Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 728537 |
| ensemblid | ENSG00000228486.11 |
| hgncid | 49272 |
| symbol | C2orf92 |
| name | chromosome 2 open reading frame 92 |
| refseq_nuc | NM_001351368.2 |
| refseq_prot | NP_001338297.1 |
| ensembl_nuc | ENST00000627399.4 |
| ensembl_prot | ENSP00000490587.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 97669713 |
| end | 97703066 |
| strand | + |
| ver | v1.2 |
| region | chr2:97669713-97703066 |
| region5000 | chr2:97664713-97708066 |
| regionname0 | C2orf92_chr2_97669713_97703066 |
| regionname5000 | C2orf92_chr2_97664713_97708066 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 265 | 172 | 65 | 31 | 52 | 3 | 19 | 42 | C2orf92_chr2_97664713_97708066 | C2orf92 | MSRAM others(260): Show |
chr2 | 97664713 | 97708066 |
| a0002 | 0/0 | 265 | 86 | 9 | 23 | 41 | 5 | 8 | 31 | C2orf92_chr2_97664713_97708066 | C2orf92 | MSRAM others(260): Show |
chr2 | 97664713 | 97708066 |
| a0003 | 0/0 | 265 | 29 | 1 | 2 | 23 | 0 | 3 | 17 | C2orf92_chr2_97664713_97708066 | C2orf92 | MSRAM others(260): Show |
chr2 | 97664713 | 97708066 |
| a0004 | 0/0 | 258 | 14 | 12 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | MSRAM others(253): Show |
chr2 | 97664713 | 97708066 |
| a0005 | 0/0 | 265 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | MSRAM others(260): Show |
chr2 | 97664713 | 97708066 |
| a0006 | 0/0 | 254 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | MSRAM others(249): Show |
chr2 | 97664713 | 97708066 |
| a0007 | 0/0 | 265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | MSRAM others(260): Show |
chr2 | 97664713 | 97708066 |
| a0008 | 0/0 | 265 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | MSRAM others(260): Show |
chr2 | 97664713 | 97708066 |
| a0009 | 0/0 | 264 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | MSRAM others(259): Show |
chr2 | 97664713 | 97708066 |
| a0010 | 0/0 | 258 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | MSRAM others(253): Show |
chr2 | 97664713 | 97708066 |
| a0011 | 0/0 | 265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | MSRAM others(260): Show |
chr2 | 97664713 | 97708066 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 795 | 172 | 65 | 31 | 52 | 3 | 19 | C2orf92_chr2_97664713_97708066 | C2orf92 | ATGAG others(790): Show |
chr2 | 97664713 | 97708066 | ||
| a0002c0002 | 0/0 | 795 | 83 | 9 | 23 | 38 | 5 | 8 | C2orf92_chr2_97664713_97708066 | C2orf92 | ATGAG others(790): Show |
chr2 | 97664713 | 97708066 | ||
| a0002c0005 | 0/0 | 795 | 3 | 0 | 0 | 3 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | ATGAG others(790): Show |
chr2 | 97664713 | 97708066 | ||
| a0003c0003 | 0/0 | 795 | 29 | 1 | 2 | 23 | 0 | 3 | C2orf92_chr2_97664713_97708066 | C2orf92 | ATGAG others(790): Show |
chr2 | 97664713 | 97708066 | ||
| a0004c0004 | 0/0 | 794 | 14 | 12 | 2 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | ATGAG others(789): Show |
chr2 | 97664713 | 97708066 | ||
| a0005c0006 | 0/0 | 795 | 3 | 3 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | ATGAG others(790): Show |
chr2 | 97664713 | 97708066 | ||
| a0006c0011 | 0/0 | 762 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | ATGAG others(757): Show |
chr2 | 97664713 | 97708066 | ||
| a0007c0009 | 0/0 | 795 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | ATGAG others(790): Show |
chr2 | 97664713 | 97708066 | ||
| a0008c0012 | 0/0 | 795 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | ATGAG others(790): Show |
chr2 | 97664713 | 97708066 | ||
| a0009c0007 | 0/0 | 792 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | ATGAG others(787): Show |
chr2 | 97664713 | 97708066 | ||
| a0010c0010 | 0/0 | 794 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | ATGAG others(789): Show |
chr2 | 97664713 | 97708066 | ||
| a0011c0008 | 0/0 | 795 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | ATGAG others(790): Show |
chr2 | 97664713 | 97708066 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1139 | 63 | 50 | 10 | 1 | 1 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1134): Show |
chr2 | 97664713 | 97708066 |
| a0001c0001t0002 | 1/1 | 1139 | 109 | 15 | 21 | 51 | 2 | 18 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1134): Show |
chr2 | 97664713 | 97708066 |
| a0002c0002t0001 | 0/0 | 1139 | 83 | 9 | 23 | 38 | 5 | 8 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1134): Show |
chr2 | 97664713 | 97708066 |
| a0002c0005t0001 | 0/0 | 1139 | 3 | 0 | 0 | 3 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1134): Show |
chr2 | 97664713 | 97708066 |
| a0003c0003t0001 | 0/0 | 1139 | 2 | 0 | 2 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1134): Show |
chr2 | 97664713 | 97708066 |
| a0003c0003t0003 | 0/0 | 1139 | 17 | 0 | 0 | 17 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1134): Show |
chr2 | 97664713 | 97708066 |
| a0003c0003t0004 | 0/0 | 1139 | 7 | 0 | 0 | 4 | 0 | 3 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1134): Show |
chr2 | 97664713 | 97708066 |
| a0003c0003t0005 | 0/0 | 1139 | 3 | 1 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1134): Show |
chr2 | 97664713 | 97708066 |
| a0004c0004t0001 | 0/0 | 1138 | 14 | 12 | 2 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1133): Show |
chr2 | 97664713 | 97708066 |
| a0005c0006t0002 | 0/0 | 1139 | 3 | 3 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1134): Show |
chr2 | 97664713 | 97708066 |
| a0006c0011t0002 | 0/0 | 1106 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1101): Show |
chr2 | 97664713 | 97708066 |
| a0007c0009t0002 | 0/0 | 1139 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1134): Show |
chr2 | 97664713 | 97708066 |
| a0008c0012t0003 | 0/0 | 1139 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1134): Show |
chr2 | 97664713 | 97708066 |
| a0009c0007t0001 | 0/0 | 1136 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1131): Show |
chr2 | 97664713 | 97708066 |
| a0010c0010t0001 | 0/0 | 1138 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1133): Show |
chr2 | 97664713 | 97708066 |
| a0011c0008t0002 | 0/0 | 1139 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | GGAGT others(1134): Show |
chr2 | 97664713 | 97708066 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0001 | 1/0 | 20 | 2 | 2 | 11 | 0 | 4 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0002 | 0/0 | 16 | 0 | 4 | 9 | 2 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0004 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0009 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0002c0005t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0003g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0003c0003t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0004c0004t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0004c0004t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0004c0004t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0004c0004t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0004c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0004c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0004c0004t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0004c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0004c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0004c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0004c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0004c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0004c0004t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0005c0006t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0005c0006t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0006c0011t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0007c0009t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0008c0012t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0009c0007t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0010c0010t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| a0011c0008t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0198 | EUR | GBR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0055 | EUR | GBR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0199 | EUR | GBR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00597 | hp2 | a0003 | c0003 | t0003 | g0222 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0068 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01243 | hp1 | a0004 | c0004 | t0001 | g0092 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0053 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0073 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01358 | hp1 | a0004 | c0004 | t0001 | g0081 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0072 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0058 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0050 | EUR | IBS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0070 | EUR | IBS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0054 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02040 | hp2 | a0003 | c0003 | t0005 | g0095 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02056 | hp1 | a0003 | c0003 | t0004 | g0103 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02056 | hp2 | a0003 | c0003 | t0004 | g0097 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02071 | hp1 | a0003 | c0003 | t0004 | g0098 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02083 | hp1 | a0003 | c0003 | t0004 | g0099 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02451 | hp1 | a0004 | c0004 | t0001 | g0083 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0059 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02717 | hp2 | a0005 | c0006 | t0002 | g0144 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02895 | hp1 | a0006 | c0011 | t0002 | g0171 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02895 | hp2 | a0004 | c0004 | t0001 | g0084 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0036 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02897 | hp1 | a0004 | c0004 | t0001 | g0086 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02965 | hp2 | a0005 | c0006 | t0002 | g0023 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02970 | hp2 | a0004 | c0004 | t0001 | g0082 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03098 | hp1 | a0004 | c0004 | t0001 | g0080 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03130 | hp1 | a0004 | c0004 | t0001 | g0020 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03209 | hp1 | a0004 | c0004 | t0001 | g0085 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03225 | hp1 | a0005 | c0006 | t0002 | g0023 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03453 | hp1 | a0004 | c0004 | t0001 | g0087 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03453 | hp2 | a0004 | c0004 | t0001 | g0090 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03486 | hp2 | a0003 | c0003 | t0005 | g0096 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03579 | hp1 | a0004 | c0004 | t0001 | g0079 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0069 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0051 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03834 | hp1 | a0003 | c0003 | t0004 | g0102 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG04115 | hp1 | a0003 | c0003 | t0004 | g0100 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG04204 | hp2 | a0003 | c0003 | t0004 | g0101 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0049 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | CHB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18906 | hp2 | a0004 | c0004 | t0001 | g0091 | AFR | YRI | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18940 | hp1 | a0003 | c0003 | t0003 | g0221 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18941 | hp2 | a0008 | c0012 | t0003 | g0013 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18947 | hp1 | a0002 | c0005 | t0001 | g0057 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18951 | hp1 | a0003 | c0003 | t0003 | g0223 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18956 | hp2 | a0003 | c0003 | t0003 | g0215 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18960 | hp1 | a0002 | c0005 | t0001 | g0075 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18965 | hp2 | a0003 | c0003 | t0003 | g0216 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18966 | hp1 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18966 | hp2 | a0009 | c0007 | t0001 | g0094 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18967 | hp2 | a0003 | c0003 | t0003 | g0224 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18970 | hp2 | a0003 | c0003 | t0003 | g0217 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18971 | hp1 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18973 | hp1 | a0003 | c0003 | t0003 | g0225 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18983 | hp2 | a0003 | c0003 | t0003 | g0013 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18999 | hp1 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19010 | hp1 | a0002 | c0005 | t0001 | g0074 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19043 | hp1 | a0010 | c0010 | t0001 | g0088 | AFR | LWK | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19054 | hp2 | a0003 | c0003 | t0003 | g0218 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19070 | hp1 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19083 | hp1 | a0003 | c0003 | t0003 | g0220 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19084 | hp1 | a0003 | c0003 | t0005 | g0226 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19085 | hp1 | a0003 | c0003 | t0003 | g0219 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19088 | hp1 | a0003 | c0003 | t0003 | g0013 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | YRI | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ASW | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA20129 | hp2 | a0004 | c0004 | t0001 | g0020 | AFR | ASW | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | GIH | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | GIH | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | USA | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| HG06807 | hp2 | a0007 | c0009 | t0002 | g0181 | AFR | USA | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | USA | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | USA | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| NA21309 | hp2 | a0011 | c0008 | t0002 | g0174 | AFR | LWK | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0165 | REF | REF | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0001 | REF | REF | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:97690264 | A | G | 3 | a0003 a0004 a0008 |
44 | HG00597.hp2 HG01243.hp1 HG01346.hp1 others(41): Show |
missense_variant | MODERATE | c.340A>G | p.Ile114Val | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/8 | 416/1139 | 340/798 | 114/265 | chr2 | 97690264 | |||
| chr2:97699070 | G | A | 1 | a0008 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.448G>A | p.Asp150Asn | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/8 | 524/1139 | 448/798 | 150/265 | chr2 | 97699070 | |||
| chr2:97701148 | ATTTAGAT others(31): Show |
A | 1 | a0006 | 1 | HG02895.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.515-3_549delTAGATG others(32): Show |
p.Asp172fs | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/8 | 515/798 | 172/265 | INFO_REALIGN_3_PRIME | chr2 | 97701148 | |||
| chr2:97701202 | A | T | 2 | a0004 a0010 |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
missense_variant | MODERATE | c.563A>T | p.Gln188Leu | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/8 | 639/1139 | 563/798 | 188/265 | chr2 | 97701202 | |||
| chr2:97701222 | G | A | 2 | a0002 a0009 |
87 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(84): Show |
missense_variant | MODERATE | c.583G>A | p.Ala195Thr | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/8 | 659/1139 | 583/798 | 195/265 | chr2 | 97701222 | |||
| chr2:97701225 | G | A | 1 | a0011 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.586G>A | p.Val196Ile | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/8 | 662/1139 | 586/798 | 196/265 | chr2 | 97701225 | |||
| chr2:97702728 | A | C | 1 | a0005 | 3 | HG02717.hp2 HG02965.hp2 HG03225.hp1 |
missense_variant | MODERATE | c.725A>C | p.His242Pro | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 8/8 | 801/1139 | 725/798 | 242/265 | chr2 | 97702728 | |||
| chr2:97702739 | GA | G | 2 | a0004 a0010 |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
frameshift_variant | HIGH | c.743delA | p.Asn248fs | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 8/8 | 819/1139 | 743/798 | 248/265 | INFO_REALIGN_3_PRIME | chr2 | 97702739 | ||
| chr2:97702758 | T | C | 1 | a0007 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.755T>C | p.Leu252Pro | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 8/8 | 831/1139 | 755/798 | 252/265 | chr2 | 97702758 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:97674490 | G | A | 1 | a0002c0005 | 3 | NA18947.hp1 NA18960.hp1 NA19010.hp1 |
synonymous_variant | LOW | c.81G>A | p.Pro27Pro | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 2/8 | 157/1139 | 81/798 | 27/265 | chr2 | 97674490 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:97669772 | T | C | 11 | a0001c0001t0001 a0002c0002t0001 a0002c0005t0001 others(8): Show |
195 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(192): Show |
5_prime_UTR_variant | MODIFIER | c.-17T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/8 | 17 | chr2 | 97669772 | ||||||
| chr2:97702887 | T | C | 1 | a0003c0003t0004 | 7 | HG02056.hp1 HG02056.hp2 HG02071.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*86T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 8/8 | 86 | chr2 | 97702887 | ||||||
| chr2:97702901 | G | A | 1 | a0003c0003t0005 | 3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*100G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 8/8 | 100 | chr2 | 97702901 | ||||||
| chr2:97703015 | G | A | 3 | a0003c0003t0003 a0003c0003t0004 a0008c0012t0003 |
25 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*214G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 8/8 | 214 | chr2 | 97703015 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:97669979 | G | T | 1 | a0001c0001t0002g0227 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.46+145G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97669979 | |||||||
| chr2:97670070 | C | T | 1 | a0003c0003t0005g0226 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.46+236C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97670070 | |||||||
| chr2:97670093 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0032 others(1): Show |
5 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+259G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97670093 | |||||||
| chr2:97670135 | A | G | 14 | a0003c0003t0003g0007 a0003c0003t0003g0013 a0003c0003t0003g0215 others(11): Show |
18 | HG00597.hp2 NA18940.hp1 NA18941.hp2 others(15): Show |
intron_variant | MODIFIER | c.46+301A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97670135 | |||||||
| chr2:97670491 | C | CA | 54 | a0001c0001t0001g0048 a0001c0001t0001g0077 a0002c0002t0001g0002 others(51): Show |
89 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.46+669dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 97670491 | ||||||
| chr2:97670667 | G | A | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46+833G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97670667 | |||||||
| chr2:97670933 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0032 others(1): Show |
5 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+1099A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97670933 | |||||||
| chr2:97670982 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0032 others(1): Show |
5 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+1148C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97670982 | |||||||
| chr2:97671020 | T | C | 99 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0032 others(96): Show |
140 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.46+1186T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97671020 | |||||||
| chr2:97671109 | G | C | 16 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0004c0004t0001g0020 others(13): Show |
17 | HG01243.hp1 HG01261.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.46+1275G>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97671109 | |||||||
| chr2:97671334 | C | CG | 94 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0021 others(91): Show |
134 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.46+1505dupG | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 97671334 | ||||||
| chr2:97671334 | C | CGG | 5 | a0002c0002t0001g0015 a0002c0002t0001g0016 a0002c0002t0001g0034 others(2): Show |
7 | HG02109.hp2 HG02818.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+1504_46+1505dup others(2): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 97671334 | ||||||
| chr2:97671437 | G | A | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46+1603G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97671437 | |||||||
| chr2:97671687 | A | G | 3 | a0001c0001t0001g0093 a0004c0004t0001g0091 a0004c0004t0001g0092 |
3 | HG01243.hp1 HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.46+1853A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97671687 | |||||||
| chr2:97672028 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.46+2194A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672028 | |||||||
| chr2:97672039 | G | C | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46+2205G>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672039 | |||||||
| chr2:97672065 | C | T | 3 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0003c0003t0003g0225 |
