): Show |
20 | HG00438.hp2 HG00741.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-281-1545dupA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184479 | |||||||
| chr2:70184479 | AT | A | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(163): Show |
178 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.-281-1545delA | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184479 | |||||||
| chr2:70184479 | ATT | A | 17 | a0001c0001t0001g0074 a0001c0001t0001g0169 a0001c0001t0001g0198 others(14): Show |
17 | HG00438.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-281-1546_-281-154 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184479 | |||||||
| chr2:70184479 | ATTT | A | 22 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0276 others(19): Show |
24 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.-281-1547_-281-154 others(7): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184479 | |||||||
| chr2:70184479 | ATTTT | A | 8 | a0001c0001t0001g0093 a0001c0001t0001g0300 a0001c0001t0001g0301 others(5): Show |
8 | HG01192.hp2 HG02630.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-281-1548_-281-154 others(8): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184479 | |||||||
| chr2:70184479 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-281-1558_-281-154 others(18): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184479 | |||||||
| chr2:70184510 | CAG | C | 188 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
200 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.-281-1577_-281-157 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184510 | |||||||
| chr2:70184617 | A | T | 1 | a0001c0001t0001g0292 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-281-1682T>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184617 | |||||||
| chr2:70184634 | C | G | 1 | a0006c0013t0001g0205 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-281-1699G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184634 | |||||||
| chr2:70184732 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-281-1797G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184732 | |||||||
| chr2:70184817 | G | A | 24 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(21): Show |
27 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-281-1882C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184817 | |||||||
| chr2:70184828 | T | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0142 |
3 | HG01243.hp2 HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-281-1893A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70184828 | |||||||
| chr2:70185014 | C | A | 1 | a0001c0001t0001g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-281-2079G>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185014 | |||||||
| chr2:70185039 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-281-2104C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185039 | |||||||
| chr2:70185079 | G | A | 1 | a0002c0002t0001g0064 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-281-2144C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185079 | |||||||
| chr2:70185202 | A | C | 22 | a0001c0001t0001g0015 a0001c0001t0001g0278 a0001c0001t0001g0279 others(19): Show |
23 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.-281-2267T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185202 | |||||||
| chr2:70185302 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-281-2367C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185302 | |||||||
| chr2:70185381 | A | G | 248 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
262 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(259): Show |
intron_variant | MODIFIER | c.-281-2446T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185381 | |||||||
| chr2:70185404 | G | A | 30 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0093 others(27): Show |
32 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.-281-2469C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185404 | |||||||
| chr2:70185408 | CA | C | 193 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(190): Show |
205 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.-281-2474delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185408 | |||||||
| chr2:70185425 | A | G | 26 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0276 others(23): Show |
28 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.-281-2490T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185425 | |||||||
| chr2:70185447 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-281-2512G>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185447 | |||||||
| chr2:70185471 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-281-2536C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185471 | |||||||
| chr2:70185565 | G | T | 1 | a0001c0001t0001g0100 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-281-2630C>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185565 | |||||||
| chr2:70185667 | C | T | 22 | a0001c0001t0001g0015 a0001c0001t0001g0278 a0001c0001t0001g0279 others(19): Show |
23 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.-281-2732G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185667 | |||||||
| chr2:70185701 | A | C | 9 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0308 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-281-2766T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185701 | |||||||
| chr2:70185714 | A | C | 1 | a0001c0001t0001g0009 | 2 | NA19004.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-281-2779T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185714 | |||||||
| chr2:70185720 | A | T | 9 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0075 others(6): Show |
9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-281-2785T>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185720 | |||||||
| chr2:70185722 | T | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0301 a0001c0001t0001g0302 others(1): Show |
4 | HG02630.hp1 HG03453.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-281-2787A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185722 | |||||||
| chr2:70185734 | C | T | 44 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0093 others(41): Show |
46 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.-281-2799G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185734 | |||||||
| chr2:70185786 | T | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0199 a0001c0001t0001g0201 others(1): Show |
7 | HG00597.hp2 HG02523.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-2851A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185786 | |||||||
| chr2:70185786 | T | TAC | 3 | a0001c0001t0001g0014 a0001c0001t0001g0276 a0001c0001t0001g0298 |
4 | HG02109.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-281-2853_-281-285 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185786 | |||||||