3 | HG01168.hp1 HG02738.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.46+2231C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672065 | |||||||
| chr2:97672086 | A | G | 44 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0021 others(41): Show |
51 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.46+2252A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672086 | |||||||
| chr2:97672336 | G | A | 2 | a0005c0006t0002g0023 a0005c0006t0002g0144 |
3 | HG02717.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.47-2120G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672336 | |||||||
| chr2:97672388 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.47-2068C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672388 | |||||||
| chr2:97672459 | C | T | 1 | a0002c0002t0001g0019 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.47-1997C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672459 | |||||||
| chr2:97672679 | C | T | 44 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0032 others(41): Show |
50 | HG00597.hp2 HG01243.hp1 HG01261.hp1 others(47): Show |
intron_variant | MODIFIER | c.47-1777C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672679 | |||||||
| chr2:97672734 | G | A | 3 | a0003c0003t0005g0095 a0003c0003t0005g0096 a0003c0003t0005g0226 |
3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.47-1722G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672734 | |||||||
| chr2:97672841 | C | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.47-1615C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672841 | |||||||
| chr2:97672917 | A | G | 1 | a0003c0003t0004g0103 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.47-1539A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672917 | |||||||
| chr2:97673217 | C | T | 7 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(4): Show |
7 | HG01123.hp1 HG01175.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-1239C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97673217 | |||||||
| chr2:97673345 | G | A | 1 | a0002c0002t0001g0008 | 3 | HG01123.hp2 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.47-1111G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97673345 | |||||||
| chr2:97673376 | G | C | 54 | a0001c0001t0001g0048 a0002c0002t0001g0002 a0002c0002t0001g0003 others(51): Show |
89 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.47-1080G>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97673376 | |||||||
| chr2:97673534 | C | T | 44 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0021 others(41): Show |
51 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.47-922C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97673534 | |||||||
| chr2:97673625 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.47-831G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97673625 | |||||||
| chr2:97673719 | C | T | 1 | a0004c0004t0001g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.47-737C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97673719 | |||||||
| chr2:97674030 | G | A | 2 | a0001c0001t0002g0148 a0001c0001t0002g0149 |
2 | HG00408.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.47-426G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97674030 | |||||||
| chr2:97674211 | T | C | 1 | a0002c0002t0001g0037 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.47-245T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97674211 | |||||||
| chr2:97674261 | C | A | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.47-195C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97674261 | |||||||
| chr2:97674398 | T | C | 3 | a0003c0003t0005g0095 a0003c0003t0005g0096 a0003c0003t0005g0226 |
3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.47-58T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97674398 | |||||||
| chr2:97674581 | CAT | C | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+25_148+26delAT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 2/7 | chr2 | 97674581 | |||||||
| chr2:97674747 | A | G | 3 | a0003c0003t0005g0095 a0003c0003t0005g0096 a0003c0003t0005g0226 |
3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.148+190A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 2/7 | chr2 | 97674747 | |||||||
| chr2:97674946 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.148+389C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 2/7 | chr2 | 97674946 | |||||||
| chr2:97674983 | G | A | 1 | a0004c0004t0001g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.148+426G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 2/7 | chr2 | 97674983 | |||||||
| chr2:97675139 | C | T | 1 | a0002c0002t0001g0016 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.148+582C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 2/7 | chr2 | 97675139 | |||||||
| chr2:97675272 | A | C | 21 | a0003c0003t0003g0007 a0003c0003t0003g0013 a0003c0003t0003g0215 others(18): Show |
25 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.149-573A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 2/7 | chr2 | 97675272 | |||||||
| chr2:97675925 | TTTGGTAA others(49): Show |
T | 1 | a0009c0007t0001g0094 | 1 | NA18966.hp2 | splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.232+1_232+56delGTA others(53): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97675925 | ||||||
| chr2:97676386 | A | C | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.232+458A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676386 | |||||||
| chr2:97676433 | C | CA | 6 | a0001c0001t0001g0021 a0001c0001t0001g0104 a0001c0001t0001g0105 others(3): Show |
7 | HG02257.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+520dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97676433 | ||||||
| chr2:97676448 | A | G | 1 | a0001c0001t0002g0027 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.232+520A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676448 | |||||||
| chr2:97676448 | AG | A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(22): Show |
27 | HG00642.hp1 HG01123.hp1 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.232+521delG | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676448 | |||||||
| chr2:97676449 | G | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0021 others(24): Show |
30 | HG01099.hp2 HG01175.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.232+521G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676449 | |||||||
| chr2:97676449 | G | GA | 7 | a0001c0001t0001g0093 a0001c0001t0002g0154 a0001c0001t0002g0160 others(4): Show |
7 | HG00544.hp1 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+538dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97676449 | ||||||
| chr2:97676449 | GA | G | 36 | a0001c0001t0002g0151 a0001c0001t0002g0162 a0001c0001t0002g0200 others(33): Show |
41 | HG01243.hp1 HG01358.hp1 HG02056.hp1 others(38): Show |
intron_variant | MODIFIER | c.232+538delA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97676449 | ||||||
| chr2:97676449 | GAA | G | 47 | a0001c0001t0001g0048 a0002c0002t0001g0002 a0002c0002t0001g0003 others(44): Show |
82 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.232+537_232+538del others(2): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97676449 | ||||||
| chr2:97676450 | A | G | 4 | a0003c0003t0005g0095 a0003c0003t0005g0096 a0003c0003t0005g0226 others(1): Show |
4 | HG02040.hp2 HG03486.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+522A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676450 | |||||||
| chr2:97676451 | A | G | 3 | a0002c0002t0001g0076 a0002c0005t0001g0074 a0002c0005t0001g0075 |
3 | HG02300.hp2 NA18960.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.232+523A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676451 | |||||||
| chr2:97676529 | T | C | 142 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(139): Show |
190 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.232+601T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676529 | |||||||
| chr2:97676697 | A | C | 1 | a0004c0004t0001g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.232+769A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676697 | |||||||
| chr2:97676721 | A | G | 3 | a0003c0003t0005g0095 a0003c0003t0005g0096 a0003c0003t0005g0226 |
3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.232+793A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676721 | |||||||
| chr2:97676737 | A | T | 1 | a0003c0003t0003g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.232+809A>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676737 | |||||||
| chr2:97676777 | AAAAGAG | A | 39 | a0001c0001t0001g0010 a0001c0001t0001g0105 a0001c0001t0001g0106 others(36): Show |
41 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.232+851_232+856del others(6): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97676777 | ||||||
| chr2:97677000 | G | A | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0150 |
3 | HG02055.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.232+1072G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677000 | |||||||
| chr2:97677069 | T | C | 1 | a0002c0002t0001g0037 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.232+1141T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677069 | |||||||
| chr2:97677144 | C | T | 1 | a0002c0002t0001g0071 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.232+1216C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677144 | |||||||
| chr2:97677237 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.232+1309G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677237 | |||||||
| chr2:97677310 | A | T | 17 | a0003c0003t0005g0095 a0003c0003t0005g0096 a0003c0003t0005g0226 others(14): Show |
18 | HG01243.hp1 HG01358.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.232+1382A>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677310 | |||||||
| chr2:97677520 | T | C | 52 | a0001c0001t0001g0048 a0002c0002t0001g0002 a0002c0002t0001g0003 others(49): Show |
87 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.232+1592T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677520 | |||||||
| chr2:97677573 | A | T | 5 | a0002c0002t0001g0009 a0002c0002t0001g0019 a0002c0002t0001g0068 others(2): Show |
8 | HG01070.hp2 HG01071.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+1645A>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677573 | |||||||
| chr2:97677663 | C | G | 1 | a0002c0002t0001g0067 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.232+1735C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677663 | |||||||
| chr2:97677915 | G | A | 1 | a0001c0001t0002g0151 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.232+1987G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677915 | |||||||
| chr2:97678079 | A | C | 1 | a0002c0002t0001g0037 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.232+2151A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97678079 | |||||||
| chr2:97678207 | T | TA | 7 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+2290dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97678207 | ||||||
| chr2:97678278 | G | GA | 7 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0002c0002t0001g0017 others(4): Show |
8 | HG00544.hp2 HG02257.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.232+2362dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97678278 | ||||||
| chr2:97678629 | A | G | 1 | a0002c0002t0001g0041 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.232+2701A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97678629 | |||||||
| chr2:97678708 | T | G | 38 | a0003c0003t0003g0007 a0003c0003t0003g0013 a0003c0003t0003g0215 others(35): Show |
43 | HG00597.hp2 HG01243.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.232+2780T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97678708 | |||||||
| chr2:97678768 | G | A | 44 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0021 others(41): Show |
51 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.232+2840G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97678768 | |||||||
| chr2:97678807 | T | TA | 57 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(54): Show |
64 | HG00741.hp1 HG01099.hp2 HG01123.hp1 others(61): Show |
intron_variant | MODIFIER | c.232+2900dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97678807 | ||||||
| chr2:97678807 | T | TAA | 9 | a0001c0001t0001g0113 a0003c0003t0004g0097 a0003c0003t0004g0098 others(6): Show |
9 | HG02056.hp1 HG02056.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.232+2899_232+2900d others(4): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97678807 | ||||||
| chr2:97678807 | T | TAAAA | 12 | a0003c0003t0003g0007 a0003c0003t0003g0013 a0003c0003t0003g0215 others(9): Show |
16 | HG00597.hp2 NA18940.hp1 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.232+2897_232+2900d others(6): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97678807 | ||||||
| chr2:97678980 | GA | G | 21 | a0001c0001t0002g0211 a0003c0003t0003g0007 a0003c0003t0003g0013 others(18): Show |
25 | HG00597.hp2 HG01169.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.232+3067delA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97678980 | ||||||
| chr2:97678991 | A | G | 1 | a0002c0002t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.232+3063A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97678991 | |||||||
| chr2:97679022 | G | T | 1 | a0001c0001t0002g0210 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.232+3094G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679022 | |||||||
| chr2:97679121 | AAG | A | 21 | a0003c0003t0003g0007 a0003c0003t0003g0013 a0003c0003t0003g0215 others(18): Show |
25 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.232+3198_232+3199d others(4): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97679121 | ||||||
| chr2:97679174 | G | GA | 51 | a0001c0001t0001g0048 a0002c0002t0001g0002 a0002c0002t0001g0003 others(48): Show |
86 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.232+3257dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97679174 | ||||||
| chr2:97679319 | C | T | 2 | a0004c0004t0001g0091 a0004c0004t0001g0092 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.232+3391C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679319 | |||||||
| chr2:97679328 | A | C | 1 | a0002c0002t0001g0064 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.232+3400A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679328 | |||||||
| chr2:97679557 | C | T | 4 | a0001c0001t0001g0089 a0001c0001t0002g0006 a0001c0001t0002g0208 others(1): Show |
7 | HG01261.hp1 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+3629C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679557 | |||||||
| chr2:97679645 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.232+3717C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679645 | |||||||
| chr2:97679735 | C | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.232+3807C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679735 | |||||||
| chr2:97679818 | C | T | 10 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(7): Show |
11 | HG01358.hp1 HG02451.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.232+3890C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679818 | |||||||
| chr2:97679837 | C | CA | 51 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0002c0002t0001g0002 others(48): Show |
86 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.232+3925dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97679837 | ||||||
| chr2:97679858 | A | G | 1 | a0003c0003t0003g0222 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.232+3930A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679858 | |||||||
| chr2:97679901 | A | G | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | NA18951.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.232+3973A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679901 | |||||||
| chr2:97679936 | C | T | 3 | a0003c0003t0004g0100 a0003c0003t0004g0101 a0003c0003t0004g0102 |
3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.232+4008C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679936 | |||||||
| chr2:97680018 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.232+4090G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680018 | |||||||
| chr2:97680083 | T | G | 1 | a0002c0002t0001g0016 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.232+4155T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680083 | |||||||
| chr2:97680159 | C | T | 1 | a0002c0002t0001g0063 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.232+4231C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680159 | |||||||
| chr2:97680198 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+4270C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680198 | |||||||
| chr2:97680251 | A | T | 3 | a0003c0003t0005g0095 a0003c0003t0005g0096 a0003c0003t0005g0226 |
3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.232+4323A>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680251 | |||||||
| chr2:97680539 | T | A | 1 | a0001c0001t0002g0206 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.232+4611T>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680539 | |||||||
| chr2:97680594 | T | C | 13 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(10): Show |
14 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.232+4666T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680594 | |||||||
| chr2:97680692 | C | T | 10 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(7): Show |
11 | HG01358.hp1 HG02451.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.232+4764C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680692 | |||||||
| chr2:97680853 | G | T | 3 | a0003c0003t0005g0095 a0003c0003t0005g0096 a0003c0003t0005g0226 |
3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.232+4925G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680853 | |||||||
| chr2:97680923 | C | CT | 3 | a0003c0003t0004g0100 a0003c0003t0004g0101 a0003c0003t0004g0102 |
3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.232+4996dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97680923 | ||||||
| chr2:97680925 | C | A | 3 | a0003c0003t0004g0100 a0003c0003t0004g0101 a0003c0003t0004g0102 |
3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.232+4997C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680925 | |||||||
| chr2:97680925 | C | CA | 4 | a0001c0001t0002g0025 a0001c0001t0002g0155 a0002c0002t0001g0034 others(1): Show |
5 | HG01934.hp1 HG02109.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+5006dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97680925 | ||||||
| chr2:97681017 | G | A | 1 | a0001c0001t0002g0206 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.232+5089G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681017 | |||||||
| chr2:97681018 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.232+5090A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681018 | |||||||
| chr2:97681090 | G | A | 2 | a0001c0001t0002g0147 a0001c0001t0002g0156 |
2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.232+5162G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681090 | |||||||
| chr2:97681106 | C | CA | 39 | a0001c0001t0001g0093 a0001c0001t0001g0107 a0001c0001t0001g0109 others(36): Show |
42 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.232+5205dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97681106 | ||||||
| chr2:97681106 | C | CAA | 34 | a0001c0001t0001g0010 a0001c0001t0001g0077 a0001c0001t0001g0106 others(31): Show |
37 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.232+5204_232+5205d others(4): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97681106 | ||||||
| chr2:97681106 | C | CAAA | 20 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0137 others(17): Show |
24 | HG00597.hp2 HG01175.hp2 HG01981.hp2 others(21): Show |
intron_variant | MODIFIER | c.232+5203_232+5205d others(5): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97681106 | ||||||
| chr2:97681106 | CA | C | 8 | a0001c0001t0001g0033 a0001c0001t0002g0203 a0001c0001t0002g0204 others(5): Show |
8 | HG01070.hp1 HG02896.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+5205delA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97681106 | ||||||
| chr2:97681106 | CAAAAAA | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0108 |
7 | HG02257.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+5200_232+5205d others(8): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97681106 | ||||||
| chr2:97681186 | A | C | 1 | a0001c0001t0002g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.232+5258A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681186 | |||||||
| chr2:97681408 | A | C | 14 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0114 others(11): Show |
14 | HG01099.hp2 HG01123.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.232+5480A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681408 | |||||||
| chr2:97681536 | C | T | 1 | a0001c0001t0002g0164 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.232+5608C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681536 | |||||||
| chr2:97681646 | C | T | 1 | a0004c0004t0001g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.232+5718C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681646 | |||||||
| chr2:97681675 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0143 |
2 | HG01175.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.232+5747G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681675 | |||||||
| chr2:97681885 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.232+5957A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681885 | |||||||
| chr2:97681930 | A | C | 1 | a0002c0002t0001g0043 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.232+6002A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681930 | |||||||