| chr2:70185796 | C | CAT | 10 | a0001c0001t0001g0055 a0001c0001t0001g0304 a0001c0001t0001g0305 others(7): Show |
10 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-281-2863_-281-286 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185796 | |||||||
| chr2:70185796 | C | CATAT | 5 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0320 others(2): Show |
5 | HG01192.hp2 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-281-2865_-281-286 others(8): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185796 | |||||||
| chr2:70185798 | T | C | 27 | a0001c0001t0001g0015 a0001c0001t0001g0093 a0001c0001t0001g0277 others(24): Show |
28 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.-281-2863A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185798 | |||||||
| chr2:70185993 | T | TA | 10 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0153 others(7): Show |
10 | HG01071.hp1 HG01175.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-281-3059dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185993 | |||||||
| chr2:70185993 | TA | T | 14 | a0001c0001t0001g0021 a0001c0001t0001g0054 a0001c0001t0001g0074 others(11): Show |
14 | HG01070.hp1 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-281-3059delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185993 | |||||||
| chr2:70185993 | TAA | T | 37 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0093 others(34): Show |
39 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.-281-3060_-281-305 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70185993 | |||||||
| chr2:70186220 | C | T | 44 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0093 others(41): Show |
46 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.-281-3285G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186220 | |||||||
| chr2:70186281 | C | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-281-3346G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186281 | |||||||
| chr2:70186300 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-281-3365C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186300 | |||||||
| chr2:70186309 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-281-3374A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186309 | |||||||
| chr2:70186313 | T | TAC | 5 | a0001c0001t0001g0204 a0001c0001t0001g0218 a0001c0001t0001g0227 others(2): Show |
5 | HG00621.hp1 NA18940.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.-281-3380_-281-337 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186313 | |||||||
| chr2:70186315 | C | T | 14 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0308 others(11): Show |
14 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-281-3380G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186315 | |||||||
| chr2:70186334 | A | G | 10 | a0002c0002t0001g0008 a0002c0002t0001g0025 a0002c0002t0001g0026 others(7): Show |
11 | HG01257.hp2 HG01258.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.-281-3399T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186334 | |||||||
| chr2:70186406 | T | TATC | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
255 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.-281-3474_-281-347 others(7): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186406 | |||||||
| chr2:70186515 | A | G | 237 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(234): Show |
251 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.-281-3580T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186515 | |||||||
| chr2:70186720 | T | A | 1 | a0001c0001t0003g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-281-3785A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186720 | |||||||
| chr2:70186727 | G | T | 5 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0320 others(2): Show |
5 | HG01192.hp2 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-281-3792C>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186727 | |||||||
| chr2:70186755 | A | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-281-3820T>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186755 | |||||||
| chr2:70186912 | A | C | 1 | a0003c0003t0001g0016 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-281-3977T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186912 | |||||||
| chr2:70186959 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-282+4014C>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186959 | |||||||
| chr2:70186992 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-282+3981A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70186992 | |||||||
| chr2:70187127 | C | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+3846G>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187127 | |||||||
| chr2:70187132 | A | C | 3 | a0001c0001t0001g0240 a0001c0001t0001g0260 a0001c0001t0001g0299 |
3 | HG00438.hp1 HG00558.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-282+3841T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187132 | |||||||
| chr2:70187217 | C | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-282+3756G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187217 | |||||||
| chr2:70187232 | C | T | 1 | a0003c0003t0001g0016 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-282+3741G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187232 | |||||||
| chr2:70187233 | T | C | 1 | a0003c0003t0001g0016 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-282+3740A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187233 | |||||||
| chr2:70187252 | TTTG | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(105): Show |
113 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-282+3718_-282+372 others(7): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187252 | |||||||
| chr2:70187337 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG02622.hp1 HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-282+3636C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187337 | |||||||
| chr2:70187343 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-282+3630G>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187343 | |||||||
| chr2:70187353 | T | C | 44 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0093 others(41): Show |
46 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.-282+3620A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187353 | |||||||
| chr2:70187400 | G | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0071 |
4 | HG01884.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+3573C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187400 | |||||||
| chr2:70187454 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-282+3519A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187454 | |||||||
| chr2:70187504 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0048 a0001c0001t0001g0069 |