| chr2:97681962 | A | G | 4 | a0001c0001t0002g0025 a0001c0001t0002g0030 a0001c0001t0002g0163 others(1): Show |
6 | NA18947.hp2 NA18960.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+6034A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681962 | |||||||
| chr2:97682140 | T | C | 1 | a0002c0002t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.232+6212T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682140 | |||||||
| chr2:97682151 | TAGAA | T | 5 | a0001c0001t0002g0029 a0001c0001t0002g0162 a0001c0001t0002g0200 others(2): Show |
6 | NA18943.hp1 NA18972.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+6226_232+6229d others(6): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97682151 | ||||||
| chr2:97682158 | C | T | 2 | a0003c0003t0001g0072 a0003c0003t0001g0073 |
2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.232+6230C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682158 | |||||||
| chr2:97682567 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.233-6328A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682567 | |||||||
| chr2:97682643 | A | ATAAAT | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-6252_233-6251i others(7): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682643 | |||||||
| chr2:97682644 | G | T | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-6251G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682644 | |||||||
| chr2:97682645 | G | T | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-6250G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682645 | |||||||
| chr2:97682648 | G | T | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-6247G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682648 | |||||||
| chr2:97682649 | G | T | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-6246G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682649 | |||||||
| chr2:97682650 | T | C | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-6245T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682650 | |||||||
| chr2:97682667 | C | T | 1 | a0004c0004t0001g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.233-6228C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682667 | |||||||
| chr2:97682769 | GA | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
10 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.233-6116delA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97682769 | ||||||
| chr2:97682824 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-6071G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682824 | |||||||
| chr2:97682861 | C | T | 2 | a0001c0001t0002g0198 a0001c0001t0002g0199 |
2 | HG00099.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.233-6034C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682861 | |||||||
| chr2:97683076 | C | A | 1 | a0004c0004t0001g0080 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.233-5819C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683076 | |||||||
| chr2:97683076 | C | CCA | 25 | a0001c0001t0001g0077 a0001c0001t0001g0113 a0001c0001t0001g0116 others(22): Show |
25 | HG00408.hp1 HG00408.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.233-5782_233-5781d others(4): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | ||||||
| chr2:97683076 | C | CCACA | 33 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0114 others(30): Show |
35 | HG01099.hp2 HG01175.hp2 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.233-5784_233-5781d others(6): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | ||||||
| chr2:97683076 | C | CCACACA | 61 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(58): Show |
92 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.233-5786_233-5781d others(8): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | ||||||
| chr2:97683076 | C | CCACACAC others(1): Show |
29 | a0001c0001t0001g0128 a0001c0001t0001g0140 a0001c0001t0001g0150 others(26): Show |
38 | HG01106.hp2 HG01123.hp1 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.233-5788_233-5781d others(10): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | ||||||
| chr2:97683076 | C | CCACACAC others(3): Show |
5 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0002c0002t0001g0060 others(2): Show |
5 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-5790_233-5781d others(12): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | ||||||
| chr2:97683076 | C | CCACACAC others(5): Show |
4 | a0003c0003t0003g0220 a0003c0003t0003g0223 a0004c0004t0001g0092 others(1): Show |
4 | HG01243.hp1 NA18951.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-5792_233-5781d others(14): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | ||||||
| chr2:97683076 | C | CCACACAC others(7): Show |
1 | a0003c0003t0004g0099 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.233-5794_233-5781d others(16): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | ||||||
| chr2:97683076 | CCA | C | 9 | a0001c0001t0001g0093 a0001c0001t0002g0166 a0001c0001t0002g0167 others(6): Show |
16 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.233-5782_233-5781d others(4): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | ||||||
| chr2:97683097 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.233-5798C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683097 | |||||||
| chr2:97683115 | A | C | 1 | a0003c0003t0004g0103 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.233-5780A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683115 | |||||||
| chr2:97683282 | A | G | 3 | a0003c0003t0005g0095 a0003c0003t0005g0096 a0003c0003t0005g0226 |
3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.233-5613A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683282 | |||||||
| chr2:97683319 | C | T | 1 | a0001c0001t0002g0201 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.233-5576C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683319 | |||||||
| chr2:97683520 | A | G | 137 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(134): Show |
178 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.233-5375A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683520 | |||||||
| chr2:97683538 | T | TA | 58 | a0001c0001t0001g0093 a0001c0001t0002g0148 a0002c0002t0001g0002 others(55): Show |
86 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.233-5341dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683538 | ||||||
| chr2:97683538 | TA | T | 8 | a0002c0002t0001g0078 a0003c0003t0004g0097 a0003c0003t0004g0098 others(5): Show |
8 | HG02056.hp1 HG02056.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-5341delA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683538 | ||||||
| chr2:97683548 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.233-5347A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683548 | |||||||
| chr2:97683704 | G | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
10 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.233-5191G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683704 | |||||||
| chr2:97683883 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.233-5012G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683883 | |||||||
| chr2:97683926 | G | A | 1 | a0002c0002t0001g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.233-4969G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683926 | |||||||
| chr2:97683927 | C | T | 1 | a0002c0002t0001g0056 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.233-4968C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683927 | |||||||
| chr2:97683967 | C | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0120 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.233-4928C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683967 | |||||||
| chr2:97684031 | A | AT | 39 | a0001c0001t0001g0127 a0001c0001t0001g0142 a0001c0001t0002g0024 others(36): Show |
45 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.233-4842dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97684031 | ||||||
| chr2:97684031 | A | ATT | 6 | a0001c0001t0002g0185 a0001c0001t0002g0193 a0001c0001t0002g0199 others(3): Show |
6 | HG00140.hp2 HG01175.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-4843_233-4842d others(4): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97684031 | ||||||
| chr2:97684031 | AT | A | 24 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(21): Show |
26 | HG01243.hp1 HG01358.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.233-4842delT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97684031 | ||||||
| chr2:97684454 | C | T | 1 | a0002c0002t0001g0055 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.233-4441C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684454 | |||||||
| chr2:97684514 | T | G | 1 | a0001c0001t0002g0026 | 2 | HG00558.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.233-4381T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684514 | |||||||
| chr2:97684582 | T | A | 1 | a0001c0001t0002g0151 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.233-4313T>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684582 | |||||||
| chr2:97684783 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.233-4112A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684783 | |||||||
| chr2:97684851 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.233-4044A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684851 | |||||||
| chr2:97684924 | T | A | 1 | a0002c0002t0001g0041 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.233-3971T>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684924 | |||||||
| chr2:97684936 | A | AT | 59 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(56): Show |
93 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.233-3954dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97684936 | ||||||
| chr2:97684936 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.233-3959A>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684936 | |||||||
| chr2:97684942 | A | T | 140 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(137): Show |
188 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.233-3953A>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684942 | |||||||
| chr2:97685008 | C | T | 2 | a0004c0004t0001g0091 a0004c0004t0001g0092 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.233-3887C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685008 | |||||||
| chr2:97685141 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.233-3754G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685141 | |||||||
| chr2:97685195 | T | C | 38 | a0003c0003t0003g0007 a0003c0003t0003g0013 a0003c0003t0003g0215 others(35): Show |
43 | HG00597.hp2 HG01243.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.233-3700T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685195 | |||||||
| chr2:97685269 | C | CT | 10 | a0001c0001t0002g0192 a0002c0002t0001g0041 a0002c0002t0001g0043 others(7): Show |
11 | HG04115.hp2 NA18941.hp2 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-3612dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97685269 | ||||||
| chr2:97685269 | CT | C | 15 | a0001c0001t0001g0122 a0001c0001t0002g0170 a0003c0003t0005g0096 others(12): Show |
16 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.233-3612delT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97685269 | ||||||
| chr2:97685366 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.233-3529C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685366 | |||||||
| chr2:97685512 | G | A | 10 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(7): Show |
11 | HG01358.hp1 HG02451.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.233-3383G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685512 | |||||||
| chr2:97685673 | C | T | 44 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0021 others(41): Show |
51 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.233-3222C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685673 | |||||||
| chr2:97685674 | T | C | 14 | a0003c0003t0003g0007 a0003c0003t0003g0013 a0003c0003t0003g0215 others(11): Show |
18 | HG00597.hp2 NA18940.hp1 NA18941.hp2 others(15): Show |
intron_variant | MODIFIER | c.233-3221T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685674 | |||||||
| chr2:97685701 | T | A | 1 | a0002c0002t0001g0043 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.233-3194T>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685701 | |||||||
| chr2:97685784 | A | G | 38 | a0003c0003t0003g0007 a0003c0003t0003g0013 a0003c0003t0003g0215 others(35): Show |
43 | HG00597.hp2 HG01243.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.233-3111A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685784 | |||||||
| chr2:97685824 | A | G | 5 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG01884.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-3071A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685824 | |||||||
| chr2:97685878 | T | C | 1 | a0002c0002t0001g0008 | 3 | HG01123.hp2 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.233-3017T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685878 | |||||||
| chr2:97686315 | C | A | 1 | a0002c0002t0001g0043 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.233-2580C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97686315 | |||||||
| chr2:97686422 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233-2473T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97686422 | |||||||
| chr2:97686749 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.233-2146C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97686749 | |||||||
| chr2:97687144 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233-1751C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687144 | |||||||
| chr2:97687148 | TGAGG | T | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-1746_233-1743d others(6): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687148 | |||||||
| chr2:97687153 | C | T | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-1742C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687153 | |||||||
| chr2:97687272 | C | T | 22 | a0002c0002t0001g0054 a0003c0003t0003g0007 a0003c0003t0003g0013 others(19): Show |
26 | HG00597.hp2 HG01943.hp1 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.233-1623C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687272 | |||||||
| chr2:97687673 | G | A | 1 | a0003c0003t0003g0217 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.233-1222G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687673 | |||||||
| chr2:97687736 | G | A | 1 | a0002c0002t0001g0050 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.233-1159G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687736 | |||||||
| chr2:97687752 | G | A | 1 | a0010c0010t0001g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.233-1143G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687752 | |||||||
| chr2:97687851 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.233-1044G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687851 | |||||||
| chr2:97687875 | T | C | 43 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0002g0172 others(40): Show |
48 | HG00597.hp2 HG01168.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.233-1020T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687875 | |||||||
| chr2:97687900 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.233-995G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687900 | |||||||
| chr2:97687977 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.233-918T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687977 | |||||||
| chr2:97688046 | C | G | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.233-849C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688046 | |||||||
| chr2:97688095 | T | C | 1 | a0011c0008t0002g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.233-800T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688095 | |||||||
| chr2:97688213 | A | G | 39 | a0001c0001t0001g0105 a0003c0003t0003g0007 a0003c0003t0003g0013 others(36): Show |
44 | HG00597.hp2 HG01243.hp1 HG01358.hp1 others(41): Show |
intron_variant | MODIFIER | c.233-682A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688213 | |||||||
| chr2:97688257 | C | A | 1 | a0001c0001t0001g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.233-638C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688257 | |||||||
| chr2:97688334 | A | C | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-561A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688334 | |||||||
| chr2:97688409 | G | A | 6 | a0001c0001t0002g0029 a0001c0001t0002g0162 a0001c0001t0002g0200 others(3): Show |
7 | HG01192.hp1 NA18943.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-486G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688409 | |||||||
| chr2:97688455 | G | A | 3 | a0002c0005t0001g0057 a0002c0005t0001g0074 a0002c0005t0001g0075 |
3 | NA18947.hp1 NA18960.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.233-440G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688455 | |||||||
| chr2:97688649 | G | A | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-246G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688649 | |||||||
| chr2:97688785 | C | T | 1 | a0002c0002t0001g0019 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.233-110C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688785 | |||||||
| chr2:97688786 | G | A | 1 | a0001c0001t0002g0175 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.233-109G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688786 | |||||||
| chr2:97688792 | G | A | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02280.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.233-103G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688792 | |||||||
| chr2:97688857 | G | A | 1 | a0001c0001t0002g0206 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.233-38G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688857 | |||||||
| chr2:97688878 | T | G | 1 | a0002c0002t0001g0043 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.233-17T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688878 | |||||||
| chr2:97688879 | G | T | 1 | a0002c0002t0001g0043 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.233-16G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688879 | |||||||
| chr2:97689339 | C | G | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.331+346C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97689339 | |||||||
| chr2:97689470 | A | C | 26 | a0003c0003t0001g0072 a0003c0003t0001g0073 a0003c0003t0003g0007 others(23): Show |
30 | HG00597.hp2 HG01346.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.331+477A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97689470 | |||||||
| chr2:97689601 | G | A | 3 | a0003c0003t0005g0095 a0003c0003t0005g0096 a0003c0003t0005g0226 |
3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.331+608G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97689601 | |||||||
| chr2:97689758 | G | A | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.332-498G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97689758 | |||||||
| chr2:97689950 | G | A | 2 | a0003c0003t0001g0072 a0003c0003t0001g0073 |
2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.332-306G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97689950 | |||||||
| chr2:97690005 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0032 others(5): Show |
9 | HG02055.hp2 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.332-251C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97690005 | |||||||
| chr2:97690031 | T | C | 4 | a0001c0001t0001g0089 a0001c0001t0002g0006 a0001c0001t0002g0208 others(1): Show |
7 | HG01261.hp1 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.332-225T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97690031 | |||||||
| chr2:97690072 | C | A | 39 | a0003c0003t0001g0072 a0003c0003t0001g0073 a0003c0003t0003g0007 others(36): Show |
44 | HG00597.hp2 HG01243.hp1 HG01346.hp1 others(41): Show |
intron_variant | MODIFIER | c.332-184C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97690072 | |||||||
| chr2:97690145 | C | A | 47 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0008 others(44): Show |
75 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.332-111C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97690145 | |||||||
| chr2:97690147 | A | G | 2 | a0003c0003t0001g0072 a0003c0003t0001g0073 |
2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.332-109A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97690147 | |||||||
| chr2:97690157 | C | A | 1 | a0003c0003t0003g0221 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.332-99C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97690157 | |||||||
| chr2:97690157 | C | G | 2 | a0003c0003t0001g0072 a0003c0003t0001g0073 |
2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.332-99C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97690157 | |||||||
| chr2:97690454 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.403+127C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690454 | |||||||
| chr2:97690537 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.403+210C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690537 | |||||||
| chr2:97690563 | A | G | 1 | a0002c0002t0001g0042 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.403+236A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690563 | |||||||
| chr2:97690571 | C | T | 1 | a0002c0002t0001g0059 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.403+244C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690571 | |||||||
| chr2:97690772 | G | GT | 11 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(8): Show |
16 | HG01496.hp2 HG01884.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.403+458dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97690772 | ||||||