3 | HG02647.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-282+3469G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187504 | |||||||
| chr2:70187609 | T | C | 22 | a0001c0001t0001g0015 a0001c0001t0001g0278 a0001c0001t0001g0279 others(19): Show |
23 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.-282+3364A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187609 | |||||||
| chr2:70187751 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-282+3222G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187751 | |||||||
| chr2:70187777 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0071 |
4 | HG01884.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+3196C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187777 | |||||||
| chr2:70187910 | C | T | 1 | a0002c0002t0001g0023 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-282+3063G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70187910 | |||||||
| chr2:70188210 | C | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02630.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-282+2763G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188210 | |||||||
| chr2:70188277 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-282+2696A>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188277 | |||||||
| chr2:70188333 | G | A | 9 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0308 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-282+2640C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188333 | |||||||
| chr2:70188343 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-282+2630T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188343 | |||||||
| chr2:70188349 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0071 |
4 | HG01884.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+2624C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188349 | |||||||
| chr2:70188378 | C | T | 30 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0093 others(27): Show |
32 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.-282+2595G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188378 | |||||||
| chr2:70188401 | G | T | 1 | a0003c0003t0001g0016 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-282+2572C>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188401 | |||||||
| chr2:70188442 | G | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+2531C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188442 | |||||||
| chr2:70188762 | C | T | 3 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0155 |
3 | HG02738.hp1 HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-282+2211G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188762 | |||||||
| chr2:70188806 | G | C | 5 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0320 others(2): Show |
5 | HG01192.hp2 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-282+2167C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188806 | |||||||
| chr2:70188809 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0276 a0001c0001t0001g0298 |
4 | HG02109.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+2164C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188809 | |||||||
| chr2:70188883 | G | T | 1 | a0001c0001t0001g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+2090C>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188883 | |||||||
| chr2:70188884 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+2089T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188884 | |||||||
| chr2:70188885 | T | A | 1 | a0001c0001t0001g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+2088A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188885 | |||||||
| chr2:70188977 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-282+1996G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70188977 | |||||||
| chr2:70189026 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-282+1947G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189026 | |||||||
| chr2:70189032 | A | G | 1 | a0003c0003t0001g0016 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-282+1941T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189032 | |||||||
| chr2:70189065 | C | T | 51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0273 others(48): Show |
53 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-282+1908G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189065 | |||||||
| chr2:70189088 | A | T | 1 | a0001c0001t0001g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+1885T>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189088 | |||||||
| chr2:70189089 | T | A | 1 | a0001c0001t0001g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+1884A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189089 | |||||||
| chr2:70189094 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | NA18612.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-282+1879A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189094 | |||||||
| chr2:70189296 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
5 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+1677G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189296 | |||||||
| chr2:70189330 | C | T | 1 | a0001c0001t0001g0017 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-282+1643G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189330 | |||||||
| chr2:70189336 | C | G | 14 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(11): Show |
14 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-282+1637G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189336 | |||||||
| chr2:70189341 | G | C | 23 | a0001c0001t0001g0015 a0001c0001t0001g0277 a0001c0001t0001g0278 others(20): Show |
24 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.-282+1632C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189341 | |||||||
| chr2:70189347 | G | C | 1 | a0002c0002t0001g0047 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-282+1626C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189347 | |||||||
| chr2:70189406 | C | CA | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
145 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.-282+1566dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189406 | |||||||
| chr2:70189406 | C | CAA | 51 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0206 others(48): Show |
51 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-282+1565_-282+156 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189406 | |||||||
| chr2:70189406 | C | CAAA | 6 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0313 others(3): Show |
6 | HG02970.hp2 HG03130.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-282+1564_-282+156 others(7): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189406 | |||||||
| chr2:70189406 | CA | C | 6 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-282+1566delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189406 | |||||||