| chr2:97690781 | T | G | 2 | a0003c0003t0001g0072 a0003c0003t0001g0073 |
2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.403+454T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690781 | |||||||
| chr2:97690786 | G | T | 1 | a0002c0002t0001g0046 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.403+459G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690786 | |||||||
| chr2:97690790 | T | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.403+463T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690790 | |||||||
| chr2:97690791 | T | G | 6 | a0001c0001t0002g0186 a0003c0003t0001g0072 a0003c0003t0001g0073 others(3): Show |
6 | HG00408.hp2 HG01346.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.403+464T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690791 | |||||||
| chr2:97691241 | T | C | 1 | a0002c0002t0001g0008 | 3 | HG01123.hp2 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.403+914T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691241 | |||||||
| chr2:97691249 | C | T | 21 | a0003c0003t0003g0007 a0003c0003t0003g0013 a0003c0003t0003g0215 others(18): Show |
25 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.403+922C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691249 | |||||||
| chr2:97691360 | C | T | 47 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0008 others(44): Show |
75 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.403+1033C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691360 | |||||||
| chr2:97691397 | C | T | 1 | a0007c0009t0002g0181 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.403+1070C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691397 | |||||||
| chr2:97691532 | A | C | 1 | a0002c0002t0001g0060 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.403+1205A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691532 | |||||||
| chr2:97691620 | C | A | 7 | a0003c0003t0004g0097 a0003c0003t0004g0098 a0003c0003t0004g0099 others(4): Show |
7 | HG02056.hp1 HG02056.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+1293C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691620 | |||||||
| chr2:97691665 | C | T | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.403+1338C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691665 | |||||||
| chr2:97691831 | C | T | 40 | a0003c0003t0001g0072 a0003c0003t0001g0073 a0003c0003t0003g0007 others(37): Show |
45 | HG00597.hp2 HG01243.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.403+1504C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691831 | |||||||
| chr2:97692025 | T | C | 1 | a0004c0004t0001g0083 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.403+1698T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97692025 | |||||||
| chr2:97692203 | T | C | 2 | a0001c0001t0002g0147 a0001c0001t0002g0156 |
2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.403+1876T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97692203 | |||||||
| chr2:97692323 | G | C | 1 | a0001c0001t0002g0153 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.403+1996G>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97692323 | |||||||
| chr2:97692407 | C | CT | 21 | a0001c0001t0001g0093 a0001c0001t0001g0130 a0001c0001t0001g0137 others(18): Show |
22 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.403+2100dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97692407 | ||||||
| chr2:97692407 | CT | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(20): Show |
29 | HG01070.hp1 HG01243.hp1 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.403+2100delT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97692407 | ||||||
| chr2:97692701 | T | C | 1 | a0001c0001t0002g0186 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.403+2374T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97692701 | |||||||
| chr2:97692726 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.403+2399C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97692726 | |||||||
| chr2:97692943 | A | C | 10 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(7): Show |
11 | HG01358.hp1 HG02451.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.403+2616A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97692943 | |||||||
| chr2:97693002 | G | A | 40 | a0003c0003t0001g0072 a0003c0003t0001g0073 a0003c0003t0003g0007 others(37): Show |
45 | HG00597.hp2 HG01243.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.403+2675G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97693002 | |||||||
| chr2:97693011 | T | G | 1 | a0003c0003t0003g0221 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.403+2684T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97693011 | |||||||
| chr2:97693323 | A | G | 13 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(10): Show |
13 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.403+2996A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97693323 | |||||||
| chr2:97693367 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
10 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.403+3040G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97693367 | |||||||
| chr2:97693419 | C | T | 47 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0008 others(44): Show |
75 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.403+3092C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97693419 | |||||||
| chr2:97694036 | A | G | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0150 |
3 | HG02055.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.403+3709A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694036 | |||||||
| chr2:97694139 | C | T | 5 | a0001c0001t0001g0137 a0001c0001t0001g0139 a0001c0001t0001g0141 others(2): Show |
5 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+3812C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694139 | |||||||
| chr2:97694214 | G | A | 1 | a0001c0001t0002g0189 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.403+3887G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694214 | |||||||
| chr2:97694248 | C | CT | 5 | a0002c0002t0001g0015 a0002c0002t0001g0034 a0002c0002t0001g0035 others(2): Show |
6 | HG02109.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.403+3935dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97694248 | ||||||
| chr2:97694284 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.403+3957G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694284 | |||||||
| chr2:97694300 | C | T | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.403+3973C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694300 | |||||||
| chr2:97694302 | C | T | 45 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0021 others(42): Show |
52 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(49): Show |
intron_variant | MODIFIER | c.403+3975C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694302 | |||||||
| chr2:97694409 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0132 a0001c0001t0001g0136 |
3 | HG01261.hp2 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.403+4082C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694409 | |||||||
| chr2:97694415 | A | AT | 25 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(22): Show |
32 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.403+4106dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97694415 | ||||||
| chr2:97694415 | A | ATTT | 19 | a0003c0003t0003g0007 a0003c0003t0003g0013 a0003c0003t0003g0215 others(16): Show |
24 | HG00597.hp2 HG01243.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.403+4104_403+4106d others(5): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97694415 | ||||||
| chr2:97694415 | A | ATTTT | 8 | a0003c0003t0001g0072 a0003c0003t0001g0073 a0003c0003t0003g0224 others(5): Show |
8 | HG01346.hp1 HG01361.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.403+4103_403+4106d others(6): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97694415 | ||||||
| chr2:97694415 | ATTT | A | 7 | a0003c0003t0004g0097 a0003c0003t0004g0098 a0003c0003t0004g0099 others(4): Show |
7 | HG02056.hp1 HG02056.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+4104_403+4106d others(5): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97694415 | ||||||
| chr2:97694583 | C | T | 6 | a0001c0001t0002g0027 a0001c0001t0002g0148 a0001c0001t0002g0149 others(3): Show |
7 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+4256C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694583 | |||||||
| chr2:97694802 | A | C | 143 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(140): Show |
191 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.404-4224A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694802 | |||||||
| chr2:97694803 | C | G | 1 | a0004c0004t0001g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.404-4223C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694803 | |||||||
| chr2:97695088 | T | C | 1 | a0001c0001t0002g0179 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.404-3938T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97695088 | |||||||
| chr2:97695141 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.404-3885C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97695141 | |||||||
| chr2:97695493 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.404-3533C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97695493 | |||||||
| chr2:97695736 | C | CTTTCT | 5 | a0002c0002t0001g0067 a0002c0005t0001g0057 a0002c0005t0001g0074 others(2): Show |
5 | HG00621.hp2 HG03486.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-3266_404-3262d others(7): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97695736 | ||||||
| chr2:97695736 | C | CTTTCTTT others(3): Show |
12 | a0003c0003t0005g0095 a0003c0003t0005g0226 a0004c0004t0001g0020 others(9): Show |
13 | HG01358.hp1 HG02040.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.404-3271_404-3262d others(12): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97695736 | ||||||
| chr2:97695736 | C | CTTTCTTT others(8): Show |
2 | a0004c0004t0001g0083 a0004c0004t0001g0092 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.404-3276_404-3262d others(17): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97695736 | ||||||
| chr2:97695736 | C | CTTTCTTT others(23): Show |
1 | a0010c0010t0001g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.404-3262_404-3261i others(32): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97695736 | ||||||
| chr2:97696007 | C | A | 2 | a0003c0003t0001g0072 a0003c0003t0001g0073 |
2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.404-3019C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696007 | |||||||
| chr2:97696054 | T | G | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.404-2972T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696054 | |||||||
| chr2:97696199 | A | G | 1 | a0003c0003t0005g0095 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.404-2827A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696199 | |||||||
| chr2:97696436 | C | CA | 23 | a0001c0001t0002g0164 a0001c0001t0002g0177 a0003c0003t0003g0007 others(20): Show |
27 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.404-2580dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97696436 | ||||||
| chr2:97696445 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0132 |
2 | HG01261.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.404-2581A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696445 | |||||||
| chr2:97696534 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0032 others(1): Show |
5 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-2492G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696534 | |||||||
| chr2:97696667 | T | C | 40 | a0003c0003t0001g0072 a0003c0003t0001g0073 a0003c0003t0003g0007 others(37): Show |
45 | HG00597.hp2 HG01243.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.404-2359T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696667 | |||||||
| chr2:97696693 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.404-2333G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696693 | |||||||
| chr2:97696778 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.404-2248C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696778 | |||||||
| chr2:97696873 | T | C | 1 | a0002c0002t0001g0016 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.404-2153T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696873 | |||||||
| chr2:97697239 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.404-1787C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97697239 | |||||||
| chr2:97697295 | G | A | 1 | a0003c0003t0004g0103 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.404-1731G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97697295 | |||||||
| chr2:97697351 | A | G | 4 | a0002c0002t0001g0015 a0002c0002t0001g0034 a0002c0002t0001g0035 others(1): Show |
5 | HG02109.hp2 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-1675A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97697351 | |||||||
| chr2:97697454 | G | A | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.404-1572G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97697454 | |||||||
| chr2:97697982 | C | T | 5 | a0003c0003t0001g0072 a0003c0003t0001g0073 a0003c0003t0005g0095 others(2): Show |
5 | HG01346.hp1 HG01361.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-1044C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97697982 | |||||||
| chr2:97697984 | CTG | C | 5 | a0001c0001t0002g0012 a0001c0001t0002g0152 a0001c0001t0002g0157 others(2): Show |
7 | HG00741.hp1 HG01070.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-1039_404-1038d others(4): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97697984 | ||||||
| chr2:97698000 | G | C | 5 | a0003c0003t0001g0072 a0003c0003t0001g0073 a0003c0003t0005g0095 others(2): Show |
5 | HG01346.hp1 HG01361.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-1026G>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97698000 | |||||||
| chr2:97698059 | T | G | 21 | a0003c0003t0003g0007 a0003c0003t0003g0013 a0003c0003t0003g0215 others(18): Show |
25 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.404-967T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97698059 | |||||||
| chr2:97698176 | C | A | 3 | a0001c0001t0002g0164 a0001c0001t0002g0178 a0001c0001t0002g0183 |
3 | NA18952.hp2 NA18961.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.404-850C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97698176 | |||||||
| chr2:97698446 | T | C | 143 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(140): Show |
191 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.404-580T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97698446 | |||||||
| chr2:97698514 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.404-512G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97698514 | |||||||
| chr2:97698566 | A | G | 2 | a0004c0004t0001g0091 a0004c0004t0001g0092 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.404-460A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97698566 | |||||||
| chr2:97698708 | T | C | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.404-318T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97698708 | |||||||
| chr2:97699345 | C | T | 1 | a0010c0010t0001g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.514+209C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97699345 | |||||||
| chr2:97699495 | G | A | 27 | a0001c0001t0002g0001 a0001c0001t0002g0028 a0001c0001t0002g0159 others(24): Show |
31 | HG00597.hp2 HG01106.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.514+359G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97699495 | |||||||
| chr2:97699515 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.514+379G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97699515 | |||||||
| chr2:97699612 | T | A | 2 | a0001c0001t0002g0166 a0003c0003t0003g0218 |
2 | HG01993.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.514+476T>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97699612 | |||||||
| chr2:97699933 | C | T | 1 | a0001c0001t0002g0210 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.514+797C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97699933 | |||||||
| chr2:97700028 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0002g0175 |
2 | HG01106.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.514+892G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700028 | |||||||
| chr2:97700331 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0185 |
2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.515-823G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700331 | |||||||
| chr2:97700609 | C | G | 2 | a0001c0001t0001g0121 a0001c0001t0002g0203 |
2 | NA18906.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.515-545C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700609 | |||||||
| chr2:97700629 | C | T | 1 | a0002c0002t0001g0040 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.515-525C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700629 | |||||||
| chr2:97700729 | TG | T | 19 | a0003c0003t0003g0007 a0003c0003t0003g0013 a0003c0003t0003g0215 others(16): Show |
23 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.515-424delG | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700729 | |||||||
| chr2:97700730 | G | GT | 51 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(48): Show |
84 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.515-413dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 97700730 | ||||||
| chr2:97700730 | G | T | 2 | a0003c0003t0003g0224 a0003c0003t0004g0100 |
2 | HG04115.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.515-424G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700730 | |||||||
| chr2:97700787 | G | A | 14 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(11): Show |
15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.515-367G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700787 | |||||||
| chr2:97700791 | T | G | 2 | a0003c0003t0001g0072 a0003c0003t0001g0073 |
2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.515-363T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700791 | |||||||
| chr2:97700800 | G | A | 10 | a0004c0004t0001g0020 a0004c0004t0001g0079 a0004c0004t0001g0080 others(7): Show |
11 | HG01358.hp1 HG02451.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.515-354G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700800 | |||||||
| chr2:97700891 | G | A | 3 | a0001c0001t0002g0161 a0001c0001t0002g0188 a0001c0001t0002g0190 |
3 | HG02055.hp1 HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.515-263G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700891 | |||||||
| chr2:97700953 | G | A | 2 | a0003c0003t0001g0072 a0003c0003t0001g0073 |
2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.515-201G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700953 | |||||||
| chr2:97700977 | C | T | 1 | a0002c0002t0001g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.515-177C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700977 | |||||||
| chr2:97700983 | A | G | 40 | a0003c0003t0001g0072 a0003c0003t0001g0073 a0003c0003t0003g0007 others(37): Show |
45 | HG00597.hp2 HG01243.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.515-171A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700983 | |||||||
| chr2:97701027 | G | A | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0150 |
3 | HG02055.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.515-127G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97701027 | |||||||
| chr2:97701308 | C | A | 143 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(140): Show |
191 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(188): Show |
splice_region_variant&intron_variant | LOW | c.665+4C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97701308 | |||||||
| chr2:97701483 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.665+179G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97701483 | |||||||
| chr2:97701494 | G | A | 1 | a0011c0008t0002g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665+190G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97701494 | |||||||
| chr2:97701503 | G | A | 1 | a0004c0004t0001g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.665+199G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97701503 | |||||||
| chr2:97701514 | G | A | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.665+210G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97701514 | |||||||
| chr2:97701888 | T | A | 1 | a0001c0001t0002g0202 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.665+584T>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97701888 | |||||||
| chr2:97701888 | TGTCTACA others(5): Show |
T | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.665+594_665+605del others(12): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 97701888 | ||||||
| chr2:97702181 | G | A | 44 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0021 others(41): Show |
51 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.666-488G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97702181 | |||||||
| chr2:97702572 | C | A | 1 | a0002c0002t0001g0044 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.666-97C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97702572 | |||||||
| chr2:97702572 | C | T | 26 | a0003c0003t0001g0072 a0003c0003t0001g0073 a0003c0003t0003g0007 others(23): Show |
30 | HG00597.hp2 HG01346.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.666-97C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97702572 | |||||||
| chr2:97702618 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
10 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.666-51G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97702618 |