| chr2:70189406 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 |
3 | HG03453.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-282+1557_-282+156 others(14): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189406 | |||||||
| chr2:70189406 | CAAAAAAA others(4): Show |
C | 17 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(14): Show |
17 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.-282+1556_-282+156 others(15): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189406 | |||||||
| chr2:70189434 | T | A | 4 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG02976.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+1539A>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189434 | |||||||
| chr2:70189439 | C | T | 14 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(11): Show |
14 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-282+1534G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189439 | |||||||
| chr2:70189461 | T | G | 1 | a0003c0003t0001g0016 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-282+1512A>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189461 | |||||||
| chr2:70189462 | A | T | 1 | a0003c0003t0001g0016 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-282+1511T>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189462 | |||||||
| chr2:70189663 | A | G | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-282+1310T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189663 | |||||||
| chr2:70189696 | C | T | 14 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(11): Show |
14 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-282+1277G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189696 | |||||||
| chr2:70189715 | C | CA | 38 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(35): Show |
38 | HG00423.hp1 HG01074.hp1 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.-282+1257dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189715 | |||||||
| chr2:70189715 | CA | C | 86 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0014 others(83): Show |
95 | HG00609.hp2 HG00673.hp1 HG00741.hp1 others(92): Show |
intron_variant | MODIFIER | c.-282+1257delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189715 | |||||||
| chr2:70189814 | T | C | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+1159A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189814 | |||||||
| chr2:70189861 | T | TA | 7 | a0001c0001t0001g0165 a0001c0001t0001g0232 a0001c0001t0001g0317 others(4): Show |
7 | HG01192.hp2 HG01884.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+1111dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189861 | |||||||
| chr2:70189861 | TA | T | 8 | a0001c0001t0001g0021 a0001c0001t0001g0167 a0001c0001t0001g0233 others(5): Show |
8 | HG01169.hp1 HG02602.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-282+1111delT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189861 | |||||||
| chr2:70189889 | T | C | 3 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 |
3 | HG03453.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-282+1084A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189889 | |||||||
| chr2:70189922 | C | T | 5 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0320 others(2): Show |
5 | HG01192.hp2 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-282+1051G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189922 | |||||||
| chr2:70189943 | GAA | G | 19 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(16): Show |
19 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-282+1028_-282+102 others(6): Show |
C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70189943 | |||||||
| chr2:70190003 | T | C | 1 | a0002c0002t0001g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-282+970A>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70190003 | |||||||
| chr2:70190006 | A | G | 32 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0273 others(29): Show |
34 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.-282+967T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70190006 | |||||||
| chr2:70190013 | C | G | 68 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0167 others(65): Show |
71 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-282+960G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70190013 | |||||||
| chr2:70190237 | C | T | 5 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0320 others(2): Show |
5 | HG01192.hp2 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-282+736G>A | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70190237 | |||||||
| chr2:70190242 | G | A | 14 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(11): Show |
14 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-282+731C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70190242 | |||||||
| chr2:70190274 | T | TA | 5 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0320 others(2): Show |
5 | HG01192.hp2 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-282+698dupT | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70190274 | |||||||
| chr2:70190405 | G | A | 109 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(106): Show |
114 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-282+568C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70190405 | |||||||
| chr2:70190590 | G | C | 1 | a0003c0003t0001g0316 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-282+383C>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70190590 | |||||||
| chr2:70190598 | A | G | 51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0273 others(48): Show |
53 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-282+375T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70190598 | |||||||
| chr2:70190640 | C | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 |
4 | HG03098.hp2 HG03139.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+333G>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70190640 | |||||||
| chr2:70190734 | A | G | 1 | a0001c0001t0001g0017 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-282+239T>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70190734 | |||||||
| chr2:70190829 | G | A | 5 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0320 others(2): Show |
5 | HG01192.hp2 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-282+144C>T | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70190829 | |||||||
| chr2:70190856 | A | C | 1 | a0003c0003t0001g0016 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-282+117T>G | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70190856 | |||||||
| chr2:70190907 | T | G | 51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0273 others(48): Show |
53 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-282+66A>C | C2orf42 | ENSG00000115998.8 | transcript | ENST00000264434.7 | protein_coding | 1/9 | chr2 | 70190907 |